Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.7669589_7676614delCA2499224945TP53c.-19_*21del
c.-21-1377_*21del
c.-19_*310del
c.-19_*222del
c.-253_*21del
c.-136_*222del
c.-136_*21del
c.-136_*310del
c.-136_983+1021del
 ClinVar
17g.7669609_7676594delCA2581463470TP53c.1_1182del
c.-21-1358_786del
c.1_903del
c.1_1161del
c.1_994-3365del
c.1_782+4572del
c.1_*289del
c.1_*201del
c.-234_1065del
c.-117_*201del
c.1_1149del
c.-117_1065del
c.-117_*289del
c.-117_983+1000del
17g.7673473_7673539dupCA2535386204TP53c.991_993+64dup
c.595_597+64dup
c.712_714+64dup
c.970_972+64dup
c.782+644_782+710dup (n.782+644_782+710dup)
c.51_53+64dup
c.874_876+64dup
c.514_516+64dup
c.958_960+64dup
 gnomAD v4
17g.7673504C>ACA2733125473TP53c.993+31G>T (n.993+31G>T)
c.597+31G>T (n.597+31G>T)
c.714+31G>T (n.714+31G>T)
c.972+31G>T (n.972+31G>T)
c.782+677G>T (n.782+677G>T)
c.53+31G>T
c.876+31G>T (n.876+31G>T)
c.516+31G>T (n.516+31G>T)
c.960+31G>T (n.960+31G>T)
 dbSNP
17g.7673504C>TCA2733125471TP53c.993+31G>A (n.993+31G>A)
c.597+31G>A (n.597+31G>A)
c.714+31G>A (n.714+31G>A)
c.972+31G>A (n.972+31G>A)
c.782+677G>A (n.782+677G>A)
c.53+31G>A
c.876+31G>A (n.876+31G>A)
c.516+31G>A (n.516+31G>A)
c.960+31G>A (n.960+31G>A)
 dbSNP
17g.7673505C>ACA2732985595TP53c.993+30G>T (n.993+30G>T)
c.597+30G>T (n.597+30G>T)
c.714+30G>T (n.714+30G>T)
c.972+30G>T (n.972+30G>T)
c.782+676G>T (n.782+676G>T)
c.53+30G>T
c.876+30G>T (n.876+30G>T)
c.516+30G>T (n.516+30G>T)
c.960+30G>T (n.960+30G>T)
 dbSNP
17g.7673505C=CA2245947248TP53c.993+30G= (n.993+30G=)
c.597+30G= (n.597+30G=)
c.714+30G= (n.714+30G=)
c.972+30G= (n.972+30G=)
c.782+676G= (n.782+676G=)
c.53+30G=
c.876+30G= (n.876+30G=)
c.516+30G= (n.516+30G=)
c.960+30G= (n.960+30G=)
17g.7673505C>GCA2732985596TP53c.993+30G>C (n.993+30G>C)
c.597+30G>C (n.597+30G>C)
c.714+30G>C (n.714+30G>C)
c.972+30G>C (n.972+30G>C)
c.782+676G>C (n.782+676G>C)
c.53+30G>C
c.876+30G>C (n.876+30G>C)
c.516+30G>C (n.516+30G>C)
c.960+30G>C (n.960+30G>C)
 dbSNP
17g.7673505C>TCA981209202TP53c.993+30G>A (n.993+30G>A)
c.597+30G>A (n.597+30G>A)
c.714+30G>A (n.714+30G>A)
c.972+30G>A (n.972+30G>A)
c.782+676G>A (n.782+676G>A)
c.53+30G>A
c.876+30G>A (n.876+30G>A)
c.516+30G>A (n.516+30G>A)
c.960+30G>A (n.960+30G>A)
 dbSNP gnomAD v3 gnomAD v4
17g.7673506A>CCA2733125477TP53c.993+29T>G (n.993+29T>G)
c.597+29T>G (n.597+29T>G)
c.714+29T>G (n.714+29T>G)
c.972+29T>G (n.972+29T>G)
c.782+675T>G (n.782+675T>G)
c.53+29T>G
c.876+29T>G (n.876+29T>G)
c.516+29T>G (n.516+29T>G)
c.960+29T>G (n.960+29T>G)
 dbSNP
17g.7673506A>GCA2733125478TP53c.993+29T>C (n.993+29T>C)
c.597+29T>C (n.597+29T>C)
c.714+29T>C (n.714+29T>C)
c.972+29T>C (n.972+29T>C)
c.782+675T>C (n.782+675T>C)
c.53+29T>C
c.876+29T>C (n.876+29T>C)
c.516+29T>C (n.516+29T>C)
c.960+29T>C (n.960+29T>C)
 dbSNP
17g.7673506A>TCA2733125479TP53c.993+29T>A (n.993+29T>A)
c.597+29T>A (n.597+29T>A)
c.714+29T>A (n.714+29T>A)
c.972+29T>A (n.972+29T>A)
c.782+675T>A (n.782+675T>A)
c.53+29T>A
c.876+29T>A (n.876+29T>A)
c.516+29T>A (n.516+29T>A)
c.960+29T>A (n.960+29T>A)
 dbSNP
17g.7673507C>ACA2732954355TP53c.993+28G>T (n.993+28G>T)
c.597+28G>T (n.597+28G>T)
c.714+28G>T (n.714+28G>T)
c.972+28G>T (n.972+28G>T)
c.782+674G>T (n.782+674G>T)
c.53+28G>T
c.876+28G>T (n.876+28G>T)
c.516+28G>T (n.516+28G>T)
c.960+28G>T (n.960+28G>T)
 dbSNP
17g.7673507C=CA2245947251TP53c.993+28G= (n.993+28G=)
c.597+28G= (n.597+28G=)
c.714+28G= (n.714+28G=)
c.972+28G= (n.972+28G=)
c.782+674G= (n.782+674G=)
c.53+28G=
c.876+28G= (n.876+28G=)
c.516+28G= (n.516+28G=)
c.960+28G= (n.960+28G=)
17g.7673507C>GCA624865100TP53c.993+28G>C (n.993+28G>C)
c.597+28G>C (n.597+28G>C)
c.714+28G>C (n.714+28G>C)
c.972+28G>C (n.972+28G>C)
c.782+674G>C (n.782+674G>C)
c.53+28G>C
c.876+28G>C (n.876+28G>C)
c.516+28G>C (n.516+28G>C)
c.960+28G>C (n.960+28G>C)
 dbSNP gnomAD v2 gnomAD v4
17g.7673507C>TCA2732954353TP53c.993+28G>A (n.993+28G>A)
c.597+28G>A (n.597+28G>A)
c.714+28G>A (n.714+28G>A)
c.972+28G>A (n.972+28G>A)
c.782+674G>A (n.782+674G>A)
c.53+28G>A
c.876+28G>A (n.876+28G>A)
c.516+28G>A (n.516+28G>A)
c.960+28G>A (n.960+28G>A)
 dbSNP
17g.7673508T>ACA2732985603TP53c.993+27A>T (n.993+27A>T)
c.597+27A>T (n.597+27A>T)
c.714+27A>T (n.714+27A>T)
c.972+27A>T (n.972+27A>T)
c.782+673A>T (n.782+673A>T)
c.53+27A>T
c.876+27A>T (n.876+27A>T)
c.516+27A>T (n.516+27A>T)
c.960+27A>T (n.960+27A>T)
 dbSNP
17g.7673508T>CCA981209208TP53c.993+27A>G (n.993+27A>G)
c.597+27A>G (n.597+27A>G)
c.714+27A>G (n.714+27A>G)
c.972+27A>G (n.972+27A>G)
c.782+673A>G (n.782+673A>G)
c.53+27A>G
c.876+27A>G (n.876+27A>G)
c.516+27A>G (n.516+27A>G)
c.960+27A>G (n.960+27A>G)
 ClinVar dbSNP gnomAD v3 gnomAD v4
17g.7673508T=CA2245947256TP53c.993+27A= (n.993+27A=)
c.597+27A= (n.597+27A=)
c.714+27A= (n.714+27A=)
c.972+27A= (n.972+27A=)
c.782+673A= (n.782+673A=)
c.53+27A=
c.876+27A= (n.876+27A=)
c.516+27A= (n.516+27A=)
c.960+27A= (n.960+27A=)
17g.7673509T>ACA2732985604TP53c.993+26A>T (n.993+26A>T)
c.597+26A>T (n.597+26A>T)
c.714+26A>T (n.714+26A>T)
c.972+26A>T (n.972+26A>T)
c.782+672A>T (n.782+672A>T)
c.53+26A>T
c.876+26A>T (n.876+26A>T)
c.516+26A>T (n.516+26A>T)
c.960+26A>T (n.960+26A>T)
 dbSNP
17g.7673509T>CCA981209211TP53c.993+26A>G (n.993+26A>G)
c.597+26A>G (n.597+26A>G)
c.714+26A>G (n.714+26A>G)
c.972+26A>G (n.972+26A>G)
c.782+672A>G (n.782+672A>G)
c.53+26A>G
c.876+26A>G (n.876+26A>G)
c.516+26A>G (n.516+26A>G)
c.960+26A>G (n.960+26A>G)
 dbSNP gnomAD v3 gnomAD v4
17g.7673509T>GCA2566747584TP53c.993+26A>C (n.993+26A>C)
c.597+26A>C (n.597+26A>C)
c.714+26A>C (n.714+26A>C)
c.972+26A>C (n.972+26A>C)
c.782+672A>C (n.782+672A>C)
c.53+26A>C
c.876+26A>C (n.876+26A>C)
c.516+26A>C (n.516+26A>C)
c.960+26A>C (n.960+26A>C)
17g.7673509T=CA2245947259TP53c.993+26A= (n.993+26A=)
c.597+26A= (n.597+26A=)
c.714+26A= (n.714+26A=)
c.972+26A= (n.972+26A=)
c.782+672A= (n.782+672A=)
c.53+26A=
c.876+26A= (n.876+26A=)
c.516+26A= (n.516+26A=)
c.960+26A= (n.960+26A=)
17g.7673510G>ACA2733125482TP53c.993+25C>T (n.993+25C>T)
c.597+25C>T (n.597+25C>T)
c.714+25C>T (n.714+25C>T)
c.972+25C>T (n.972+25C>T)
c.782+671C>T (n.782+671C>T)
c.53+25C>T
c.876+25C>T (n.876+25C>T)
c.516+25C>T (n.516+25C>T)
c.960+25C>T (n.960+25C>T)
 dbSNP
17g.7673510G>CCA2733125502TP53c.993+25C>G (n.993+25C>G)
c.597+25C>G (n.597+25C>G)
c.714+25C>G (n.714+25C>G)
c.972+25C>G (n.972+25C>G)
c.782+671C>G (n.782+671C>G)
c.53+25C>G
c.876+25C>G (n.876+25C>G)
c.516+25C>G (n.516+25C>G)
c.960+25C>G (n.960+25C>G)
 dbSNP
17g.7673510G>TCA2733125584TP53c.993+25C>A (n.993+25C>A)
c.597+25C>A (n.597+25C>A)
c.714+25C>A (n.714+25C>A)
c.972+25C>A (n.972+25C>A)
c.782+671C>A (n.782+671C>A)
c.53+25C>A
c.876+25C>A (n.876+25C>A)
c.516+25C>A (n.516+25C>A)
c.960+25C>A (n.960+25C>A)
 dbSNP
17g.7673510_7673534delCA645587336TP53c.993+1_993+25del (n.993+1_993+25del)
c.597+1_597+25del (n.597+1_597+25del)
c.714+1_714+25del (n.714+1_714+25del)
c.972+1_972+25del (n.972+1_972+25del)
c.782+647_782+671del (n.782+647_782+671del)
c.53+1_53+25del
c.876+1_876+25del (n.876+1_876+25del)
c.516+1_516+25del (n.516+1_516+25del)
c.960+1_960+25del (n.960+1_960+25del)
 COSMIC COSMIC COSMIC COSMIC
17g.7673511A=CA2245947261TP53c.993+24T= (n.993+24T=)
c.597+24T= (n.597+24T=)
c.714+24T= (n.714+24T=)
c.972+24T= (n.972+24T=)
c.782+670T= (n.782+670T=)
c.53+24T=
c.876+24T= (n.876+24T=)
c.516+24T= (n.516+24T=)
c.960+24T= (n.960+24T=)
17g.7673511A>GCA287486485TP53c.993+24T>C (n.993+24T>C)
c.597+24T>C (n.597+24T>C)
c.714+24T>C (n.714+24T>C)
c.972+24T>C (n.972+24T>C)
c.782+670T>C (n.782+670T>C)
c.53+24T>C
c.876+24T>C (n.876+24T>C)
c.516+24T>C (n.516+24T>C)
c.960+24T>C (n.960+24T>C)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.7673511A>TCA2732942237TP53c.993+24T>A (n.993+24T>A)
c.597+24T>A (n.597+24T>A)
c.714+24T>A (n.714+24T>A)
c.972+24T>A (n.972+24T>A)
c.782+670T>A (n.782+670T>A)
c.53+24T>A
c.876+24T>A (n.876+24T>A)
c.516+24T>A (n.516+24T>A)
c.960+24T>A (n.960+24T>A)
 dbSNP
17g.7673512_7673515dupCA2635874035TP53c.993+20_993+23dup (n.993+20_993+23dup)
c.597+20_597+23dup (n.597+20_597+23dup)
c.714+20_714+23dup (n.714+20_714+23dup)
c.972+20_972+23dup (n.972+20_972+23dup)
c.782+666_782+669dup (n.782+666_782+669dup)
c.53+20_53+23dup
c.876+20_876+23dup (n.876+20_876+23dup)
c.516+20_516+23dup (n.516+20_516+23dup)
c.960+20_960+23dup (n.960+20_960+23dup)
 gnomAD v4
17g.7673513A>GCA2544471111TP53c.993+22T>C (n.993+22T>C)
c.597+22T>C (n.597+22T>C)
c.714+22T>C (n.714+22T>C)
c.972+22T>C (n.972+22T>C)
c.782+668T>C (n.782+668T>C)
c.53+22T>C
c.876+22T>C (n.876+22T>C)
c.516+22T>C (n.516+22T>C)
c.960+22T>C (n.960+22T>C)
 dbSNP
17g.7673513A>TCA2733125597TP53c.993+22T>A (n.993+22T>A)
c.597+22T>A (n.597+22T>A)
c.714+22T>A (n.714+22T>A)
c.972+22T>A (n.972+22T>A)
c.782+668T>A (n.782+668T>A)
c.53+22T>A
c.876+22T>A (n.876+22T>A)
c.516+22T>A (n.516+22T>A)
c.960+22T>A (n.960+22T>A)
 dbSNP
17g.7673514A>GCA2576230608TP53c.993+21T>C (n.993+21T>C)
c.597+21T>C (n.597+21T>C)
c.714+21T>C (n.714+21T>C)
c.972+21T>C (n.972+21T>C)
c.782+667T>C (n.782+667T>C)
c.53+21T>C
c.876+21T>C (n.876+21T>C)
c.516+21T>C (n.516+21T>C)
c.960+21T>C (n.960+21T>C)
 dbSNP
17g.7673514A>TCA2733125743TP53c.993+21T>A (n.993+21T>A)
c.597+21T>A (n.597+21T>A)
c.714+21T>A (n.714+21T>A)
c.972+21T>A (n.972+21T>A)
c.782+667T>A (n.782+667T>A)
c.53+21T>A
c.876+21T>A (n.876+21T>A)
c.516+21T>A (n.516+21T>A)
c.960+21T>A (n.960+21T>A)
 dbSNP
17g.7673515G>ACA2580094890TP53c.993+20C>T (n.993+20C>T)
c.597+20C>T (n.597+20C>T)
c.714+20C>T (n.714+20C>T)
c.972+20C>T (n.972+20C>T)
c.782+666C>T (n.782+666C>T)
c.53+20C>T
c.876+20C>T (n.876+20C>T)
c.516+20C>T (n.516+20C>T)
c.960+20C>T (n.960+20C>T)
 ClinVar dbSNP
17g.7673515G>CCA2245947265TP53c.993+20C>G (n.993+20C>G)
c.597+20C>G (n.597+20C>G)
c.714+20C>G (n.714+20C>G)
c.972+20C>G (n.972+20C>G)
c.782+666C>G (n.782+666C>G)
c.53+20C>G
c.876+20C>G (n.876+20C>G)
c.516+20C>G (n.516+20C>G)
c.960+20C>G (n.960+20C>G)
 dbSNP
17g.7673515G=CA2245947264TP53c.993+20C= (n.993+20C=)
c.597+20C= (n.597+20C=)
c.714+20C= (n.714+20C=)
c.972+20C= (n.972+20C=)
c.782+666C= (n.782+666C=)
c.53+20C=
c.876+20C= (n.876+20C=)
c.516+20C= (n.516+20C=)
c.960+20C= (n.960+20C=)
17g.7673515G>TCA2732985607TP53c.993+20C>A (n.993+20C>A)
c.597+20C>A (n.597+20C>A)
c.714+20C>A (n.714+20C>A)
c.972+20C>A (n.972+20C>A)
c.782+666C>A (n.782+666C>A)
c.53+20C>A
c.876+20C>A (n.876+20C>A)
c.516+20C>A (n.516+20C>A)
c.960+20C>A (n.960+20C>A)
 dbSNP
17g.7673516A=CA2245947269TP53c.993+19T= (n.993+19T=)
c.597+19T= (n.597+19T=)
c.714+19T= (n.714+19T=)
c.972+19T= (n.972+19T=)
c.782+665T= (n.782+665T=)
c.53+19T=
c.876+19T= (n.876+19T=)
c.516+19T= (n.516+19T=)
c.960+19T= (n.960+19T=)
17g.7673516A>GCA2732925963TP53c.993+19T>C (n.993+19T>C)
c.597+19T>C (n.597+19T>C)
c.714+19T>C (n.714+19T>C)
c.972+19T>C (n.972+19T>C)
c.782+665T>C (n.782+665T>C)
c.53+19T>C
c.876+19T>C (n.876+19T>C)
c.516+19T>C (n.516+19T>C)
c.960+19T>C (n.960+19T>C)
 dbSNP
17g.7673516A>TCA001165TP53c.993+19T>A (n.993+19T>A)
c.597+19T>A (n.597+19T>A)
c.714+19T>A (n.714+19T>A)
c.972+19T>A (n.972+19T>A)
c.782+665T>A (n.782+665T>A)
c.53+19T>A
c.876+19T>A (n.876+19T>A)
c.516+19T>A (n.516+19T>A)
c.960+19T>A (n.960+19T>A)
 ClinVar dbSNP ExAC gnomAD v2
17g.7673517G>ACA001171TP53c.993+18C>T (n.993+18C>T)
c.597+18C>T (n.597+18C>T)
c.714+18C>T (n.714+18C>T)
c.972+18C>T (n.972+18C>T)
c.782+664C>T (n.782+664C>T)
c.53+18C>T
c.876+18C>T (n.876+18C>T)
c.516+18C>T (n.516+18C>T)
c.960+18C>T (n.960+18C>T)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.7673517G>CCA2732926315TP53c.993+18C>G (n.993+18C>G)
c.597+18C>G (n.597+18C>G)
c.714+18C>G (n.714+18C>G)
c.972+18C>G (n.972+18C>G)
c.782+664C>G (n.782+664C>G)
c.53+18C>G
c.876+18C>G (n.876+18C>G)
c.516+18C>G (n.516+18C>G)
c.960+18C>G (n.960+18C>G)
 dbSNP
17g.7673517G=CA2245947274TP53c.993+18C= (n.993+18C=)
c.597+18C= (n.597+18C=)
c.714+18C= (n.714+18C=)
c.972+18C= (n.972+18C=)
c.782+664C= (n.782+664C=)
c.53+18C=
c.876+18C= (n.876+18C=)
c.516+18C= (n.516+18C=)
c.960+18C= (n.960+18C=)
17g.7673517G>TCA2695202234TP53c.993+18C>A (n.993+18C>A)
c.597+18C>A (n.597+18C>A)
c.714+18C>A (n.714+18C>A)
c.972+18C>A (n.972+18C>A)
c.782+664C>A (n.782+664C>A)
c.53+18C>A
c.876+18C>A (n.876+18C>A)
c.516+18C>A (n.516+18C>A)
c.960+18C>A (n.960+18C>A)
 dbSNP
17g.7673518G>ACA2580094892TP53c.993+17C>T (n.993+17C>T)
c.597+17C>T (n.597+17C>T)
c.714+17C>T (n.714+17C>T)
c.972+17C>T (n.972+17C>T)
c.782+663C>T (n.782+663C>T)
c.53+17C>T
c.876+17C>T (n.876+17C>T)
c.516+17C>T (n.516+17C>T)
c.960+17C>T (n.960+17C>T)
 ClinVar dbSNP
17g.7673518G>CCA2732931740TP53c.993+17C>G (n.993+17C>G)
c.597+17C>G (n.597+17C>G)
c.714+17C>G (n.714+17C>G)
c.972+17C>G (n.972+17C>G)
c.782+663C>G (n.782+663C>G)
c.53+17C>G
c.876+17C>G (n.876+17C>G)
c.516+17C>G (n.516+17C>G)
c.960+17C>G (n.960+17C>G)
 dbSNP
17g.7673518G=CA2245947277TP53c.993+17C= (n.993+17C=)
c.597+17C= (n.597+17C=)
c.714+17C= (n.714+17C=)
c.972+17C= (n.972+17C=)
c.782+663C= (n.782+663C=)
c.53+17C=
c.876+17C= (n.876+17C=)
c.516+17C= (n.516+17C=)
c.960+17C= (n.960+17C=)
17g.7673518G>TCA287486489TP53c.993+17C>A (n.993+17C>A)
c.597+17C>A (n.597+17C>A)
c.714+17C>A (n.714+17C>A)
c.972+17C>A (n.972+17C>A)
c.782+663C>A (n.782+663C>A)
c.53+17C>A
c.876+17C>A (n.876+17C>A)
c.516+17C>A (n.516+17C>A)
c.960+17C>A (n.960+17C>A)
 dbSNP
17g.7673519T>ACA2733125754TP53c.993+16A>T (n.993+16A>T)
c.597+16A>T (n.597+16A>T)
c.714+16A>T (n.714+16A>T)
c.972+16A>T (n.972+16A>T)
c.782+662A>T (n.782+662A>T)
c.53+16A>T
c.876+16A>T (n.876+16A>T)
c.516+16A>T (n.516+16A>T)
c.960+16A>T (n.960+16A>T)
 dbSNP
17g.7673519T>CCA2733125771TP53c.993+16A>G (n.993+16A>G)
c.597+16A>G (n.597+16A>G)
c.714+16A>G (n.714+16A>G)
c.972+16A>G (n.972+16A>G)
c.782+662A>G (n.782+662A>G)
c.53+16A>G
c.876+16A>G (n.876+16A>G)
c.516+16A>G (n.516+16A>G)
c.960+16A>G (n.960+16A>G)
 dbSNP
17g.7673519T>GCA2733125788TP53c.993+16A>C (n.993+16A>C)
c.597+16A>C (n.597+16A>C)
c.714+16A>C (n.714+16A>C)
c.972+16A>C (n.972+16A>C)
c.782+662A>C (n.782+662A>C)
c.53+16A>C
c.876+16A>C (n.876+16A>C)
c.516+16A>C (n.516+16A>C)
c.960+16A>C (n.960+16A>C)
 dbSNP
17g.7673520C>ACA658683979TP53c.993+15G>T (n.993+15G>T)
c.597+15G>T (n.597+15G>T)
c.714+15G>T (n.714+15G>T)
c.972+15G>T (n.972+15G>T)
c.782+661G>T (n.782+661G>T)
c.53+15G>T
c.876+15G>T (n.876+15G>T)
c.516+15G>T (n.516+15G>T)
c.960+15G>T (n.960+15G>T)
 ClinVar dbSNP
17g.7673520C=CA2245947284TP53c.993+15G= (n.993+15G=)
c.597+15G= (n.597+15G=)
c.714+15G= (n.714+15G=)
c.972+15G= (n.972+15G=)
c.782+661G= (n.782+661G=)
c.53+15G=
c.876+15G= (n.876+15G=)
c.516+15G= (n.516+15G=)
c.960+15G= (n.960+15G=)
17g.7673520C>GCA2635874040TP53c.993+15G>C (n.993+15G>C)
c.597+15G>C (n.597+15G>C)
c.714+15G>C (n.714+15G>C)
c.972+15G>C (n.972+15G>C)
c.782+661G>C (n.782+661G>C)
c.53+15G>C
c.876+15G>C (n.876+15G>C)
c.516+15G>C (n.516+15G>C)
c.960+15G>C (n.960+15G>C)
 ClinVar dbSNP gnomAD v4
17g.7673520C>TCA2732963321TP53c.993+15G>A (n.993+15G>A)
c.597+15G>A (n.597+15G>A)
c.714+15G>A (n.714+15G>A)
c.972+15G>A (n.972+15G>A)
c.782+661G>A (n.782+661G>A)
c.53+15G>A
c.876+15G>A (n.876+15G>A)
c.516+15G>A (n.516+15G>A)
c.960+15G>A (n.960+15G>A)
 ClinVar dbSNP
17g.7673521C>ACA2733125832TP53c.993+14G>T (n.993+14G>T)
c.597+14G>T (n.597+14G>T)
c.714+14G>T (n.714+14G>T)
c.972+14G>T (n.972+14G>T)
c.782+660G>T (n.782+660G>T)
c.53+14G>T
c.876+14G>T (n.876+14G>T)
c.516+14G>T (n.516+14G>T)
c.960+14G>T (n.960+14G>T)
 dbSNP
17g.7673521C>GCA2573154621TP53c.993+14G>C (n.993+14G>C)
c.597+14G>C (n.597+14G>C)
c.714+14G>C (n.714+14G>C)
c.972+14G>C (n.972+14G>C)
c.782+660G>C (n.782+660G>C)
c.53+14G>C
c.876+14G>C (n.876+14G>C)
c.516+14G>C (n.516+14G>C)
c.960+14G>C (n.960+14G>C)
 ClinVar dbSNP gnomAD v4
17g.7673521C>TCA2733125800TP53c.993+14G>A (n.993+14G>A)
c.597+14G>A (n.597+14G>A)
c.714+14G>A (n.714+14G>A)
c.972+14G>A (n.972+14G>A)
c.782+660G>A (n.782+660G>A)
c.53+14G>A
c.876+14G>A (n.876+14G>A)
c.516+14G>A (n.516+14G>A)
c.960+14G>A (n.960+14G>A)
 dbSNP
17g.7673522C>ACA2732925964TP53c.993+13G>T (n.993+13G>T)
c.597+13G>T (n.597+13G>T)
c.714+13G>T (n.714+13G>T)
c.972+13G>T (n.972+13G>T)
c.782+659G>T (n.782+659G>T)
c.53+13G>T
c.876+13G>T (n.876+13G>T)
c.516+13G>T (n.516+13G>T)
c.960+13G>T (n.960+13G>T)
 dbSNP
17g.7673522C=CA2245947294TP53c.993+13G= (n.993+13G=)
c.597+13G= (n.597+13G=)
c.714+13G= (n.714+13G=)
c.972+13G= (n.972+13G=)
c.782+659G= (n.782+659G=)
c.53+13G=
c.876+13G= (n.876+13G=)
c.516+13G= (n.516+13G=)
c.960+13G= (n.960+13G=)
17g.7673522C>GCA000522TP53c.993+13G>C (n.993+13G>C)
c.597+13G>C (n.597+13G>C)
c.714+13G>C (n.714+13G>C)
c.972+13G>C (n.972+13G>C)
c.782+659G>C (n.782+659G>C)
c.53+13G>C
c.876+13G>C (n.876+13G>C)
c.516+13G>C (n.516+13G>C)
c.960+13G>C (n.960+13G>C)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.7673522C>TCA2573154623TP53c.993+13G>A (n.993+13G>A)
c.597+13G>A (n.597+13G>A)
c.714+13G>A (n.714+13G>A)
c.972+13G>A (n.972+13G>A)
c.782+659G>A (n.782+659G>A)
c.53+13G>A
c.876+13G>A (n.876+13G>A)
c.516+13G>A (n.516+13G>A)
c.960+13G>A (n.960+13G>A)
 ClinVar dbSNP gnomAD v4
17g.7673522_7673523delinsTGCA2573154622TP53c.993+12_993+13delinsCA (n.993+12_993+13delinsCA)
c.597+12_597+13delinsCA (n.597+12_597+13delinsCA)
c.714+12_714+13delinsCA (n.714+12_714+13delinsCA)
c.972+12_972+13delinsCA (n.972+12_972+13delinsCA)
c.782+658_782+659delinsCA (n.782+658_782+659delinsCA)
c.53+12_53+13delinsCA
c.876+12_876+13delinsCA (n.876+12_876+13delinsCA)
c.516+12_516+13delinsCA (n.516+12_516+13delinsCA)
c.960+12_960+13delinsCA (n.960+12_960+13delinsCA)
 ClinVar
17g.7673523A=CA2245947305TP53c.993+12T= (n.993+12T=)
c.597+12T= (n.597+12T=)
c.714+12T= (n.714+12T=)
c.972+12T= (n.972+12T=)
c.782+658T= (n.782+658T=)
c.53+12T=
c.876+12T= (n.876+12T=)
c.516+12T= (n.516+12T=)
c.960+12T= (n.960+12T=)
17g.7673523A>CCA2580574841TP53c.993+12T>G (n.993+12T>G)
c.597+12T>G (n.597+12T>G)
c.714+12T>G (n.714+12T>G)
c.972+12T>G (n.972+12T>G)
c.782+658T>G (n.782+658T>G)
c.53+12T>G
c.876+12T>G (n.876+12T>G)
c.516+12T>G (n.516+12T>G)
c.960+12T>G (n.960+12T>G)
17g.7673523A>GCA000520TP53c.993+12T>C (n.993+12T>C)
c.597+12T>C (n.597+12T>C)
c.714+12T>C (n.714+12T>C)
c.972+12T>C (n.972+12T>C)
c.782+658T>C (n.782+658T>C)
c.53+12T>C
c.876+12T>C (n.876+12T>C)
c.516+12T>C (n.516+12T>C)
c.960+12T>C (n.960+12T>C)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.7673523A>TCA2580574842TP53c.993+12T>A (n.993+12T>A)
c.597+12T>A (n.597+12T>A)
c.714+12T>A (n.714+12T>A)
c.972+12T>A (n.972+12T>A)
c.782+658T>A (n.782+658T>A)
c.53+12T>A
c.876+12T>A (n.876+12T>A)
c.516+12T>A (n.516+12T>A)
c.960+12T>A (n.960+12T>A)
 dbSNP
17g.7673524A=CA2245947313TP53c.993+11T= (n.993+11T=)
c.597+11T= (n.597+11T=)
c.714+11T= (n.714+11T=)
c.972+11T= (n.972+11T=)
c.782+657T= (n.782+657T=)
c.53+11T=
c.876+11T= (n.876+11T=)
c.516+11T= (n.516+11T=)
c.960+11T= (n.960+11T=)
17g.7673524A>GCA001188TP53c.993+11T>C (n.993+11T>C)
c.597+11T>C (n.597+11T>C)
c.714+11T>C (n.714+11T>C)
c.972+11T>C (n.972+11T>C)
c.782+657T>C (n.782+657T>C)
c.53+11T>C
c.876+11T>C (n.876+11T>C)
c.516+11T>C (n.516+11T>C)
c.960+11T>C (n.960+11T>C)
 dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
17g.7673524A>TCA2732930950TP53c.993+11T>A (n.993+11T>A)
c.597+11T>A (n.597+11T>A)
c.714+11T>A (n.714+11T>A)
c.972+11T>A (n.972+11T>A)
c.782+657T>A (n.782+657T>A)
c.53+11T>A
c.876+11T>A (n.876+11T>A)
c.516+11T>A (n.516+11T>A)
c.960+11T>A (n.960+11T>A)
 dbSNP
17g.7673525G>ACA2733125845TP53c.993+10C>T (n.993+10C>T)
c.597+10C>T (n.597+10C>T)
c.714+10C>T (n.714+10C>T)
c.972+10C>T (n.972+10C>T)
c.782+656C>T (n.782+656C>T)
c.53+10C>T
c.876+10C>T (n.876+10C>T)
c.516+10C>T (n.516+10C>T)
c.960+10C>T (n.960+10C>T)
 dbSNP
17g.7673525G>CCA2635874081TP53c.993+10C>G (n.993+10C>G)
c.597+10C>G (n.597+10C>G)
c.714+10C>G (n.714+10C>G)
c.972+10C>G (n.972+10C>G)
c.782+656C>G (n.782+656C>G)
c.53+10C>G
c.876+10C>G (n.876+10C>G)
c.516+10C>G (n.516+10C>G)
c.960+10C>G (n.960+10C>G)
 dbSNP gnomAD v4
17g.7673525G>TCA2733125848TP53c.993+10C>A (n.993+10C>A)
c.597+10C>A (n.597+10C>A)
c.714+10C>A (n.714+10C>A)
c.972+10C>A (n.972+10C>A)
c.782+656C>A (n.782+656C>A)
c.53+10C>A
c.876+10C>A (n.876+10C>A)
c.516+10C>A (n.516+10C>A)
c.960+10C>A (n.960+10C>A)
 dbSNP
17g.7673525_7673526insGGTGCA2635874080TP53c.993+10_993+11insACCC (n.993+10_993+11insACCC)
c.597+10_597+11insACCC (n.597+10_597+11insACCC)
c.714+10_714+11insACCC (n.714+10_714+11insACCC)
c.972+10_972+11insACCC (n.972+10_972+11insACCC)
c.782+656_782+657insACCC (n.782+656_782+657insACCC)
c.53+10_53+11insACCC
c.876+10_876+11insACCC (n.876+10_876+11insACCC)
c.516+10_516+11insACCC (n.516+10_516+11insACCC)
c.960+10_960+11insACCC (n.960+10_960+11insACCC)
 gnomAD v4
17g.7673526A>GCA2576230614TP53c.993+9T>C (n.993+9T>C)
c.597+9T>C (n.597+9T>C)
c.714+9T>C (n.714+9T>C)
c.972+9T>C (n.972+9T>C)
c.782+655T>C (n.782+655T>C)
c.53+9T>C
c.876+9T>C (n.876+9T>C)
c.516+9T>C (n.516+9T>C)
c.960+9T>C (n.960+9T>C)
 ClinVar dbSNP
17g.7673526A>TCA2733125877TP53c.993+9T>A (n.993+9T>A)
c.597+9T>A (n.597+9T>A)
c.714+9T>A (n.714+9T>A)
c.972+9T>A (n.972+9T>A)
c.782+655T>A (n.782+655T>A)
c.53+9T>A
c.876+9T>A (n.876+9T>A)
c.516+9T>A (n.516+9T>A)
c.960+9T>A (n.960+9T>A)
 dbSNP
17g.7673527C>ACA2732943608TP53c.993+8G>T (n.993+8G>T)
c.597+8G>T (n.597+8G>T)
c.714+8G>T (n.714+8G>T)
c.972+8G>T (n.972+8G>T)
c.782+654G>T (n.782+654G>T)
c.53+8G>T
c.876+8G>T (n.876+8G>T)
c.516+8G>T (n.516+8G>T)
c.960+8G>T (n.960+8G>T)
 dbSNP
17g.7673527C=CA2245947326TP53c.993+8G= (n.993+8G=)
c.597+8G= (n.597+8G=)
c.714+8G= (n.714+8G=)
c.972+8G= (n.972+8G=)
c.782+654G= (n.782+654G=)
c.53+8G=
c.876+8G= (n.876+8G=)
c.516+8G= (n.516+8G=)
c.960+8G= (n.960+8G=)
17g.7673527C>GCA2576230615TP53c.993+8G>C (n.993+8G>C)
c.597+8G>C (n.597+8G>C)
c.714+8G>C (n.714+8G>C)
c.972+8G>C (n.972+8G>C)
c.782+654G>C (n.782+654G>C)
c.53+8G>C
c.876+8G>C (n.876+8G>C)
c.516+8G>C (n.516+8G>C)
c.960+8G>C (n.960+8G>C)
 ClinVar gnomAD v4
17g.7673527C>TCA16615685TP53c.993+8G>A (n.993+8G>A)
c.597+8G>A (n.597+8G>A)
c.714+8G>A (n.714+8G>A)
c.972+8G>A (n.972+8G>A)
c.782+654G>A (n.782+654G>A)
c.53+8G>A
c.876+8G>A (n.876+8G>A)
c.516+8G>A (n.516+8G>A)
c.960+8G>A (n.960+8G>A)
 ClinVar dbSNP
17g.7673527_7673529delCA2635874085TP53c.993+6_993+8del (n.993+6_993+8del)
c.597+6_597+8del (n.597+6_597+8del)
c.714+6_714+8del (n.714+6_714+8del)
c.972+6_972+8del (n.972+6_972+8del)
c.782+652_782+654del (n.782+652_782+654del)
c.53+6_53+8del
c.876+6_876+8del (n.876+6_876+8del)
c.516+6_516+8del (n.516+6_516+8del)
c.960+6_960+8del (n.960+6_960+8del)
 gnomAD v4
17g.7673528T>ACA2732941348TP53c.993+7A>T (n.993+7A>T)
c.597+7A>T (n.597+7A>T)
c.714+7A>T (n.714+7A>T)
c.972+7A>T (n.972+7A>T)
c.782+653A>T (n.782+653A>T)
c.53+7A>T
c.876+7A>T (n.876+7A>T)
c.516+7A>T (n.516+7A>T)
c.960+7A>T (n.960+7A>T)
 dbSNP
17g.7673528T>CCA287486495TP53c.993+7A>G (n.993+7A>G)
c.597+7A>G (n.597+7A>G)
c.714+7A>G (n.714+7A>G)
c.972+7A>G (n.972+7A>G)
c.782+653A>G (n.782+653A>G)
c.53+7A>G
c.876+7A>G (n.876+7A>G)
c.516+7A>G (n.516+7A>G)
c.960+7A>G (n.960+7A>G)
 ClinVar dbSNP gnomAD v4
17g.7673528T>GCA2732941347TP53c.993+7A>C (n.993+7A>C)
c.597+7A>C (n.597+7A>C)
c.714+7A>C (n.714+7A>C)
c.972+7A>C (n.972+7A>C)
c.782+653A>C (n.782+653A>C)
c.53+7A>C
c.876+7A>C (n.876+7A>C)
c.516+7A>C (n.516+7A>C)
c.960+7A>C (n.960+7A>C)
 dbSNP
17g.7673528T=CA2245947329TP53c.993+7A= (n.993+7A=)
c.597+7A= (n.597+7A=)
c.714+7A= (n.714+7A=)
c.972+7A= (n.972+7A=)
c.782+653A= (n.782+653A=)
c.53+7A=
c.876+7A= (n.876+7A=)
c.516+7A= (n.516+7A=)
c.960+7A= (n.960+7A=)
17g.7673529_7673532dupCA2573154625TP53c.993+4_993+7dup (n.993+4_993+7dup)
c.597+4_597+7dup (n.597+4_597+7dup)
c.714+4_714+7dup (n.714+4_714+7dup)
c.972+4_972+7dup (n.972+4_972+7dup)
c.782+650_782+653dup (n.782+650_782+653dup)
c.53+4_53+7dup
c.876+4_876+7dup (n.876+4_876+7dup)
c.516+4_516+7dup (n.516+4_516+7dup)
c.960+4_960+7dup (n.960+4_960+7dup)
 ClinVar dbSNP
17g.7673528_7673536delCA2573154624TP53c.992_993+7del
c.596_597+7del
c.713_714+7del
c.971_972+7del
c.782+645_782+653del (n.782+645_782+653del)
c.52_53+7del
c.875_876+7del
c.515_516+7del
c.959_960+7del
 dbSNP
17g.7673528_7673529insGCA2576230616TP53c.993+6_993+7insC (n.993+6_993+7insC)
c.597+6_597+7insC (n.597+6_597+7insC)
c.714+6_714+7insC (n.714+6_714+7insC)
c.972+6_972+7insC (n.972+6_972+7insC)
c.782+652_782+653insC (n.782+652_782+653insC)
c.53+6_53+7insC
c.876+6_876+7insC (n.876+6_876+7insC)
c.516+6_516+7insC (n.516+6_516+7insC)
c.960+6_960+7insC (n.960+6_960+7insC)
17g.7673529T>ACA2576230617TP53c.993+6A>T (n.993+6A>T)
c.597+6A>T (n.597+6A>T)
c.714+6A>T (n.714+6A>T)
c.972+6A>T (n.972+6A>T)
c.782+652A>T (n.782+652A>T)
c.53+6A>T
c.876+6A>T (n.876+6A>T)
c.516+6A>T (n.516+6A>T)
c.960+6A>T (n.960+6A>T)
17g.7673529T>CCA2573154626TP53c.993+6A>G (n.993+6A>G)
c.597+6A>G (n.597+6A>G)
c.714+6A>G (n.714+6A>G)
c.972+6A>G (n.972+6A>G)
c.782+652A>G (n.782+652A>G)
c.53+6A>G
c.876+6A>G (n.876+6A>G)
c.516+6A>G (n.516+6A>G)
c.960+6A>G (n.960+6A>G)
 ClinVar dbSNP gnomAD v4
17g.7673529T>GCA2733125928TP53c.993+6A>C (n.993+6A>C)
c.597+6A>C (n.597+6A>C)
c.714+6A>C (n.714+6A>C)
c.972+6A>C (n.972+6A>C)
c.782+652A>C (n.782+652A>C)
c.53+6A>C
c.876+6A>C (n.876+6A>C)
c.516+6A>C (n.516+6A>C)
c.960+6A>C (n.960+6A>C)
 dbSNP
17g.7673529_7673541delCA645587337TP53c.987_993+6del
c.591_597+6del
c.708_714+6del
c.966_972+6del
c.782+640_782+652del (n.782+640_782+652del)
c.47_53+6del
c.870_876+6del
c.510_516+6del
c.954_960+6del
 COSMIC COSMIC COSMIC COSMIC
17g.7673530A=CA2245947338TP53c.993+5T= (n.993+5T=)
c.597+5T= (n.597+5T=)
c.714+5T= (n.714+5T=)
c.972+5T= (n.972+5T=)
c.782+651T= (n.782+651T=)
c.53+5T=
c.876+5T= (n.876+5T=)
c.516+5T= (n.516+5T=)
c.960+5T= (n.960+5T=)
17g.7673530A>CCA915949513TP53c.993+5T>G (n.993+5T>G)
c.597+5T>G (n.597+5T>G)
c.714+5T>G (n.714+5T>G)
c.972+5T>G (n.972+5T>G)
c.782+651T>G (n.782+651T>G)
c.53+5T>G
c.876+5T>G (n.876+5T>G)
c.516+5T>G (n.516+5T>G)
c.960+5T>G (n.960+5T>G)
 ClinVar dbSNP gnomAD v4
17g.7673530A>GCA658656522TP53c.993+5T>C (n.993+5T>C)
c.597+5T>C (n.597+5T>C)
c.714+5T>C (n.714+5T>C)
c.972+5T>C (n.972+5T>C)
c.782+651T>C (n.782+651T>C)
c.53+5T>C
c.876+5T>C (n.876+5T>C)
c.516+5T>C (n.516+5T>C)
c.960+5T>C (n.960+5T>C)
 ClinVar dbSNP gnomAD v3 gnomAD v4
17g.7673530A>TCA2732953019TP53c.993+5T>A (n.993+5T>A)
c.597+5T>A (n.597+5T>A)
c.714+5T>A (n.714+5T>A)
c.972+5T>A (n.972+5T>A)
c.782+651T>A (n.782+651T>A)
c.53+5T>A
c.876+5T>A (n.876+5T>A)
c.516+5T>A (n.516+5T>A)
c.960+5T>A (n.960+5T>A)
 dbSNP
17g.7673530_7673531delinsAGCA2245947337TP53c.993+4_993+5delinsCT (n.993+4_993+5delinsCT)
c.597+4_597+5delinsCT (n.597+4_597+5delinsCT)
c.714+4_714+5delinsCT (n.714+4_714+5delinsCT)
c.972+4_972+5delinsCT (n.972+4_972+5delinsCT)
c.782+650_782+651delinsCT (n.782+650_782+651delinsCT)
c.53+4_53+5delinsCT
c.876+4_876+5delinsCT (n.876+4_876+5delinsCT)
c.516+4_516+5delinsCT (n.516+4_516+5delinsCT)
c.960+4_960+5delinsCT (n.960+4_960+5delinsCT)
17g.7673531delCA10580907TP53c.993+4del (n.993+4del)
c.597+4del (n.597+4del)
c.714+4del (n.714+4del)
c.972+4del (n.972+4del)
c.782+650del (n.782+650del)
c.53+4del
c.876+4del (n.876+4del)
c.516+4del (n.516+4del)
c.960+4del (n.960+4del)
 ClinVar dbSNP
17g.7673531G>ACA658798695TP53c.993+4C>T (n.993+4C>T)
c.597+4C>T (n.597+4C>T)
c.714+4C>T (n.714+4C>T)
c.972+4C>T (n.972+4C>T)
c.782+650C>T (n.782+650C>T)
c.53+4C>T
c.876+4C>T (n.876+4C>T)
c.516+4C>T (n.516+4C>T)
c.960+4C>T (n.960+4C>T)
 ClinVar dbSNP gnomAD v4
17g.7673531G>CCA913188777TP53c.993+4C>G (n.993+4C>G)
c.597+4C>G (n.597+4C>G)
c.714+4C>G (n.714+4C>G)
c.972+4C>G (n.972+4C>G)
c.782+650C>G (n.782+650C>G)
c.53+4C>G
c.876+4C>G (n.876+4C>G)
c.516+4C>G (n.516+4C>G)
c.960+4C>G (n.960+4C>G)
 ClinVar dbSNP
17g.7673531G=CA2245947358TP53c.993+4C= (n.993+4C=)
c.597+4C= (n.597+4C=)
c.714+4C= (n.714+4C=)
c.972+4C= (n.972+4C=)
c.782+650C= (n.782+650C=)
c.53+4C=
c.876+4C= (n.876+4C=)
c.516+4C= (n.516+4C=)
c.960+4C= (n.960+4C=)
17g.7673531G>TCA2732963322TP53c.993+4C>A (n.993+4C>A)
c.597+4C>A (n.597+4C>A)
c.714+4C>A (n.714+4C>A)
c.972+4C>A (n.972+4C>A)
c.782+650C>A (n.782+650C>A)
c.53+4C>A
c.876+4C>A (n.876+4C>A)
c.516+4C>A (n.516+4C>A)
c.960+4C>A (n.960+4C>A)
 dbSNP
17g.7673532_7673541delCA645587338TP53c.988_993+4del
c.592_597+4del
c.709_714+4del
c.967_972+4del
c.782+641_782+650del (n.782+641_782+650del)
c.48_53+4del
c.871_876+4del
c.511_516+4del
c.955_960+4del
 COSMIC COSMIC COSMIC COSMIC
17g.7673532T>ACA2573154627TP53c.993+3A>T (n.993+3A>T)
c.597+3A>T (n.597+3A>T)
c.714+3A>T (n.714+3A>T)
c.972+3A>T (n.972+3A>T)
c.782+649A>T (n.782+649A>T)
c.53+3A>T
c.876+3A>T (n.876+3A>T)
c.516+3A>T (n.516+3A>T)
c.960+3A>T (n.960+3A>T)
 ClinVar dbSNP gnomAD v4
17g.7673532T>CCA2733126018TP53c.993+3A>G (n.993+3A>G)
c.597+3A>G (n.597+3A>G)
c.714+3A>G (n.714+3A>G)
c.972+3A>G (n.972+3A>G)
c.782+649A>G (n.782+649A>G)
c.53+3A>G
c.876+3A>G (n.876+3A>G)
c.516+3A>G (n.516+3A>G)
c.960+3A>G (n.960+3A>G)
 dbSNP
17g.7673532T>GCA2733126009TP53c.993+3A>C (n.993+3A>C)
c.597+3A>C (n.597+3A>C)
c.714+3A>C (n.714+3A>C)
c.972+3A>C (n.972+3A>C)
c.782+649A>C (n.782+649A>C)
c.53+3A>C
c.876+3A>C (n.876+3A>C)
c.516+3A>C (n.516+3A>C)
c.960+3A>C (n.960+3A>C)
 dbSNP
17g.7673532_7673534delinsGCA645587339TP53c.993+1_993+3delinsC (n.993+1_993+3delinsC)
c.597+1_597+3delinsC (n.597+1_597+3delinsC)
c.714+1_714+3delinsC (n.714+1_714+3delinsC)
c.972+1_972+3delinsC (n.972+1_972+3delinsC)
c.782+647_782+649delinsC (n.782+647_782+649delinsC)
c.53+1_53+3delinsC
c.876+1_876+3delinsC (n.876+1_876+3delinsC)
c.516+1_516+3delinsC (n.516+1_516+3delinsC)
c.960+1_960+3delinsC (n.960+1_960+3delinsC)
 COSMIC
17g.7673533A=CA2245947371TP53c.993+2T= (n.993+2T=)
c.597+2T= (n.597+2T=)
c.714+2T= (n.714+2T=)
c.972+2T= (n.972+2T=)
c.782+648T= (n.782+648T=)
c.53+2T=
c.876+2T= (n.876+2T=)
c.516+2T= (n.516+2T=)
c.960+2T= (n.960+2T=)
17g.7673533A>CCA397835626TP53c.993+2T>G (n.993+2T>G)
c.597+2T>G (n.597+2T>G)
c.714+2T>G (n.714+2T>G)
c.972+2T>G (n.972+2T>G)
c.782+648T>G (n.782+648T>G)
c.53+2T>G
c.876+2T>G (n.876+2T>G)
c.516+2T>G (n.516+2T>G)
c.960+2T>G (n.960+2T>G)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC
17g.7673533A>GCA397835629TP53c.993+2T>C (n.993+2T>C)
c.597+2T>C (n.597+2T>C)
c.714+2T>C (n.714+2T>C)
c.972+2T>C (n.972+2T>C)
c.782+648T>C (n.782+648T>C)
c.53+2T>C
c.876+2T>C (n.876+2T>C)
c.516+2T>C (n.516+2T>C)
c.960+2T>C (n.960+2T>C)
 ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC
17g.7673533A>TCA397835635TP53c.993+2T>A (n.993+2T>A)
c.597+2T>A (n.597+2T>A)
c.714+2T>A (n.714+2T>A)
c.972+2T>A (n.972+2T>A)
c.782+648T>A (n.782+648T>A)
c.53+2T>A
c.876+2T>A (n.876+2T>A)
c.516+2T>A (n.516+2T>A)
c.960+2T>A (n.960+2T>A)
 dbSNP COSMIC COSMIC COSMIC COSMIC
17g.7673533_7673534delinsACCA2245947369TP53c.993+1_993+2delinsGT (n.993+1_993+2delinsGT)
c.597+1_597+2delinsGT (n.597+1_597+2delinsGT)
c.714+1_714+2delinsGT (n.714+1_714+2delinsGT)
c.972+1_972+2delinsGT (n.972+1_972+2delinsGT)
c.782+647_782+648delinsGT (n.782+647_782+648delinsGT)
c.53+1_53+2delinsGT
c.876+1_876+2delinsGT (n.876+1_876+2delinsGT)
c.516+1_516+2delinsGT (n.516+1_516+2delinsGT)
c.960+1_960+2delinsGT (n.960+1_960+2delinsGT)
17g.7673533_7673541delinsTACA2580094895TP53c.987_993+2delinsTA
c.591_597+2delinsTA
c.708_714+2delinsTA
c.966_972+2delinsTA
c.782+640_782+648delinsTA (n.782+640_782+648delinsTA)
c.47_53+2delinsTA
c.870_876+2delinsTA
c.510_516+2delinsTA
c.954_960+2delinsTA
 ClinVar
17g.7673534C>ACA287486498TP53c.993+1G>T (n.993+1G>T)
c.597+1G>T (n.597+1G>T)
c.714+1G>T (n.714+1G>T)
c.972+1G>T (n.972+1G>T)
c.782+647G>T (n.782+647G>T)
c.53+1G>T
c.876+1G>T (n.876+1G>T)
c.516+1G>T (n.516+1G>T)
c.960+1G>T (n.960+1G>T)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC
17g.7673534C=CA2245947398TP53c.993+1G= (n.993+1G=)
c.597+1G= (n.597+1G=)
c.714+1G= (n.714+1G=)
c.972+1G= (n.972+1G=)
c.782+647G= (n.782+647G=)
c.53+1G=
c.876+1G= (n.876+1G=)
c.516+1G= (n.516+1G=)
c.960+1G= (n.960+1G=)
17g.7673534C>GCA16607519TP53c.993+1G>C (n.993+1G>C)
c.597+1G>C (n.597+1G>C)
c.714+1G>C (n.714+1G>C)
c.972+1G>C (n.972+1G>C)
c.782+647G>C (n.782+647G>C)
c.53+1G>C
c.876+1G>C (n.876+1G>C)
c.516+1G>C (n.516+1G>C)
c.960+1G>C (n.960+1G>C)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC
17g.7673534C>TCA397835645TP53c.993+1G>A (n.993+1G>A)
c.597+1G>A (n.597+1G>A)
c.714+1G>A (n.714+1G>A)
c.972+1G>A (n.972+1G>A)
c.782+647G>A (n.782+647G>A)
c.53+1G>A
c.876+1G>A (n.876+1G>A)
c.516+1G>A (n.516+1G>A)
c.960+1G>A (n.960+1G>A)
 ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC COSMIC COSMIC
17g.7673535delCA645369685TP53c.993+1del
c.597+1del
c.714+1del
c.972+1del
c.782+647del (n.782+647del)
c.53+1del
c.876+1del
c.516+1del
c.960+1del
 ClinVar dbSNP
17g.7673534_7673538delinsCCTGACA2245947390TP53c.990_993+1delinsTCAGG
c.594_597+1delinsTCAGG
c.711_714+1delinsTCAGG
c.969_972+1delinsTCAGG
c.782+643_782+647delinsTCAGG (n.782+643_782+647delinsTCAGG)
c.50_53+1delinsTCAGG
c.873_876+1delinsTCAGG
c.513_516+1delinsTCAGG
c.957_960+1delinsTCAGG
17g.7673535C>ACA287486501TP53c.993G>T (p.Gln331His)
c.597G>T (p.Gln199His)
c.714G>T (p.Gln238His)
c.972G>T (p.Gln324His)
c.782+646G>T (n.782+646G>T)
c.53G>T
c.876G>T (p.Gln292His)
c.516G>T (p.Gln172His)
c.960G>T (p.Gln320His)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC
17g.7673535C=CA2245947419TP53c.993G= (p.Gln331=)
c.597G= (p.Gln199=)
c.714G= (p.Gln238=)
c.972G= (p.Gln324=)
c.782+646G= (n.782+646G=)
c.53G=
c.876G= (p.Gln292=)
c.516G= (p.Gln172=)
c.960G= (p.Gln320=)
17g.7673535C>GCA397835662TP53c.993G>C (p.Gln331His)
c.597G>C (p.Gln199His)
c.714G>C (p.Gln238His)
c.972G>C (p.Gln324His)
c.782+646G>C (n.782+646G>C)
c.53G>C
c.876G>C (p.Gln292His)
c.516G>C (p.Gln172His)
c.960G>C (p.Gln320His)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC
17g.7673535C>TCA10590137TP53c.993G>A (p.Gln331=)
c.597G>A (p.Gln199=)
c.714G>A (p.Gln238=)
c.972G>A (p.Gln324=)
c.782+646G>A (n.782+646G>A)
c.53G>A
c.876G>A (p.Gln292=)
c.516G>A (p.Gln172=)
c.960G>A (p.Gln320=)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC
17g.7673535_7673536delCA645587344TP53c.992_993del (p.Gln331HisfsTer5)
c.596_597del (p.Gln199HisfsTer5)
c.713_714del (p.Gln238HisfsTer5)
c.971_972del (p.Gln324HisfsTer5)
c.992_993del (p.Lys332AsnfsTer?)
c.782+645_782+646del (n.782+645_782+646del)
c.992_993del (p.Gln331ArgfsTer15)
c.992_993del (p.Gln331HisfsTer4)
c.596_597del (p.Gln199HisfsTer4)
c.596_597del (p.Gln199=)
c.596_597del (p.Gln199ArgfsTer15)
c.52_53del
c.875_876del (p.Gln292HisfsTer5)
c.875_876del (p.Gln292HisfsTer4)
c.515_516del (p.Gln172HisfsTer4)
c.959_960del (p.Gln320HisfsTer5)
c.515_516del (p.Gln172ArgfsTer15)
c.515_516del (p.Gln172HisfsTer5)
c.875_876del (p.Gln292ArgfsTer15)
 COSMIC
17g.7673535_7673536delinsTGCA645587342TP53c.992_993delinsCA (p.Gln331Pro)
c.596_597delinsCA (p.Gln199Pro)
c.713_714delinsCA (p.Gln238Pro)
c.971_972delinsCA (p.Gln324Pro)
c.782+645_782+646delinsCA (n.782+645_782+646delinsCA)
c.52_53delinsCA
c.875_876delinsCA (p.Gln292Pro)
c.515_516delinsCA (p.Gln172Pro)
c.959_960delinsCA (p.Gln320Pro)
 COSMIC
17g.7673535_7673538delCA658656523TP53c.990_993del (p.Gln331SerfsTer13)
c.594_597del (p.Gln199SerfsTer13)
c.711_714del (p.Gln238SerfsTer13)
c.969_972del (p.Gln324SerfsTer13)
c.990_993del (p.Gln331LysfsTer20)
c.782+643_782+646del (n.782+643_782+646del)
c.990_993del (p.Gln331ThrfsTer19)
c.990_993del (p.Gln331CysfsTer11)
c.594_597del (p.Gln199CysfsTer11)
c.594_597del (p.Leu198=)
c.594_597del (p.Gln199ThrfsTer19)
c.50_53del
c.873_876del (p.Gln292SerfsTer13)
c.873_876del (p.Gln292CysfsTer11)
c.513_516del (p.Gln172CysfsTer11)
c.957_960del (p.Gln320SerfsTer13)
c.513_516del (p.Gln172ThrfsTer19)
c.513_516del (p.Gln172SerfsTer13)
c.873_876del (p.Gln292ThrfsTer19)
 ClinVar dbSNP
17g.7673536T>ACA397835673TP53c.992A>T (p.Gln331Leu)
c.596A>T (p.Gln199Leu)
c.713A>T (p.Gln238Leu)
c.971A>T (p.Gln324Leu)
c.782+645A>T (n.782+645A>T)
c.52A>T
c.875A>T (p.Gln292Leu)
c.515A>T (p.Gln172Leu)
c.959A>T (p.Gln320Leu)
17g.7673536T>CCA16620611TP53c.992A>G (p.Gln331Arg)
c.596A>G (p.Gln199Arg)
c.713A>G (p.Gln238Arg)
c.971A>G (p.Gln324Arg)
c.782+645A>G (n.782+645A>G)
c.52A>G
c.875A>G (p.Gln292Arg)
c.515A>G (p.Gln172Arg)
c.959A>G (p.Gln320Arg)
 ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC
17g.7673536T>GCA397835672TP53c.992A>C (p.Gln331Pro)
c.596A>C (p.Gln199Pro)
c.713A>C (p.Gln238Pro)
c.971A>C (p.Gln324Pro)
c.782+645A>C (n.782+645A>C)
c.52A>C
c.875A>C (p.Gln292Pro)
c.515A>C (p.Gln172Pro)
c.959A>C (p.Gln320Pro)
 COSMIC
17g.7673536T=CA2245947430TP53c.992A= (p.Gln331=)
c.596A= (p.Gln199=)
c.713A= (p.Gln238=)
c.971A= (p.Gln324=)
c.782+645A= (n.782+645A=)
c.52A=
c.875A= (p.Gln292=)
c.515A= (p.Gln172=)
c.959A= (p.Gln320=)
17g.7673536_7673594dupCA2499224956TP53c.934_992dup (p.Ile332ProfsTer33)
c.538_596dup (p.Ile200ProfsTer33)
c.655_713dup (p.Ile239ProfsTer33)
c.913_971dup (p.Ile325ProfsTer33)
c.934_992dup (p.Lys332ProfsTer40)
c.782+587_782+645dup (n.782+587_782+645dup)
c.934_992dup (p.Asp332ProfsTer39)
c.934_992dup (p.Met332ProfsTer31)
c.538_596dup (p.Met200ProfsTer31)
c.538_596dup (p.Gln199=)
c.538_596dup (p.Asp200ProfsTer39)
c.817_875dup (p.Ile293ProfsTer33)
c.817_875dup (p.Met293ProfsTer31)
c.457_515dup (p.Met173ProfsTer31)
c.901_959dup (p.Ile321ProfsTer33)
c.457_515dup (p.Asp173ProfsTer39)
c.457_515dup (p.Ile173ProfsTer33)
c.817_875dup (p.Asp293ProfsTer39)
 ClinVar dbSNP
17g.7673537G>ACA397835674TP53c.991C>T (p.Gln331Ter)
c.595C>T (p.Gln199Ter)
c.712C>T (p.Gln238Ter)
c.970C>T (p.Gln324Ter)
c.782+644C>T (n.782+644C>T)
c.51C>T
c.874C>T (p.Gln292Ter)
c.514C>T (p.Gln172Ter)
c.958C>T (p.Gln320Ter)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC
17g.7673537G>CCA397835677TP53c.991C>G (p.Gln331Glu)
c.595C>G (p.Gln199Glu)
c.712C>G (p.Gln238Glu)
c.970C>G (p.Gln324Glu)
c.782+644C>G (n.782+644C>G)
c.51C>G
c.874C>G (p.Gln292Glu)
c.514C>G (p.Gln172Glu)
c.958C>G (p.Gln320Glu)
 ClinVar
17g.7673537G=CA2245947449TP53c.991C= (p.Gln331=)
c.595C= (p.Gln199=)
c.712C= (p.Gln238=)
c.970C= (p.Gln324=)
c.782+644C= (n.782+644C=)
c.51C=
c.874C= (p.Gln292=)
c.514C= (p.Gln172=)
c.958C= (p.Gln320=)
17g.7673537G>TCA397835679TP53c.991C>A (p.Gln331Lys)
c.595C>A (p.Gln199Lys)
c.712C>A (p.Gln238Lys)
c.970C>A (p.Gln324Lys)
c.782+644C>A (n.782+644C>A)
c.51C>A
c.874C>A (p.Gln292Lys)
c.514C>A (p.Gln172Lys)
c.958C>A (p.Gln320Lys)
 ClinVar dbSNP
17g.7673538A>CCA497713725TP53c.990T>G (p.Leu330=)
c.594T>G (p.Leu198=)
c.711T>G (p.Leu237=)
c.969T>G (p.Leu323=)
c.782+643T>G (n.782+643T>G)
c.50T>G
c.873T>G (p.Leu291=)
c.513T>G (p.Leu171=)
c.957T>G (p.Leu319=)
 dbSNP
17g.7673538A>GCA497713729TP53c.990T>C (p.Leu330=)
c.594T>C (p.Leu198=)
c.711T>C (p.Leu237=)
c.969T>C (p.Leu323=)
c.782+643T>C (n.782+643T>C)
c.50T>C
c.873T>C (p.Leu291=)
c.513T>C (p.Leu171=)
c.957T>C (p.Leu319=)
 dbSNP
17g.7673538A>TCA497713734TP53c.990T>A (p.Leu330=)
c.594T>A (p.Leu198=)
c.711T>A (p.Leu237=)
c.969T>A (p.Leu323=)
c.782+643T>A (n.782+643T>A)
c.50T>A
c.873T>A (p.Leu291=)
c.513T>A (p.Leu171=)
c.957T>A (p.Leu319=)
 dbSNP
17g.7673539dupCA645587345TP53c.990dup (p.Gln331SerfsTer6)
c.594dup (p.Gln199SerfsTer6)
c.711dup (p.Gln238SerfsTer6)
c.969dup (p.Gln324SerfsTer6)
c.990dup (p.Gln331SerfsTer?)
c.782+643dup (n.782+643dup)
c.990dup (p.Gln331SerfsTer16)
c.990dup (p.Gln331SerfsTer5)
c.594dup (p.Gln199SerfsTer5)
c.594dup (p.Gln199SerfsTer?)
c.594dup (p.Gln199SerfsTer16)
c.50dup
c.873dup (p.Gln292SerfsTer6)
c.873dup (p.Gln292SerfsTer5)
c.513dup (p.Gln172SerfsTer5)
c.957dup (p.Gln320SerfsTer6)
c.513dup (p.Gln172SerfsTer16)
c.513dup (p.Gln172SerfsTer6)
c.873dup (p.Gln292SerfsTer16)
 COSMIC COSMIC
17g.7673539delCA497713744TP53c.990del (p.Gln331ArgfsTer14)
c.594del (p.Gln199ArgfsTer14)
c.711del (p.Gln238ArgfsTer14)
c.969del (p.Gln324ArgfsTer14)
c.990del (p.Gln331ArgfsTer21)
c.782+643del (n.782+643del)
c.990del (p.Gln331ArgfsTer20)
c.990del (p.Gln331ArgfsTer12)
c.594del (p.Gln199ArgfsTer12)
c.594del (p.Leu198=)
c.594del (p.Gln199ArgfsTer20)
c.50del
c.873del (p.Gln292ArgfsTer14)
c.873del (p.Gln292ArgfsTer12)
c.513del (p.Gln172ArgfsTer12)
c.957del (p.Gln320ArgfsTer14)
c.513del (p.Gln172ArgfsTer20)
c.513del (p.Gln172ArgfsTer14)
c.873del (p.Gln292ArgfsTer20)
 ClinVar dbSNP COSMIC
17g.7673538_7673539insTCA497713747TP53c.989_990insA (p.Gln331SerfsTer6)
c.593_594insA (p.Gln199SerfsTer6)
c.710_711insA (p.Gln238SerfsTer6)
c.968_969insA (p.Gln324SerfsTer6)
c.989_990insA (p.Gln331SerfsTer?)
c.782+642_782+643insA (n.782+642_782+643insA)
c.989_990insA (p.Gln331SerfsTer16)
c.989_990insA (p.Gln331SerfsTer5)
c.593_594insA (p.Gln199SerfsTer5)
c.593_594insA (p.Gln199SerfsTer?)
c.593_594insA (p.Gln199SerfsTer16)
c.49_50insA
c.872_873insA (p.Gln292SerfsTer6)
c.872_873insA (p.Gln292SerfsTer5)
c.512_513insA (p.Gln172SerfsTer5)
c.956_957insA (p.Gln320SerfsTer6)
c.512_513insA (p.Gln172SerfsTer16)
c.512_513insA (p.Gln172SerfsTer6)
c.872_873insA (p.Gln292SerfsTer16)
17g.7673539A=CA2245947462TP53c.989T= (p.Leu330=)
c.593T= (p.Leu198=)
c.710T= (p.Leu237=)
c.968T= (p.Leu323=)
c.782+642T= (n.782+642T=)
c.49T=
c.872T= (p.Leu291=)
c.512T= (p.Leu171=)
c.956T= (p.Leu319=)
17g.7673539A>CCA397835702TP53c.989T>G (p.Leu330Arg)
c.593T>G (p.Leu198Arg)
c.710T>G (p.Leu237Arg)
c.968T>G (p.Leu323Arg)
c.782+642T>G (n.782+642T>G)
c.49T>G
c.872T>G (p.Leu291Arg)
c.512T>G (p.Leu171Arg)
c.956T>G (p.Leu319Arg)
 ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC
17g.7673539A>GCA397835704TP53c.989T>C (p.Leu330Pro)
c.593T>C (p.Leu198Pro)
c.710T>C (p.Leu237Pro)
c.968T>C (p.Leu323Pro)
c.782+642T>C (n.782+642T>C)
c.49T>C
c.872T>C (p.Leu291Pro)
c.512T>C (p.Leu171Pro)
c.956T>C (p.Leu319Pro)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC
17g.7673539A>TCA397835707TP53c.989T>A (p.Leu330His)
c.593T>A (p.Leu198His)
c.710T>A (p.Leu237His)
c.968T>A (p.Leu323His)
c.782+642T>A (n.782+642T>A)
c.49T>A
c.872T>A (p.Leu291His)
c.512T>A (p.Leu171His)
c.956T>A (p.Leu319His)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC
17g.7673539_7673540delinsAGCA2245947468TP53c.988_989delinsCT (p.Leu330=)
c.592_593delinsCT (p.Leu198=)
c.709_710delinsCT (p.Leu237=)
c.967_968delinsCT (p.Leu323=)
c.782+641_782+642delinsCT (n.782+641_782+642delinsCT)
c.48_49delinsCT
c.871_872delinsCT (p.Leu291=)
c.511_512delinsCT (p.Leu171=)
c.955_956delinsCT (p.Leu319=)
17g.7673540G>ACA397835712TP53c.988C>T (p.Leu330Phe)
c.592C>T (p.Leu198Phe)
c.709C>T (p.Leu237Phe)
c.967C>T (p.Leu323Phe)
c.782+641C>T (n.782+641C>T)
c.48C>T
c.871C>T (p.Leu291Phe)
c.511C>T (p.Leu171Phe)
c.955C>T (p.Leu319Phe)
 ClinVar dbSNP
17g.7673540G>CCA397835714TP53c.988C>G (p.Leu330Val)
c.592C>G (p.Leu198Val)
c.709C>G (p.Leu237Val)
c.967C>G (p.Leu323Val)
c.782+641C>G (n.782+641C>G)
c.48C>G
c.871C>G (p.Leu291Val)
c.511C>G (p.Leu171Val)
c.955C>G (p.Leu319Val)
 dbSNP
17g.7673540G=CA2245947485TP53c.988C= (p.Leu330=)
c.592C= (p.Leu198=)
c.709C= (p.Leu237=)
c.967C= (p.Leu323=)
c.782+641C= (n.782+641C=)
c.48C=
c.871C= (p.Leu291=)
c.511C= (p.Leu171=)
c.955C= (p.Leu319=)
17g.7673540G>TCA397835718TP53c.988C>A (p.Leu330Ile)
c.592C>A (p.Leu198Ile)
c.709C>A (p.Leu237Ile)
c.967C>A (p.Leu323Ile)
c.782+641C>A (n.782+641C>A)
c.48C>A
c.871C>A (p.Leu291Ile)
c.511C>A (p.Leu171Ile)
c.955C>A (p.Leu319Ile)
 dbSNP
17g.7673542delCA497713751TP53c.988del (p.Leu330PhefsTer15)
c.592del (p.Leu198PhefsTer15)
c.709del (p.Leu237PhefsTer15)
c.967del (p.Leu323PhefsTer15)
c.988del (p.Leu330PhefsTer22)
c.782+641del (n.782+641del)
c.988del (p.Leu330PhefsTer21)
c.988del (p.Leu330PhefsTer13)
c.592del (p.Leu198PhefsTer13)
c.592del (p.Leu198PhefsTer?)
c.592del (p.Leu198PhefsTer21)
c.48del
c.871del (p.Leu291PhefsTer15)
c.871del (p.Leu291PhefsTer13)
c.511del (p.Leu171PhefsTer13)
c.955del (p.Leu319PhefsTer15)
c.511del (p.Leu171PhefsTer21)
c.511del (p.Leu171PhefsTer15)
c.871del (p.Leu291PhefsTer21)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7673541G>ACA497713763TP53c.987C>T (p.Thr329=)
c.591C>T (p.Thr197=)
c.708C>T (p.Thr236=)
c.966C>T (p.Thr322=)
c.782+640C>T (n.782+640C>T)
c.47C>T
c.870C>T (p.Thr290=)
c.510C>T (p.Thr170=)
c.954C>T (p.Thr318=)
 ClinVar dbSNP gnomAD v4 COSMIC
17g.7673541G>CCA497713766TP53c.987C>G (p.Thr329=)
c.591C>G (p.Thr197=)
c.708C>G (p.Thr236=)
c.966C>G (p.Thr322=)
c.782+640C>G (n.782+640C>G)
c.47C>G
c.870C>G (p.Thr290=)
c.510C>G (p.Thr170=)
c.954C>G (p.Thr318=)
 dbSNP
17g.7673541G>TCA497713769TP53c.987C>A (p.Thr329=)
c.591C>A (p.Thr197=)
c.708C>A (p.Thr236=)
c.966C>A (p.Thr322=)
c.782+640C>A (n.782+640C>A)
c.47C>A
c.870C>A (p.Thr290=)
c.510C>A (p.Thr170=)
c.954C>A (p.Thr318=)
 ClinVar dbSNP COSMIC
17g.7673541_7673542delinsAACA645587346TP53c.986_987delinsTT (p.Thr329Ile)
c.590_591delinsTT (p.Thr197Ile)
c.707_708delinsTT (p.Thr236Ile)
c.965_966delinsTT (p.Thr322Ile)
c.782+639_782+640delinsTT (n.782+639_782+640delinsTT)
c.46_47delinsTT
c.869_870delinsTT (p.Thr290Ile)
c.509_510delinsTT (p.Thr170Ile)
c.953_954delinsTT (p.Thr318Ile)
 COSMIC COSMIC
17g.7673541_7673560delinsGGTGAAATATTCTCCATCCACA2245947495TP53c.968_987delinsTGGATGGAGAATATTTCACC (p.Leu323=)
c.572_591delinsTGGATGGAGAATATTTCACC (p.Leu191=)
c.689_708delinsTGGATGGAGAATATTTCACC (p.Leu230=)
c.947_966delinsTGGATGGAGAATATTTCACC (p.Leu316=)
c.782+621_782+640delinsTGGATGGAGAATATTTCACC (n.782+621_782+640delinsTGGATGGAGAATATTTCACC)
c.28_47delinsTGGATGGAGAATATTTCACC
c.851_870delinsTGGATGGAGAATATTTCACC (p.Leu284=)
c.491_510delinsTGGATGGAGAATATTTCACC (p.Leu164=)
c.935_954delinsTGGATGGAGAATATTTCACC (p.Leu312=)
17g.7673542G>ACA287486504TP53c.986C>T (p.Thr329Ile)
c.590C>T (p.Thr197Ile)
c.707C>T (p.Thr236Ile)
c.965C>T (p.Thr322Ile)
c.782+639C>T (n.782+639C>T)
c.46C>T
c.869C>T (p.Thr290Ile)
c.509C>T (p.Thr170Ile)
c.953C>T (p.Thr318Ile)
 ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC
17g.7673542G>CCA397835725TP53c.986C>G (p.Thr329Ser)
c.590C>G (p.Thr197Ser)
c.707C>G (p.Thr236Ser)
c.965C>G (p.Thr322Ser)
c.782+639C>G (n.782+639C>G)
c.46C>G
c.869C>G (p.Thr290Ser)
c.509C>G (p.Thr170Ser)
c.953C>G (p.Thr318Ser)
 dbSNP
17g.7673542G=CA2245947503TP53c.986C= (p.Thr329=)
c.590C= (p.Thr197=)
c.707C= (p.Thr236=)
c.965C= (p.Thr322=)
c.782+639C= (n.782+639C=)
c.46C=
c.869C= (p.Thr290=)
c.509C= (p.Thr170=)
c.953C= (p.Thr318=)
17g.7673542G>TCA397835730TP53c.986C>A (p.Thr329Asn)
c.590C>A (p.Thr197Asn)
c.707C>A (p.Thr236Asn)
c.965C>A (p.Thr322Asn)
c.782+639C>A (n.782+639C>A)
c.46C>A
c.869C>A (p.Thr290Asn)
c.509C>A (p.Thr170Asn)
c.953C>A (p.Thr318Asn)
 dbSNP
17g.7673545_7673563delCA913188778TP53c.968_986del (p.Leu323ProfsTer16)
c.572_590del (p.Leu191ProfsTer16)
c.689_707del (p.Leu230ProfsTer16)
c.947_965del (p.Leu316ProfsTer16)
c.968_986del (p.Leu323ProfsTer23)
c.782+621_782+639del (n.782+621_782+639del)
c.968_986del (p.Leu323ProfsTer22)
c.968_986del (p.Leu323ProfsTer14)
c.572_590del (p.Leu191ProfsTer14)
c.572_590del (p.Leu191ProfsTer?)
c.572_590del (p.Leu191ProfsTer22)
c.28_46del
c.851_869del (p.Leu284ProfsTer16)
c.851_869del (p.Leu284ProfsTer14)
c.491_509del (p.Leu164ProfsTer14)
c.935_953del (p.Leu312ProfsTer16)
c.491_509del (p.Leu164ProfsTer22)
c.491_509del (p.Leu164ProfsTer16)
c.851_869del (p.Leu284ProfsTer22)
 ClinVar dbSNP
17g.7673543T>ACA397835737TP53c.985A>T (p.Thr329Ser)
c.589A>T (p.Thr197Ser)
c.706A>T (p.Thr236Ser)
c.964A>T (p.Thr322Ser)
c.782+638A>T (n.782+638A>T)
c.45A>T
c.868A>T (p.Thr290Ser)
c.508A>T (p.Thr170Ser)
c.952A>T (p.Thr318Ser)
 dbSNP
17g.7673543T>CCA397835735TP53c.985A>G (p.Thr329Ala)
c.589A>G (p.Thr197Ala)
c.706A>G (p.Thr236Ala)
c.964A>G (p.Thr322Ala)
c.782+638A>G (n.782+638A>G)
c.45A>G
c.868A>G (p.Thr290Ala)
c.508A>G (p.Thr170Ala)
c.952A>G (p.Thr318Ala)
 ClinVar dbSNP gnomAD v4
17g.7673543T>GCA397835733TP53c.985A>C (p.Thr329Pro)
c.589A>C (p.Thr197Pro)
c.706A>C (p.Thr236Pro)
c.964A>C (p.Thr322Pro)
c.782+638A>C (n.782+638A>C)
c.45A>C
c.868A>C (p.Thr290Pro)
c.508A>C (p.Thr170Pro)
c.952A>C (p.Thr318Pro)
 dbSNP
17g.7673543T=CA2245947510TP53c.985A= (p.Thr329=)
c.589A= (p.Thr197=)
c.706A= (p.Thr236=)
c.964A= (p.Thr322=)
c.782+638A= (n.782+638A=)
c.45A=
c.868A= (p.Thr290=)
c.508A= (p.Thr170=)
c.952A= (p.Thr318=)
17g.7673544G>ACA16608656TP53c.984C>T (p.Phe328=)
c.588C>T (p.Phe196=)
c.705C>T (p.Phe235=)
c.963C>T (p.Phe321=)
c.782+637C>T (n.782+637C>T)
c.44C>T
c.867C>T (p.Phe289=)
c.507C>T (p.Phe169=)
c.951C>T (p.Phe317=)
 ClinVar dbSNP COSMIC
17g.7673544G>CCA397835743TP53c.984C>G (p.Phe328Leu)
c.588C>G (p.Phe196Leu)
c.705C>G (p.Phe235Leu)
c.963C>G (p.Phe321Leu)
c.782+637C>G (n.782+637C>G)
c.44C>G
c.867C>G (p.Phe289Leu)
c.507C>G (p.Phe169Leu)
c.951C>G (p.Phe317Leu)
 dbSNP
17g.7673544G=CA2245947520TP53c.984C= (p.Phe328=)
c.588C= (p.Phe196=)
c.705C= (p.Phe235=)
c.963C= (p.Phe321=)
c.782+637C= (n.782+637C=)
c.44C=
c.867C= (p.Phe289=)
c.507C= (p.Phe169=)
c.951C= (p.Phe317=)
17g.7673544G>TCA397835745TP53c.984C>A (p.Phe328Leu)
c.588C>A (p.Phe196Leu)
c.705C>A (p.Phe235Leu)
c.963C>A (p.Phe321Leu)
c.782+637C>A (n.782+637C>A)
c.44C>A
c.867C>A (p.Phe289Leu)
c.507C>A (p.Phe169Leu)
c.951C>A (p.Phe317Leu)
 dbSNP
17g.7673544_7673545insTCA645587347TP53c.983_984insA (p.Phe328LeufsTer9)
c.587_588insA (p.Phe196LeufsTer9)
c.704_705insA (p.Phe235LeufsTer9)
c.962_963insA (p.Phe321LeufsTer9)
c.983_984insA (p.Phe328LeufsTer?)
c.782+636_782+637insA (n.782+636_782+637insA)
c.983_984insA (p.Phe328LeufsTer19)
c.983_984insA (p.Phe328LeufsTer8)
c.587_588insA (p.Phe196LeufsTer8)
c.587_588insA (p.Phe196LeufsTer?)
c.587_588insA (p.Phe196LeufsTer19)
c.43_44insA
c.866_867insA (p.Phe289LeufsTer9)
c.866_867insA (p.Phe289LeufsTer8)
c.506_507insA (p.Phe169LeufsTer8)
c.950_951insA (p.Phe317LeufsTer9)
c.506_507insA (p.Phe169LeufsTer19)
c.506_507insA (p.Phe169LeufsTer9)
c.866_867insA (p.Phe289LeufsTer19)
 COSMIC
17g.7673545A=CA2245947539TP53c.983T= (p.Phe328=)
c.587T= (p.Phe196=)
c.704T= (p.Phe235=)
c.962T= (p.Phe321=)
c.782+636T= (n.782+636T=)
c.43T=
c.866T= (p.Phe289=)
c.506T= (p.Phe169=)
c.950T= (p.Phe317=)
17g.7673545A>CCA397835749TP53c.983T>G (p.Phe328Cys)
c.587T>G (p.Phe196Cys)
c.704T>G (p.Phe235Cys)
c.962T>G (p.Phe321Cys)
c.782+636T>G (n.782+636T>G)
c.43T>G
c.866T>G (p.Phe289Cys)
c.506T>G (p.Phe169Cys)
c.950T>G (p.Phe317Cys)
17g.7673545A>GCA397835751TP53c.983T>C (p.Phe328Ser)
c.587T>C (p.Phe196Ser)
c.704T>C (p.Phe235Ser)
c.962T>C (p.Phe321Ser)
c.782+636T>C (n.782+636T>C)
c.43T>C
c.866T>C (p.Phe289Ser)
c.506T>C (p.Phe169Ser)
c.950T>C (p.Phe317Ser)
 ClinVar dbSNP COSMIC
17g.7673545A>TCA397835754TP53c.983T>A (p.Phe328Tyr)
c.587T>A (p.Phe196Tyr)
c.704T>A (p.Phe235Tyr)
c.962T>A (p.Phe321Tyr)
c.782+636T>A (n.782+636T>A)
c.43T>A
c.866T>A (p.Phe289Tyr)
c.506T>A (p.Phe169Tyr)
c.950T>A (p.Phe317Tyr)
 dbSNP
17g.7673547dupCA10603410TP53c.983dup (p.Thr329HisfsTer8)
c.587dup (p.Thr197HisfsTer8)
c.704dup (p.Thr236HisfsTer8)
c.962dup (p.Thr322HisfsTer8)
c.983dup (p.Thr329HisfsTer?)
c.782+636dup (n.782+636dup)
c.983dup (p.Thr329HisfsTer18)
c.983dup (p.Thr329HisfsTer7)
c.587dup (p.Thr197HisfsTer7)
c.587dup (p.Thr197HisfsTer?)
c.587dup (p.Thr197HisfsTer18)
c.43dup
c.866dup (p.Thr290HisfsTer8)
c.866dup (p.Thr290HisfsTer7)
c.506dup (p.Thr170HisfsTer7)
c.950dup (p.Thr318HisfsTer8)
c.506dup (p.Thr170HisfsTer18)
c.506dup (p.Thr170HisfsTer8)
c.866dup (p.Thr290HisfsTer18)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC
17g.7673546_7673547dupCA2573154629TP53c.982_983dup (p.Thr329SerfsTer17)
c.586_587dup (p.Thr197SerfsTer17)
c.703_704dup (p.Thr236SerfsTer17)
c.961_962dup (p.Thr322SerfsTer17)
c.982_983dup (p.Thr329SerfsTer24)
c.782+635_782+636dup (n.782+635_782+636dup)
c.982_983dup (p.Thr329SerfsTer23)
c.982_983dup (p.Thr329SerfsTer15)
c.586_587dup (p.Thr197SerfsTer15)
c.586_587dup (p.Thr197SerfsTer?)
c.586_587dup (p.Thr197SerfsTer23)
c.42_43dup
c.865_866dup (p.Thr290SerfsTer17)
c.865_866dup (p.Thr290SerfsTer15)
c.505_506dup (p.Thr170SerfsTer15)
c.949_950dup (p.Thr318SerfsTer17)
c.505_506dup (p.Thr170SerfsTer23)
c.505_506dup (p.Thr170SerfsTer17)
c.865_866dup (p.Thr290SerfsTer23)
 ClinVar dbSNP
17g.7673547delCA497713799TP53c.983del (p.Phe328SerfsTer17)
c.587del (p.Phe196SerfsTer17)
c.704del (p.Phe235SerfsTer17)
c.962del (p.Phe321SerfsTer17)
c.983del (p.Phe328SerfsTer24)
c.782+636del (n.782+636del)
c.983del (p.Phe328SerfsTer23)
c.983del (p.Phe328SerfsTer15)
c.587del (p.Phe196SerfsTer15)
c.587del (p.Phe196SerfsTer?)
c.587del (p.Phe196SerfsTer23)
c.43del
c.866del (p.Phe289SerfsTer17)
c.866del (p.Phe289SerfsTer15)
c.506del (p.Phe169SerfsTer15)
c.950del (p.Phe317SerfsTer17)
c.506del (p.Phe169SerfsTer23)
c.506del (p.Phe169SerfsTer17)
c.866del (p.Phe289SerfsTer23)
 COSMIC COSMIC COSMIC COSMIC
17g.7673545_7673546insTCA497713806TP53c.982_983insA (p.Phe328TyrfsTer9)
c.586_587insA (p.Phe196TyrfsTer9)
c.703_704insA (p.Phe235TyrfsTer9)
c.961_962insA (p.Phe321TyrfsTer9)
c.982_983insA (p.Phe328TyrfsTer?)
c.782+635_782+636insA (n.782+635_782+636insA)
c.982_983insA (p.Phe328TyrfsTer19)
c.982_983insA (p.Phe328TyrfsTer8)
c.586_587insA (p.Phe196TyrfsTer8)
c.586_587insA (p.Phe196TyrfsTer?)
c.586_587insA (p.Phe196TyrfsTer19)
c.42_43insA
c.865_866insA (p.Phe289TyrfsTer9)
c.865_866insA (p.Phe289TyrfsTer8)
c.505_506insA (p.Phe169TyrfsTer8)
c.949_950insA (p.Phe317TyrfsTer9)
c.505_506insA (p.Phe169TyrfsTer19)
c.505_506insA (p.Phe169TyrfsTer9)
c.865_866insA (p.Phe289TyrfsTer19)
17g.7673546A>CCA397835758TP53c.982T>G (p.Phe328Val)
c.586T>G (p.Phe196Val)
c.703T>G (p.Phe235Val)
c.961T>G (p.Phe321Val)
c.782+635T>G (n.782+635T>G)
c.42T>G
c.865T>G (p.Phe289Val)
c.505T>G (p.Phe169Val)
c.949T>G (p.Phe317Val)
 COSMIC
17g.7673546A>GCA397835759TP53c.982T>C (p.Phe328Leu)
c.586T>C (p.Phe196Leu)
c.703T>C (p.Phe235Leu)
c.961T>C (p.Phe321Leu)
c.782+635T>C (n.782+635T>C)
c.42T>C
c.865T>C (p.Phe289Leu)
c.505T>C (p.Phe169Leu)
c.949T>C (p.Phe317Leu)
17g.7673546A>TCA397835761TP53c.982T>A (p.Phe328Ile)
c.586T>A (p.Phe196Ile)
c.703T>A (p.Phe235Ile)
c.961T>A (p.Phe321Ile)
c.782+635T>A (n.782+635T>A)
c.42T>A
c.865T>A (p.Phe289Ile)
c.505T>A (p.Phe169Ile)
c.949T>A (p.Phe317Ile)
 dbSNP
17g.7673546_7673548delinsAATCA2245947548TP53c.980_982delinsATT (p.Tyr327=)
c.584_586delinsATT (p.Tyr195=)
c.701_703delinsATT (p.Tyr234=)
c.959_961delinsATT (p.Tyr320=)
c.782+633_782+635delinsATT (n.782+633_782+635delinsATT)
c.40_42delinsATT
c.863_865delinsATT (p.Tyr288=)
c.503_505delinsATT (p.Tyr168=)
c.947_949delinsATT (p.Tyr316=)
17g.7673547A=CA2245947559TP53c.981T= (p.Tyr327=)
c.585T= (p.Tyr195=)
c.702T= (p.Tyr234=)
c.960T= (p.Tyr320=)
c.782+634T= (n.782+634T=)
c.41T=
c.864T= (p.Tyr288=)
c.504T= (p.Tyr168=)
c.948T= (p.Tyr316=)
17g.7673547A>CCA10584585TP53c.981T>G (p.Tyr327Ter)
c.585T>G (p.Tyr195Ter)
c.702T>G (p.Tyr234Ter)
c.960T>G (p.Tyr320Ter)
c.782+634T>G (n.782+634T>G)
c.41T>G
c.864T>G (p.Tyr288Ter)
c.504T>G (p.Tyr168Ter)
c.948T>G (p.Tyr316Ter)
 ClinVar dbSNP COSMIC COSMIC
17g.7673547A>GCA497713821TP53c.981T>C (p.Tyr327=)
c.585T>C (p.Tyr195=)
c.702T>C (p.Tyr234=)
c.960T>C (p.Tyr320=)
c.782+634T>C (n.782+634T>C)
c.41T>C
c.864T>C (p.Tyr288=)
c.504T>C (p.Tyr168=)
c.948T>C (p.Tyr316=)
 dbSNP
17g.7673547A>TCA397835766TP53c.981T>A (p.Tyr327Ter)
c.585T>A (p.Tyr195Ter)
c.702T>A (p.Tyr234Ter)
c.960T>A (p.Tyr320Ter)
c.782+634T>A (n.782+634T>A)
c.41T>A
c.864T>A (p.Tyr288Ter)
c.504T>A (p.Tyr168Ter)
c.948T>A (p.Tyr316Ter)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC
17g.7673549_7673550delCA645587348TP53c.980_981del (p.Tyr327PhefsTer9)
c.584_585del (p.Tyr195PhefsTer9)
c.701_702del (p.Tyr234PhefsTer9)
c.959_960del (p.Tyr320PhefsTer9)
c.980_981del (p.Tyr327PhefsTer?)
c.782+633_782+634del (n.782+633_782+634del)
c.980_981del (p.Tyr327PhefsTer19)
c.980_981del (p.Tyr327PhefsTer8)
c.584_585del (p.Tyr195PhefsTer8)
c.584_585del (p.Tyr195PhefsTer?)
c.584_585del (p.Tyr195PhefsTer19)
c.40_41del
c.863_864del (p.Tyr288PhefsTer9)
c.863_864del (p.Tyr288PhefsTer8)
c.503_504del (p.Tyr168PhefsTer8)
c.947_948del (p.Tyr316PhefsTer9)
c.503_504del (p.Tyr168PhefsTer19)
c.503_504del (p.Tyr168PhefsTer9)
c.863_864del (p.Tyr288PhefsTer19)
 ClinVar dbSNP COSMIC
17g.7673548T>ACA397835768TP53c.980A>T (p.Tyr327Phe)
c.584A>T (p.Tyr195Phe)
c.701A>T (p.Tyr234Phe)
c.959A>T (p.Tyr320Phe)
c.782+633A>T (n.782+633A>T)
c.40A>T
c.863A>T (p.Tyr288Phe)
c.503A>T (p.Tyr168Phe)
c.947A>T (p.Tyr316Phe)
 dbSNP
17g.7673548T>CCA397835771TP53c.980A>G (p.Tyr327Cys)
c.584A>G (p.Tyr195Cys)
c.701A>G (p.Tyr234Cys)
c.959A>G (p.Tyr320Cys)
c.782+633A>G (n.782+633A>G)
c.40A>G
c.863A>G (p.Tyr288Cys)
c.503A>G (p.Tyr168Cys)
c.947A>G (p.Tyr316Cys)
 ClinVar dbSNP
17g.7673548T>GCA397835778TP53c.980A>C (p.Tyr327Ser)
c.584A>C (p.Tyr195Ser)
c.701A>C (p.Tyr234Ser)
c.959A>C (p.Tyr320Ser)
c.782+633A>C (n.782+633A>C)
c.40A>C
c.863A>C (p.Tyr288Ser)
c.503A>C (p.Tyr168Ser)
c.947A>C (p.Tyr316Ser)
 dbSNP
17g.7673548_7673549insTTCA645587349TP53c.980_981insAA (p.Tyr327Ter)
c.584_585insAA (p.Tyr195Ter)
c.701_702insAA (p.Tyr234Ter)
c.959_960insAA (p.Tyr320Ter)
c.782+633_782+634insAA (n.782+633_782+634insAA)
c.40_41insAA
c.863_864insAA (p.Tyr288Ter)
c.503_504insAA (p.Tyr168Ter)
c.947_948insAA (p.Tyr316Ter)
 COSMIC
17g.7673549A>CCA397835781TP53c.979T>G (p.Tyr327Asp)
c.583T>G (p.Tyr195Asp)
c.700T>G (p.Tyr234Asp)
c.958T>G (p.Tyr320Asp)
c.782+632T>G (n.782+632T>G)
c.39T>G
c.862T>G (p.Tyr288Asp)
c.502T>G (p.Tyr168Asp)
c.946T>G (p.Tyr316Asp)
 dbSNP COSMIC
17g.7673549A>GCA397835786TP53c.979T>C (p.Tyr327His)
c.583T>C (p.Tyr195His)
c.700T>C (p.Tyr234His)
c.958T>C (p.Tyr320His)
c.782+632T>C (n.782+632T>C)
c.39T>C
c.862T>C (p.Tyr288His)
c.502T>C (p.Tyr168His)
c.946T>C (p.Tyr316His)
17g.7673549A>TCA397835783TP53c.979T>A (p.Tyr327Asn)
c.583T>A (p.Tyr195Asn)
c.700T>A (p.Tyr234Asn)
c.958T>A (p.Tyr320Asn)
c.782+632T>A (n.782+632T>A)
c.39T>A
c.862T>A (p.Tyr288Asn)
c.502T>A (p.Tyr168Asn)
c.946T>A (p.Tyr316Asn)
 dbSNP
17g.7673550T>ACA287486513TP53c.978A>T (p.Glu326Asp)
c.582A>T (p.Glu194Asp)
c.699A>T (p.Glu233Asp)
c.957A>T (p.Glu319Asp)
c.782+631A>T (n.782+631A>T)
c.38A>T
c.861A>T (p.Glu287Asp)
c.501A>T (p.Glu167Asp)
c.945A>T (p.Glu315Asp)
 ClinVar dbSNP gnomAD v4
17g.7673550T>CCA497713840TP53c.978A>G (p.Glu326=)
c.582A>G (p.Glu194=)
c.699A>G (p.Glu233=)
c.957A>G (p.Glu319=)
c.782+631A>G (n.782+631A>G)
c.38A>G
c.861A>G (p.Glu287=)
c.501A>G (p.Glu167=)
c.945A>G (p.Glu315=)
 ClinVar dbSNP
17g.7673550T>GCA397835791TP53c.978A>C (p.Glu326Asp)
c.582A>C (p.Glu194Asp)
c.699A>C (p.Glu233Asp)
c.957A>C (p.Glu319Asp)
c.782+631A>C (n.782+631A>C)
c.38A>C
c.861A>C (p.Glu287Asp)
c.501A>C (p.Glu167Asp)
c.945A>C (p.Glu315Asp)
 dbSNP gnomAD v2 gnomAD v4
17g.7673550T=CA2245947569TP53c.978A= (p.Glu326=)
c.582A= (p.Glu194=)
c.699A= (p.Glu233=)
c.957A= (p.Glu319=)
c.782+631A= (n.782+631A=)
c.38A=
c.861A= (p.Glu287=)
c.501A= (p.Glu167=)
c.945A= (p.Glu315=)
17g.7673551_7673553delCA2635874179TP53c.976_978del (p.Glu326del)
c.580_582del (p.Glu194del)
c.697_699del (p.Glu233del)
c.955_957del (p.Glu319del)
c.782+629_782+631del (n.782+629_782+631del)
c.36_38del
c.859_861del (p.Glu287del)
c.499_501del (p.Glu167del)
c.943_945del (p.Glu315del)
 gnomAD v4
17g.7673551T>ACA397835794TP53c.977A>T (p.Glu326Val)
c.581A>T (p.Glu194Val)
c.698A>T (p.Glu233Val)
c.956A>T (p.Glu319Val)
c.782+630A>T (n.782+630A>T)
c.37A>T
c.860A>T (p.Glu287Val)
c.500A>T (p.Glu167Val)
c.944A>T (p.Glu315Val)
 ClinVar dbSNP
17g.7673551T>CCA397835798TP53c.977A>G (p.Glu326Gly)
c.581A>G (p.Glu194Gly)
c.698A>G (p.Glu233Gly)
c.956A>G (p.Glu319Gly)
c.782+630A>G (n.782+630A>G)
c.37A>G
c.860A>G (p.Glu287Gly)
c.500A>G (p.Glu167Gly)
c.944A>G (p.Glu315Gly)
 dbSNP
17g.7673551T>GCA397835801TP53c.977A>C (p.Glu326Ala)
c.581A>C (p.Glu194Ala)
c.698A>C (p.Glu233Ala)
c.956A>C (p.Glu319Ala)
c.782+630A>C (n.782+630A>C)
c.37A>C
c.860A>C (p.Glu287Ala)
c.500A>C (p.Glu167Ala)
c.944A>C (p.Glu315Ala)
 dbSNP
17g.7673553_7673554dupCA915949514TP53c.976_977dup (p.Tyr327AsnfsTer19)
c.580_581dup (p.Tyr195AsnfsTer19)
c.697_698dup (p.Tyr234AsnfsTer19)
c.955_956dup (p.Tyr320AsnfsTer19)
c.976_977dup (p.Tyr327AsnfsTer26)
c.782+629_782+630dup (n.782+629_782+630dup)
c.976_977dup (p.Tyr327AsnfsTer25)
c.976_977dup (p.Tyr327AsnfsTer17)
c.580_581dup (p.Tyr195AsnfsTer17)
c.580_581dup (p.Tyr195AsnfsTer?)
c.580_581dup (p.Tyr195AsnfsTer25)
c.36_37dup
c.859_860dup (p.Tyr288AsnfsTer19)
c.859_860dup (p.Tyr288AsnfsTer17)
c.499_500dup (p.Tyr168AsnfsTer17)
c.943_944dup (p.Tyr316AsnfsTer19)
c.499_500dup (p.Tyr168AsnfsTer25)
c.499_500dup (p.Tyr168AsnfsTer19)
c.859_860dup (p.Tyr288AsnfsTer25)
 ClinVar dbSNP
17g.7673552C>ACA10580908TP53c.976G>T (p.Glu326Ter)
c.580G>T (p.Glu194Ter)
c.697G>T (p.Glu233Ter)
c.955G>T (p.Glu319Ter)
c.782+629G>T (n.782+629G>T)
c.36G>T
c.859G>T (p.Glu287Ter)
c.499G>T (p.Glu167Ter)
c.943G>T (p.Glu315Ter)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC
17g.7673552C=CA2245947579TP53c.976G= (p.Glu326=)
c.580G= (p.Glu194=)
c.697G= (p.Glu233=)
c.955G= (p.Glu319=)
c.782+629G= (n.782+629G=)
c.36G=
c.859G= (p.Glu287=)
c.499G= (p.Glu167=)
c.943G= (p.Glu315=)
17g.7673552C>GCA397835806TP53c.976G>C (p.Glu326Gln)
c.580G>C (p.Glu194Gln)
c.697G>C (p.Glu233Gln)
c.955G>C (p.Glu319Gln)
c.782+629G>C (n.782+629G>C)
c.36G>C
c.859G>C (p.Glu287Gln)
c.499G>C (p.Glu167Gln)
c.943G>C (p.Glu315Gln)
 dbSNP
17g.7673552C>TCA397835809TP53c.976G>A (p.Glu326Lys)
c.580G>A (p.Glu194Lys)
c.697G>A (p.Glu233Lys)
c.955G>A (p.Glu319Lys)
c.782+629G>A (n.782+629G>A)
c.36G>A
c.859G>A (p.Glu287Lys)
c.499G>A (p.Glu167Lys)
c.943G>A (p.Glu315Lys)
 dbSNP COSMIC COSMIC COSMIC COSMIC
17g.7673553T>ACA497713884TP53c.975A>T (p.Gly325=)
c.579A>T (p.Gly193=)
c.696A>T (p.Gly232=)
c.954A>T (p.Gly318=)
c.782+628A>T (n.782+628A>T)
c.35A>T
c.858A>T (p.Gly286=)
c.498A>T (p.Gly166=)
c.942A>T (p.Gly314=)
17g.7673553T>CCA497713893TP53c.975A>G (p.Gly325=)
c.579A>G (p.Gly193=)
c.696A>G (p.Gly232=)
c.954A>G (p.Gly318=)
c.782+628A>G (n.782+628A>G)
c.35A>G
c.858A>G (p.Gly286=)
c.498A>G (p.Gly166=)
c.942A>G (p.Gly314=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
17g.7673553T>GCA497713894TP53c.975A>C (p.Gly325=)
c.579A>C (p.Gly193=)
c.696A>C (p.Gly232=)
c.954A>C (p.Gly318=)
c.782+628A>C (n.782+628A>C)
c.35A>C
c.858A>C (p.Gly286=)
c.498A>C (p.Gly166=)
c.942A>C (p.Gly314=)
17g.7673553T=CA2245947582TP53c.975A= (p.Gly325=)
c.579A= (p.Gly193=)
c.696A= (p.Gly232=)
c.954A= (p.Gly318=)
c.782+628A= (n.782+628A=)
c.35A=
c.858A= (p.Gly286=)
c.498A= (p.Gly166=)
c.942A= (p.Gly314=)
17g.7673554C>ACA000516TP53c.974G>T (p.Gly325Val)
c.578G>T (p.Gly193Val)
c.695G>T (p.Gly232Val)
c.953G>T (p.Gly318Val)
c.782+627G>T (n.782+627G>T)
c.34G>T
c.857G>T (p.Gly286Val)
c.497G>T (p.Gly166Val)
c.941G>T (p.Gly314Val)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
17g.7673554C=CA2245947593TP53c.974G= (p.Gly325=)
c.578G= (p.Gly193=)
c.695G= (p.Gly232=)
c.953G= (p.Gly318=)
c.782+627G= (n.782+627G=)
c.34G=
c.857G= (p.Gly286=)
c.497G= (p.Gly166=)
c.941G= (p.Gly314=)
17g.7673554C>GCA397835813TP53c.974G>C (p.Gly325Ala)
c.578G>C (p.Gly193Ala)
c.695G>C (p.Gly232Ala)
c.953G>C (p.Gly318Ala)
c.782+627G>C (n.782+627G>C)
c.34G>C
c.857G>C (p.Gly286Ala)
c.497G>C (p.Gly166Ala)
c.941G>C (p.Gly314Ala)
 dbSNP COSMIC
17g.7673554C>TCA397835817TP53c.974G>A (p.Gly325Glu)
c.578G>A (p.Gly193Glu)
c.695G>A (p.Gly232Glu)
c.953G>A (p.Gly318Glu)
c.782+627G>A (n.782+627G>A)
c.34G>A
c.857G>A (p.Gly286Glu)
c.497G>A (p.Gly166Glu)
c.941G>A (p.Gly314Glu)
 ClinVar dbSNP COSMIC
17g.7673555C>ACA335679TP53c.973G>T (p.Gly325Ter)
c.577G>T (p.Gly193Ter)
c.694G>T (p.Gly232Ter)
c.952G>T (p.Gly318Ter)
c.782+626G>T (n.782+626G>T)
c.33G>T
c.856G>T (p.Gly286Ter)
c.496G>T (p.Gly166Ter)
c.940G>T (p.Gly314Ter)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC
17g.7673555C=CA2245947602TP53c.973G= (p.Gly325=)
c.577G= (p.Gly193=)
c.694G= (p.Gly232=)
c.952G= (p.Gly318=)
c.782+626G= (n.782+626G=)
c.33G=
c.856G= (p.Gly286=)
c.496G= (p.Gly166=)
c.940G= (p.Gly314=)
17g.7673555C>GCA397835825TP53c.973G>C (p.Gly325Arg)
c.577G>C (p.Gly193Arg)
c.694G>C (p.Gly232Arg)
c.952G>C (p.Gly318Arg)
c.782+626G>C (n.782+626G>C)
c.33G>C
c.856G>C (p.Gly286Arg)
c.496G>C (p.Gly166Arg)
c.940G>C (p.Gly314Arg)
 dbSNP
17g.7673555C>TCA397835820TP53c.973G>A (p.Gly325Arg)
c.577G>A (p.Gly193Arg)
c.694G>A (p.Gly232Arg)
c.952G>A (p.Gly318Arg)
c.782+626G>A (n.782+626G>A)
c.33G>A
c.856G>A (p.Gly286Arg)
c.496G>A (p.Gly166Arg)
c.940G>A (p.Gly314Arg)
 ClinVar dbSNP
17g.7673556A>CCA397835833TP53c.972T>G (p.Asp324Glu)
c.576T>G (p.Asp192Glu)
c.693T>G (p.Asp231Glu)
c.951T>G (p.Asp317Glu)
c.782+625T>G (n.782+625T>G)
c.32T>G
c.855T>G (p.Asp285Glu)
c.495T>G (p.Asp165Glu)
c.939T>G (p.Asp313Glu)
 dbSNP COSMIC
17g.7673556A>GCA497713910TP53c.972T>C (p.Asp324=)
c.576T>C (p.Asp192=)
c.693T>C (p.Asp231=)
c.951T>C (p.Asp317=)
c.782+625T>C (n.782+625T>C)
c.32T>C
c.855T>C (p.Asp285=)
c.495T>C (p.Asp165=)
c.939T>C (p.Asp313=)
 dbSNP COSMIC
17g.7673556A>TCA397835829TP53c.972T>A (p.Asp324Glu)
c.576T>A (p.Asp192Glu)
c.693T>A (p.Asp231Glu)
c.951T>A (p.Asp317Glu)
c.782+625T>A (n.782+625T>A)
c.32T>A
c.855T>A (p.Asp285Glu)
c.495T>A (p.Asp165Glu)
c.939T>A (p.Asp313Glu)
 ClinVar dbSNP COSMIC
17g.7673557delCA497713915TP53c.971del (p.Asp324ValfsTer21)
c.575del (p.Asp192ValfsTer21)
c.692del (p.Asp231ValfsTer21)
c.950del (p.Asp317ValfsTer21)
c.971del (p.Asp324ValfsTer28)
c.782+624del (n.782+624del)
c.971del (p.Asp324ValfsTer27)
c.971del (p.Asp324ValfsTer19)
c.575del (p.Asp192ValfsTer19)
c.575del (p.Asp192ValfsTer?)
c.575del (p.Asp192ValfsTer27)
c.31del
c.854del (p.Asp285ValfsTer21)
c.854del (p.Asp285ValfsTer19)
c.494del (p.Asp165ValfsTer19)
c.938del (p.Asp313ValfsTer21)
c.494del (p.Asp165ValfsTer27)
c.494del (p.Asp165ValfsTer21)
c.854del (p.Asp285ValfsTer27)
 COSMIC
17g.7673557T>ACA397835834TP53c.971A>T (p.Asp324Val)
c.575A>T (p.Asp192Val)
c.692A>T (p.Asp231Val)
c.950A>T (p.Asp317Val)
c.782+624A>T (n.782+624A>T)
c.31A>T
c.854A>T (p.Asp285Val)
c.494A>T (p.Asp165Val)
c.938A>T (p.Asp313Val)
17g.7673557T>CCA397835837TP53c.971A>G (p.Asp324Gly)
c.575A>G (p.Asp192Gly)
c.692A>G (p.Asp231Gly)
c.950A>G (p.Asp317Gly)
c.782+624A>G (n.782+624A>G)
c.31A>G
c.854A>G (p.Asp285Gly)
c.494A>G (p.Asp165Gly)
c.938A>G (p.Asp313Gly)
 dbSNP gnomAD v2 gnomAD v4
17g.7673557T>GCA397835840TP53c.971A>C (p.Asp324Ala)
c.575A>C (p.Asp192Ala)
c.692A>C (p.Asp231Ala)
c.950A>C (p.Asp317Ala)
c.782+624A>C (n.782+624A>C)
c.31A>C
c.854A>C (p.Asp285Ala)
c.494A>C (p.Asp165Ala)
c.938A>C (p.Asp313Ala)
 dbSNP
17g.7673557T=CA2245947614TP53c.971A= (p.Asp324=)
c.575A= (p.Asp192=)
c.692A= (p.Asp231=)
c.950A= (p.Asp317=)
c.782+624A= (n.782+624A=)
c.31A=
c.854A= (p.Asp285=)
c.494A= (p.Asp165=)
c.938A= (p.Asp313=)
17g.7673557_7673558delinsCTCA645587350TP53c.970_971delinsAG (p.Asp324Ser)
c.574_575delinsAG (p.Asp192Ser)
c.691_692delinsAG (p.Asp231Ser)
c.949_950delinsAG (p.Asp317Ser)
c.782+623_782+624delinsAG (n.782+623_782+624delinsAG)
c.30_31delinsAG
c.853_854delinsAG (p.Asp285Ser)
c.493_494delinsAG (p.Asp165Ser)
c.937_938delinsAG (p.Asp313Ser)
 COSMIC
17g.7673557_7673558delinsTCCA2245947611TP53c.970_971delinsGA (p.Asp324=)
c.574_575delinsGA (p.Asp192=)
c.691_692delinsGA (p.Asp231=)
c.949_950delinsGA (p.Asp317=)
c.782+623_782+624delinsGA (n.782+623_782+624delinsGA)
c.30_31delinsGA
c.853_854delinsGA (p.Asp285=)
c.493_494delinsGA (p.Asp165=)
c.937_938delinsGA (p.Asp313=)
17g.7673558C>ACA397835843TP53c.970G>T (p.Asp324Tyr)
c.574G>T (p.Asp192Tyr)
c.691G>T (p.Asp231Tyr)
c.949G>T (p.Asp317Tyr)
c.782+623G>T (n.782+623G>T)
c.30G>T
c.853G>T (p.Asp285Tyr)
c.493G>T (p.Asp165Tyr)
c.937G>T (p.Asp313Tyr)
 ClinVar dbSNP
17g.7673558C=CA2245947625TP53c.970G= (p.Asp324=)
c.574G= (p.Asp192=)
c.691G= (p.Asp231=)
c.949G= (p.Asp317=)
c.782+623G= (n.782+623G=)
c.30G=
c.853G= (p.Asp285=)
c.493G= (p.Asp165=)
c.937G= (p.Asp313=)
17g.7673558C>GCA16620612TP53c.970G>C (p.Asp324His)
c.574G>C (p.Asp192His)
c.691G>C (p.Asp231His)
c.949G>C (p.Asp317His)
c.782+623G>C (n.782+623G>C)
c.30G>C
c.853G>C (p.Asp285His)
c.493G>C (p.Asp165His)
c.937G>C (p.Asp313His)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.7673558C>TCA397835847TP53c.970G>A (p.Asp324Asn)
c.574G>A (p.Asp192Asn)
c.691G>A (p.Asp231Asn)
c.949G>A (p.Asp317Asn)
c.782+623G>A (n.782+623G>A)
c.30G>A
c.853G>A (p.Asp285Asn)
c.493G>A (p.Asp165Asn)
c.937G>A (p.Asp313Asn)
 ClinVar dbSNP gnomAD v2 gnomAD v4
17g.7673559delCA658683980TP53c.970del (p.Asp324MetfsTer21)
c.574del (p.Asp192MetfsTer21)
c.691del (p.Asp231MetfsTer21)
c.949del (p.Asp317MetfsTer21)
c.970del (p.Asp324MetfsTer28)
c.782+623del (n.782+623del)
c.970del (p.Asp324MetfsTer27)
c.970del (p.Asp324MetfsTer19)
c.574del (p.Asp192MetfsTer19)
c.574del (p.Asp192MetfsTer?)
c.574del (p.Asp192MetfsTer27)
c.30del
c.853del (p.Asp285MetfsTer21)
c.853del (p.Asp285MetfsTer19)
c.493del (p.Asp165MetfsTer19)
c.937del (p.Asp313MetfsTer21)
c.493del (p.Asp165MetfsTer27)
c.493del (p.Asp165MetfsTer21)
c.853del (p.Asp285MetfsTer27)
 ClinVar dbSNP
17g.7673558_7673580dupCA645587351TP53c.948_970dup (p.Asp324AlafsTer29)
c.552_574dup (p.Asp192AlafsTer29)
c.669_691dup (p.Asp231AlafsTer29)
c.927_949dup (p.Asp317AlafsTer29)
c.948_970dup (p.Asp324AlafsTer36)
c.782+601_782+623dup (n.782+601_782+623dup)
c.948_970dup (p.Asp324AlafsTer35)
c.948_970dup (p.Asp324AlafsTer27)
c.552_574dup (p.Asp192AlafsTer27)
c.552_574dup (p.Asp192AlafsTer?)
c.552_574dup (p.Asp192AlafsTer35)
c.8_30dup
c.831_853dup (p.Asp285AlafsTer29)
c.831_853dup (p.Asp285AlafsTer27)
c.471_493dup (p.Asp165AlafsTer27)
c.915_937dup (p.Asp313AlafsTer29)
c.471_493dup (p.Asp165AlafsTer35)
c.471_493dup (p.Asp165AlafsTer29)
c.831_853dup (p.Asp285AlafsTer35)
 COSMIC
17g.7673559C>ACA497713919TP53c.969G>T (p.Leu323=)
c.573G>T (p.Leu191=)
c.690G>T (p.Leu230=)
c.948G>T (p.Leu316=)
c.782+622G>T (n.782+622G>T)
c.29G>T
c.852G>T (p.Leu284=)
c.492G>T (p.Leu164=)
c.936G>T (p.Leu312=)
 dbSNP
17g.7673559C=CA2245947634TP53c.969G= (p.Leu323=)
c.573G= (p.Leu191=)
c.690G= (p.Leu230=)
c.948G= (p.Leu316=)
c.782+622G= (n.782+622G=)
c.29G=
c.852G= (p.Leu284=)
c.492G= (p.Leu164=)
c.936G= (p.Leu312=)
17g.7673559C>GCA497713923TP53c.969G>C (p.Leu323=)
c.573G>C (p.Leu191=)
c.690G>C (p.Leu230=)
c.948G>C (p.Leu316=)
c.782+622G>C (n.782+622G>C)
c.29G>C
c.852G>C (p.Leu284=)
c.492G>C (p.Leu164=)
c.936G>C (p.Leu312=)
 ClinVar dbSNP
17g.7673559C>TCA000512TP53c.969G>A (p.Leu323=)
c.573G>A (p.Leu191=)
c.690G>A (p.Leu230=)
c.948G>A (p.Leu316=)
c.782+622G>A (n.782+622G>A)
c.29G>A
c.852G>A (p.Leu284=)
c.492G>A (p.Leu164=)
c.936G>A (p.Leu312=)
 ClinVar dbSNP gnomAD v3 gnomAD v4
17g.7673560A=CA2245947643TP53c.968T= (p.Leu323=)
c.572T= (p.Leu191=)
c.689T= (p.Leu230=)
c.947T= (p.Leu316=)
c.782+621T= (n.782+621T=)
c.28T=
c.851T= (p.Leu284=)
c.491T= (p.Leu164=)
c.935T= (p.Leu312=)
17g.7673560A>CCA397835852TP53c.968T>G (p.Leu323Arg)
c.572T>G (p.Leu191Arg)
c.689T>G (p.Leu230Arg)
c.947T>G (p.Leu316Arg)
c.782+621T>G (n.782+621T>G)
c.28T>G
c.851T>G (p.Leu284Arg)
c.491T>G (p.Leu164Arg)
c.935T>G (p.Leu312Arg)
 COSMIC
17g.7673560A>GCA397835853TP53c.968T>C (p.Leu323Pro)
c.572T>C (p.Leu191Pro)
c.689T>C (p.Leu230Pro)
c.947T>C (p.Leu316Pro)
c.782+621T>C (n.782+621T>C)
c.28T>C
c.851T>C (p.Leu284Pro)
c.491T>C (p.Leu164Pro)
c.935T>C (p.Leu312Pro)
 ClinVar dbSNP COSMIC
17g.7673560A>TCA397835857TP53c.968T>A (p.Leu323Gln)
c.572T>A (p.Leu191Gln)
c.689T>A (p.Leu230Gln)
c.947T>A (p.Leu316Gln)
c.782+621T>A (n.782+621T>A)
c.28T>A
c.851T>A (p.Leu284Gln)
c.491T>A (p.Leu164Gln)
c.935T>A (p.Leu312Gln)
 dbSNP
17g.7673560_7673561delinsCCCA645587352TP53c.967_968delinsGG (p.Leu323Gly)
c.571_572delinsGG (p.Leu191Gly)
c.688_689delinsGG (p.Leu230Gly)
c.946_947delinsGG (p.Leu316Gly)
c.782+620_782+621delinsGG (n.782+620_782+621delinsGG)
c.27_28delinsGG
c.850_851delinsGG (p.Leu284Gly)
c.490_491delinsGG (p.Leu164Gly)
c.934_935delinsGG (p.Leu312Gly)
 COSMIC
17g.7673562_7673586delCA645587353TP53c.944_968del (p.Ser315TrpfsTer22)
c.548_572del (p.Ser183TrpfsTer22)
c.665_689del (p.Ser222TrpfsTer22)
c.923_947del (p.Ser308TrpfsTer22)
c.944_968del (p.Ser315TrpfsTer29)
c.782+597_782+621del (n.782+597_782+621del)
c.944_968del (p.Ser315TrpfsTer28)
c.944_968del (p.Ser315TrpfsTer20)
c.548_572del (p.Ser183TrpfsTer20)
c.548_572del (p.Ser183TrpfsTer?)
c.548_572del (p.Ser183TrpfsTer28)
c.4_28del
c.827_851del (p.Ser276TrpfsTer22)
c.827_851del (p.Ser276TrpfsTer20)
c.467_491del (p.Ser156TrpfsTer20)
c.911_935del (p.Ser304TrpfsTer22)
c.467_491del (p.Ser156TrpfsTer28)
c.467_491del (p.Ser156TrpfsTer22)
c.827_851del (p.Ser276TrpfsTer28)
 COSMIC
17g.7673561delCA497713940TP53c.967del (p.Leu323TrpfsTer22)
c.571del (p.Leu191TrpfsTer22)
c.688del (p.Leu230TrpfsTer22)
c.946del (p.Leu316TrpfsTer22)
c.967del (p.Leu323TrpfsTer29)
c.782+620del (n.782+620del)
c.967del (p.Leu323TrpfsTer28)
c.967del (p.Leu323TrpfsTer20)
c.571del (p.Leu191TrpfsTer20)
c.571del (p.Leu191TrpfsTer?)
c.571del (p.Leu191TrpfsTer28)
c.27del
c.850del (p.Leu284TrpfsTer22)
c.850del (p.Leu284TrpfsTer20)
c.490del (p.Leu164TrpfsTer20)
c.934del (p.Leu312TrpfsTer22)
c.490del (p.Leu164TrpfsTer28)
c.490del (p.Leu164TrpfsTer22)
c.850del (p.Leu284TrpfsTer28)
 COSMIC
17g.7673561G>ACA497713934TP53c.967C>T (p.Leu323=)
c.571C>T (p.Leu191=)
c.688C>T (p.Leu230=)
c.946C>T (p.Leu316=)
c.782+620C>T (n.782+620C>T)
c.27C>T
c.850C>T (p.Leu284=)
c.490C>T (p.Leu164=)
c.934C>T (p.Leu312=)
 dbSNP
17g.7673561G>CCA397835860TP53c.967C>G (p.Leu323Val)
c.571C>G (p.Leu191Val)
c.688C>G (p.Leu230Val)
c.946C>G (p.Leu316Val)
c.782+620C>G (n.782+620C>G)
c.27C>G
c.850C>G (p.Leu284Val)
c.490C>G (p.Leu164Val)
c.934C>G (p.Leu312Val)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
17g.7673561G=CA2245947652TP53c.967C= (p.Leu323=)
c.571C= (p.Leu191=)
c.688C= (p.Leu230=)
c.946C= (p.Leu316=)
c.782+620C= (n.782+620C=)
c.27C=
c.850C= (p.Leu284=)
c.490C= (p.Leu164=)
c.934C= (p.Leu312=)
17g.7673561G>TCA397835867TP53c.967C>A (p.Leu323Met)
c.571C>A (p.Leu191Met)
c.688C>A (p.Leu230Met)
c.946C>A (p.Leu316Met)
c.782+620C>A (n.782+620C>A)
c.27C>A
c.850C>A (p.Leu284Met)
c.490C>A (p.Leu164Met)
c.934C>A (p.Leu312Met)
 dbSNP COSMIC
17g.7673562T>ACA497713943TP53c.966A>T (p.Pro322=)
c.570A>T (p.Pro190=)
c.687A>T (p.Pro229=)
c.945A>T (p.Pro315=)
c.782+619A>T (n.782+619A>T)
c.26A>T
c.849A>T (p.Pro283=)
c.489A>T (p.Pro163=)
c.933A>T (p.Pro311=)
17g.7673562T>CCA497713945TP53c.966A>G (p.Pro322=)
c.570A>G (p.Pro190=)
c.687A>G (p.Pro229=)
c.945A>G (p.Pro315=)
c.782+619A>G (n.782+619A>G)
c.26A>G
c.849A>G (p.Pro283=)
c.489A>G (p.Pro163=)
c.933A>G (p.Pro311=)
 ClinVar
17g.7673562T>GCA497713950TP53c.966A>C (p.Pro322=)
c.570A>C (p.Pro190=)
c.687A>C (p.Pro229=)
c.945A>C (p.Pro315=)
c.782+619A>C (n.782+619A>C)
c.26A>C
c.849A>C (p.Pro283=)
c.489A>C (p.Pro163=)
c.933A>C (p.Pro311=)
 ClinVar
17g.7673562dupCA2245947657TP53c.966dup (p.Leu323ThrfsTer14)
c.570dup (p.Leu191ThrfsTer14)
c.687dup (p.Leu230ThrfsTer14)
c.945dup (p.Leu316ThrfsTer14)
c.966dup (p.Leu323ThrfsTer?)
c.782+619dup (n.782+619dup)
c.966dup (p.Leu323ThrfsTer24)
c.966dup (p.Leu323ThrfsTer13)
c.570dup (p.Leu191ThrfsTer13)
c.570dup (p.Leu191ThrfsTer?)
c.570dup (p.Leu191ThrfsTer24)
c.26dup
c.849dup (p.Leu284ThrfsTer14)
c.849dup (p.Leu284ThrfsTer13)
c.489dup (p.Leu164ThrfsTer13)
c.933dup (p.Leu312ThrfsTer14)
c.489dup (p.Leu164ThrfsTer24)
c.489dup (p.Leu164ThrfsTer14)
c.849dup (p.Leu284ThrfsTer24)
 dbSNP
17g.7673563G>ACA397835873TP53c.965C>T (p.Pro322Leu)
c.569C>T (p.Pro190Leu)
c.686C>T (p.Pro229Leu)
c.944C>T (p.Pro315Leu)
c.782+618C>T (n.782+618C>T)
c.25C>T
c.848C>T (p.Pro283Leu)
c.488C>T (p.Pro163Leu)
c.932C>T (p.Pro311Leu)
 dbSNP COSMIC
17g.7673563G>CCA397835872TP53c.965C>G (p.Pro322Arg)
c.569C>G (p.Pro190Arg)
c.686C>G (p.Pro229Arg)
c.944C>G (p.Pro315Arg)
c.782+618C>G (n.782+618C>G)
c.25C>G
c.848C>G (p.Pro283Arg)
c.488C>G (p.Pro163Arg)
c.932C>G (p.Pro311Arg)
 ClinVar dbSNP COSMIC
17g.7673563G>TCA397835870TP53c.965C>A (p.Pro322Gln)
c.569C>A (p.Pro190Gln)
c.686C>A (p.Pro229Gln)
c.944C>A (p.Pro315Gln)
c.782+618C>A (n.782+618C>A)
c.25C>A
c.848C>A (p.Pro283Gln)
c.488C>A (p.Pro163Gln)
c.932C>A (p.Pro311Gln)
 dbSNP
17g.7673564delCA497713957TP53c.965del (p.Pro322HisfsTer23)
c.569del (p.Pro190HisfsTer23)
c.686del (p.Pro229HisfsTer23)
c.944del (p.Pro315HisfsTer23)
c.965del (p.Pro322HisfsTer30)
c.782+618del (n.782+618del)
c.965del (p.Pro322HisfsTer29)
c.965del (p.Pro322HisfsTer21)
c.569del (p.Pro190HisfsTer21)
c.569del (p.Pro190HisfsTer?)
c.569del (p.Pro190HisfsTer29)
c.25del
c.848del (p.Pro283HisfsTer23)
c.848del (p.Pro283HisfsTer21)
c.488del (p.Pro163HisfsTer21)
c.932del (p.Pro311HisfsTer23)
c.488del (p.Pro163HisfsTer29)
c.488del (p.Pro163HisfsTer23)
c.848del (p.Pro283HisfsTer29)
 ClinVar COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7673564G>ACA336073TP53c.964C>T (p.Pro322Ser)
c.568C>T (p.Pro190Ser)
c.685C>T (p.Pro229Ser)
c.943C>T (p.Pro315Ser)
c.782+617C>T (n.782+617C>T)
c.24C>T
c.847C>T (p.Pro283Ser)
c.487C>T (p.Pro163Ser)
c.931C>T (p.Pro311Ser)
 ClinVar dbSNP gnomAD v4
17g.7673564G>CCA397835876TP53c.964C>G (p.Pro322Ala)
c.568C>G (p.Pro190Ala)
c.685C>G (p.Pro229Ala)
c.943C>G (p.Pro315Ala)
c.782+617C>G (n.782+617C>G)
c.24C>G
c.847C>G (p.Pro283Ala)
c.487C>G (p.Pro163Ala)
c.931C>G (p.Pro311Ala)
 ClinVar dbSNP
17g.7673564G=CA2245947670TP53c.964C= (p.Pro322=)
c.568C= (p.Pro190=)
c.685C= (p.Pro229=)
c.943C= (p.Pro315=)
c.782+617C= (n.782+617C=)
c.24C=
c.847C= (p.Pro283=)
c.487C= (p.Pro163=)
c.931C= (p.Pro311=)
17g.7673564G>TCA10580909TP53c.964C>A (p.Pro322Thr)
c.568C>A (p.Pro190Thr)
c.685C>A (p.Pro229Thr)
c.943C>A (p.Pro315Thr)
c.782+617C>A (n.782+617C>A)
c.24C>A
c.847C>A (p.Pro283Thr)
c.487C>A (p.Pro163Thr)
c.931C>A (p.Pro311Thr)
 ClinVar dbSNP
17g.7673565T>ACA397835878TP53c.963A>T (p.Lys321Asn)
c.567A>T (p.Lys189Asn)
c.684A>T (p.Lys228Asn)
c.942A>T (p.Lys314Asn)
c.782+616A>T (n.782+616A>T)
c.23A>T
c.846A>T (p.Lys282Asn)
c.486A>T (p.Lys162Asn)
c.930A>T (p.Lys310Asn)
 dbSNP
17g.7673565T>CCA497713967TP53c.963A>G (p.Lys321=)
c.567A>G (p.Lys189=)
c.684A>G (p.Lys228=)
c.942A>G (p.Lys314=)
c.782+616A>G (n.782+616A>G)
c.23A>G
c.846A>G (p.Lys282=)
c.486A>G (p.Lys162=)
c.930A>G (p.Lys310=)
 ClinVar dbSNP COSMIC
17g.7673565T>GCA397835879TP53c.963A>C (p.Lys321Asn)
c.567A>C (p.Lys189Asn)
c.684A>C (p.Lys228Asn)
c.942A>C (p.Lys314Asn)
c.782+616A>C (n.782+616A>C)
c.23A>C
c.846A>C (p.Lys282Asn)
c.486A>C (p.Lys162Asn)
c.930A>C (p.Lys310Asn)
 dbSNP
17g.7673567dupCA645587355TP53c.963dup (p.Pro322ThrfsTer15)
c.567dup (p.Pro190ThrfsTer15)
c.684dup (p.Pro229ThrfsTer15)
c.942dup (p.Pro315ThrfsTer15)
c.963dup (p.Pro322ThrfsTer?)
c.782+616dup (n.782+616dup)
c.963dup (p.Pro322ThrfsTer25)
c.963dup (p.Pro322ThrfsTer14)
c.567dup (p.Pro190ThrfsTer14)
c.567dup (p.Pro190ThrfsTer?)
c.567dup (p.Pro190ThrfsTer25)
c.23dup
c.846dup (p.Pro283ThrfsTer15)
c.846dup (p.Pro283ThrfsTer14)
c.486dup (p.Pro163ThrfsTer14)
c.930dup (p.Pro311ThrfsTer15)
c.486dup (p.Pro163ThrfsTer25)
c.486dup (p.Pro163ThrfsTer15)
c.846dup (p.Pro283ThrfsTer25)
 COSMIC COSMIC COSMIC COSMIC
17g.7673567delCA497713971TP53c.963del (p.Lys321AsnfsTer24)
c.567del (p.Lys189AsnfsTer24)
c.684del (p.Lys228AsnfsTer24)
c.942del (p.Lys314AsnfsTer24)
c.963del (p.Lys321AsnfsTer?)
c.782+616del (n.782+616del)
c.963del (p.Lys321AsnfsTer30)
c.963del (p.Lys321AsnfsTer22)
c.567del (p.Lys189AsnfsTer22)
c.567del (p.Lys189AsnfsTer?)
c.567del (p.Lys189AsnfsTer30)
c.23del
c.846del (p.Lys282AsnfsTer24)
c.846del (p.Lys282AsnfsTer22)
c.486del (p.Lys162AsnfsTer22)
c.930del (p.Lys310AsnfsTer24)
c.486del (p.Lys162AsnfsTer30)
c.486del (p.Lys162AsnfsTer24)
c.846del (p.Lys282AsnfsTer30)
 COSMIC
17g.7673565_7673568delinsTTTCCA2245947676TP53c.960_963delinsGAAA (p.Lys320=)
c.564_567delinsGAAA (p.Lys188=)
c.681_684delinsGAAA (p.Lys227=)
c.939_942delinsGAAA (p.Lys313=)
c.782+613_782+616delinsGAAA (n.782+613_782+616delinsGAAA)
c.20_23delinsGAAA
c.843_846delinsGAAA (p.Lys281=)
c.483_486delinsGAAA (p.Lys161=)
c.927_930delinsGAAA (p.Lys309=)
17g.7673565_7673605delCA645587356TP53c.923_963del (p.Leu308ProfsTer15)
c.527_567del (p.Leu176ProfsTer15)
c.644_684del (p.Leu215ProfsTer15)
c.902_942del (p.Leu301ProfsTer15)
c.923_963del (p.Leu308ProfsTer?)
c.782+576_782+616del (n.782+576_782+616del)
c.923_963del (p.Leu308ProfsTer25)
c.923_963del (p.Leu308ProfsTer14)
c.527_567del (p.Leu176ProfsTer14)
c.527_567del (p.Leu176ProfsTer?)
c.527_567del (p.Leu176ProfsTer25)
c.806_846del (p.Leu269ProfsTer15)
c.806_846del (p.Leu269ProfsTer14)
c.446_486del (p.Leu149ProfsTer14)
c.890_930del (p.Leu297ProfsTer15)
c.446_486del (p.Leu149ProfsTer25)
c.446_486del (p.Leu149ProfsTer15)
c.806_846del (p.Leu269ProfsTer25)
 COSMIC
17g.7673566T>ACA397835881TP53c.962A>T (p.Lys321Ile)
c.566A>T (p.Lys189Ile)
c.683A>T (p.Lys228Ile)
c.941A>T (p.Lys314Ile)
c.782+615A>T (n.782+615A>T)
c.22A>T
c.845A>T (p.Lys282Ile)
c.485A>T (p.Lys162Ile)
c.929A>T (p.Lys310Ile)
 dbSNP
17g.7673566T>CCA397835882TP53c.962A>G (p.Lys321Arg)
c.566A>G (p.Lys189Arg)
c.683A>G (p.Lys228Arg)
c.941A>G (p.Lys314Arg)
c.782+615A>G (n.782+615A>G)
c.22A>G
c.845A>G (p.Lys282Arg)
c.485A>G (p.Lys162Arg)
c.929A>G (p.Lys310Arg)
 dbSNP
17g.7673566T>GCA397835886TP53c.962A>C (p.Lys321Thr)
c.566A>C (p.Lys189Thr)
c.683A>C (p.Lys228Thr)
c.941A>C (p.Lys314Thr)
c.782+615A>C (n.782+615A>C)
c.22A>C
c.845A>C (p.Lys282Thr)
c.485A>C (p.Lys162Thr)
c.929A>C (p.Lys310Thr)
 dbSNP
17g.7673571_7673573dupCA645587357TP53c.960_962dup (p.Lys321_Pro322insLys)
c.564_566dup (p.Lys189_Pro190insLys)
c.681_683dup (p.Lys228_Pro229insLys)
c.939_941dup (p.Lys314_Pro315insLys)
c.782+613_782+615dup (n.782+613_782+615dup)
c.20_22dup
c.843_845dup (p.Lys282_Pro283insLys)
c.483_485dup (p.Lys162_Pro163insLys)
c.927_929dup (p.Lys310_Pro311insLys)
 COSMIC COSMIC
17g.7673571_7673573delCA891844039TP53c.960_962del (p.Lys321del)
c.564_566del (p.Lys189del)
c.681_683del (p.Lys228del)
c.939_941del (p.Lys314del)
c.782+613_782+615del (n.782+613_782+615del)
c.20_22del
c.843_845del (p.Lys282del)
c.483_485del (p.Lys162del)
c.927_929del (p.Lys310del)
 ClinVar dbSNP
17g.7673567T>ACA397835889TP53c.961A>T (p.Lys321Ter)
c.565A>T (p.Lys189Ter)
c.682A>T (p.Lys228Ter)
c.940A>T (p.Lys314Ter)
c.782+614A>T (n.782+614A>T)
c.21A>T
c.844A>T (p.Lys282Ter)
c.484A>T (p.Lys162Ter)
c.928A>T (p.Lys310Ter)
 ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC
17g.7673567T>CCA397835893TP53c.961A>G (p.Lys321Glu)
c.565A>G (p.Lys189Glu)
c.682A>G (p.Lys228Glu)
c.940A>G (p.Lys314Glu)
c.782+614A>G (n.782+614A>G)
c.21A>G
c.844A>G (p.Lys282Glu)
c.484A>G (p.Lys162Glu)
c.928A>G (p.Lys310Glu)
17g.7673567T>GCA397835894TP53c.961A>C (p.Lys321Gln)
c.565A>C (p.Lys189Gln)
c.682A>C (p.Lys228Gln)
c.940A>C (p.Lys314Gln)
c.782+614A>C (n.782+614A>C)
c.21A>C
c.844A>C (p.Lys282Gln)
c.484A>C (p.Lys162Gln)
c.928A>C (p.Lys310Gln)
17g.7673567T=CA2245947687TP53c.961A= (p.Lys321=)
c.565A= (p.Lys189=)
c.682A= (p.Lys228=)
c.940A= (p.Lys314=)
c.782+614A= (n.782+614A=)
c.21A=
c.844A= (p.Lys282=)
c.484A= (p.Lys162=)
c.928A= (p.Lys310=)
17g.7673568delCA645587358TP53c.960del (p.Lys321AsnfsTer24)
c.564del (p.Lys189AsnfsTer24)
c.681del (p.Lys228AsnfsTer24)
c.939del (p.Lys314AsnfsTer24)
c.960del (p.Lys321AsnfsTer?)
c.782+613del (n.782+613del)
c.960del (p.Lys321AsnfsTer22)
c.564del (p.Lys189AsnfsTer22)
c.564del (p.Lys189AsnfsTer?)
c.20del
c.843del (p.Lys282AsnfsTer24)
c.843del (p.Lys282AsnfsTer22)
c.483del (p.Lys162AsnfsTer22)
c.927del (p.Lys310AsnfsTer24)
c.483del (p.Lys162AsnfsTer?)
c.483del (p.Lys162AsnfsTer24)
c.843del (p.Lys282AsnfsTer?)
 ClinVar COSMIC COSMIC COSMIC COSMIC
17g.7673568C>ACA397835895TP53c.960G>T (p.Lys320Asn)
c.564G>T (p.Lys188Asn)
c.681G>T (p.Lys227Asn)
c.939G>T (p.Lys313Asn)
c.782+613G>T (n.782+613G>T)
c.20G>T
c.843G>T (p.Lys281Asn)
c.483G>T (p.Lys161Asn)
c.927G>T (p.Lys309Asn)
 dbSNP
17g.7673568C>GCA397835897TP53c.960G>C (p.Lys320Asn)
c.564G>C (p.Lys188Asn)
c.681G>C (p.Lys227Asn)
c.939G>C (p.Lys313Asn)
c.782+613G>C (n.782+613G>C)
c.20G>C
c.843G>C (p.Lys281Asn)
c.483G>C (p.Lys161Asn)
c.927G>C (p.Lys309Asn)
 dbSNP COSMIC
17g.7673568C>TCA497713987TP53c.960G>A (p.Lys320=)
c.564G>A (p.Lys188=)
c.681G>A (p.Lys227=)
c.939G>A (p.Lys313=)
c.782+613G>A (n.782+613G>A)
c.20G>A
c.843G>A (p.Lys281=)
c.483G>A (p.Lys161=)
c.927G>A (p.Lys309=)
 dbSNP COSMIC COSMIC COSMIC COSMIC
17g.7673569T>ACA397835903TP53c.959A>T (p.Lys320Met)
c.563A>T (p.Lys188Met)
c.680A>T (p.Lys227Met)
c.938A>T (p.Lys313Met)
c.782+612A>T (n.782+612A>T)
c.19A>T
c.842A>T (p.Lys281Met)
c.482A>T (p.Lys161Met)
c.926A>T (p.Lys309Met)
 dbSNP
17g.7673569T>CCA397835905TP53c.959A>G (p.Lys320Arg)
c.563A>G (p.Lys188Arg)
c.680A>G (p.Lys227Arg)
c.938A>G (p.Lys313Arg)
c.782+612A>G (n.782+612A>G)
c.19A>G
c.842A>G (p.Lys281Arg)
c.482A>G (p.Lys161Arg)
c.926A>G (p.Lys309Arg)
 dbSNP
17g.7673569T>GCA397835900TP53c.959A>C (p.Lys320Thr)
c.563A>C (p.Lys188Thr)
c.680A>C (p.Lys227Thr)
c.938A>C (p.Lys313Thr)
c.782+612A>C (n.782+612A>C)
c.19A>C
c.842A>C (p.Lys281Thr)
c.482A>C (p.Lys161Thr)
c.926A>C (p.Lys309Thr)
17g.7673570delCA497714003TP53c.959del (p.Lys320ArgfsTer25)
c.563del (p.Lys188ArgfsTer25)
c.680del (p.Lys227ArgfsTer25)
c.938del (p.Lys313ArgfsTer25)
c.959del (p.Lys320ArgfsTer?)
c.782+612del (n.782+612del)
c.959del (p.Lys320ArgfsTer23)
c.563del (p.Lys188ArgfsTer23)
c.563del (p.Lys188ArgfsTer?)
c.19del
c.842del (p.Lys281ArgfsTer25)
c.842del (p.Lys281ArgfsTer23)
c.482del (p.Lys161ArgfsTer23)
c.926del (p.Lys309ArgfsTer25)
c.482del (p.Lys161ArgfsTer?)
c.482del (p.Lys161ArgfsTer25)
c.842del (p.Lys281ArgfsTer?)
 COSMIC
17g.7673570T>ACA397835908TP53c.958A>T (p.Lys320Ter)
c.562A>T (p.Lys188Ter)
c.679A>T (p.Lys227Ter)
c.937A>T (p.Lys313Ter)
c.782+611A>T (n.782+611A>T)
c.18A>T
c.841A>T (p.Lys281Ter)
c.481A>T (p.Lys161Ter)
c.925A>T (p.Lys309Ter)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC
17g.7673570T>CCA397835912TP53c.958A>G (p.Lys320Glu)
c.562A>G (p.Lys188Glu)
c.679A>G (p.Lys227Glu)
c.937A>G (p.Lys313Glu)
c.782+611A>G (n.782+611A>G)
c.18A>G
c.841A>G (p.Lys281Glu)
c.481A>G (p.Lys161Glu)
c.925A>G (p.Lys309Glu)
 dbSNP
17g.7673570T>GCA397835915TP53c.958A>C (p.Lys320Gln)
c.562A>C (p.Lys188Gln)
c.679A>C (p.Lys227Gln)
c.937A>C (p.Lys313Gln)
c.782+611A>C (n.782+611A>C)
c.18A>C
c.841A>C (p.Lys281Gln)
c.481A>C (p.Lys161Gln)
c.925A>C (p.Lys309Gln)
17g.7673570_7673587delCA645587360TP53c.941_958del (p.Ser314Ter)
c.545_562del (p.Ser182Ter)
c.662_679del (p.Ser221Ter)
c.920_937del (p.Ser307Ter)
c.782+594_782+611del (n.782+594_782+611del)
c.1_18del
c.824_841del (p.Ser275Ter)
c.464_481del (p.Ser155Ter)
c.908_925del (p.Ser303Ter)
 COSMIC COSMIC COSMIC COSMIC
17g.7673570_7673588delCA645587363TP53c.940_958del (p.Ser314ArgfsTer25)
c.544_562del (p.Ser182ArgfsTer25)
c.661_679del (p.Ser221ArgfsTer25)
c.919_937del (p.Ser307ArgfsTer25)
c.940_958del (p.Ser314ArgfsTer?)
c.782+593_782+611del (n.782+593_782+611del)
c.940_958del (p.Ser314ArgfsTer23)
c.544_562del (p.Ser182ArgfsTer23)
c.544_562del (p.Ser182ArgfsTer?)
c.823_841del (p.Ser275ArgfsTer25)
c.823_841del (p.Ser275ArgfsTer23)
c.463_481del (p.Ser155ArgfsTer23)
c.907_925del (p.Ser303ArgfsTer25)
c.463_481del (p.Ser155ArgfsTer?)
c.463_481del (p.Ser155ArgfsTer25)
c.823_841del (p.Ser275ArgfsTer?)
 COSMIC
17g.7673571delCA645587364TP53c.957del (p.Lys320ArgfsTer25)
c.561del (p.Lys188ArgfsTer25)
c.678del (p.Lys227ArgfsTer25)
c.936del (p.Lys313ArgfsTer25)
c.957del (p.Lys320ArgfsTer?)
c.782+610del (n.782+610del)
c.957del (p.Lys320ArgfsTer23)
c.561del (p.Lys188ArgfsTer23)
c.561del (p.Lys188ArgfsTer?)
c.17del
c.840del (p.Lys281ArgfsTer25)
c.840del (p.Lys281ArgfsTer23)
c.480del (p.Lys161ArgfsTer23)
c.924del (p.Lys309ArgfsTer25)
c.480del (p.Lys161ArgfsTer?)
c.480del (p.Lys161ArgfsTer25)
c.840del (p.Lys281ArgfsTer?)
 COSMIC COSMIC COSMIC COSMIC
17g.7673571C>ACA397835919TP53c.957G>T (p.Lys319Asn)
c.561G>T (p.Lys187Asn)
c.678G>T (p.Lys226Asn)
c.936G>T (p.Lys312Asn)
c.782+610G>T (n.782+610G>T)
c.17G>T
c.840G>T (p.Lys280Asn)
c.480G>T (p.Lys160Asn)
c.924G>T (p.Lys308Asn)
 dbSNP COSMIC
17g.7673571C>GCA397835921TP53c.957G>C (p.Lys319Asn)
c.561G>C (p.Lys187Asn)
c.678G>C (p.Lys226Asn)
c.936G>C (p.Lys312Asn)
c.782+610G>C (n.782+610G>C)
c.17G>C
c.840G>C (p.Lys280Asn)
c.480G>C (p.Lys160Asn)
c.924G>C (p.Lys308Asn)
 dbSNP COSMIC COSMIC COSMIC COSMIC
17g.7673571C>TCA497714016TP53c.957G>A (p.Lys319=)
c.561G>A (p.Lys187=)
c.678G>A (p.Lys226=)
c.936G>A (p.Lys312=)
c.782+610G>A (n.782+610G>A)
c.17G>A
c.840G>A (p.Lys280=)
c.480G>A (p.Lys160=)
c.924G>A (p.Lys308=)
 dbSNP COSMIC
17g.7673572T>ACA397835924TP53c.956A>T (p.Lys319Met)
c.560A>T (p.Lys187Met)
c.677A>T (p.Lys226Met)
c.935A>T (p.Lys312Met)
c.782+609A>T (n.782+609A>T)
c.16A>T
c.839A>T (p.Lys280Met)
c.479A>T (p.Lys160Met)
c.923A>T (p.Lys308Met)
 dbSNP
17g.7673572T>CCA397835927TP53c.956A>G (p.Lys319Arg)
c.560A>G (p.Lys187Arg)
c.677A>G (p.Lys226Arg)
c.935A>G (p.Lys312Arg)
c.782+609A>G (n.782+609A>G)
c.16A>G
c.839A>G (p.Lys280Arg)
c.479A>G (p.Lys160Arg)
c.923A>G (p.Lys308Arg)
 dbSNP COSMIC
17g.7673572T>GCA397835930TP53c.956A>C (p.Lys319Thr)
c.560A>C (p.Lys187Thr)
c.677A>C (p.Lys226Thr)
c.935A>C (p.Lys312Thr)
c.782+609A>C (n.782+609A>C)
c.16A>C
c.839A>C (p.Lys280Thr)
c.479A>C (p.Lys160Thr)
c.923A>C (p.Lys308Thr)
17g.7673573T>ACA397835934TP53c.955A>T (p.Lys319Ter)
c.559A>T (p.Lys187Ter)
c.676A>T (p.Lys226Ter)
c.934A>T (p.Lys312Ter)
c.782+608A>T (n.782+608A>T)
c.15A>T
c.838A>T (p.Lys280Ter)
c.478A>T (p.Lys160Ter)
c.922A>T (p.Lys308Ter)
 dbSNP COSMIC COSMIC COSMIC COSMIC
17g.7673573T>CCA397835937TP53c.955A>G (p.Lys319Glu)
c.559A>G (p.Lys187Glu)
c.676A>G (p.Lys226Glu)
c.934A>G (p.Lys312Glu)
c.782+608A>G (n.782+608A>G)
c.15A>G
c.838A>G (p.Lys280Glu)
c.478A>G (p.Lys160Glu)
c.922A>G (p.Lys308Glu)
 COSMIC
17g.7673573T>GCA397835940TP53c.955A>C (p.Lys319Gln)
c.559A>C (p.Lys187Gln)
c.676A>C (p.Lys226Gln)
c.934A>C (p.Lys312Gln)
c.782+608A>C (n.782+608A>C)
c.15A>C
c.838A>C (p.Lys280Gln)
c.478A>C (p.Lys160Gln)
c.922A>C (p.Lys308Gln)
17g.7673573_7673577delinsTTGGCCA2245947690TP53c.951_955delinsGCCAA (p.Gln317=)
c.555_559delinsGCCAA (p.Gln185=)
c.672_676delinsGCCAA (p.Gln224=)
c.930_934delinsGCCAA (p.Gln310=)
c.782+604_782+608delinsGCCAA (n.782+604_782+608delinsGCCAA)
c.11_15delinsGCCAA
c.834_838delinsGCCAA (p.Gln278=)
c.474_478delinsGCCAA (p.Gln158=)
c.918_922delinsGCCAA (p.Gln306=)
17g.7673574T>ACA497714040TP53c.954A>T (p.Pro318=)
c.558A>T (p.Pro186=)
c.675A>T (p.Pro225=)
c.933A>T (p.Pro311=)
c.782+607A>T (n.782+607A>T)
c.14A>T
c.837A>T (p.Pro279=)
c.477A>T (p.Pro159=)
c.921A>T (p.Pro307=)
 ClinVar
17g.7673574T>CCA497714031TP53c.954A>G (p.Pro318=)
c.558A>G (p.Pro186=)
c.675A>G (p.Pro225=)
c.933A>G (p.Pro311=)
c.782+607A>G (n.782+607A>G)
c.14A>G
c.837A>G (p.Pro279=)
c.477A>G (p.Pro159=)
c.921A>G (p.Pro307=)
 ClinVar dbSNP
17g.7673574T>GCA001195TP53c.954A>C (p.Pro318=)
c.558A>C (p.Pro186=)
c.675A>C (p.Pro225=)
c.933A>C (p.Pro311=)
c.782+607A>C (n.782+607A>C)
c.14A>C
c.837A>C (p.Pro279=)
c.477A>C (p.Pro159=)
c.921A>C (p.Pro307=)
 dbSNP ExAC gnomAD v2 gnomAD v4
17g.7673574T=CA2245947701TP53c.954A= (p.Pro318=)
c.558A= (p.Pro186=)
c.675A= (p.Pro225=)
c.933A= (p.Pro311=)
c.782+607A= (n.782+607A=)
c.14A=
c.837A= (p.Pro279=)
c.477A= (p.Pro159=)
c.921A= (p.Pro307=)
17g.7673577_7673580dupCA645587367TP53c.951_954dup (p.Lys319AlafsTer19)
c.555_558dup (p.Lys187AlafsTer19)
c.672_675dup (p.Lys226AlafsTer19)
c.930_933dup (p.Lys312AlafsTer19)
c.951_954dup (p.Lys319AlafsTer?)
c.782+604_782+607dup (n.782+604_782+607dup)
c.951_954dup (p.Lys319AlafsTer29)
c.951_954dup (p.Lys319AlafsTer18)
c.555_558dup (p.Lys187AlafsTer18)
c.555_558dup (p.Lys187AlafsTer?)
c.555_558dup (p.Lys187AlafsTer29)
c.11_14dup
c.834_837dup (p.Lys280AlafsTer19)
c.834_837dup (p.Lys280AlafsTer18)
c.474_477dup (p.Lys160AlafsTer18)
c.918_921dup (p.Lys308AlafsTer19)
c.474_477dup (p.Lys160AlafsTer29)
c.474_477dup (p.Lys160AlafsTer19)
c.834_837dup (p.Lys280AlafsTer29)
 COSMIC COSMIC
17g.7673577_7673580delCA915949515TP53c.951_954del (p.Pro318ArgfsTer26)
c.555_558del (p.Pro186ArgfsTer26)
c.672_675del (p.Pro225ArgfsTer26)
c.930_933del (p.Pro311ArgfsTer26)
c.951_954del (p.Pro318ArgfsTer?)
c.782+604_782+607del (n.782+604_782+607del)
c.951_954del (p.Pro318ArgfsTer24)
c.555_558del (p.Pro186ArgfsTer24)
c.555_558del (p.Pro186ArgfsTer?)
c.11_14del
c.834_837del (p.Pro279ArgfsTer26)
c.834_837del (p.Pro279ArgfsTer24)
c.474_477del (p.Pro159ArgfsTer24)
c.918_921del (p.Pro307ArgfsTer26)
c.474_477del (p.Pro159ArgfsTer?)
c.474_477del (p.Pro159ArgfsTer26)
c.834_837del (p.Pro279ArgfsTer?)
 ClinVar dbSNP
17g.7673575G>ACA397835952TP53c.953C>T (p.Pro318Leu)
c.557C>T (p.Pro186Leu)
c.674C>T (p.Pro225Leu)
c.932C>T (p.Pro311Leu)
c.782+606C>T (n.782+606C>T)
c.13C>T
c.836C>T (p.Pro279Leu)
c.476C>T (p.Pro159Leu)
c.920C>T (p.Pro307Leu)
 ClinVar dbSNP gnomAD v4
17g.7673575G>CCA397835946TP53c.953C>G (p.Pro318Arg)
c.557C>G (p.Pro186Arg)
c.674C>G (p.Pro225Arg)
c.932C>G (p.Pro311Arg)
c.782+606C>G (n.782+606C>G)
c.13C>G
c.836C>G (p.Pro279Arg)
c.476C>G (p.Pro159Arg)
c.920C>G (p.Pro307Arg)
 ClinVar dbSNP
17g.7673575G=CA2245947708TP53c.953C= (p.Pro318=)
c.557C= (p.Pro186=)
c.674C= (p.Pro225=)
c.932C= (p.Pro311=)
c.782+606C= (n.782+606C=)
c.13C=
c.836C= (p.Pro279=)
c.476C= (p.Pro159=)
c.920C= (p.Pro307=)
17g.7673575G>TCA397835949TP53c.953C>A (p.Pro318Gln)
c.557C>A (p.Pro186Gln)
c.674C>A (p.Pro225Gln)
c.932C>A (p.Pro311Gln)
c.782+606C>A (n.782+606C>A)
c.13C>A
c.836C>A (p.Pro279Gln)
c.476C>A (p.Pro159Gln)
c.920C>A (p.Pro307Gln)
 dbSNP
17g.7673576G>ACA397835955TP53c.952C>T (p.Pro318Ser)
c.556C>T (p.Pro186Ser)
c.673C>T (p.Pro225Ser)
c.931C>T (p.Pro311Ser)
c.782+605C>T (n.782+605C>T)
c.12C>T
c.835C>T (p.Pro279Ser)
c.475C>T (p.Pro159Ser)
c.919C>T (p.Pro307Ser)
 ClinVar dbSNP
17g.7673576G>CCA397835958TP53c.952C>G (p.Pro318Ala)
c.556C>G (p.Pro186Ala)
c.673C>G (p.Pro225Ala)
c.931C>G (p.Pro311Ala)
c.782+605C>G (n.782+605C>G)
c.12C>G
c.835C>G (p.Pro279Ala)
c.475C>G (p.Pro159Ala)
c.919C>G (p.Pro307Ala)
 dbSNP COSMIC
17g.7673576G>TCA397835961TP53c.952C>A (p.Pro318Thr)
c.556C>A (p.Pro186Thr)
c.673C>A (p.Pro225Thr)
c.931C>A (p.Pro311Thr)
c.782+605C>A (n.782+605C>A)
c.12C>A
c.835C>A (p.Pro279Thr)
c.475C>A (p.Pro159Thr)
c.919C>A (p.Pro307Thr)
 dbSNP
17g.7673577delCA645587368TP53c.951del (p.Gln317HisfsTer28)
c.555del (p.Gln185HisfsTer28)
c.672del (p.Gln224HisfsTer28)
c.930del (p.Gln310HisfsTer28)
c.951del (p.Gln317HisfsTer?)
c.782+604del (n.782+604del)
c.951del (p.Gln317HisfsTer26)
c.555del (p.Gln185HisfsTer26)
c.555del (p.Gln185HisfsTer?)
c.11del
c.834del (p.Gln278HisfsTer28)
c.834del (p.Gln278HisfsTer26)
c.474del (p.Gln158HisfsTer26)
c.918del (p.Gln306HisfsTer28)
c.474del (p.Gln158HisfsTer?)
c.474del (p.Gln158HisfsTer28)
c.834del (p.Gln278HisfsTer?)
 COSMIC COSMIC COSMIC COSMIC
17g.7673577C>ACA16615689TP53c.951G>T (p.Gln317His)
c.555G>T (p.Gln185His)
c.672G>T (p.Gln224His)
c.930G>T (p.Gln310His)
c.782+604G>T (n.782+604G>T)
c.11G>T
c.834G>T (p.Gln278His)
c.474G>T (p.Gln158His)
c.918G>T (p.Gln306His)
 ClinVar dbSNP
17g.7673577C=CA2245947719TP53c.951G= (p.Gln317=)
c.555G= (p.Gln185=)
c.672G= (p.Gln224=)
c.930G= (p.Gln310=)
c.782+604G= (n.782+604G=)
c.11G=
c.834G= (p.Gln278=)
c.474G= (p.Gln158=)
c.918G= (p.Gln306=)
17g.7673577C>GCA397835964TP53c.951G>C (p.Gln317His)
c.555G>C (p.Gln185His)
c.672G>C (p.Gln224His)
c.930G>C (p.Gln310His)
c.782+604G>C (n.782+604G>C)
c.11G>C
c.834G>C (p.Gln278His)
c.474G>C (p.Gln158His)
c.918G>C (p.Gln306His)
 dbSNP
17g.7673577C>TCA497714069TP53c.951G>A (p.Gln317=)
c.555G>A (p.Gln185=)
c.672G>A (p.Gln224=)
c.930G>A (p.Gln310=)
c.782+604G>A (n.782+604G>A)
c.11G>A
c.834G>A (p.Gln278=)
c.474G>A (p.Gln158=)
c.918G>A (p.Gln306=)
 ClinVar dbSNP
17g.7673577_7673578delinsCTCA2245947725TP53c.950_951delinsAG (p.Gln317=)
c.554_555delinsAG (p.Gln185=)
c.671_672delinsAG (p.Gln224=)
c.929_930delinsAG (p.Gln310=)
c.782+603_782+604delinsAG (n.782+603_782+604delinsAG)
c.10_11delinsAG
c.833_834delinsAG (p.Gln278=)
c.473_474delinsAG (p.Gln158=)
c.917_918delinsAG (p.Gln306=)
17g.7673578delCA645587369TP53c.950del (p.Gln317ArgfsTer28)
c.554del (p.Gln185ArgfsTer28)
c.671del (p.Gln224ArgfsTer28)
c.929del (p.Gln310ArgfsTer28)
c.950del (p.Gln317ArgfsTer?)
c.782+603del (n.782+603del)
c.950del (p.Gln317ArgfsTer26)
c.554del (p.Gln185ArgfsTer26)
c.554del (p.Gln185ArgfsTer?)
c.10del
c.833del (p.Gln278ArgfsTer28)
c.833del (p.Gln278ArgfsTer26)
c.473del (p.Gln158ArgfsTer26)
c.917del (p.Gln306ArgfsTer28)
c.473del (p.Gln158ArgfsTer?)
c.473del (p.Gln158ArgfsTer28)
c.833del (p.Gln278ArgfsTer?)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC
17g.7673578T>ACA397835969TP53c.950A>T (p.Gln317Leu)
c.554A>T (p.Gln185Leu)
c.671A>T (p.Gln224Leu)
c.929A>T (p.Gln310Leu)
c.782+603A>T (n.782+603A>T)
c.10A>T
c.833A>T (p.Gln278Leu)
c.473A>T (p.Gln158Leu)
c.917A>T (p.Gln306Leu)
 ClinVar dbSNP
17g.7673578T>CCA397835971TP53c.950A>G (p.Gln317Arg)
c.554A>G (p.Gln185Arg)
c.671A>G (p.Gln224Arg)
c.929A>G (p.Gln310Arg)
c.782+603A>G (n.782+603A>G)
c.10A>G
c.833A>G (p.Gln278Arg)
c.473A>G (p.Gln158Arg)
c.917A>G (p.Gln306Arg)
 ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC COSMIC COSMIC
17g.7673578T>GCA397835972TP53c.950A>C (p.Gln317Pro)
c.554A>C (p.Gln185Pro)
c.671A>C (p.Gln224Pro)
c.929A>C (p.Gln310Pro)
c.782+603A>C (n.782+603A>C)
c.10A>C
c.833A>C (p.Gln278Pro)
c.473A>C (p.Gln158Pro)
c.917A>C (p.Gln306Pro)
 COSMIC
17g.7673578T=CA2245947747TP53c.950A= (p.Gln317=)
c.554A= (p.Gln185=)
c.671A= (p.Gln224=)
c.929A= (p.Gln310=)
c.782+603A= (n.782+603A=)
c.10A=
c.833A= (p.Gln278=)
c.473A= (p.Gln158=)
c.917A= (p.Gln306=)
17g.7673578_7673579delinsTGCA2245947741TP53c.949_950delinsCA (p.Gln317=)
c.553_554delinsCA (p.Gln185=)
c.670_671delinsCA (p.Gln224=)
c.928_929delinsCA (p.Gln310=)
c.782+602_782+603delinsCA (n.782+602_782+603delinsCA)
c.9_10delinsCA
c.832_833delinsCA (p.Gln278=)
c.472_473delinsCA (p.Gln158=)
c.916_917delinsCA (p.Gln306=)
17g.7673578_7673582delCA645587370TP53c.946_950del (p.Pro316AlafsTer19)
c.550_554del (p.Pro184AlafsTer19)
c.667_671del (p.Pro223AlafsTer19)
c.925_929del (p.Pro309AlafsTer19)
c.946_950del (p.Pro316AlafsTer?)
c.782+599_782+603del (n.782+599_782+603del)
c.946_950del (p.Pro316AlafsTer29)
c.946_950del (p.Pro316AlafsTer18)
c.550_554del (p.Pro184AlafsTer18)
c.550_554del (p.Pro184AlafsTer?)
c.550_554del (p.Pro184AlafsTer29)
c.6_10del
c.829_833del (p.Pro277AlafsTer19)
c.829_833del (p.Pro277AlafsTer18)
c.469_473del (p.Pro157AlafsTer18)
c.913_917del (p.Pro305AlafsTer19)
c.469_473del (p.Pro157AlafsTer29)
c.469_473del (p.Pro157AlafsTer19)
c.829_833del (p.Pro277AlafsTer29)
 COSMIC
17g.7673579G>ACA397835973TP53c.949C>T (p.Gln317Ter)
c.553C>T (p.Gln185Ter)
c.670C>T (p.Gln224Ter)
c.928C>T (p.Gln310Ter)
c.782+602C>T (n.782+602C>T)
c.9C>T
c.832C>T (p.Gln278Ter)
c.472C>T (p.Gln158Ter)
c.916C>T (p.Gln306Ter)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC
17g.7673579G>CCA397835975TP53c.949C>G (p.Gln317Glu)
c.553C>G (p.Gln185Glu)
c.670C>G (p.Gln224Glu)
c.928C>G (p.Gln310Glu)
c.782+602C>G (n.782+602C>G)
c.9C>G
c.832C>G (p.Gln278Glu)
c.472C>G (p.Gln158Glu)
c.916C>G (p.Gln306Glu)
 dbSNP
17g.7673579G=CA2245947768TP53c.949C= (p.Gln317=)
c.553C= (p.Gln185=)
c.670C= (p.Gln224=)
c.928C= (p.Gln310=)
c.782+602C= (n.782+602C=)
c.9C=
c.832C= (p.Gln278=)
c.472C= (p.Gln158=)
c.916C= (p.Gln306=)
17g.7673579G>TCA001204TP53c.949C>A (p.Gln317Lys)
c.553C>A (p.Gln185Lys)
c.670C>A (p.Gln224Lys)
c.928C>A (p.Gln310Lys)
c.782+602C>A (n.782+602C>A)
c.9C>A
c.832C>A (p.Gln278Lys)
c.472C>A (p.Gln158Lys)
c.916C>A (p.Gln306Lys)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
17g.7673579_7673580delinsAACA645587373TP53c.948_949delinsTT (p.Pro317Ter)
c.552_553delinsTT (p.Pro185Ter)
c.669_670delinsTT (p.Pro224Ter)
c.927_928delinsTT (p.Pro310Ter)
c.782+601_782+602delinsTT (n.782+601_782+602delinsTT)
c.8_9delinsTT
c.831_832delinsTT (p.Pro278Ter)
c.471_472delinsTT (p.Pro158Ter)
c.915_916delinsTT (p.Pro306Ter)
 COSMIC
17g.7673582dupCA645587372TP53c.949dup (p.Gln317ProfsTer20)
c.553dup (p.Gln185ProfsTer20)
c.670dup (p.Gln224ProfsTer20)
c.928dup (p.Gln310ProfsTer20)
c.949dup (p.Gln317ProfsTer?)
c.782+602dup (n.782+602dup)
c.949dup (p.Gln317ProfsTer30)
c.949dup (p.Gln317ProfsTer19)
c.553dup (p.Gln185ProfsTer19)
c.553dup (p.Gln185ProfsTer?)
c.553dup (p.Gln185ProfsTer30)
c.9dup
c.832dup (p.Gln278ProfsTer20)
c.832dup (p.Gln278ProfsTer19)
c.472dup (p.Gln158ProfsTer19)
c.916dup (p.Gln306ProfsTer20)
c.472dup (p.Gln158ProfsTer30)
c.472dup (p.Gln158ProfsTer20)
c.832dup (p.Gln278ProfsTer30)
 COSMIC COSMIC COSMIC COSMIC
17g.7673582delCA497714083TP53c.949del (p.Gln317SerfsTer28)
c.553del (p.Gln185SerfsTer28)
c.670del (p.Gln224SerfsTer28)
c.928del (p.Gln310SerfsTer28)
c.949del (p.Gln317SerfsTer?)
c.782+602del (n.782+602del)
c.949del (p.Gln317SerfsTer26)
c.553del (p.Gln185SerfsTer26)
c.553del (p.Gln185SerfsTer?)
c.9del
c.832del (p.Gln278SerfsTer28)
c.832del (p.Gln278SerfsTer26)
c.472del (p.Gln158SerfsTer26)
c.916del (p.Gln306SerfsTer28)
c.472del (p.Gln158SerfsTer?)
c.472del (p.Gln158SerfsTer28)
c.832del (p.Gln278SerfsTer?)
 ClinVar dbSNP COSMIC COSMIC COSMIC
17g.7673581_7673582delCA645587371TP53c.948_949del (p.Gln317AlafsTer19)
c.552_553del (p.Gln185AlafsTer19)
c.669_670del (p.Gln224AlafsTer19)
c.927_928del (p.Gln310AlafsTer19)
c.948_949del (p.Gln317AlafsTer?)
c.782+601_782+602del (n.782+601_782+602del)
c.948_949del (p.Gln317AlafsTer29)
c.948_949del (p.Gln317AlafsTer18)
c.552_553del (p.Gln185AlafsTer18)
c.552_553del (p.Gln185AlafsTer?)
c.552_553del (p.Gln185AlafsTer29)
c.8_9del
c.831_832del (p.Gln278AlafsTer19)
c.831_832del (p.Gln278AlafsTer18)
c.471_472del (p.Gln158AlafsTer18)
c.915_916del (p.Gln306AlafsTer19)
c.471_472del (p.Gln158AlafsTer29)
c.471_472del (p.Gln158AlafsTer19)
c.831_832del (p.Gln278AlafsTer29)
 COSMIC
17g.7673580G>ACA497714095TP53c.948C>T (p.Pro316=)
c.552C>T (p.Pro184=)
c.669C>T (p.Pro223=)
c.927C>T (p.Pro309=)
c.782+601C>T (n.782+601C>T)
c.8C>T
c.831C>T (p.Pro277=)
c.471C>T (p.Pro157=)
c.915C>T (p.Pro305=)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC
17g.7673580G>CCA497714109TP53c.948C>G (p.Pro316=)
c.552C>G (p.Pro184=)
c.669C>G (p.Pro223=)
c.927C>G (p.Pro309=)
c.782+601C>G (n.782+601C>G)
c.8C>G
c.831C>G (p.Pro277=)
c.471C>G (p.Pro157=)
c.915C>G (p.Pro305=)
 ClinVar dbSNP
17g.7673580G=CA2245947794TP53c.948C= (p.Pro316=)
c.552C= (p.Pro184=)
c.669C= (p.Pro223=)
c.927C= (p.Pro309=)
c.782+601C= (n.782+601C=)
c.8C=
c.831C= (p.Pro277=)
c.471C= (p.Pro157=)
c.915C= (p.Pro305=)
17g.7673580G>TCA497714113TP53c.948C>A (p.Pro316=)
c.552C>A (p.Pro184=)
c.669C>A (p.Pro223=)
c.927C>A (p.Pro309=)
c.782+601C>A (n.782+601C>A)
c.8C>A
c.831C>A (p.Pro277=)
c.471C>A (p.Pro157=)
c.915C>A (p.Pro305=)
17g.7673581G>ACA397835981TP53c.947C>T (p.Pro316Leu)
c.551C>T (p.Pro184Leu)
c.668C>T (p.Pro223Leu)
c.926C>T (p.Pro309Leu)
c.782+600C>T (n.782+600C>T)
c.7C>T
c.830C>T (p.Pro277Leu)
c.470C>T (p.Pro157Leu)
c.914C>T (p.Pro305Leu)
 ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC
17g.7673581G>CCA397835984TP53c.947C>G (p.Pro316Arg)
c.551C>G (p.Pro184Arg)
c.668C>G (p.Pro223Arg)
c.926C>G (p.Pro309Arg)
c.782+600C>G (n.782+600C>G)
c.7C>G
c.830C>G (p.Pro277Arg)
c.470C>G (p.Pro157Arg)
c.914C>G (p.Pro305Arg)
17g.7673581G=CA2245947801TP53c.947C= (p.Pro316=)
c.551C= (p.Pro184=)
c.668C= (p.Pro223=)
c.926C= (p.Pro309=)
c.782+600C= (n.782+600C=)
c.7C=
c.830C= (p.Pro277=)
c.470C= (p.Pro157=)
c.914C= (p.Pro305=)
17g.7673581G>TCA397835980TP53c.947C>A (p.Pro316His)
c.551C>A (p.Pro184His)
c.668C>A (p.Pro223His)
c.926C>A (p.Pro309His)
c.782+600C>A (n.782+600C>A)
c.7C>A
c.830C>A (p.Pro277His)
c.470C>A (p.Pro157His)
c.914C>A (p.Pro305His)
 dbSNP
17g.7673581_7673591delinsGGAGAGGAGCTCA2245947806TP53c.937_947delinsAGCTCCTCTCC (p.Ser313=)
c.541_551delinsAGCTCCTCTCC (p.Ser181=)
c.658_668delinsAGCTCCTCTCC (p.Ser220=)
c.916_926delinsAGCTCCTCTCC (p.Ser306=)
c.782+590_782+600delinsAGCTCCTCTCC (n.782+590_782+600delinsAGCTCCTCTCC)
c.820_830delinsAGCTCCTCTCC (p.Ser274=)
c.460_470delinsAGCTCCTCTCC (p.Ser154=)
c.904_914delinsAGCTCCTCTCC (p.Ser302=)
17g.7673582G>ACA397835996TP53c.946C>T (p.Pro316Ser)
c.550C>T (p.Pro184Ser)
c.667C>T (p.Pro223Ser)
c.925C>T (p.Pro309Ser)
c.782+599C>T (n.782+599C>T)
c.6C>T
c.829C>T (p.Pro277Ser)
c.469C>T (p.Pro157Ser)
c.913C>T (p.Pro305Ser)
 ClinVar dbSNP
17g.7673582G>CCA397835999TP53c.946C>G (p.Pro316Ala)
c.550C>G (p.Pro184Ala)
c.667C>G (p.Pro223Ala)
c.925C>G (p.Pro309Ala)
c.782+599C>G (n.782+599C>G)
c.6C>G
c.829C>G (p.Pro277Ala)
c.469C>G (p.Pro157Ala)
c.913C>G (p.Pro305Ala)
 dbSNP
17g.7673582G=CA2245947821TP53c.946C= (p.Pro316=)
c.550C= (p.Pro184=)
c.667C= (p.Pro223=)
c.925C= (p.Pro309=)
c.782+599C= (n.782+599C=)
c.6C=
c.829C= (p.Pro277=)
c.469C= (p.Pro157=)
c.913C= (p.Pro305=)
17g.7673582G>TCA001212TP53c.946C>A (p.Pro316Thr)
c.550C>A (p.Pro184Thr)
c.667C>A (p.Pro223Thr)
c.925C>A (p.Pro309Thr)
c.782+599C>A (n.782+599C>A)
c.6C>A
c.829C>A (p.Pro277Thr)
c.469C>A (p.Pro157Thr)
c.913C>A (p.Pro305Thr)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.7673582_7673583delinsGACA2245947828TP53c.945_946delinsTC (p.Ser315=)
c.549_550delinsTC (p.Ser183=)
c.666_667delinsTC (p.Ser222=)
c.924_925delinsTC (p.Ser308=)
c.782+598_782+599delinsTC (n.782+598_782+599delinsTC)
c.5_6delinsTC
c.828_829delinsTC (p.Ser276=)
c.468_469delinsTC (p.Ser156=)
c.912_913delinsTC (p.Ser304=)
17g.7673585_7673586dupCA2573102338TP53c.945_946dup (p.Pro316LeufsTer30)
c.549_550dup (p.Pro184LeufsTer30)
c.666_667dup (p.Pro223LeufsTer30)
c.924_925dup (p.Pro309LeufsTer30)
c.945_946dup (p.Pro316LeufsTer?)
c.782+598_782+599dup (n.782+598_782+599dup)
c.945_946dup (p.Pro316LeufsTer28)
c.549_550dup (p.Pro184LeufsTer28)
c.549_550dup (p.Pro184LeufsTer?)
c.5_6dup
c.828_829dup (p.Pro277LeufsTer30)
c.828_829dup (p.Pro277LeufsTer28)
c.468_469dup (p.Pro157LeufsTer28)
c.912_913dup (p.Pro305LeufsTer30)
c.468_469dup (p.Pro157LeufsTer?)
c.468_469dup (p.Pro157LeufsTer30)
c.828_829dup (p.Pro277LeufsTer?)
17g.7673585_7673586delCA645587374TP53c.945_946del (p.Gln317AlafsTer19)
c.549_550del (p.Gln185AlafsTer19)
c.666_667del (p.Gln224AlafsTer19)
c.924_925del (p.Gln310AlafsTer19)
c.945_946del (p.Gln317AlafsTer?)
c.782+598_782+599del (n.782+598_782+599del)
c.945_946del (p.Gln317AlafsTer18)
c.549_550del (p.Gln185AlafsTer18)
c.549_550del (p.Gln185AlafsTer?)
c.5_6del
c.828_829del (p.Gln278AlafsTer19)
c.828_829del (p.Gln278AlafsTer18)
c.468_469del (p.Gln158AlafsTer18)
c.912_913del (p.Gln306AlafsTer19)
c.468_469del (p.Gln158AlafsTer?)
c.468_469del (p.Gln158AlafsTer19)
c.828_829del (p.Gln278AlafsTer?)
 ClinVar dbSNP COSMIC COSMIC
17g.7673583_7673592delCA913190577TP53c.937_946del (p.Ser313ProfsTer29)
c.541_550del (p.Ser181ProfsTer29)
c.658_667del (p.Ser220ProfsTer29)
c.916_925del (p.Ser306ProfsTer29)
c.937_946del (p.Ser313ProfsTer?)
c.782+590_782+599del (n.782+590_782+599del)
c.937_946del (p.Ser313ProfsTer27)
c.541_550del (p.Ser181ProfsTer27)
c.541_550del (p.Ser181ProfsTer?)
c.820_829del (p.Ser274ProfsTer29)
c.820_829del (p.Ser274ProfsTer27)
c.460_469del (p.Ser154ProfsTer27)
c.904_913del (p.Ser302ProfsTer29)
c.460_469del (p.Ser154ProfsTer?)
c.460_469del (p.Ser154ProfsTer29)
c.820_829del (p.Ser274ProfsTer?)
 ClinVar dbSNP
17g.7673583delCA915949516TP53c.945del (p.Gln317SerfsTer28)
c.549del (p.Gln185SerfsTer28)
c.666del (p.Gln224SerfsTer28)
c.924del (p.Gln310SerfsTer28)
c.945del (p.Gln317SerfsTer?)
c.782+598del (n.782+598del)
c.945del (p.Gln317SerfsTer26)
c.549del (p.Gln185SerfsTer26)
c.549del (p.Gln185SerfsTer?)
c.5del
c.828del (p.Gln278SerfsTer28)
c.828del (p.Gln278SerfsTer26)
c.468del (p.Gln158SerfsTer26)
c.912del (p.Gln306SerfsTer28)
c.468del (p.Gln158SerfsTer?)
c.468del (p.Gln158SerfsTer28)
c.828del (p.Gln278SerfsTer?)
 ClinVar dbSNP
17g.7673583A>CCA497714137TP53c.945T>G (p.Ser315=)
c.549T>G (p.Ser183=)
c.666T>G (p.Ser222=)
c.924T>G (p.Ser308=)
c.782+598T>G (n.782+598T>G)
c.5T>G
c.828T>G (p.Ser276=)
c.468T>G (p.Ser156=)
c.912T>G (p.Ser304=)
 COSMIC
17g.7673583A>GCA497714150TP53c.945T>C (p.Ser315=)
c.549T>C (p.Ser183=)
c.666T>C (p.Ser222=)
c.924T>C (p.Ser308=)
c.782+598T>C (n.782+598T>C)
c.5T>C
c.828T>C (p.Ser276=)
c.468T>C (p.Ser156=)
c.912T>C (p.Ser304=)
 dbSNP
17g.7673583A>TCA497714154TP53c.945T>A (p.Ser315=)
c.549T>A (p.Ser183=)
c.666T>A (p.Ser222=)
c.924T>A (p.Ser308=)
c.782+598T>A (n.782+598T>A)
c.5T>A
c.828T>A (p.Ser276=)
c.468T>A (p.Ser156=)
c.912T>A (p.Ser304=)
 dbSNP
17g.7673583dupCA645587375TP53c.945dup (p.Pro316SerfsTer21)
c.549dup (p.Pro184SerfsTer21)
c.666dup (p.Pro223SerfsTer21)
c.924dup (p.Pro309SerfsTer21)
c.945dup (p.Pro316SerfsTer?)
c.782+598dup (n.782+598dup)
c.945dup (p.Pro316SerfsTer20)
c.549dup (p.Pro184SerfsTer20)
c.549dup (p.Pro184SerfsTer?)
c.5dup
c.828dup (p.Pro277SerfsTer21)
c.828dup (p.Pro277SerfsTer20)
c.468dup (p.Pro157SerfsTer20)
c.912dup (p.Pro305SerfsTer21)
c.468dup (p.Pro157SerfsTer?)
c.468dup (p.Pro157SerfsTer21)
c.828dup (p.Pro277SerfsTer?)
 ClinVar dbSNP COSMIC
17g.7673583_7673584insTCA497714157TP53c.944_945insA (p.Pro316SerfsTer21)
c.548_549insA (p.Pro184SerfsTer21)
c.665_666insA (p.Pro223SerfsTer21)
c.923_924insA (p.Pro309SerfsTer21)
c.944_945insA (p.Pro316SerfsTer?)
c.782+597_782+598insA (n.782+597_782+598insA)
c.944_945insA (p.Pro316SerfsTer20)
c.548_549insA (p.Pro184SerfsTer20)
c.548_549insA (p.Pro184SerfsTer?)
c.4_5insA
c.827_828insA (p.Pro277SerfsTer21)
c.827_828insA (p.Pro277SerfsTer20)
c.467_468insA (p.Pro157SerfsTer20)
c.911_912insA (p.Pro305SerfsTer21)
c.467_468insA (p.Pro157SerfsTer?)
c.467_468insA (p.Pro157SerfsTer21)
c.827_828insA (p.Pro277SerfsTer?)
17g.7673584G>ACA397836004TP53c.944C>T (p.Ser315Phe)
c.548C>T (p.Ser183Phe)
c.665C>T (p.Ser222Phe)
c.923C>T (p.Ser308Phe)
c.782+597C>T (n.782+597C>T)
c.4C>T
c.827C>T (p.Ser276Phe)
c.467C>T (p.Ser156Phe)
c.911C>T (p.Ser304Phe)
 ClinVar dbSNP
17g.7673584G>CCA397836006TP53c.944C>G (p.Ser315Cys)
c.548C>G (p.Ser183Cys)
c.665C>G (p.Ser222Cys)
c.923C>G (p.Ser308Cys)
c.782+597C>G (n.782+597C>G)
c.4C>G
c.827C>G (p.Ser276Cys)
c.467C>G (p.Ser156Cys)
c.911C>G (p.Ser304Cys)
 ClinVar dbSNP gnomAD v4 COSMIC
17g.7673584G=CA2245947848TP53c.944C= (p.Ser315=)
c.548C= (p.Ser183=)
c.665C= (p.Ser222=)
c.923C= (p.Ser308=)
c.782+597C= (n.782+597C=)
c.4C=
c.827C= (p.Ser276=)
c.467C= (p.Ser156=)
c.911C= (p.Ser304=)
17g.7673584G>TCA397836013TP53c.944C>A (p.Ser315Tyr)
c.548C>A (p.Ser183Tyr)
c.665C>A (p.Ser222Tyr)
c.923C>A (p.Ser308Tyr)
c.782+597C>A (n.782+597C>A)
c.4C>A
c.827C>A (p.Ser276Tyr)
c.467C>A (p.Ser156Tyr)
c.911C>A (p.Ser304Tyr)
 dbSNP
17g.7673585A=CA2245947858TP53c.943T= (p.Ser315=)
c.547T= (p.Ser183=)
c.664T= (p.Ser222=)
c.922T= (p.Ser308=)
c.782+596T= (n.782+596T=)
c.3T=
c.826T= (p.Ser276=)
c.466T= (p.Ser156=)
c.910T= (p.Ser304=)
17g.7673585A>CCA397836018TP53c.943T>G (p.Ser315Ala)
c.547T>G (p.Ser183Ala)
c.664T>G (p.Ser222Ala)
c.922T>G (p.Ser308Ala)
c.782+596T>G (n.782+596T>G)
c.3T>G
c.826T>G (p.Ser276Ala)
c.466T>G (p.Ser156Ala)
c.910T>G (p.Ser304Ala)
17g.7673585A>GCA397836023TP53c.943T>C (p.Ser315Pro)
c.547T>C (p.Ser183Pro)
c.664T>C (p.Ser222Pro)
c.922T>C (p.Ser308Pro)
c.782+596T>C (n.782+596T>C)
c.3T>C
c.826T>C (p.Ser276Pro)
c.466T>C (p.Ser156Pro)
c.910T>C (p.Ser304Pro)
 ClinVar dbSNP COSMIC
17g.7673585A>TCA000506TP53c.943T>A (p.Ser315Thr)
c.547T>A (p.Ser183Thr)
c.664T>A (p.Ser222Thr)
c.922T>A (p.Ser308Thr)
c.782+596T>A (n.782+596T>A)
c.3T>A
c.826T>A (p.Ser276Thr)
c.466T>A (p.Ser156Thr)
c.910T>A (p.Ser304Thr)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
17g.7673586G>ACA497714190TP53c.942C>T (p.Ser314=)
c.546C>T (p.Ser182=)
c.663C>T (p.Ser221=)
c.921C>T (p.Ser307=)
c.782+595C>T (n.782+595C>T)
c.2C>T
c.825C>T (p.Ser275=)
c.465C>T (p.Ser155=)
c.909C>T (p.Ser303=)
 dbSNP
17g.7673586G>CCA497714198TP53c.942C>G (p.Ser314=)
c.546C>G (p.Ser182=)
c.663C>G (p.Ser221=)
c.921C>G (p.Ser307=)
c.782+595C>G (n.782+595C>G)
c.2C>G
c.825C>G (p.Ser275=)
c.465C>G (p.Ser155=)
c.909C>G (p.Ser303=)
 ClinVar dbSNP
17g.7673586G=CA2245947870TP53c.942C= (p.Ser314=)
c.546C= (p.Ser182=)
c.663C= (p.Ser221=)
c.921C= (p.Ser307=)
c.782+595C= (n.782+595C=)
c.2C=
c.825C= (p.Ser275=)
c.465C= (p.Ser155=)
c.909C= (p.Ser303=)
17g.7673586G>TCA001225TP53c.942C>A (p.Ser314=)
c.546C>A (p.Ser182=)
c.663C>A (p.Ser221=)
c.921C>A (p.Ser307=)
c.782+595C>A (n.782+595C>A)
c.2C>A
c.825C>A (p.Ser275=)
c.465C>A (p.Ser155=)
c.909C>A (p.Ser303=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
17g.7673587G>ACA001234TP53c.941C>T (p.Ser314Phe)
c.545C>T (p.Ser182Phe)
c.662C>T (p.Ser221Phe)
c.920C>T (p.Ser307Phe)
c.782+594C>T (n.782+594C>T)
c.1C>T
c.824C>T (p.Ser275Phe)
c.464C>T (p.Ser155Phe)
c.908C>T (p.Ser303Phe)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
17g.7673587G>CCA397836031TP53c.941C>G (p.Ser314Cys)
c.545C>G (p.Ser182Cys)
c.662C>G (p.Ser221Cys)
c.920C>G (p.Ser307Cys)
c.782+594C>G (n.782+594C>G)
c.1C>G
c.824C>G (p.Ser275Cys)
c.464C>G (p.Ser155Cys)
c.908C>G (p.Ser303Cys)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC
17g.7673587G=CA2245947882TP53c.941C= (p.Ser314=)
c.545C= (p.Ser182=)
c.662C= (p.Ser221=)
c.920C= (p.Ser307=)
c.782+594C= (n.782+594C=)
c.1C=
c.824C= (p.Ser275=)
c.464C= (p.Ser155=)
c.908C= (p.Ser303=)
17g.7673587G>TCA397836036TP53c.941C>A (p.Ser314Tyr)
c.545C>A (p.Ser182Tyr)
c.662C>A (p.Ser221Tyr)
c.920C>A (p.Ser307Tyr)
c.782+594C>A (n.782+594C>A)
c.1C>A
c.824C>A (p.Ser275Tyr)
c.464C>A (p.Ser155Tyr)
c.908C>A (p.Ser303Tyr)
 dbSNP
17g.7673588A>CCA397836044TP53c.940T>G (p.Ser314Ala)
c.544T>G (p.Ser182Ala)
c.661T>G (p.Ser221Ala)
c.919T>G (p.Ser307Ala)
c.782+593T>G (n.782+593T>G)
c.823T>G (p.Ser275Ala)
c.463T>G (p.Ser155Ala)
c.907T>G (p.Ser303Ala)
17g.7673588A>GCA397836042TP53c.940T>C (p.Ser314Pro)
c.544T>C (p.Ser182Pro)
c.661T>C (p.Ser221Pro)
c.919T>C (p.Ser307Pro)
c.782+593T>C (n.782+593T>C)
c.823T>C (p.Ser275Pro)
c.463T>C (p.Ser155Pro)
c.907T>C (p.Ser303Pro)
17g.7673588A>TCA397836039TP53c.940T>A (p.Ser314Thr)
c.544T>A (p.Ser182Thr)
c.661T>A (p.Ser221Thr)
c.919T>A (p.Ser307Thr)
c.782+593T>A (n.782+593T>A)
c.823T>A (p.Ser275Thr)
c.463T>A (p.Ser155Thr)
c.907T>A (p.Ser303Thr)
 dbSNP
17g.7673589G>ACA497714209TP53c.939C>T (p.Ser313=)
c.543C>T (p.Ser181=)
c.660C>T (p.Ser220=)
c.918C>T (p.Ser306=)
c.782+592C>T (n.782+592C>T)
c.822C>T (p.Ser274=)
c.462C>T (p.Ser154=)
c.906C>T (p.Ser302=)
 dbSNP
17g.7673589G>CCA397836048TP53c.939C>G (p.Ser313Arg)
c.543C>G (p.Ser181Arg)
c.660C>G (p.Ser220Arg)
c.918C>G (p.Ser306Arg)
c.782+592C>G (n.782+592C>G)
c.822C>G (p.Ser274Arg)
c.462C>G (p.Ser154Arg)
c.906C>G (p.Ser302Arg)
 dbSNP
17g.7673589G=CA2245947895TP53c.939C= (p.Ser313=)
c.543C= (p.Ser181=)
c.660C= (p.Ser220=)
c.918C= (p.Ser306=)
c.782+592C= (n.782+592C=)
c.822C= (p.Ser274=)
c.462C= (p.Ser154=)
c.906C= (p.Ser302=)
17g.7673589G>TCA397836050TP53c.939C>A (p.Ser313Arg)
c.543C>A (p.Ser181Arg)
c.660C>A (p.Ser220Arg)
c.918C>A (p.Ser306Arg)
c.782+592C>A (n.782+592C>A)
c.822C>A (p.Ser274Arg)
c.462C>A (p.Ser154Arg)
c.906C>A (p.Ser302Arg)
 dbSNP
17g.7673592_7673610delCA645587376TP53c.921_939del
c.525_543del
c.642_660del
c.900_918del
c.782+574_782+592del (n.782+574_782+592del)
c.804_822del
c.444_462del
c.888_906del
 COSMIC
17g.7673590delCA891842223TP53c.938del (p.Ser313ThrfsTer?)
c.542del (p.Ser181ThrfsTer?)
c.659del (p.Ser220ThrfsTer?)
c.917del (p.Ser306ThrfsTer?)
c.782+591del (n.782+591del)
c.938del (p.Ser313ThrfsTer30)
c.542del (p.Ser181ThrfsTer30)
c.821del (p.Ser274ThrfsTer?)
c.821del (p.Ser274ThrfsTer30)
c.461del (p.Ser154ThrfsTer30)
c.905del (p.Ser302ThrfsTer?)
c.461del (p.Ser154ThrfsTer?)
17g.7673590C>ACA397836053TP53c.938G>T (p.Ser313Ile)
c.542G>T (p.Ser181Ile)
c.659G>T (p.Ser220Ile)
c.917G>T (p.Ser306Ile)
c.782+591G>T (n.782+591G>T)
c.821G>T (p.Ser274Ile)
c.461G>T (p.Ser154Ile)
c.905G>T (p.Ser302Ile)
 dbSNP
17g.7673590C>GCA397836056TP53c.938G>C (p.Ser313Thr)
c.542G>C (p.Ser181Thr)
c.659G>C (p.Ser220Thr)
c.917G>C (p.Ser306Thr)
c.782+591G>C (n.782+591G>C)
c.821G>C (p.Ser274Thr)
c.461G>C (p.Ser154Thr)
c.905G>C (p.Ser302Thr)
 dbSNP
17g.7673590C>TCA397836058TP53c.938G>A (p.Ser313Asn)
c.542G>A (p.Ser181Asn)
c.659G>A (p.Ser220Asn)
c.917G>A (p.Ser306Asn)
c.782+591G>A (n.782+591G>A)
c.821G>A (p.Ser274Asn)
c.461G>A (p.Ser154Asn)
c.905G>A (p.Ser302Asn)
 ClinVar dbSNP COSMIC
17g.7673592_7673702delCA645587377TP53c.919+1_938del
c.523+1_542del
c.640+1_659del
c.898+1_917del
c.782+481_782+591del (n.782+481_782+591del)
c.802+1_821del
c.442+1_461del
c.886+1_905del
 COSMIC
17g.7673591T>ACA397836061TP53c.937A>T (p.Ser313Cys)
c.541A>T (p.Ser181Cys)
c.658A>T (p.Ser220Cys)
c.916A>T (p.Ser306Cys)
c.782+590A>T (n.782+590A>T)
c.820A>T (p.Ser274Cys)
c.460A>T (p.Ser154Cys)
c.904A>T (p.Ser302Cys)
 COSMIC
17g.7673591T>CCA397836063TP53c.937A>G (p.Ser313Gly)
c.541A>G (p.Ser181Gly)
c.658A>G (p.Ser220Gly)
c.916A>G (p.Ser306Gly)
c.782+590A>G (n.782+590A>G)
c.820A>G (p.Ser274Gly)
c.460A>G (p.Ser154Gly)
c.904A>G (p.Ser302Gly)
17g.7673591T>GCA397836065TP53c.937A>C (p.Ser313Arg)
c.541A>C (p.Ser181Arg)
c.658A>C (p.Ser220Arg)
c.916A>C (p.Ser306Arg)
c.782+590A>C (n.782+590A>C)
c.820A>C (p.Ser274Arg)
c.460A>C (p.Ser154Arg)
c.904A>C (p.Ser302Arg)
17g.7673592G>ACA497714260TP53c.936C>T (p.Thr312=)
c.540C>T (p.Thr180=)
c.657C>T (p.Thr219=)
c.915C>T (p.Thr305=)
c.782+589C>T (n.782+589C>T)
c.819C>T (p.Thr273=)
c.459C>T (p.Thr153=)
c.903C>T (p.Thr301=)
 COSMIC
17g.7673592G>CCA497714258TP53c.936C>G (p.Thr312=)
c.540C>G (p.Thr180=)
c.657C>G (p.Thr219=)
c.915C>G (p.Thr305=)
c.782+589C>G (n.782+589C>G)
c.819C>G (p.Thr273=)
c.459C>G (p.Thr153=)
c.903C>G (p.Thr301=)
 ClinVar dbSNP gnomAD v4
17g.7673592G=CA2245947902TP53c.936C= (p.Thr312=)
c.540C= (p.Thr180=)
c.657C= (p.Thr219=)
c.915C= (p.Thr305=)
c.782+589C= (n.782+589C=)
c.819C= (p.Thr273=)
c.459C= (p.Thr153=)
c.903C= (p.Thr301=)
17g.7673592G>TCA497714264TP53c.936C>A (p.Thr312=)
c.540C>A (p.Thr180=)
c.657C>A (p.Thr219=)
c.915C>A (p.Thr305=)
c.782+589C>A (n.782+589C>A)
c.819C>A (p.Thr273=)
c.459C>A (p.Thr153=)
c.903C>A (p.Thr301=)
 ClinVar dbSNP COSMIC
17g.7673593delCA497714256TP53c.936del (p.Ser313AlafsTer?)
c.540del (p.Ser181AlafsTer?)
c.657del (p.Ser220AlafsTer?)
c.915del (p.Ser306AlafsTer?)
c.782+589del (n.782+589del)
c.819del (p.Ser274AlafsTer?)
c.459del (p.Ser154AlafsTer?)
c.903del (p.Ser302AlafsTer?)
 COSMIC COSMIC COSMIC
17g.7673593G>ACA397836069TP53c.935C>T (p.Thr312Ile)
c.539C>T (p.Thr180Ile)
c.656C>T (p.Thr219Ile)
c.914C>T (p.Thr305Ile)
c.782+588C>T (n.782+588C>T)
c.818C>T (p.Thr273Ile)
c.458C>T (p.Thr153Ile)
c.902C>T (p.Thr301Ile)
 ClinVar dbSNP COSMIC
17g.7673593G>CCA000505TP53c.935C>G (p.Thr312Ser)
c.539C>G (p.Thr180Ser)
c.656C>G (p.Thr219Ser)
c.914C>G (p.Thr305Ser)
c.782+588C>G (n.782+588C>G)
c.818C>G (p.Thr273Ser)
c.458C>G (p.Thr153Ser)
c.902C>G (p.Thr301Ser)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
17g.7673593G=CA2245947910TP53c.935C= (p.Thr312=)
c.539C= (p.Thr180=)
c.656C= (p.Thr219=)
c.914C= (p.Thr305=)
c.782+588C= (n.782+588C=)
c.818C= (p.Thr273=)
c.458C= (p.Thr153=)
c.902C= (p.Thr301=)
17g.7673593G>TCA397836074TP53c.935C>A (p.Thr312Asn)
c.539C>A (p.Thr180Asn)
c.656C>A (p.Thr219Asn)
c.914C>A (p.Thr305Asn)
c.782+588C>A (n.782+588C>A)
c.818C>A (p.Thr273Asn)
c.458C>A (p.Thr153Asn)
c.902C>A (p.Thr301Asn)
 ClinVar dbSNP
17g.7673593_7673594insACTTAGTACCTGAAGGGTGAAATATTCTCCATCCAGTGCA645587378TP53c.935_936insACTGGATGGAGAATATTTCACCCTTCAGGTACTAAGTC (p.Ser313LeufsTer?)
c.539_540insACTGGATGGAGAATATTTCACCCTTCAGGTACTAAGTC (p.Ser181LeufsTer?)
c.656_657insACTGGATGGAGAATATTTCACCCTTCAGGTACTAAGTC (p.Ser220LeufsTer?)
c.914_915insACTGGATGGAGAATATTTCACCCTTCAGGTACTAAGTC (p.Ser306LeufsTer?)
c.782+588_782+589insACTGGATGGAGAATATTTCACCCTTCAGGTACTAAGTC (n.782+588_782+589insACTGGATGGAGAATATTTCACCCTTCAGGTACTAAGTC)
c.818_819insACTGGATGGAGAATATTTCACCCTTCAGGTACTAAGTC (p.Ser274LeufsTer?)
c.458_459insACTGGATGGAGAATATTTCACCCTTCAGGTACTAAGTC (p.Ser154LeufsTer?)
c.902_903insACTGGATGGAGAATATTTCACCCTTCAGGTACTAAGTC (p.Ser302LeufsTer?)
 COSMIC COSMIC COSMIC COSMIC
17g.7673594delCA497714281TP53c.934del (p.Thr312ProfsTer?)
c.538del (p.Thr180ProfsTer?)
c.655del (p.Thr219ProfsTer?)
c.913del (p.Thr305ProfsTer?)
c.782+587del (n.782+587del)
c.817del (p.Thr273ProfsTer?)
c.457del (p.Thr153ProfsTer?)
c.901del (p.Thr301ProfsTer?)
 COSMIC
17g.7673594T>ACA397836079TP53c.934A>T (p.Thr312Ser)
c.538A>T (p.Thr180Ser)
c.655A>T (p.Thr219Ser)
c.913A>T (p.Thr305Ser)
c.782+587A>T (n.782+587A>T)
c.817A>T (p.Thr273Ser)
c.457A>T (p.Thr153Ser)
c.901A>T (p.Thr301Ser)
 dbSNP COSMIC
17g.7673594T>CCA397836082TP53c.934A>G (p.Thr312Ala)
c.538A>G (p.Thr180Ala)
c.655A>G (p.Thr219Ala)
c.913A>G (p.Thr305Ala)
c.782+587A>G (n.782+587A>G)
c.817A>G (p.Thr273Ala)
c.457A>G (p.Thr153Ala)
c.901A>G (p.Thr301Ala)
 ClinVar dbSNP gnomAD v4 COSMIC
17g.7673594T>GCA397836085TP53c.934A>C (p.Thr312Pro)
c.538A>C (p.Thr180Pro)
c.655A>C (p.Thr219Pro)
c.913A>C (p.Thr305Pro)
c.782+587A>C (n.782+587A>C)
c.817A>C (p.Thr273Pro)
c.457A>C (p.Thr153Pro)
c.901A>C (p.Thr301Pro)
 dbSNP
17g.7673594dupCA645587379TP53c.934dup (p.Thr312AsnfsTer25)
c.538dup (p.Thr180AsnfsTer25)
c.655dup (p.Thr219AsnfsTer25)
c.913dup (p.Thr305AsnfsTer25)
c.934dup (p.Thr312AsnfsTer?)
c.782+587dup (n.782+587dup)
c.934dup (p.Thr312AsnfsTer24)
c.538dup (p.Thr180AsnfsTer24)
c.538dup (p.Thr180AsnfsTer?)
c.817dup (p.Thr273AsnfsTer25)
c.817dup (p.Thr273AsnfsTer24)
c.457dup (p.Thr153AsnfsTer24)
c.901dup (p.Thr301AsnfsTer25)
c.457dup (p.Thr153AsnfsTer?)
c.457dup (p.Thr153AsnfsTer25)
c.817dup (p.Thr273AsnfsTer?)
 COSMIC COSMIC COSMIC COSMIC
17g.7673594_7673595delinsTGCA2245947916TP53c.933_934delinsCA (p.Asn311=)
c.537_538delinsCA (p.Asn179=)
c.654_655delinsCA (p.Asn218=)
c.912_913delinsCA (p.Asn304=)
c.782+586_782+587delinsCA (n.782+586_782+587delinsCA)
c.816_817delinsCA (p.Asn272=)
c.456_457delinsCA (p.Asn152=)
c.900_901delinsCA (p.Asn300=)
17g.7673595delCA497714310TP53c.933del (p.Asn311LysfsTer?)
c.537del (p.Asn179LysfsTer?)
c.654del (p.Asn218LysfsTer?)
c.912del (p.Asn304LysfsTer?)
c.782+586del (n.782+586del)
c.816del (p.Asn272LysfsTer?)
c.456del (p.Asn152LysfsTer?)
c.900del (p.Asn300LysfsTer?)
 ClinVar dbSNP COSMIC
17g.7673595G>ACA16607849TP53c.933C>T (p.Asn311=)
c.537C>T (p.Asn179=)
c.654C>T (p.Asn218=)
c.912C>T (p.Asn304=)
c.782+586C>T (n.782+586C>T)
c.816C>T (p.Asn272=)
c.456C>T (p.Asn152=)
c.900C>T (p.Asn300=)
 ClinVar dbSNP
17g.7673595G>CCA397836091TP53c.933C>G (p.Asn311Lys)
c.537C>G (p.Asn179Lys)
c.654C>G (p.Asn218Lys)
c.912C>G (p.Asn304Lys)
c.782+586C>G (n.782+586C>G)
c.816C>G (p.Asn272Lys)
c.456C>G (p.Asn152Lys)
c.900C>G (p.Asn300Lys)
 dbSNP COSMIC
17g.7673595G=CA2245947932TP53c.933C= (p.Asn311=)
c.537C= (p.Asn179=)
c.654C= (p.Asn218=)
c.912C= (p.Asn304=)
c.782+586C= (n.782+586C=)
c.816C= (p.Asn272=)
c.456C= (p.Asn152=)
c.900C= (p.Asn300=)
17g.7673595G>TCA397836089TP53c.933C>A (p.Asn311Lys)
c.537C>A (p.Asn179Lys)
c.654C>A (p.Asn218Lys)
c.912C>A (p.Asn304Lys)
c.782+586C>A (n.782+586C>A)
c.816C>A (p.Asn272Lys)
c.456C>A (p.Asn152Lys)
c.900C>A (p.Asn300Lys)
17g.7673596T>ACA397836095TP53c.932A>T (p.Asn311Ile)
c.536A>T (p.Asn179Ile)
c.653A>T (p.Asn218Ile)
c.911A>T (p.Asn304Ile)
c.782+585A>T (n.782+585A>T)
c.815A>T (p.Asn272Ile)
c.455A>T (p.Asn152Ile)
c.899A>T (p.Asn300Ile)
 dbSNP
17g.7673596T>CCA16615690TP53c.932A>G (p.Asn311Ser)
c.536A>G (p.Asn179Ser)
c.653A>G (p.Asn218Ser)
c.911A>G (p.Asn304Ser)
c.782+585A>G (n.782+585A>G)
c.815A>G (p.Asn272Ser)
c.455A>G (p.Asn152Ser)
c.899A>G (p.Asn300Ser)
 ClinVar dbSNP gnomAD v4
17g.7673596T>GCA349248TP53c.932A>C (p.Asn311Thr)
c.536A>C (p.Asn179Thr)
c.653A>C (p.Asn218Thr)
c.911A>C (p.Asn304Thr)
c.782+585A>C (n.782+585A>C)
c.815A>C (p.Asn272Thr)
c.455A>C (p.Asn152Thr)
c.899A>C (p.Asn300Thr)
 ClinVar dbSNP gnomAD v4
17g.7673596T=CA2245947945TP53c.932A= (p.Asn311=)
c.536A= (p.Asn179=)
c.653A= (p.Asn218=)
c.911A= (p.Asn304=)
c.782+585A= (n.782+585A=)
c.815A= (p.Asn272=)
c.455A= (p.Asn152=)
c.899A= (p.Asn300=)
17g.7673597dupCA891842224TP53c.932dup (p.Asn311LysfsTer26)
c.536dup (p.Asn179LysfsTer26)
c.653dup (p.Asn218LysfsTer26)
c.911dup (p.Asn304LysfsTer26)
c.932dup (p.Asn311LysfsTer?)
c.782+585dup (n.782+585dup)
c.932dup (p.Asn311LysfsTer25)
c.536dup (p.Asn179LysfsTer25)
c.536dup (p.Asn179LysfsTer?)
c.815dup (p.Asn272LysfsTer26)
c.815dup (p.Asn272LysfsTer25)
c.455dup (p.Asn152LysfsTer25)
c.899dup (p.Asn300LysfsTer26)
c.455dup (p.Asn152LysfsTer?)
c.455dup (p.Asn152LysfsTer26)
c.815dup (p.Asn272LysfsTer?)
 ClinVar
17g.7673597T>ACA397836102TP53c.931A>T (p.Asn311Tyr)
c.535A>T (p.Asn179Tyr)
c.652A>T (p.Asn218Tyr)
c.910A>T (p.Asn304Tyr)
c.782+584A>T (n.782+584A>T)
c.814A>T (p.Asn272Tyr)
c.454A>T (p.Asn152Tyr)
c.898A>T (p.Asn300Tyr)
 dbSNP COSMIC
17g.7673597T>CCA397836104TP53c.931A>G (p.Asn311Asp)
c.535A>G (p.Asn179Asp)
c.652A>G (p.Asn218Asp)
c.910A>G (p.Asn304Asp)
c.782+584A>G (n.782+584A>G)
c.814A>G (p.Asn272Asp)
c.454A>G (p.Asn152Asp)
c.898A>G (p.Asn300Asp)
17g.7673597T>GCA397836105TP53c.931A>C (p.Asn311His)
c.535A>C (p.Asn179His)
c.652A>C (p.Asn218His)
c.910A>C (p.Asn304His)
c.782+584A>C (n.782+584A>C)
c.814A>C (p.Asn272His)
c.454A>C (p.Asn152His)
c.898A>C (p.Asn300His)
 ClinVar dbSNP gnomAD v4 COSMIC
17g.7673597T=CA2245947959TP53c.931A= (p.Asn311=)
c.535A= (p.Asn179=)
c.652A= (p.Asn218=)
c.910A= (p.Asn304=)
c.782+584A= (n.782+584A=)
c.814A= (p.Asn272=)
c.454A= (p.Asn152=)
c.898A= (p.Asn300=)
17g.7673598_7673702delCA645587380TP53c.919_931del
c.523_535del
c.640_652del
c.898_910del
c.782+480_782+584del (n.782+480_782+584del)
c.802_814del
c.442_454del
c.886_898del
 COSMIC
17g.7673598G>ACA497714331TP53c.930C>T (p.Asn310=)
c.534C>T (p.Asn178=)
c.651C>T (p.Asn217=)
c.909C>T (p.Asn303=)
c.782+583C>T (n.782+583C>T)
c.813C>T (p.Asn271=)
c.453C>T (p.Asn151=)
c.897C>T (p.Asn299=)
 ClinVar dbSNP
17g.7673598G>CCA397836109TP53c.930C>G (p.Asn310Lys)
c.534C>G (p.Asn178Lys)
c.651C>G (p.Asn217Lys)
c.909C>G (p.Asn303Lys)
c.782+583C>G (n.782+583C>G)
c.813C>G (p.Asn271Lys)
c.453C>G (p.Asn151Lys)
c.897C>G (p.Asn299Lys)
 ClinVar dbSNP gnomAD v2 gnomAD v4
17g.7673598G=CA2245947967TP53c.930C= (p.Asn310=)
c.534C= (p.Asn178=)
c.651C= (p.Asn217=)
c.909C= (p.Asn303=)
c.782+583C= (n.782+583C=)
c.813C= (p.Asn271=)
c.453C= (p.Asn151=)
c.897C= (p.Asn299=)
17g.7673598G>TCA10580910TP53c.930C>A (p.Asn310Lys)
c.534C>A (p.Asn178Lys)
c.651C>A (p.Asn217Lys)
c.909C>A (p.Asn303Lys)
c.782+583C>A (n.782+583C>A)
c.813C>A (p.Asn271Lys)
c.453C>A (p.Asn151Lys)
c.897C>A (p.Asn299Lys)
 ClinVar dbSNP
17g.7673598_7673600delinsCAACA645587381TP53c.928_930delinsTTG (p.Asn310Leu)
c.532_534delinsTTG (p.Asn178Leu)
c.649_651delinsTTG (p.Asn217Leu)
c.907_909delinsTTG (p.Asn303Leu)
c.782+581_782+583delinsTTG (n.782+581_782+583delinsTTG)
c.811_813delinsTTG (p.Asn271Leu)
c.451_453delinsTTG (p.Asn151Leu)
c.895_897delinsTTG (p.Asn299Leu)
 COSMIC
17g.7673598_7673599insACA645587383TP53c.929_930insT (p.Asn311GlnfsTer26)
c.533_534insT (p.Asn179GlnfsTer26)
c.650_651insT (p.Asn218GlnfsTer26)
c.908_909insT (p.Asn304GlnfsTer26)
c.929_930insT (p.Asn311GlnfsTer?)
c.782+582_782+583insT (n.782+582_782+583insT)
c.929_930insT (p.Asn311GlnfsTer25)
c.533_534insT (p.Asn179GlnfsTer25)
c.533_534insT (p.Asn179GlnfsTer?)
c.812_813insT (p.Asn272GlnfsTer26)
c.812_813insT (p.Asn272GlnfsTer25)
c.452_453insT (p.Asn152GlnfsTer25)
c.896_897insT (p.Asn300GlnfsTer26)
c.452_453insT (p.Asn152GlnfsTer?)
c.452_453insT (p.Asn152GlnfsTer26)
c.812_813insT (p.Asn272GlnfsTer?)
 COSMIC
17g.7673599T>ACA397836112TP53c.929A>T (p.Asn310Ile)
c.533A>T (p.Asn178Ile)
c.650A>T (p.Asn217Ile)
c.908A>T (p.Asn303Ile)
c.782+582A>T (n.782+582A>T)
c.812A>T (p.Asn271Ile)
c.452A>T (p.Asn151Ile)
c.896A>T (p.Asn299Ile)
 ClinVar dbSNP
17g.7673599T>CCA397836116TP53c.929A>G (p.Asn310Ser)
c.533A>G (p.Asn178Ser)
c.650A>G (p.Asn217Ser)
c.908A>G (p.Asn303Ser)
c.782+582A>G (n.782+582A>G)
c.812A>G (p.Asn271Ser)
c.452A>G (p.Asn151Ser)
c.896A>G (p.Asn299Ser)
 ClinVar dbSNP
17g.7673599T>GCA397836117TP53c.929A>C (p.Asn310Thr)
c.533A>C (p.Asn178Thr)
c.650A>C (p.Asn217Thr)
c.908A>C (p.Asn303Thr)
c.782+582A>C (n.782+582A>C)
c.812A>C (p.Asn271Thr)
c.452A>C (p.Asn151Thr)
c.896A>C (p.Asn299Thr)
 dbSNP COSMIC
17g.7673600dupCA497714339TP53c.929dup (p.Asn310LysfsTer27)
c.533dup (p.Asn178LysfsTer27)
c.650dup (p.Asn217LysfsTer27)
c.908dup (p.Asn303LysfsTer27)
c.929dup (p.Asn310LysfsTer?)
c.782+582dup (n.782+582dup)
c.929dup (p.Asn310LysfsTer26)
c.533dup (p.Asn178LysfsTer26)
c.533dup (p.Asn178LysfsTer?)
c.812dup (p.Asn271LysfsTer27)
c.812dup (p.Asn271LysfsTer26)
c.452dup (p.Asn151LysfsTer26)
c.896dup (p.Asn299LysfsTer27)
c.452dup (p.Asn151LysfsTer?)
c.452dup (p.Asn151LysfsTer27)
c.812dup (p.Asn271LysfsTer?)
17g.7673600T>ACA397836121TP53c.928A>T (p.Asn310Tyr)
c.532A>T (p.Asn178Tyr)
c.649A>T (p.Asn217Tyr)
c.907A>T (p.Asn303Tyr)
c.782+581A>T (n.782+581A>T)
c.811A>T (p.Asn271Tyr)
c.451A>T (p.Asn151Tyr)
c.895A>T (p.Asn299Tyr)
17g.7673600T>CCA397836124TP53c.928A>G (p.Asn310Asp)
c.532A>G (p.Asn178Asp)
c.649A>G (p.Asn217Asp)
c.907A>G (p.Asn303Asp)
c.782+581A>G (n.782+581A>G)
c.811A>G (p.Asn271Asp)
c.451A>G (p.Asn151Asp)
c.895A>G (p.Asn299Asp)
 ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC
17g.7673600T>GCA397836126TP53c.928A>C (p.Asn310His)
c.532A>C (p.Asn178His)
c.649A>C (p.Asn217His)
c.907A>C (p.Asn303His)
c.782+581A>C (n.782+581A>C)
c.811A>C (p.Asn271His)
c.451A>C (p.Asn151His)
c.895A>C (p.Asn299His)
 ClinVar COSMIC COSMIC COSMIC COSMIC
17g.7673600T=CA2245947978TP53c.928A= (p.Asn310=)
c.532A= (p.Asn178=)
c.649A= (p.Asn217=)
c.907A= (p.Asn303=)
c.782+581A= (n.782+581A=)
c.811A= (p.Asn271=)
c.451A= (p.Asn151=)
c.895A= (p.Asn299=)
17g.7673600_7673601delinsTGCA2245947981TP53c.927_928delinsCA (p.Pro309=)
c.531_532delinsCA (p.Pro177=)
c.648_649delinsCA (p.Pro216=)
c.906_907delinsCA (p.Pro302=)
c.782+580_782+581delinsCA (n.782+580_782+581delinsCA)
c.810_811delinsCA (p.Pro270=)
c.450_451delinsCA (p.Pro150=)
c.894_895delinsCA (p.Pro298=)
17g.7673600_7673604delCA645587385TP53c.924_928del (p.Pro309GlnfsTer26)
c.528_532del (p.Pro177GlnfsTer26)
c.645_649del (p.Pro216GlnfsTer26)
c.903_907del (p.Pro302GlnfsTer26)
c.924_928del (p.Pro309GlnfsTer?)
c.782+577_782+581del (n.782+577_782+581del)
c.924_928del (p.Pro309GlnfsTer25)
c.528_532del (p.Pro177GlnfsTer25)
c.528_532del (p.Pro177GlnfsTer?)
c.807_811del (p.Pro270GlnfsTer26)
c.807_811del (p.Pro270GlnfsTer25)
c.447_451del (p.Pro150GlnfsTer25)
c.891_895del (p.Pro298GlnfsTer26)
c.447_451del (p.Pro150GlnfsTer?)
c.447_451del (p.Pro150GlnfsTer26)
c.807_811del (p.Pro270GlnfsTer?)
 COSMIC
17g.7673600_7673614delCA645587386TP53c.920-6_928del
c.524-6_532del
c.641-6_649del
c.899-6_907del
c.782+567_782+581del (n.782+567_782+581del)
c.803-6_811del
c.443-6_451del
c.887-6_895del
 COSMIC
17g.7673601G>ACA497714349TP53c.927C>T (p.Pro309=)
c.531C>T (p.Pro177=)
c.648C>T (p.Pro216=)
c.906C>T (p.Pro302=)
c.782+580C>T (n.782+580C>T)
c.810C>T (p.Pro270=)
c.450C>T (p.Pro150=)
c.894C>T (p.Pro298=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
17g.7673601G>CCA497714350TP53c.927C>G (p.Pro309=)
c.531C>G (p.Pro177=)
c.648C>G (p.Pro216=)
c.906C>G (p.Pro302=)
c.782+580C>G (n.782+580C>G)
c.810C>G (p.Pro270=)
c.450C>G (p.Pro150=)
c.894C>G (p.Pro298=)
 dbSNP
17g.7673601G=CA2245947993TP53c.927C= (p.Pro309=)
c.531C= (p.Pro177=)
c.648C= (p.Pro216=)
c.906C= (p.Pro302=)
c.782+580C= (n.782+580C=)
c.810C= (p.Pro270=)
c.450C= (p.Pro150=)
c.894C= (p.Pro298=)
17g.7673601G>TCA497714352TP53c.927C>A (p.Pro309=)
c.531C>A (p.Pro177=)
c.648C>A (p.Pro216=)
c.906C>A (p.Pro302=)
c.782+580C>A (n.782+580C>A)
c.810C>A (p.Pro270=)
c.450C>A (p.Pro150=)
c.894C>A (p.Pro298=)
 ClinVar dbSNP COSMIC
17g.7673603delCA497714355TP53c.927del (p.Asn310ThrfsTer?)
c.531del (p.Asn178ThrfsTer?)
c.648del (p.Asn217ThrfsTer?)
c.906del (p.Asn303ThrfsTer?)
c.782+580del (n.782+580del)
c.810del (p.Asn271ThrfsTer?)
c.450del (p.Asn151ThrfsTer?)
c.894del (p.Asn299ThrfsTer?)
 ClinVar dbSNP COSMIC COSMIC
17g.7673602G>ACA397836130TP53c.926C>T (p.Pro309Leu)
c.530C>T (p.Pro177Leu)
c.647C>T (p.Pro216Leu)
c.905C>T (p.Pro302Leu)
c.782+579C>T (n.782+579C>T)
c.809C>T (p.Pro270Leu)
c.449C>T (p.Pro150Leu)
c.893C>T (p.Pro298Leu)
 ClinVar dbSNP
17g.7673602G>CCA397836137TP53c.926C>G (p.Pro309Arg)
c.530C>G (p.Pro177Arg)
c.647C>G (p.Pro216Arg)
c.905C>G (p.Pro302Arg)
c.782+579C>G (n.782+579C>G)
c.809C>G (p.Pro270Arg)
c.449C>G (p.Pro150Arg)
c.893C>G (p.Pro298Arg)
 dbSNP COSMIC
17g.7673602G>TCA397836134TP53c.926C>A (p.Pro309His)
c.530C>A (p.Pro177His)
c.647C>A (p.Pro216His)
c.905C>A (p.Pro302His)
c.782+579C>A (n.782+579C>A)
c.809C>A (p.Pro270His)
c.449C>A (p.Pro150His)
c.893C>A (p.Pro298His)
 dbSNP
17g.7673606_7673622delCA645587387TP53c.920-10_926del
c.524-10_530del
c.641-10_647del
c.899-10_905del
c.782+563_782+579del (n.782+563_782+579del)
c.803-10_809del
c.443-10_449del
c.887-10_893del
 COSMIC COSMIC COSMIC COSMIC
17g.7673603G>ACA397836140TP53c.925C>T (p.Pro309Ser)
c.529C>T (p.Pro177Ser)
c.646C>T (p.Pro216Ser)
c.904C>T (p.Pro302Ser)
c.782+578C>T (n.782+578C>T)
c.808C>T (p.Pro270Ser)
c.448C>T (p.Pro150Ser)
c.892C>T (p.Pro298Ser)
 ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC
17g.7673603G>CCA397836142TP53c.925C>G (p.Pro309Ala)
c.529C>G (p.Pro177Ala)
c.646C>G (p.Pro216Ala)
c.904C>G (p.Pro302Ala)
c.782+578C>G (n.782+578C>G)
c.808C>G (p.Pro270Ala)
c.448C>G (p.Pro150Ala)
c.892C>G (p.Pro298Ala)
 dbSNP
17g.7673603G=CA2245948005TP53c.925C= (p.Pro309=)
c.529C= (p.Pro177=)
c.646C= (p.Pro216=)
c.904C= (p.Pro302=)
c.782+578C= (n.782+578C=)
c.808C= (p.Pro270=)
c.448C= (p.Pro150=)
c.892C= (p.Pro298=)
17g.7673603G>TCA397836145TP53c.925C>A (p.Pro309Thr)
c.529C>A (p.Pro177Thr)
c.646C>A (p.Pro216Thr)
c.904C>A (p.Pro302Thr)
c.782+578C>A (n.782+578C>A)
c.808C>A (p.Pro270Thr)
c.448C>A (p.Pro150Thr)
c.892C>A (p.Pro298Thr)
 dbSNP
17g.7673604C>ACA497714384TP53c.924G>T (p.Leu308=)
c.528G>T (p.Leu176=)
c.645G>T (p.Leu215=)
c.903G>T (p.Leu301=)
c.782+577G>T (n.782+577G>T)
c.807G>T (p.Leu269=)
c.447G>T (p.Leu149=)
c.891G>T (p.Leu297=)
 ClinVar
17g.7673604C=CA2245948012TP53c.924G= (p.Leu308=)
c.528G= (p.Leu176=)
c.645G= (p.Leu215=)
c.903G= (p.Leu301=)
c.782+577G= (n.782+577G=)
c.807G= (p.Leu269=)
c.447G= (p.Leu149=)
c.891G= (p.Leu297=)
17g.7673604C>GCA16615992TP53c.924G>C (p.Leu308=)
c.528G>C (p.Leu176=)
c.645G>C (p.Leu215=)
c.903G>C (p.Leu301=)
c.782+577G>C (n.782+577G>C)
c.807G>C (p.Leu269=)
c.447G>C (p.Leu149=)
c.891G>C (p.Leu297=)
 ClinVar dbSNP gnomAD v4 COSMIC
17g.7673604C>TCA000503TP53c.924G>A (p.Leu308=)
c.528G>A (p.Leu176=)
c.645G>A (p.Leu215=)
c.903G>A (p.Leu301=)
c.782+577G>A (n.782+577G>A)
c.807G>A (p.Leu269=)
c.447G>A (p.Leu149=)
c.891G>A (p.Leu297=)
 ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC
17g.7673610_7673611insCAACAGTGCTCA645587389TP53c.924_925insTTGAGCACTG
c.528_529insTTGAGCACTG
c.645_646insTTGAGCACTG
c.903_904insTTGAGCACTG
c.782+577_782+578insTTGAGCACTG (n.782+577_782+578insTTGAGCACTG)
c.807_808insTTGAGCACTG
c.447_448insTTGAGCACTG
c.891_892insTTGAGCACTG
 COSMIC COSMIC COSMIC COSMIC

Number of alleles fetched