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.7674861_7676624dupCA2573130640TP53c.-28_672dup
c.-21-1386_276dup
c.-28_393dup
c.-28_651dup
c.-25-3_672dup
n.112_928dup
c.-262_555dup
c.-145_555dup
c.-142-3_555dup
17g.7675197_7676153delCA645589160TP53c.216_415del
c.-21-917_19del
c.96+229_136del
c.216_394del
n.472_671del
c.99_298del
c.216_382del
 COSMIC
17g.7675226_7676561delCA645589205TP53c.36_388del
c.-21-1323_-9del
c.36_109del
c.36_376-9del
n.175_644del
c.-199_271del
c.-82_271del
c.36_355del
 COSMIC
17g.7675995_7676194delCA645589234TP53c.179_375+3del
c.-21-954_-21-755del (n.-21-954_-21-755del)
c.96+192_96+391del (n.96+192_96+391del)
n.435_631+3del
c.62_258+3del
c.179_340+34del
 COSMIC
17g.7675995_7676272delCA645589239TP53c.97_374del (p.Ser33ValfsTer23)
c.-21-1036_-21-759del (n.-21-1036_-21-759del)
c.96+110_96+387del (n.96+110_96+387del)
c.97_374del (p.Ser33AspfsTer16)
c.97_374del (p.Ser33ValfsTer?)
n.353_630del
c.-21_257del
c.97_340+30del
 COSMIC
17g.7676074_7676129delCA645589310TP53c.240_295del (p.Thr81ProfsTer?)
c.-21-893_-21-838del (n.-21-893_-21-838del)
c.96+253_96+308del (n.96+253_96+308del)
n.496_551del
c.123_178del (p.Thr42ProfsTer?)
 COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7676079_7676104delCA2695223133TP53c.269_294del (p.Ser90PhefsTer?)
c.-21-864_-21-839del (n.-21-864_-21-839del)
c.96+282_96+307del (n.96+282_96+307del)
n.525_550del
c.152_177del (p.Ser51PhefsTer?)
17g.7676081_7676122dupCA645589315TP53c.248_289dup (p.Ser96_Val97insAlaAlaProAlaProAlaProSerTrpProLeuSerSerSer)
c.-21-885_-21-844dup (n.-21-885_-21-844dup)
c.96+261_96+302dup (n.96+261_96+302dup)
n.504_545dup
c.131_172dup (p.Ser57_Val58insAlaAlaProAlaProAlaProSerTrpProLeuSerSerSer)
 COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7676089_7676111delCA645589322TP53c.258_280del (p.Pro87IlefsTer?)
c.-21-875_-21-853del (n.-21-875_-21-853del)
c.96+271_96+293del (n.96+271_96+293del)
n.514_536del
c.141_163del (p.Pro48IlefsTer?)
 COSMIC
17g.7676089_7676112delinsACAGGGGCCAGGAGGGGGCTGGTGCA2245933930TP53c.257_280delinsCACCAGCCCCCTCCTGGCCCCTGT (p.Ala86=)
c.-21-876_-21-853delinsCACCAGCCCCCTCCTGGCCCCTGT (n.-21-876_-21-853delinsCACCAGCCCCCTCCTGGCCCCTGT)
c.96+270_96+293delinsCACCAGCCCCCTCCTGGCCCCTGT (n.96+270_96+293delinsCACCAGCCCCCTCCTGGCCCCTGT)
n.513_536delinsCACCAGCCCCCTCCTGGCCCCTGT
c.140_163delinsCACCAGCCCCCTCCTGGCCCCTGT (p.Ala47=)
17g.7676089_7676142delinsACAGGGGCCAGGAGGGGGCTGGTGCAGGGGCCGCCGGTGTAGGAGCTGCTGGTGCA2245933936TP53c.227_280delinsCACCAGCAGCTCCTACACCGGCGGCCCCTGCACCAGCCCCCTCCTGGCCCCTGT (p.Ala76=)
c.-21-906_-21-853delinsCACCAGCAGCTCCTACACCGGCGGCCCCTGCACCAGCCCCCTCCTGGCCCCTGT (n.-21-906_-21-853delinsCACCAGCAGCTCCTACACCGGCGGCCCCTGCACCAGCCCCCTCCTGGCCCCTGT)
c.96+240_96+293delinsCACCAGCAGCTCCTACACCGGCGGCCCCTGCACCAGCCCCCTCCTGGCCCCTGT (n.96+240_96+293delinsCACCAGCAGCTCCTACACCGGCGGCCCCTGCACCAGCCCCCTCCTGGCCCCTGT)
n.483_536delinsCACCAGCAGCTCCTACACCGGCGGCCCCTGCACCAGCCCCCTCCTGGCCCCTGT
c.110_163delinsCACCAGCAGCTCCTACACCGGCGGCCCCTGCACCAGCCCCCTCCTGGCCCCTGT (p.Ala37=)
17g.7676098_7676120delCA10603324TP53c.257_279del (p.Ala86ValfsTer?)
c.-21-876_-21-854del (n.-21-876_-21-854del)
c.96+270_96+292del (n.96+270_96+292del)
n.513_535del
c.140_162del (p.Ala47ValfsTer?)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7676099_7676151delCA645369690TP53c.227_279del (p.Ala76ValfsTer?)
c.-21-906_-21-854del (n.-21-906_-21-854del)
c.96+240_96+292del (n.96+240_96+292del)
n.483_535del
c.110_162del (p.Ala37ValfsTer?)
 ClinVar dbSNP
17g.7676097_7676107delCA2580095100TP53c.267_277del (p.Ser90ValfsTer?)
c.-21-866_-21-856del (n.-21-866_-21-856del)
c.96+280_96+290del (n.96+280_96+290del)
n.523_533del
c.150_160del (p.Ser51ValfsTer?)
 ClinVar
17g.7676092_7676122delCA891842280TP53c.247_277del (p.Ala83CysfsTer30)
c.-21-886_-21-856del (n.-21-886_-21-856del)
c.96+260_96+290del (n.96+260_96+290del)
n.503_533del
c.130_160del (p.Ala44CysfsTer30)
c.247_277del (p.Ala83CysfsTer?)
17g.7676096_7676232delCA645589328TP53c.141_277del (p.Asp48ValfsTer?)
c.-21-992_-21-856del (n.-21-992_-21-856del)
c.96+154_96+290del (n.96+154_96+290del)
n.397_533del
c.24_160del (p.Asp9ValfsTer?)
 COSMIC
17g.7676101_7676116delCA645589331TP53c.257_272del (p.Ala86GlyfsTer?)
c.-21-876_-21-861del (n.-21-876_-21-861del)
c.96+270_96+285del (n.96+270_96+285del)
n.513_528del
c.140_155del (p.Ala47GlyfsTer?)
 COSMIC
17g.7676098_7676109delinsAGGAGGGGGCTGCA2245934044TP53c.260_271delinsCAGCCCCCTCCT (p.Pro87=)
c.-21-873_-21-862delinsCAGCCCCCTCCT (n.-21-873_-21-862delinsCAGCCCCCTCCT)
c.96+273_96+284delinsCAGCCCCCTCCT (n.96+273_96+284delinsCAGCCCCCTCCT)
n.516_527delinsCAGCCCCCTCCT
c.143_154delinsCAGCCCCCTCCT (p.Pro48=)
17g.7676101_7676104delCA2695223136TP53c.267_270del (p.Ser90GlyfsTer?)
c.-21-866_-21-863del (n.-21-866_-21-863del)
c.96+280_96+283del (n.96+280_96+283del)
n.523_526del
c.150_153del (p.Ser51GlyfsTer?)
17g.7676101_7676110delCA645589335TP53c.261_270del (p.Ala88GlyfsTer?)
c.-21-872_-21-863del (n.-21-872_-21-863del)
c.96+274_96+283del (n.96+274_96+283del)
n.517_526del
c.144_153del (p.Ala49GlyfsTer?)
 ClinVar COSMIC COSMIC COSMIC
17g.7676100_7676110delCA913191058TP53c.260_270del (p.Pro87LeufsTer?)
c.-21-873_-21-863del (n.-21-873_-21-863del)
c.96+273_96+283del (n.96+273_96+283del)
n.516_526del
c.143_153del (p.Pro48LeufsTer?)
 ClinVar dbSNP
17g.7676101_7676117delCA645589333TP53c.254_270del (p.Pro85LeufsTer?)
c.-21-879_-21-863del (n.-21-879_-21-863del)
c.96+267_96+283del (n.96+267_96+283del)
n.510_526del
c.137_153del (p.Pro46LeufsTer?)
 COSMIC
17g.7676099_7676143delCA645589334TP53c.226_270del (p.Ala76_Ser90del)
c.-21-907_-21-863del (n.-21-907_-21-863del)
c.96+239_96+283del (n.96+239_96+283del)
n.482_526del
c.109_153del (p.Ala37_Ser51del)
 COSMIC
17g.7676101_7676102delinsAGCA2245934067TP53c.267_268delinsCT (p.Pro89=)
c.-21-866_-21-865delinsCT (n.-21-866_-21-865delinsCT)
c.96+280_96+281delinsCT (n.96+280_96+281delinsCT)
n.523_524delinsCT
c.150_151delinsCT (p.Pro50=)
17g.7676105_7676106insCAGGGGCAGGGGCCAGGAGGGGCAGGGGCA2580612886TP53c.268_269insGCCCCTCCTGGCCCCTGCCCCTGCCCCT (p.Ser90CysfsTer?)
c.-21-865_-21-864insGCCCCTCCTGGCCCCTGCCCCTGCCCCT (n.-21-865_-21-864insGCCCCTCCTGGCCCCTGCCCCTGCCCCT)
c.96+281_96+282insGCCCCTCCTGGCCCCTGCCCCTGCCCCT (n.96+281_96+282insGCCCCTCCTGGCCCCTGCCCCTGCCCCT)
n.524_525insGCCCCTCCTGGCCCCTGCCCCTGCCCCT
c.151_152insGCCCCTCCTGGCCCCTGCCCCTGCCCCT (p.Ser51CysfsTer?)
 dbSNP
17g.7676106_7676118delCA645589338TP53c.256_268del (p.Ala86ProfsTer?)
c.-21-877_-21-865del (n.-21-877_-21-865del)
c.96+269_96+281del (n.96+269_96+281del)
n.512_524del
c.139_151del (p.Ala47ProfsTer?)
 COSMIC
17g.7676102G>ACA000090TP53c.267C>T (p.Pro89=)
c.-21-866C>T (n.-21-866C>T)
c.96+280C>T (n.96+280C>T)
n.523C>T
c.150C>T (p.Pro50=)
 ClinVar dbSNP gnomAD v3 gnomAD v4
17g.7676102G>CCA497925934TP53c.267C>G (p.Pro89=)
c.-21-866C>G (n.-21-866C>G)
c.96+280C>G (n.96+280C>G)
n.523C>G
c.150C>G (p.Pro50=)
 dbSNP
17g.7676102G=CA2245934111TP53c.267C= (p.Pro89=)
c.-21-866C= (n.-21-866C=)
c.96+280C= (n.96+280C=)
n.523C=
c.150C= (p.Pro50=)
17g.7676102G>TCA16607525TP53c.267C>A (p.Pro89=)
c.-21-866C>A (n.-21-866C>A)
c.96+280C>A (n.96+280C>A)
n.523C>A
c.150C>A (p.Pro50=)
 ClinVar dbSNP gnomAD v4
17g.7676106dupCA645589339TP53c.267dup (p.Ser90LeufsTer?)
c.-21-866dup (n.-21-866dup)
c.96+280dup (n.96+280dup)
n.523dup
c.150dup (p.Ser51LeufsTer?)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7676106delCA000091TP53c.267del (p.Ser90ProfsTer?)
c.-21-866del (n.-21-866del)
c.96+280del (n.96+280del)
n.523del
c.150del (p.Ser51ProfsTer?)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7676105_7676118delCA645589340TP53c.254_267del (p.Pro85LeufsTer?)
c.-21-879_-21-866del (n.-21-879_-21-866del)
c.96+267_96+280del (n.96+267_96+280del)
n.510_523del
c.137_150del (p.Pro46LeufsTer?)
 COSMIC
17g.7676102_7676103insCCA497925935TP53c.266_267insG (p.Ser90LeufsTer?)
c.-21-867_-21-866insG (n.-21-867_-21-866insG)
c.96+279_96+280insG (n.96+279_96+280insG)
n.522_523insG
c.149_150insG (p.Ser51LeufsTer?)
17g.7676103G>ACA000089TP53c.266C>T (p.Pro89Leu)
c.-21-867C>T (n.-21-867C>T)
c.96+279C>T (n.96+279C>T)
n.522C>T
c.149C>T (p.Pro50Leu)
 ClinVar dbSNP gnomAD v4 COSMIC
17g.7676103G>CCA397845248TP53c.266C>G (p.Pro89Arg)
c.-21-867C>G (n.-21-867C>G)
c.96+279C>G (n.96+279C>G)
n.522C>G
c.149C>G (p.Pro50Arg)
 dbSNP
17g.7676103G=CA2245934130TP53c.266C= (p.Pro89=)
c.-21-867C= (n.-21-867C=)
c.96+279C= (n.96+279C=)
n.522C=
c.149C= (p.Pro50=)
17g.7676103G>TCA397845250TP53c.266C>A (p.Pro89His)
c.-21-867C>A (n.-21-867C>A)
c.96+279C>A (n.96+279C>A)
n.522C>A
c.149C>A (p.Pro50His)
 dbSNP
17g.7676103_7676104delinsAACA645589341TP53c.265_266delinsTT (p.Pro89Phe)
c.-21-868_-21-867delinsTT (n.-21-868_-21-867delinsTT)
c.96+278_96+279delinsTT (n.96+278_96+279delinsTT)
n.521_522delinsTT
c.148_149delinsTT (p.Pro50Phe)
 COSMIC
17g.7676103_7676104insCCA497925936TP53c.265_266insG (p.Pro89ArgfsTer?)
c.-21-868_-21-867insG (n.-21-868_-21-867insG)
c.96+278_96+279insG (n.96+278_96+279insG)
n.521_522insG
c.148_149insG (p.Pro50ArgfsTer?)
17g.7676104G>ACA397845278TP53c.265C>T (p.Pro89Ser)
c.-21-868C>T (n.-21-868C>T)
c.96+278C>T (n.96+278C>T)
n.521C>T
c.148C>T (p.Pro50Ser)
 dbSNP gnomAD v4 COSMIC
17g.7676104G>CCA397845274TP53c.265C>G (p.Pro89Ala)
c.-21-868C>G (n.-21-868C>G)
c.96+278C>G (n.96+278C>G)
n.521C>G
c.148C>G (p.Pro50Ala)
17g.7676104G=CA2245934138TP53c.265C= (p.Pro89=)
c.-21-868C= (n.-21-868C=)
c.96+278C= (n.96+278C=)
n.521C=
c.148C= (p.Pro50=)
17g.7676104G>TCA397845257TP53c.265C>A (p.Pro89Thr)
c.-21-868C>A (n.-21-868C>A)
c.96+278C>A (n.96+278C>A)
n.521C>A
c.148C>A (p.Pro50Thr)
 ClinVar dbSNP
17g.7676107_7676117delCA645589342TP53c.255_265del (p.Ala86LeufsTer?)
c.-21-878_-21-868del (n.-21-878_-21-868del)
c.96+268_96+278del (n.96+268_96+278del)
n.511_521del
c.138_148del (p.Ala47LeufsTer?)
 COSMIC
17g.7676105G>ACA10580954TP53c.264C>T (p.Ala88=)
c.-21-869C>T (n.-21-869C>T)
c.96+277C>T (n.96+277C>T)
n.520C>T
c.147C>T (p.Ala49=)
 ClinVar dbSNP gnomAD v4
17g.7676105G>CCA497925937TP53c.264C>G (p.Ala88=)
c.-21-869C>G (n.-21-869C>G)
c.96+277C>G (n.96+277C>G)
n.520C>G
c.147C>G (p.Ala49=)
17g.7676105G=CA2245934160TP53c.264C= (p.Ala88=)
c.-21-869C= (n.-21-869C=)
c.96+277C= (n.96+277C=)
n.520C=
c.147C= (p.Ala49=)
17g.7676105G>TCA497925938TP53c.264C>A (p.Ala88=)
c.-21-869C>A (n.-21-869C>A)
c.96+277C>A (n.96+277C>A)
n.520C>A
c.147C>A (p.Ala49=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.7676107_7676116delCA645589344TP53c.255_264del (p.Ala86ProfsTer?)
c.-21-878_-21-869del (n.-21-878_-21-869del)
c.96+268_96+277del (n.96+268_96+277del)
n.511_520del
c.138_147del (p.Ala47ProfsTer?)
 COSMIC
17g.7676105_7676134delCA645589343TP53c.235_264del (p.Ala79_Ala88del)
c.-21-898_-21-869del (n.-21-898_-21-869del)
c.96+248_96+277del (n.96+248_96+277del)
n.491_520del
c.118_147del (p.Ala40_Ala49del)
 COSMIC
17g.7676105_7676135delinsGGCTGGTGCAGGGGCCGCCGGTGTAGGAGCTCA2245934157TP53c.234_264delinsAGCTCCTACACCGGCGGCCCCTGCACCAGCC (p.Ala78=)
c.-21-899_-21-869delinsAGCTCCTACACCGGCGGCCCCTGCACCAGCC (n.-21-899_-21-869delinsAGCTCCTACACCGGCGGCCCCTGCACCAGCC)
c.96+247_96+277delinsAGCTCCTACACCGGCGGCCCCTGCACCAGCC (n.96+247_96+277delinsAGCTCCTACACCGGCGGCCCCTGCACCAGCC)
n.490_520delinsAGCTCCTACACCGGCGGCCCCTGCACCAGCC
c.117_147delinsAGCTCCTACACCGGCGGCCCCTGCACCAGCC (p.Ala39=)
17g.7676106G>ACA397845305TP53c.263C>T (p.Ala88Val)
c.-21-870C>T (n.-21-870C>T)
c.96+276C>T (n.96+276C>T)
n.519C>T
c.146C>T (p.Ala49Val)
 ClinVar dbSNP gnomAD v4
17g.7676106G>CCA397845310TP53c.263C>G (p.Ala88Gly)
c.-21-870C>G (n.-21-870C>G)
c.96+276C>G (n.96+276C>G)
n.519C>G
c.146C>G (p.Ala49Gly)
 ClinVar dbSNP
17g.7676106G=CA2245934175TP53c.263C= (p.Ala88=)
c.-21-870C= (n.-21-870C=)
c.96+276C= (n.96+276C=)
n.519C=
c.146C= (p.Ala49=)
17g.7676106G>TCA397845315TP53c.263C>A (p.Ala88Asp)
c.-21-870C>A (n.-21-870C>A)
c.96+276C>A (n.96+276C>A)
n.519C>A
c.146C>A (p.Ala49Asp)
 dbSNP
17g.7676106_7676107delCA2576155522TP53c.262_263del (p.Ala88ProfsTer?)
c.-21-871_-21-870del (n.-21-871_-21-870del)
c.96+275_96+276del (n.96+275_96+276del)
n.518_519del
c.145_146del (p.Ala49ProfsTer?)
17g.7676106_7676108delinsCAGGGGCAGGGGCCAGGAGGGGCAGGGGCCACA2582341712TP53c.261_263delinsTGGCCCCTGCCCCTCCTGGCCCCTGCCCCTG (p.Ala88GlyfsTer?)
c.-21-872_-21-870delinsTGGCCCCTGCCCCTCCTGGCCCCTGCCCCTG (n.-21-872_-21-870delinsTGGCCCCTGCCCCTCCTGGCCCCTGCCCCTG)
c.96+274_96+276delinsTGGCCCCTGCCCCTCCTGGCCCCTGCCCCTG (n.96+274_96+276delinsTGGCCCCTGCCCCTCCTGGCCCCTGCCCCTG)
n.517_519delinsTGGCCCCTGCCCCTCCTGGCCCCTGCCCCTG
c.144_146delinsTGGCCCCTGCCCCTCCTGGCCCCTGCCCCTG (p.Ala49GlyfsTer?)
 ClinVar
17g.7676121_7676150delCA002925TP53c.234_263del (p.Ala79_Ala88del)
c.-21-899_-21-870del (n.-21-899_-21-870del)
c.96+247_96+276del (n.96+247_96+276del)
n.490_519del
c.117_146del (p.Ala40_Ala49del)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.7676107delCA497925939TP53c.262del (p.Ala88ProfsTer?)
c.-21-871del (n.-21-871del)
c.96+275del (n.96+275del)
n.518del
c.145del (p.Ala49ProfsTer?)
 ClinVar dbSNP COSMIC
17g.7676107C>ACA397845325TP53c.262G>T (p.Ala88Ser)
c.-21-871G>T (n.-21-871G>T)
c.96+275G>T (n.96+275G>T)
n.518G>T
c.145G>T (p.Ala49Ser)
 dbSNP
17g.7676107C=CA2245934187TP53c.262G= (p.Ala88=)
c.-21-871G= (n.-21-871G=)
c.96+275G= (n.96+275G=)
n.518G=
c.145G= (p.Ala49=)
17g.7676107C>GCA397845323TP53c.262G>C (p.Ala88Pro)
c.-21-871G>C (n.-21-871G>C)
c.96+275G>C (n.96+275G>C)
n.518G>C
c.145G>C (p.Ala49Pro)
 ClinVar dbSNP gnomAD v4
17g.7676107C>TCA397845322TP53c.262G>A (p.Ala88Thr)
c.-21-871G>A (n.-21-871G>A)
c.96+275G>A (n.96+275G>A)
n.518G>A
c.145G>A (p.Ala49Thr)
 dbSNP
17g.7676108_7676120delCA645589346TP53c.250_262del (p.Ala84ProfsTer?)
c.-21-883_-21-871del (n.-21-883_-21-871del)
c.96+263_96+275del (n.96+263_96+275del)
n.506_518del
c.133_145del (p.Ala45ProfsTer?)
 COSMIC
17g.7676108_7676123delCA645589345TP53c.247_262del (p.Ala83ProfsTer?)
c.-21-886_-21-871del (n.-21-886_-21-871del)
c.96+260_96+275del (n.96+260_96+275del)
n.503_518del
c.130_145del (p.Ala44ProfsTer?)
 COSMIC
17g.7676108T>ACA497925940TP53c.261A>T (p.Pro87=)
c.-21-872A>T (n.-21-872A>T)
c.96+274A>T (n.96+274A>T)
n.517A>T
c.144A>T (p.Pro48=)
 ClinVar dbSNP COSMIC
17g.7676108T>CCA497925941TP53c.261A>G (p.Pro87=)
c.-21-872A>G (n.-21-872A>G)
c.96+274A>G (n.96+274A>G)
n.517A>G
c.144A>G (p.Pro48=)
 dbSNP
17g.7676108T>GCA497925942TP53c.261A>C (p.Pro87=)
c.-21-872A>C (n.-21-872A>C)
c.96+274A>C (n.96+274A>C)
n.517A>C
c.144A>C (p.Pro48=)
 ClinVar dbSNP
17g.7676109G>ACA397845331TP53c.260C>T (p.Pro87Leu)
c.-21-873C>T (n.-21-873C>T)
c.96+273C>T (n.96+273C>T)
n.516C>T
c.143C>T (p.Pro48Leu)
 ClinVar dbSNP COSMIC
17g.7676109G>CCA397845340TP53c.260C>G (p.Pro87Arg)
c.-21-873C>G (n.-21-873C>G)
c.96+273C>G (n.96+273C>G)
n.516C>G
c.143C>G (p.Pro48Arg)
 ClinVar
17g.7676109G=CA2245934197TP53c.260C= (p.Pro87=)
c.-21-873C= (n.-21-873C=)
c.96+273C= (n.96+273C=)
n.516C=
c.143C= (p.Pro48=)
17g.7676109G>TCA397845342TP53c.260C>A (p.Pro87Gln)
c.-21-873C>A (n.-21-873C>A)
c.96+273C>A (n.96+273C>A)
n.516C>A
c.143C>A (p.Pro48Gln)
 COSMIC
17g.7676110_7676125delCA2695199887TP53c.245_260del (p.Pro82GlnfsTer?)
c.-21-888_-21-873del (n.-21-888_-21-873del)
c.96+258_96+273del (n.96+258_96+273del)
n.501_516del
c.128_143del (p.Pro43GlnfsTer?)
 ClinVar
17g.7676110G>ACA397845348TP53c.259C>T (p.Pro87Ser)
c.-21-874C>T (n.-21-874C>T)
c.96+272C>T (n.96+272C>T)
n.515C>T
c.142C>T (p.Pro48Ser)
 ClinVar dbSNP
17g.7676110G>CCA397845361TP53c.259C>G (p.Pro87Ala)
c.-21-874C>G (n.-21-874C>G)
c.96+272C>G (n.96+272C>G)
n.515C>G
c.142C>G (p.Pro48Ala)
 ClinVar dbSNP
17g.7676110G=CA2245934204TP53c.259C= (p.Pro87=)
c.-21-874C= (n.-21-874C=)
c.96+272C= (n.96+272C=)
n.515C=
c.142C= (p.Pro48=)
17g.7676110G>TCA397845366TP53c.259C>A (p.Pro87Thr)
c.-21-874C>A (n.-21-874C>A)
c.96+272C>A (n.96+272C>A)
n.515C>A
c.142C>A (p.Pro48Thr)
 dbSNP
17g.7676111T>ACA497925943TP53c.258A>T (p.Ala86=)
c.-21-875A>T (n.-21-875A>T)
c.96+271A>T (n.96+271A>T)
n.514A>T
c.141A>T (p.Ala47=)
 dbSNP
17g.7676111T>CCA497925944TP53c.258A>G (p.Ala86=)
c.-21-875A>G (n.-21-875A>G)
c.96+271A>G (n.96+271A>G)
n.514A>G
c.141A>G (p.Ala47=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
17g.7676111T>GCA497925945TP53c.258A>C (p.Ala86=)
c.-21-875A>C (n.-21-875A>C)
c.96+271A>C (n.96+271A>C)
n.514A>C
c.141A>C (p.Ala47=)
 dbSNP gnomAD v2 gnomAD v4
17g.7676111T=CA2245934209TP53c.258A= (p.Ala86=)
c.-21-875A= (n.-21-875A=)
c.96+271A= (n.96+271A=)
n.514A=
c.141A= (p.Ala47=)
17g.7676112G>ACA397845372TP53c.257C>T (p.Ala86Val)
c.-21-876C>T (n.-21-876C>T)
c.96+270C>T (n.96+270C>T)
n.513C>T
c.140C>T (p.Ala47Val)
 ClinVar dbSNP COSMIC
17g.7676112G>CCA397845377TP53c.257C>G (p.Ala86Gly)
c.-21-876C>G (n.-21-876C>G)
c.96+270C>G (n.96+270C>G)
n.513C>G
c.140C>G (p.Ala47Gly)
 dbSNP
17g.7676112G=CA2245934217TP53c.257C= (p.Ala86=)
c.-21-876C= (n.-21-876C=)
c.96+270C= (n.96+270C=)
n.513C=
c.140C= (p.Ala47=)
17g.7676112G>TCA397845375TP53c.257C>A (p.Ala86Glu)
c.-21-876C>A (n.-21-876C>A)
c.96+270C>A (n.96+270C>A)
n.513C>A
c.140C>A (p.Ala47Glu)
17g.7676112_7676122delinsGCAGGGGCCGCCA2245934219TP53c.247_257delinsGCGGCCCCTGC (p.Ala83=)
c.-21-886_-21-876delinsGCGGCCCCTGC (n.-21-886_-21-876delinsGCGGCCCCTGC)
c.96+260_96+270delinsGCGGCCCCTGC (n.96+260_96+270delinsGCGGCCCCTGC)
n.503_513delinsGCGGCCCCTGC
c.130_140delinsGCGGCCCCTGC (p.Ala44=)
17g.7676113C>ACA397845382TP53c.256G>T (p.Ala86Ser)
c.-21-877G>T (n.-21-877G>T)
c.96+269G>T (n.96+269G>T)
n.512G>T
c.139G>T (p.Ala47Ser)
17g.7676113C=CA2245934230TP53c.256G= (p.Ala86=)
c.-21-877G= (n.-21-877G=)
c.96+269G= (n.96+269G=)
n.512G=
c.139G= (p.Ala47=)
17g.7676113C>GCA397845383TP53c.256G>C (p.Ala86Pro)
c.-21-877G>C (n.-21-877G>C)
c.96+269G>C (n.96+269G>C)
n.512G>C
c.139G>C (p.Ala47Pro)
 ClinVar gnomAD v4
17g.7676113C>TCA000088TP53c.256G>A (p.Ala86Thr)
c.-21-877G>A (n.-21-877G>A)
c.96+269G>A (n.96+269G>A)
n.512G>A
c.139G>A (p.Ala47Thr)
 ClinVar dbSNP gnomAD v4
17g.7676114_7676123delCA658824568TP53c.247_256del (p.Ala83HisfsTer?)
c.-21-886_-21-877del (n.-21-886_-21-877del)
c.96+260_96+269del (n.96+260_96+269del)
n.503_512del
c.130_139del (p.Ala44HisfsTer?)
 ClinVar dbSNP
17g.7676114A=CA2245934247TP53c.255T= (p.Pro85=)
c.-21-878T= (n.-21-878T=)
c.96+268T= (n.96+268T=)
n.511T=
c.138T= (p.Pro46=)
17g.7676114A>CCA497925946TP53c.255T>G (p.Pro85=)
c.-21-878T>G (n.-21-878T>G)
c.96+268T>G (n.96+268T>G)
n.511T>G
c.138T>G (p.Pro46=)
17g.7676114A>GCA000087TP53c.255T>C (p.Pro85=)
c.-21-878T>C (n.-21-878T>C)
c.96+268T>C (n.96+268T>C)
n.511T>C
c.138T>C (p.Pro46=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.7676114A>TCA000086TP53c.255T>A (p.Pro85=)
c.-21-878T>A (n.-21-878T>A)
c.96+268T>A (n.96+268T>A)
n.511T>A
c.138T>A (p.Pro46=)
 ClinVar dbSNP
17g.7676114_7676115delinsAGCA2245934257TP53c.254_255delinsCT (p.Pro85=)
c.-21-879_-21-878delinsCT (n.-21-879_-21-878delinsCT)
c.96+267_96+268delinsCT (n.96+267_96+268delinsCT)
n.510_511delinsCT
c.137_138delinsCT (p.Pro46=)
17g.7676114_7676127delCA891842281TP53c.242_255del (p.Thr81SerfsTer?)
c.-21-891_-21-878del (n.-21-891_-21-878del)
c.96+255_96+268del (n.96+255_96+268del)
n.498_511del
c.125_138del (p.Thr42SerfsTer?)
17g.7676115G>ACA397845394TP53c.254C>T (p.Pro85Leu)
c.-21-879C>T (n.-21-879C>T)
c.96+267C>T (n.96+267C>T)
n.510C>T
c.137C>T (p.Pro46Leu)
 ClinVar dbSNP COSMIC
17g.7676115G>CCA397845411TP53c.254C>G (p.Pro85Arg)
c.-21-879C>G (n.-21-879C>G)
c.96+267C>G (n.96+267C>G)
n.510C>G
c.137C>G (p.Pro46Arg)
 dbSNP
17g.7676115G>TCA397845416TP53c.254C>A (p.Pro85His)
c.-21-879C>A (n.-21-879C>A)
c.96+267C>A (n.96+267C>A)
n.510C>A
c.137C>A (p.Pro46His)
 dbSNP
17g.7676118dupCA645589347TP53c.254dup (p.Ala86CysfsTer?)
c.-21-879dup (n.-21-879dup)
c.96+267dup (n.96+267dup)
n.510dup
c.137dup (p.Ala47CysfsTer?)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7676118delCA16620639TP53c.254del (p.Pro85LeufsTer?)
c.-21-879del (n.-21-879del)
c.96+267del (n.96+267del)
n.510del
c.137del (p.Pro46LeufsTer?)
 ClinVar dbSNP
17g.7676117_7676118delCA645589348TP53c.253_254del (p.Pro85CysfsTer?)
c.-21-880_-21-879del (n.-21-880_-21-879del)
c.96+266_96+267del (n.96+266_96+267del)
n.509_510del
c.136_137del (p.Pro46CysfsTer?)
 COSMIC
17g.7676115_7676123delinsGGGGCCGCCCA2245934270TP53c.246_254delinsGGCGGCCCC (p.Pro82=)
c.-21-887_-21-879delinsGGCGGCCCC (n.-21-887_-21-879delinsGGCGGCCCC)
c.96+259_96+267delinsGGCGGCCCC (n.96+259_96+267delinsGGCGGCCCC)
n.502_510delinsGGCGGCCCC
c.129_137delinsGGCGGCCCC (p.Pro43=)
17g.7676115_7676116insCCA497925947TP53c.253_254insG (p.Pro85ArgfsTer?)
c.-21-880_-21-879insG (n.-21-880_-21-879insG)
c.96+266_96+267insG (n.96+266_96+267insG)
n.509_510insG
c.136_137insG (p.Pro46ArgfsTer?)
17g.7676116G>ACA397845420TP53c.253C>T (p.Pro85Ser)
c.-21-880C>T (n.-21-880C>T)
c.96+266C>T (n.96+266C>T)
n.509C>T
c.136C>T (p.Pro46Ser)
 ClinVar dbSNP COSMIC
17g.7676116G>CCA397845433TP53c.253C>G (p.Pro85Ala)
c.-21-880C>G (n.-21-880C>G)
c.96+266C>G (n.96+266C>G)
n.509C>G
c.136C>G (p.Pro46Ala)
 ClinVar dbSNP
17g.7676116G=CA2245934279TP53c.253C= (p.Pro85=)
c.-21-880C= (n.-21-880C=)
c.96+266C= (n.96+266C=)
n.509C=
c.136C= (p.Pro46=)
17g.7676116G>TCA397845434TP53c.253C>A (p.Pro85Thr)
c.-21-880C>A (n.-21-880C>A)
c.96+266C>A (n.96+266C>A)
n.509C>A
c.136C>A (p.Pro46Thr)
 dbSNP
17g.7676118_7676125delCA913191059TP53c.246_253del (p.Ala83CysfsTer?)
c.-21-887_-21-880del (n.-21-887_-21-880del)
c.96+259_96+266del (n.96+259_96+266del)
n.502_509del
c.129_136del (p.Ala44CysfsTer?)
 ClinVar dbSNP
17g.7676119_7676179delCA645589349TP53c.193_253del (p.Arg65LeufsTer?)
c.-21-940_-21-880del (n.-21-940_-21-880del)
c.96+206_96+266del (n.96+206_96+266del)
n.449_509del
c.76_136del (p.Arg26LeufsTer?)
 COSMIC
17g.7676117G>ACA287489058TP53c.252C>T (p.Ala84=)
c.-21-881C>T (n.-21-881C>T)
c.96+265C>T (n.96+265C>T)
n.508C>T
c.135C>T (p.Ala45=)
 dbSNP gnomAD v2 gnomAD v4 COSMIC
17g.7676117G>CCA497925948TP53c.252C>G (p.Ala84=)
c.-21-881C>G (n.-21-881C>G)
c.96+265C>G (n.96+265C>G)
n.508C>G
c.135C>G (p.Ala45=)
 dbSNP
17g.7676117G=CA2245934295TP53c.252C= (p.Ala84=)
c.-21-881C= (n.-21-881C=)
c.96+265C= (n.96+265C=)
n.508C=
c.135C= (p.Ala45=)
17g.7676117G>TCA002944TP53c.252C>A (p.Ala84=)
c.-21-881C>A (n.-21-881C>A)
c.96+265C>A (n.96+265C>A)
n.508C>A
c.135C>A (p.Ala45=)
 ClinVar dbSNP ExAC gnomAD v2 COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7676117_7676118delinsAACA645589350TP53c.251_252delinsTT (p.Ala84Val)
c.-21-882_-21-881delinsTT (n.-21-882_-21-881delinsTT)
c.96+264_96+265delinsTT (n.96+264_96+265delinsTT)
n.507_508delinsTT
c.134_135delinsTT (p.Ala45Val)
 COSMIC
17g.7676118G>ACA397845445TP53c.251C>T (p.Ala84Val)
c.-21-882C>T (n.-21-882C>T)
c.96+264C>T (n.96+264C>T)
n.507C>T
c.134C>T (p.Ala45Val)
 ClinVar dbSNP COSMIC
17g.7676118G>CCA397845453TP53c.251C>G (p.Ala84Gly)
c.-21-882C>G (n.-21-882C>G)
c.96+264C>G (n.96+264C>G)
n.507C>G
c.134C>G (p.Ala45Gly)
 dbSNP COSMIC
17g.7676118G=CA2245934309TP53c.251C= (p.Ala84=)
c.-21-882C= (n.-21-882C=)
c.96+264C= (n.96+264C=)
n.507C=
c.134C= (p.Ala45=)
17g.7676118G>TCA397845452TP53c.251C>A (p.Ala84Asp)
c.-21-882C>A (n.-21-882C>A)
c.96+264C>A (n.96+264C>A)
n.507C>A
c.134C>A (p.Ala45Asp)
 dbSNP gnomAD v3 gnomAD v4
17g.7676118_7676119delinsGCCA2245934310TP53c.250_251delinsGC (p.Ala84=)
c.-21-883_-21-882delinsGC (n.-21-883_-21-882delinsGC)
c.96+263_96+264delinsGC (n.96+263_96+264delinsGC)
n.506_507delinsGC
c.133_134delinsGC (p.Ala45=)
17g.7676118_7676119delinsTTCA2697552147TP53c.250_251delinsAA (p.Ala84Asn)
c.-21-883_-21-882delinsAA (n.-21-883_-21-882delinsAA)
c.96+263_96+264delinsAA (n.96+263_96+264delinsAA)
n.506_507delinsAA
c.133_134delinsAA (p.Ala45Asn)
 ClinVar
17g.7676118_7676119insACA645589351TP53c.250_251insT (p.Ala84ValfsTer?)
c.-21-883_-21-882insT (n.-21-883_-21-882insT)
c.96+263_96+264insT (n.96+263_96+264insT)
n.506_507insT
c.133_134insT (p.Ala45ValfsTer?)
 COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7676119C>ACA397845457TP53c.250G>T (p.Ala84Ser)
c.-21-883G>T (n.-21-883G>T)
c.96+263G>T (n.96+263G>T)
n.506G>T
c.133G>T (p.Ala45Ser)
 dbSNP
17g.7676119C=CA2245934329TP53c.250G= (p.Ala84=)
c.-21-883G= (n.-21-883G=)
c.96+263G= (n.96+263G=)
n.506G=
c.133G= (p.Ala45=)
17g.7676119C>GCA397845463TP53c.250G>C (p.Ala84Pro)
c.-21-883G>C (n.-21-883G>C)
c.96+263G>C (n.96+263G>C)
n.506G>C
c.133G>C (p.Ala45Pro)
 dbSNP
17g.7676119C>TCA000085TP53c.250G>A (p.Ala84Thr)
c.-21-883G>A (n.-21-883G>A)
c.96+263G>A (n.96+263G>A)
n.506G>A
c.133G>A (p.Ala45Thr)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
17g.7676120delCA497925949TP53c.250del (p.Ala84ProfsTer?)
c.-21-883del (n.-21-883del)
c.96+263del (n.96+263del)
n.506del
c.133del (p.Ala45ProfsTer?)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7676119_7676121delinsCCGCA2245934327TP53c.248_250delinsCGG (p.Ala83=)
c.-21-885_-21-883delinsCGG (n.-21-885_-21-883delinsCGG)
c.96+261_96+263delinsCGG (n.96+261_96+263delinsCGG)
n.504_506delinsCGG
c.131_133delinsCGG (p.Ala44=)
17g.7676120_7676123delCA645589352TP53c.247_250del (p.Ala83ProfsTer?)
c.-21-886_-21-883del (n.-21-886_-21-883del)
c.96+260_96+263del (n.96+260_96+263del)
n.503_506del
c.130_133del (p.Ala44ProfsTer?)
 COSMIC
17g.7676120C>ACA497925950TP53c.249G>T (p.Ala83=)
c.-21-884G>T (n.-21-884G>T)
c.96+262G>T (n.96+262G>T)
n.505G>T
c.132G>T (p.Ala44=)
 dbSNP
17g.7676120C=CA2245934341TP53c.249G= (p.Ala83=)
c.-21-884G= (n.-21-884G=)
c.96+262G= (n.96+262G=)
n.505G=
c.132G= (p.Ala44=)
17g.7676120C>GCA497925951TP53c.249G>C (p.Ala83=)
c.-21-884G>C (n.-21-884G>C)
c.96+262G>C (n.96+262G>C)
n.505G>C
c.132G>C (p.Ala44=)
 dbSNP
17g.7676120C>TCA000084TP53c.249G>A (p.Ala83=)
c.-21-884G>A (n.-21-884G>A)
c.96+262G>A (n.96+262G>A)
n.505G>A
c.132G>A (p.Ala44=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
17g.7676121_7676122delCA645369691TP53c.248_249del (p.Ala83GlyfsTer?)
c.-21-885_-21-884del (n.-21-885_-21-884del)
c.96+261_96+262del (n.96+261_96+262del)
n.504_505del
c.131_132del (p.Ala44GlyfsTer?)
 ClinVar dbSNP COSMIC
17g.7676121G>ACA000083TP53c.248C>T (p.Ala83Val)
c.-21-885C>T (n.-21-885C>T)
c.96+261C>T (n.96+261C>T)
n.504C>T
c.131C>T (p.Ala44Val)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.7676121G>CCA397845490TP53c.248C>G (p.Ala83Gly)
c.-21-885C>G (n.-21-885C>G)
c.96+261C>G (n.96+261C>G)
n.504C>G
c.131C>G (p.Ala44Gly)
 dbSNP
17g.7676121G=CA2245934361TP53c.248C= (p.Ala83=)
c.-21-885C= (n.-21-885C=)
c.96+261C= (n.96+261C=)
n.504C=
c.131C= (p.Ala44=)
17g.7676121G>TCA000082TP53c.248C>A (p.Ala83Glu)
c.-21-885C>A (n.-21-885C>A)
c.96+261C>A (n.96+261C>A)
n.504C>A
c.131C>A (p.Ala44Glu)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
17g.7676121_7676122delinsGCCA2245934372TP53c.247_248delinsGC (p.Ala83=)
c.-21-886_-21-885delinsGC (n.-21-886_-21-885delinsGC)
c.96+260_96+261delinsGC (n.96+260_96+261delinsGC)
n.503_504delinsGC
c.130_131delinsGC (p.Ala44=)
17g.7676122C>ACA397845499TP53c.247G>T (p.Ala83Ser)
c.-21-886G>T (n.-21-886G>T)
c.96+260G>T (n.96+260G>T)
n.503G>T
c.130G>T (p.Ala44Ser)
17g.7676122C>GCA397845501TP53c.247G>C (p.Ala83Pro)
c.-21-886G>C (n.-21-886G>C)
c.96+260G>C (n.96+260G>C)
n.503G>C
c.130G>C (p.Ala44Pro)
 dbSNP
17g.7676122C>TCA397845502TP53c.247G>A (p.Ala83Thr)
c.-21-886G>A (n.-21-886G>A)
c.96+260G>A (n.96+260G>A)
n.503G>A
c.130G>A (p.Ala44Thr)
 ClinVar dbSNP
17g.7676123dupCA287489068TP53c.247dup (p.Ala83GlyfsTer?)
c.-21-886dup (n.-21-886dup)
c.96+260dup (n.96+260dup)
n.503dup
c.130dup (p.Ala44GlyfsTer?)
 dbSNP
17g.7676123delCA913191060TP53c.247del (p.Ala83ArgfsTer?)
c.-21-886del (n.-21-886del)
c.96+260del (n.96+260del)
n.503del
c.130del (p.Ala44ArgfsTer?)
 ClinVar dbSNP
17g.7676123C>ACA497925952TP53c.246G>T (p.Pro82=)
c.-21-887G>T (n.-21-887G>T)
c.96+259G>T (n.96+259G>T)
n.502G>T
c.129G>T (p.Pro43=)
 ClinVar dbSNP
17g.7676123C=CA2245934386TP53c.246G= (p.Pro82=)
c.-21-887G= (n.-21-887G=)
c.96+259G= (n.96+259G=)
n.502G=
c.129G= (p.Pro43=)
17g.7676123C>GCA497925953TP53c.246G>C (p.Pro82=)
c.-21-887G>C (n.-21-887G>C)
c.96+259G>C (n.96+259G>C)
n.502G>C
c.129G>C (p.Pro43=)
 ClinVar dbSNP
17g.7676123C>TCA000081TP53c.246G>A (p.Pro82=)
c.-21-887G>A (n.-21-887G>A)
c.96+259G>A (n.96+259G>A)
n.502G>A
c.129G>A (p.Pro43=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
17g.7676124G>ACA000080TP53c.245C>T (p.Pro82Leu)
c.-21-888C>T (n.-21-888C>T)
c.96+258C>T (n.96+258C>T)
n.501C>T
c.128C>T (p.Pro43Leu)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC
17g.7676124G>CCA397845507TP53c.245C>G (p.Pro82Arg)
c.-21-888C>G (n.-21-888C>G)
c.96+258C>G (n.96+258C>G)
n.501C>G
c.128C>G (p.Pro43Arg)
 ClinVar dbSNP
17g.7676124G=CA2245934404TP53c.245C= (p.Pro82=)
c.-21-888C= (n.-21-888C=)
c.96+258C= (n.96+258C=)
n.501C=
c.128C= (p.Pro43=)
17g.7676124G>TCA397845510TP53c.245C>A (p.Pro82Gln)
c.-21-888C>A (n.-21-888C>A)
c.96+258C>A (n.96+258C>A)
n.501C>A
c.128C>A (p.Pro43Gln)
 dbSNP
17g.7676125delCA645589353TP53c.245del (p.Pro82ArgfsTer?)
c.-21-888del (n.-21-888del)
c.96+258del (n.96+258del)
n.501del
c.128del (p.Pro43ArgfsTer?)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7676124_7676127dupCA2825002624TP53c.242_245dup (p.Ala83ThrfsTer?)
c.-21-891_-21-888dup (n.-21-891_-21-888dup)
c.96+255_96+258dup (n.96+255_96+258dup)
n.498_501dup
c.125_128dup (p.Ala44ThrfsTer?)
 ClinVar
17g.7676126_7676131dupCA2697552148TP53c.240_245dup (p.Pro82_Ala83insThrPro)
c.-21-893_-21-888dup (n.-21-893_-21-888dup)
c.96+253_96+258dup (n.96+253_96+258dup)
n.496_501dup
c.123_128dup (p.Pro43_Ala44insThrPro)
 ClinVar
17g.7676125_7676131delCA645589354TP53c.239_245del (p.Pro80ArgfsTer?)
c.-21-894_-21-888del (n.-21-894_-21-888del)
c.96+252_96+258del (n.96+252_96+258del)
n.495_501del
c.122_128del (p.Pro41ArgfsTer?)
 COSMIC
17g.7676125G>ACA397845521TP53c.244C>T (p.Pro82Ser)
c.-21-889C>T (n.-21-889C>T)
c.96+257C>T (n.96+257C>T)
n.500C>T
c.127C>T (p.Pro43Ser)
 ClinVar dbSNP gnomAD v4
17g.7676125G>CCA397845525TP53c.244C>G (p.Pro82Ala)
c.-21-889C>G (n.-21-889C>G)
c.96+257C>G (n.96+257C>G)
n.500C>G
c.127C>G (p.Pro43Ala)
 ClinVar dbSNP gnomAD v4
17g.7676125G=CA2245934421TP53c.244C= (p.Pro82=)
c.-21-889C= (n.-21-889C=)
c.96+257C= (n.96+257C=)
n.500C=
c.127C= (p.Pro43=)
17g.7676125G>TCA397845523TP53c.244C>A (p.Pro82Thr)
c.-21-889C>A (n.-21-889C>A)
c.96+257C>A (n.96+257C>A)
n.500C>A
c.127C>A (p.Pro43Thr)
17g.7676126_7676142dupCA2573154640TP53c.228_244dup (p.Pro82HisfsTer?)
c.-21-905_-21-889dup (n.-21-905_-21-889dup)
c.96+241_96+257dup (n.96+241_96+257dup)
n.484_500dup
c.111_127dup (p.Pro43HisfsTer?)
 ClinVar dbSNP
17g.7676126T>ACA497925956TP53c.243A>T (p.Thr81=)
c.-21-890A>T (n.-21-890A>T)
c.96+256A>T (n.96+256A>T)
n.499A>T
c.126A>T (p.Thr42=)
 ClinVar dbSNP
17g.7676126T>CCA497925957TP53c.243A>G (p.Thr81=)
c.-21-890A>G (n.-21-890A>G)
c.96+256A>G (n.96+256A>G)
n.499A>G
c.126A>G (p.Thr42=)
 ClinVar dbSNP
17g.7676126T>GCA497925958TP53c.243A>C (p.Thr81=)
c.-21-890A>C (n.-21-890A>C)
c.96+256A>C (n.96+256A>C)
n.499A>C
c.126A>C (p.Thr42=)
 dbSNP
17g.7676126T=CA2245934430TP53c.243A= (p.Thr81=)
c.-21-890A= (n.-21-890A=)
c.96+256A= (n.96+256A=)
n.499A=
c.126A= (p.Thr42=)
17g.7676126_7676127insTGTAGGAGCTCA645589355TP53c.243_244insGCTCCTACAA (p.Pro82AlafsTer?)
c.-21-890_-21-889insGCTCCTACAA (n.-21-890_-21-889insGCTCCTACAA)
c.96+256_96+257insGCTCCTACAA (n.96+256_96+257insGCTCCTACAA)
n.499_500insGCTCCTACAA
c.126_127insGCTCCTACAA (p.Pro43AlafsTer?)
 COSMIC
17g.7676127delCA645589356TP53c.242del (p.Thr81AsnfsTer?)
c.-21-891del (n.-21-891del)
c.96+255del (n.96+255del)
n.498del
c.125del (p.Thr42AsnfsTer?)
 COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7676127G>ACA397845528TP53c.242C>T (p.Thr81Ile)
c.-21-891C>T (n.-21-891C>T)
c.96+255C>T (n.96+255C>T)
n.498C>T
c.125C>T (p.Thr42Ile)
 ClinVar dbSNP gnomAD v4 COSMIC
17g.7676127G>CCA397845532TP53c.242C>G (p.Thr81Arg)
c.-21-891C>G (n.-21-891C>G)
c.96+255C>G (n.96+255C>G)
n.498C>G
c.125C>G (p.Thr42Arg)
17g.7676127G=CA2245934439TP53c.242C= (p.Thr81=)
c.-21-891C= (n.-21-891C=)
c.96+255C= (n.96+255C=)
n.498C=
c.125C= (p.Thr42=)
17g.7676127G>TCA397845535TP53c.242C>A (p.Thr81Lys)
c.-21-891C>A (n.-21-891C>A)
c.96+255C>A (n.96+255C>A)
n.498C>A
c.125C>A (p.Thr42Lys)
17g.7676128_7676156delCA891842282TP53c.214_242del (p.Pro72ThrfsTer?)
c.-21-919_-21-891del (n.-21-919_-21-891del)
c.96+227_96+255del (n.96+227_96+255del)
n.470_498del
c.97_125del (p.Pro33ThrfsTer?)
17g.7676128T>ACA397845538TP53c.241A>T (p.Thr81Ser)
c.-21-892A>T (n.-21-892A>T)
c.96+254A>T (n.96+254A>T)
n.497A>T
c.124A>T (p.Thr42Ser)
 dbSNP
17g.7676128T>CCA397845540TP53c.241A>G (p.Thr81Ala)
c.-21-892A>G (n.-21-892A>G)
c.96+254A>G (n.96+254A>G)
n.497A>G
c.124A>G (p.Thr42Ala)
17g.7676128T>GCA397845542TP53c.241A>C (p.Thr81Pro)
c.-21-892A>C (n.-21-892A>C)
c.96+254A>C (n.96+254A>C)
n.497A>C
c.124A>C (p.Thr42Pro)
 dbSNP
17g.7676128dupCA645589357TP53c.241dup (p.Thr81AsnfsTer?)
c.-21-892dup (n.-21-892dup)
c.96+254dup (n.96+254dup)
n.497dup
c.124dup (p.Thr42AsnfsTer?)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7676129A>CCA497925959TP53c.240T>G (p.Pro80=)
c.-21-893T>G (n.-21-893T>G)
c.96+253T>G (n.96+253T>G)
n.496T>G
c.123T>G (p.Pro41=)
 dbSNP
17g.7676129A>GCA497925960TP53c.240T>C (p.Pro80=)
c.-21-893T>C (n.-21-893T>C)
c.96+253T>C (n.96+253T>C)
n.496T>C
c.123T>C (p.Pro41=)
 dbSNP
17g.7676129A>TCA497925961TP53c.240T>A (p.Pro80=)
c.-21-893T>A (n.-21-893T>A)
c.96+253T>A (n.96+253T>A)
n.496T>A
c.123T>A (p.Pro41=)
 dbSNP
17g.7676130G>ACA397845543TP53c.239C>T (p.Pro80Leu)
c.-21-894C>T (n.-21-894C>T)
c.96+252C>T (n.96+252C>T)
n.495C>T
c.122C>T (p.Pro41Leu)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7676130G>CCA397845545TP53c.239C>G (p.Pro80Arg)
c.-21-894C>G (n.-21-894C>G)
c.96+252C>G (n.96+252C>G)
n.495C>G
c.122C>G (p.Pro41Arg)
 dbSNP
17g.7676130G>TCA397845550TP53c.239C>A (p.Pro80His)
c.-21-894C>A (n.-21-894C>A)
c.96+252C>A (n.96+252C>A)
n.495C>A
c.122C>A (p.Pro41His)
 dbSNP
17g.7676131delCA497925962TP53c.239del (p.Pro80LeufsTer?)
c.-21-894del (n.-21-894del)
c.96+252del (n.96+252del)
n.495del
c.122del (p.Pro41LeufsTer?)
 COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7676131G>ACA16615999TP53c.238C>T (p.Pro80Ser)
c.-21-895C>T (n.-21-895C>T)
c.96+251C>T (n.96+251C>T)
n.494C>T
c.121C>T (p.Pro41Ser)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7676131G>CCA397845558TP53c.238C>G (p.Pro80Ala)
c.-21-895C>G (n.-21-895C>G)
c.96+251C>G (n.96+251C>G)
n.494C>G
c.121C>G (p.Pro41Ala)
17g.7676131G=CA2245934467TP53c.238C= (p.Pro80=)
c.-21-895C= (n.-21-895C=)
c.96+251C= (n.96+251C=)
n.494C=
c.121C= (p.Pro41=)
17g.7676131G>TCA397845552TP53c.238C>A (p.Pro80Thr)
c.-21-895C>A (n.-21-895C>A)
c.96+251C>A (n.96+251C>A)
n.494C>A
c.121C>A (p.Pro41Thr)
17g.7676132_7676139delCA645589358TP53c.231_238del (p.Ala78TyrfsTer?)
c.-21-902_-21-895del (n.-21-902_-21-895del)
c.96+244_96+251del (n.96+244_96+251del)
n.487_494del
c.114_121del (p.Ala39TyrfsTer?)
 COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7676132delCA645589359TP53c.237del (p.Pro80LeufsTer?)
c.-21-896del (n.-21-896del)
c.96+250del (n.96+250del)
n.493del
c.120del (p.Pro41LeufsTer?)
 COSMIC
17g.7676132A>CCA497925964TP53c.237T>G (p.Ala79=)
c.-21-896T>G (n.-21-896T>G)
c.96+250T>G (n.96+250T>G)
n.493T>G
c.120T>G (p.Ala40=)
 ClinVar dbSNP
17g.7676132A>GCA497925965TP53c.237T>C (p.Ala79=)
c.-21-896T>C (n.-21-896T>C)
c.96+250T>C (n.96+250T>C)
n.493T>C
c.120T>C (p.Ala40=)
 ClinVar dbSNP
17g.7676132A>TCA497925963TP53c.237T>A (p.Ala79=)
c.-21-896T>A (n.-21-896T>A)
c.96+250T>A (n.96+250T>A)
n.493T>A
c.120T>A (p.Ala40=)
 dbSNP
17g.7676133_7676151delCA2580095105TP53c.219_237del (p.Ala74LeufsTer?)
c.-21-914_-21-896del (n.-21-914_-21-896del)
c.96+232_96+250del (n.96+232_96+250del)
n.475_493del
c.102_120del (p.Ala35LeufsTer?)
 ClinVar
17g.7676133G>ACA397845562TP53c.236C>T (p.Ala79Val)
c.-21-897C>T (n.-21-897C>T)
c.96+249C>T (n.96+249C>T)
n.492C>T
c.119C>T (p.Ala40Val)
 dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7676133G>CCA397845564TP53c.236C>G (p.Ala79Gly)
c.-21-897C>G (n.-21-897C>G)
c.96+249C>G (n.96+249C>G)
n.492C>G
c.119C>G (p.Ala40Gly)
 ClinVar dbSNP
17g.7676133G=CA2245934480TP53c.236C= (p.Ala79=)
c.-21-897C= (n.-21-897C=)
c.96+249C= (n.96+249C=)
n.492C=
c.119C= (p.Ala40=)
17g.7676133G>TCA397845566TP53c.236C>A (p.Ala79Asp)
c.-21-897C>A (n.-21-897C>A)
c.96+249C>A (n.96+249C>A)
n.492C>A
c.119C>A (p.Ala40Asp)
17g.7676133_7676134delinsGCCA2245934486TP53c.235_236delinsGC (p.Ala79=)
c.-21-898_-21-897delinsGC (n.-21-898_-21-897delinsGC)
c.96+248_96+249delinsGC (n.96+248_96+249delinsGC)
n.491_492delinsGC
c.118_119delinsGC (p.Ala40=)
17g.7676134_7676140delCA645589360TP53c.230_236del (p.Pro77LeufsTer?)
c.-21-903_-21-897del (n.-21-903_-21-897del)
c.96+243_96+249del (n.96+243_96+249del)
n.486_492del
c.113_119del (p.Pro38LeufsTer?)
 COSMIC COSMIC COSMIC
17g.7676134delCA2245934496TP53c.235del (p.Ala79LeufsTer?)
c.-21-898del (n.-21-898del)
c.96+248del (n.96+248del)
n.491del
c.118del (p.Ala40LeufsTer?)
 dbSNP
17g.7676134C>ACA397845570TP53c.235G>T (p.Ala79Ser)
c.-21-898G>T (n.-21-898G>T)
c.96+248G>T (n.96+248G>T)
n.491G>T
c.118G>T (p.Ala40Ser)
17g.7676134C>GCA397845573TP53c.235G>C (p.Ala79Pro)
c.-21-898G>C (n.-21-898G>C)
c.96+248G>C (n.96+248G>C)
n.491G>C
c.118G>C (p.Ala40Pro)
17g.7676134C>TCA397845576TP53c.235G>A (p.Ala79Thr)
c.-21-898G>A (n.-21-898G>A)
c.96+248G>A (n.96+248G>A)
n.491G>A
c.118G>A (p.Ala40Thr)
 COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7676135T>ACA497925966TP53c.234A>T (p.Ala78=)
c.-21-899A>T (n.-21-899A>T)
c.96+247A>T (n.96+247A>T)
n.490A>T
c.117A>T (p.Ala39=)
 dbSNP
17g.7676135T>CCA000079TP53c.234A>G (p.Ala78=)
c.-21-899A>G (n.-21-899A>G)
c.96+247A>G (n.96+247A>G)
n.490A>G
c.117A>G (p.Ala39=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.7676135T>GCA497925967TP53c.234A>C (p.Ala78=)
c.-21-899A>C (n.-21-899A>C)
c.96+247A>C (n.96+247A>C)
n.490A>C
c.117A>C (p.Ala39=)
 dbSNP
17g.7676135T=CA2245934504TP53c.234A= (p.Ala78=)
c.-21-899A= (n.-21-899A=)
c.96+247A= (n.96+247A=)
n.490A=
c.117A= (p.Ala39=)
17g.7676136G>ACA397845581TP53c.233C>T (p.Ala78Val)
c.-21-900C>T (n.-21-900C>T)
c.96+246C>T (n.96+246C>T)
n.489C>T
c.116C>T (p.Ala39Val)
 ClinVar dbSNP COSMIC
17g.7676136G>CCA10580955TP53c.233C>G (p.Ala78Gly)
c.-21-900C>G (n.-21-900C>G)
c.96+246C>G (n.96+246C>G)
n.489C>G
c.116C>G (p.Ala39Gly)
 ClinVar dbSNP gnomAD v2 gnomAD v4
17g.7676136G=CA2245934524TP53c.233C= (p.Ala78=)
c.-21-900C= (n.-21-900C=)
c.96+246C= (n.96+246C=)
n.489C=
c.116C= (p.Ala39=)
17g.7676136G>TCA397845590TP53c.233C>A (p.Ala78Glu)
c.-21-900C>A (n.-21-900C>A)
c.96+246C>A (n.96+246C>A)
n.489C>A
c.116C>A (p.Ala39Glu)
 dbSNP
17g.7676136_7676184delinsGCTGGTGCAGGGGCCACGGGGGGAGCAGCCTCTGGCATTCTGGGAGCTTCA2245934518TP53c.185_233delinsAAGCTCCCAGAATGCCAGAGGCTGCTCCCCCCGTGGCCCCTGCACCAGC (p.Glu62=)
c.-21-948_-21-900delinsAAGCTCCCAGAATGCCAGAGGCTGCTCCCCCCGTGGCCCCTGCACCAGC (n.-21-948_-21-900delinsAAGCTCCCAGAATGCCAGAGGCTGCTCCCCCCGTGGCCCCTGCACCAGC)
c.96+198_96+246delinsAAGCTCCCAGAATGCCAGAGGCTGCTCCCCCCGTGGCCCCTGCACCAGC (n.96+198_96+246delinsAAGCTCCCAGAATGCCAGAGGCTGCTCCCCCCGTGGCCCCTGCACCAGC)
n.441_489delinsAAGCTCCCAGAATGCCAGAGGCTGCTCCCCCCGTGGCCCCTGCACCAGC
c.68_116delinsAAGCTCCCAGAATGCCAGAGGCTGCTCCCCCCGTGGCCCCTGCACCAGC (p.Glu23=)
17g.7676137C>ACA397845601TP53c.232G>T (p.Ala78Ser)
c.-21-901G>T (n.-21-901G>T)
c.96+245G>T (n.96+245G>T)
n.488G>T
c.115G>T (p.Ala39Ser)
 ClinVar dbSNP COSMIC
17g.7676137C=CA2245934538TP53c.232G= (p.Ala78=)
c.-21-901G= (n.-21-901G=)
c.96+245G= (n.96+245G=)
n.488G=
c.115G= (p.Ala39=)
17g.7676137C>GCA397845605TP53c.232G>C (p.Ala78Pro)
c.-21-901G>C (n.-21-901G>C)
c.96+245G>C (n.96+245G>C)
n.488G>C
c.115G>C (p.Ala39Pro)
 dbSNP
17g.7676137C>TCA397845606TP53c.232G>A (p.Ala78Thr)
c.-21-901G>A (n.-21-901G>A)
c.96+245G>A (n.96+245G>A)
n.488G>A
c.115G>A (p.Ala39Thr)
 ClinVar dbSNP
17g.7676137_7676143dupCA645589361TP53c.226_232dup (p.Ala78GlyfsTer?)
c.-21-907_-21-901dup (n.-21-907_-21-901dup)
c.96+239_96+245dup (n.96+239_96+245dup)
n.482_488dup
c.109_115dup (p.Ala39GlyfsTer?)
 COSMIC
17g.7676138_7676185delCA913191061TP53c.185_232del (p.Glu62_Pro77del)
c.-21-948_-21-901del (n.-21-948_-21-901del)
c.96+198_96+245del (n.96+198_96+245del)
n.441_488del
c.68_115del (p.Glu23_Pro38del)
 ClinVar dbSNP
17g.7676138T>ACA497925968TP53c.231A>T (p.Pro77=)
c.-21-902A>T (n.-21-902A>T)
c.96+244A>T (n.96+244A>T)
n.487A>T
c.114A>T (p.Pro38=)
17g.7676138T>CCA497925969TP53c.231A>G (p.Pro77=)
c.-21-902A>G (n.-21-902A>G)
c.96+244A>G (n.96+244A>G)
n.487A>G
c.114A>G (p.Pro38=)
 dbSNP
17g.7676138T>GCA497925970TP53c.231A>C (p.Pro77=)
c.-21-902A>C (n.-21-902A>C)
c.96+244A>C (n.96+244A>C)
n.487A>C
c.114A>C (p.Pro38=)
 dbSNP
17g.7676138dupCA645589362TP53c.231dup (p.Ala78SerfsTer?)
c.-21-902dup (n.-21-902dup)
c.96+244dup (n.96+244dup)
n.487dup
c.114dup (p.Ala39SerfsTer?)
 COSMIC COSMIC COSMIC
17g.7676139G>ACA397845609TP53c.230C>T (p.Pro77Leu)
c.-21-903C>T (n.-21-903C>T)
c.96+243C>T (n.96+243C>T)
n.486C>T
c.113C>T (p.Pro38Leu)
 dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7676139G>CCA397845614TP53c.230C>G (p.Pro77Arg)
c.-21-903C>G (n.-21-903C>G)
c.96+243C>G (n.96+243C>G)
n.486C>G
c.113C>G (p.Pro38Arg)
 dbSNP
17g.7676139G>TCA397845611TP53c.230C>A (p.Pro77Gln)
c.-21-903C>A (n.-21-903C>A)
c.96+243C>A (n.96+243C>A)
n.486C>A
c.113C>A (p.Pro38Gln)
17g.7676139_7676140delCA645589364TP53c.229_230del (p.Pro77SerfsTer?)
c.-21-904_-21-903del (n.-21-904_-21-903del)
c.96+242_96+243del (n.96+242_96+243del)
n.485_486del
c.112_113del (p.Pro38SerfsTer?)
 COSMIC
17g.7676140delCA497925971TP53c.230del (p.Pro77GlnfsTer?)
c.-21-903del (n.-21-903del)
c.96+243del (n.96+243del)
n.486del
c.113del (p.Pro38GlnfsTer?)
 COSMIC
17g.7676139_7676149delCA645589363TP53c.220_230del (p.Ala74SerfsTer?)
c.-21-913_-21-903del (n.-21-913_-21-903del)
c.96+233_96+243del (n.96+233_96+243del)
n.476_486del
c.103_113del (p.Ala35SerfsTer?)
 COSMIC
17g.7676139_7676140insACA497925972TP53c.229_230insT (p.Pro77LeufsTer?)
c.-21-904_-21-903insT (n.-21-904_-21-903insT)
c.96+242_96+243insT (n.96+242_96+243insT)
n.485_486insT
c.112_113insT (p.Pro38LeufsTer?)
17g.7676140G>ACA397845619TP53c.229C>T (p.Pro77Ser)
c.-21-904C>T (n.-21-904C>T)
c.96+242C>T (n.96+242C>T)
n.485C>T
c.112C>T (p.Pro38Ser)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
17g.7676140G>CCA397845624TP53c.229C>G (p.Pro77Ala)
c.-21-904C>G (n.-21-904C>G)
c.96+242C>G (n.96+242C>G)
n.485C>G
c.112C>G (p.Pro38Ala)
 ClinVar dbSNP COSMIC
17g.7676140G=CA2245934553TP53c.229C= (p.Pro77=)
c.-21-904C= (n.-21-904C=)
c.96+242C= (n.96+242C=)
n.485C=
c.112C= (p.Pro38=)
17g.7676140G>TCA003025TP53c.229C>A (p.Pro77Thr)
c.-21-904C>A (n.-21-904C>A)
c.96+242C>A (n.96+242C>A)
n.485C>A
c.112C>A (p.Pro38Thr)
 ClinVar dbSNP ExAC gnomAD v2
17g.7676141T>ACA497925974TP53c.228A>T (p.Ala76=)
c.-21-905A>T (n.-21-905A>T)
c.96+241A>T (n.96+241A>T)
n.484A>T
c.111A>T (p.Ala37=)
 dbSNP COSMIC
17g.7676141T>CCA497925975TP53c.228A>G (p.Ala76=)
c.-21-905A>G (n.-21-905A>G)
c.96+241A>G (n.96+241A>G)
n.484A>G
c.111A>G (p.Ala37=)
 ClinVar dbSNP
17g.7676141T>GCA497925973TP53c.228A>C (p.Ala76=)
c.-21-905A>C (n.-21-905A>C)
c.96+241A>C (n.96+241A>C)
n.484A>C
c.111A>C (p.Ala37=)
 dbSNP
17g.7676141_7676144dupCA645589365TP53c.225_228dup (p.Pro77CysfsTer?)
c.-21-908_-21-905dup (n.-21-908_-21-905dup)
c.96+238_96+241dup (n.96+238_96+241dup)
n.481_484dup
c.108_111dup (p.Pro38CysfsTer?)
 COSMIC COSMIC
17g.7676142_7676201delCA645589366TP53c.169_228del (p.Asp57_Ala76del)
c.-21-964_-21-905del (n.-21-964_-21-905del)
c.96+182_96+241del (n.96+182_96+241del)
n.425_484del
c.52_111del (p.Asp18_Ala37del)
 COSMIC
17g.7676142G>ACA397845636TP53c.227C>T (p.Ala76Val)
c.-21-906C>T (n.-21-906C>T)
c.96+240C>T (n.96+240C>T)
n.483C>T
c.110C>T (p.Ala37Val)
 ClinVar dbSNP COSMIC
17g.7676142G>CCA397845638TP53c.227C>G (p.Ala76Gly)
c.-21-906C>G (n.-21-906C>G)
c.96+240C>G (n.96+240C>G)
n.483C>G
c.110C>G (p.Ala37Gly)
 dbSNP
17g.7676142G=CA2245934561TP53c.227C= (p.Ala76=)
c.-21-906C= (n.-21-906C=)
c.96+240C= (n.96+240C=)
n.483C=
c.110C= (p.Ala37=)
17g.7676142G>TCA397845639TP53c.227C>A (p.Ala76Glu)
c.-21-906C>A (n.-21-906C>A)
c.96+240C>A (n.96+240C>A)
n.483C>A
c.110C>A (p.Ala37Glu)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.7676142dupCA2573154643TP53c.227dup (p.Pro77ThrfsTer?)
c.-21-906dup (n.-21-906dup)
c.96+240dup (n.96+240dup)
n.483dup
c.110dup (p.Pro38ThrfsTer?)
 ClinVar dbSNP
17g.7676143C>ACA397845645TP53c.226G>T (p.Ala76Ser)
c.-21-907G>T (n.-21-907G>T)
c.96+239G>T (n.96+239G>T)
n.482G>T
c.109G>T (p.Ala37Ser)
 dbSNP
17g.7676143C>GCA397845648TP53c.226G>C (p.Ala76Pro)
c.-21-907G>C (n.-21-907G>C)
c.96+239G>C (n.96+239G>C)
n.482G>C
c.109G>C (p.Ala37Pro)
 dbSNP
17g.7676143C>TCA397845649TP53c.226G>A (p.Ala76Thr)
c.-21-907G>A (n.-21-907G>A)
c.96+239G>A (n.96+239G>A)
n.482G>A
c.109G>A (p.Ala37Thr)
 ClinVar dbSNP gnomAD v4
17g.7676143dupCA891842283TP53c.226dup (p.Ala76GlyfsTer?)
c.-21-907dup (n.-21-907dup)
c.96+239dup (n.96+239dup)
n.482dup
c.109dup (p.Ala37GlyfsTer?)
17g.7676143_7676171delCA2580574333TP53c.198_226del (p.Met66IlefsTer?)
c.-21-935_-21-907del (n.-21-935_-21-907del)
c.96+211_96+239del (n.96+211_96+239del)
n.454_482del
c.81_109del (p.Met27IlefsTer?)
17g.7676144delCA497925979TP53c.225del (p.Ala76HisfsTer?)
c.-21-908del (n.-21-908del)
c.96+238del (n.96+238del)
n.481del
c.108del (p.Ala37HisfsTer?)
 ClinVar COSMIC
17g.7676144A=CA2245934576TP53c.225T= (p.Pro75=)
c.-21-908T= (n.-21-908T=)
c.96+238T= (n.96+238T=)
n.481T=
c.108T= (p.Pro36=)
17g.7676144A>CCA497925976TP53c.225T>G (p.Pro75=)
c.-21-908T>G (n.-21-908T>G)
c.96+238T>G (n.96+238T>G)
n.481T>G
c.108T>G (p.Pro36=)
17g.7676144A>GCA497925977TP53c.225T>C (p.Pro75=)
c.-21-908T>C (n.-21-908T>C)
c.96+238T>C (n.96+238T>C)
n.481T>C
c.108T>C (p.Pro36=)
 dbSNP
17g.7676144A>TCA497925978TP53c.225T>A (p.Pro75=)
c.-21-908T>A (n.-21-908T>A)
c.96+238T>A (n.96+238T>A)
n.481T>A
c.108T>A (p.Pro36=)
 dbSNP
17g.7676145G>ACA397845650TP53c.224C>T (p.Pro75Leu)
c.-21-909C>T (n.-21-909C>T)
c.96+237C>T (n.96+237C>T)
n.480C>T
c.107C>T (p.Pro36Leu)
 ClinVar dbSNP
17g.7676145G>CCA397845653TP53c.224C>G (p.Pro75Arg)
c.-21-909C>G (n.-21-909C>G)
c.96+237C>G (n.96+237C>G)
n.480C>G
c.107C>G (p.Pro36Arg)
 dbSNP COSMIC
17g.7676145G=CA2245934586TP53c.224C= (p.Pro75=)
c.-21-909C= (n.-21-909C=)
c.96+237C= (n.96+237C=)
n.480C=
c.107C= (p.Pro36=)
17g.7676145G>TCA397845656TP53c.224C>A (p.Pro75His)
c.-21-909C>A (n.-21-909C>A)
c.96+237C>A (n.96+237C>A)
n.480C>A
c.107C>A (p.Pro36His)
 dbSNP gnomAD v4
17g.7676148dupCA913191062TP53c.224dup (p.Ala76CysfsTer?)
c.-21-909dup (n.-21-909dup)
c.96+237dup (n.96+237dup)
n.480dup
c.107dup (p.Ala37CysfsTer?)
 ClinVar dbSNP
17g.7676148delCA497925980TP53c.224del (p.Pro75LeufsTer?)
c.-21-909del (n.-21-909del)
c.96+237del (n.96+237del)
n.480del
c.107del (p.Pro36LeufsTer?)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC
17g.7676146G>ACA397845674TP53c.223C>T (p.Pro75Ser)
c.-21-910C>T (n.-21-910C>T)
c.96+236C>T (n.96+236C>T)
n.479C>T
c.106C>T (p.Pro36Ser)
 dbSNP gnomAD v4 COSMIC
17g.7676146G>CCA397845670TP53c.223C>G (p.Pro75Ala)
c.-21-910C>G (n.-21-910C>G)
c.96+236C>G (n.96+236C>G)
n.479C>G
c.106C>G (p.Pro36Ala)
 dbSNP
17g.7676146G>TCA397845667TP53c.223C>A (p.Pro75Thr)
c.-21-910C>A (n.-21-910C>A)
c.96+236C>A (n.96+236C>A)
n.479C>A
c.106C>A (p.Pro36Thr)
 ClinVar gnomAD v4
17g.7676147G>ACA000078TP53c.222C>T (p.Ala74=)
c.-21-911C>T (n.-21-911C>T)
c.96+235C>T (n.96+235C>T)
n.478C>T
c.105C>T (p.Ala35=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
17g.7676147G>CCA497925981TP53c.222C>G (p.Ala74=)
c.-21-911C>G (n.-21-911C>G)
c.96+235C>G (n.96+235C>G)
n.478C>G
c.105C>G (p.Ala35=)
 dbSNP
17g.7676147G=CA2245934591TP53c.222C= (p.Ala74=)
c.-21-911C= (n.-21-911C=)
c.96+235C= (n.96+235C=)
n.478C=
c.105C= (p.Ala35=)
17g.7676147G>TCA497925982TP53c.222C>A (p.Ala74=)
c.-21-911C>A (n.-21-911C>A)
c.96+235C>A (n.96+235C>A)
n.478C>A
c.105C>A (p.Ala35=)
 dbSNP
17g.7676148G>ACA000077TP53c.221C>T (p.Ala74Val)
c.-21-912C>T (n.-21-912C>T)
c.96+234C>T (n.96+234C>T)
n.477C>T
c.104C>T (p.Ala35Val)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
17g.7676148G>CCA397845690TP53c.221C>G (p.Ala74Gly)
c.-21-912C>G (n.-21-912C>G)
c.96+234C>G (n.96+234C>G)
n.477C>G
c.104C>G (p.Ala35Gly)
 ClinVar dbSNP
17g.7676148G=CA2245934604TP53c.221C= (p.Ala74=)
c.-21-912C= (n.-21-912C=)
c.96+234C= (n.96+234C=)
n.477C=
c.104C= (p.Ala35=)
17g.7676148G>TCA397845686TP53c.221C>A (p.Ala74Asp)
c.-21-912C>A (n.-21-912C>A)
c.96+234C>A (n.96+234C>A)
n.477C>A
c.104C>A (p.Ala35Asp)
17g.7676149_7676153dupCA2697552149TP53c.217_221dup (p.Pro75TrpfsTer?)
c.-21-916_-21-912dup (n.-21-916_-21-912dup)
c.96+230_96+234dup (n.96+230_96+234dup)
n.473_477dup
c.100_104dup (p.Pro36TrpfsTer?)
 ClinVar
17g.7676148_7676166delinsCTCCCCA645589367TP53c.203_221delinsGGGAG (p.Glu68GlyfsTer?)
c.-21-930_-21-912delinsGGGAG (n.-21-930_-21-912delinsGGGAG)
c.96+216_96+234delinsGGGAG (n.96+216_96+234delinsGGGAG)
n.459_477delinsGGGAG
c.86_104delinsGGGAG (p.Glu29GlyfsTer?)
 COSMIC
17g.7676149C>ACA397845695TP53c.220G>T (p.Ala74Ser)
c.-21-913G>T (n.-21-913G>T)
c.96+233G>T (n.96+233G>T)
n.476G>T
c.103G>T (p.Ala35Ser)
 ClinVar dbSNP gnomAD v4
17g.7676149C>GCA397845699TP53c.220G>C (p.Ala74Pro)
c.-21-913G>C (n.-21-913G>C)
c.96+233G>C (n.96+233G>C)
n.476G>C
c.103G>C (p.Ala35Pro)
17g.7676149C>TCA397845701TP53c.220G>A (p.Ala74Thr)
c.-21-913G>A (n.-21-913G>A)
c.96+233G>A (n.96+233G>A)
n.476G>A
c.103G>A (p.Ala35Thr)
 dbSNP
17g.7676150delCA497925983TP53c.220del (p.Ala74ProfsTer?)
c.-21-913del (n.-21-913del)
c.96+233del (n.96+233del)
n.476del
c.103del (p.Ala35ProfsTer?)
 COSMIC
17g.7676150C>ACA497925985TP53c.219G>T (p.Val73=)
c.-21-914G>T (n.-21-914G>T)
c.96+232G>T (n.96+232G>T)
n.475G>T
c.102G>T (p.Val34=)
 ClinVar dbSNP
17g.7676150C=CA2245934617TP53c.219G= (p.Val73=)
c.-21-914G= (n.-21-914G=)
c.96+232G= (n.96+232G=)
n.475G=
c.102G= (p.Val34=)
17g.7676150C>GCA497925986TP53c.219G>C (p.Val73=)
c.-21-914G>C (n.-21-914G>C)
c.96+232G>C (n.96+232G>C)
n.475G>C
c.102G>C (p.Val34=)
 dbSNP
17g.7676150C>TCA497925984TP53c.219G>A (p.Val73=)
c.-21-914G>A (n.-21-914G>A)
c.96+232G>A (n.96+232G>A)
n.475G>A
c.102G>A (p.Val34=)
 ClinVar dbSNP
17g.7676150_7676151insCGCA645589368TP53c.218_219insCG (p.Ala74GlyfsTer?)
c.-21-915_-21-914insCG (n.-21-915_-21-914insCG)
c.96+231_96+232insCG (n.96+231_96+232insCG)
n.474_475insCG
c.101_102insCG (p.Ala35GlyfsTer?)
 COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7676151delCA497925987TP53c.218del (p.Val73GlyfsTer?)
c.-21-915del (n.-21-915del)
c.96+231del (n.96+231del)
n.474del
c.101del (p.Val34GlyfsTer?)
 COSMIC
17g.7676151A>CCA397845706TP53c.218T>G (p.Val73Gly)
c.-21-915T>G (n.-21-915T>G)
c.96+231T>G (n.96+231T>G)
n.474T>G
c.101T>G (p.Val34Gly)
17g.7676151A>GCA397845710TP53c.218T>C (p.Val73Ala)
c.-21-915T>C (n.-21-915T>C)
c.96+231T>C (n.96+231T>C)
n.474T>C
c.101T>C (p.Val34Ala)
 ClinVar dbSNP
17g.7676151A>TCA397845712TP53c.218T>A (p.Val73Glu)
c.-21-915T>A (n.-21-915T>A)
c.96+231T>A (n.96+231T>A)
n.474T>A
c.101T>A (p.Val34Glu)
 dbSNP COSMIC
17g.7676151_7676152insGCA645589369TP53c.217_218insC (p.Val73AlafsTer?)
c.-21-916_-21-915insC (n.-21-916_-21-915insC)
c.96+230_96+231insC (n.96+230_96+231insC)
n.473_474insC
c.100_101insC (p.Val34AlafsTer?)
 COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7676152delCA2695223137TP53c.217del (p.Val73TrpfsTer?)
c.-21-916del (n.-21-916del)
c.96+230del (n.96+230del)
n.473del
c.100del (p.Val34TrpfsTer?)
17g.7676152C>ACA397845729TP53c.217G>T (p.Val73Leu)
c.-21-916G>T (n.-21-916G>T)
c.96+230G>T (n.96+230G>T)
n.473G>T
c.100G>T (p.Val34Leu)
 COSMIC
17g.7676152C=CA2245934642TP53c.217G= (p.Val73=)
c.-21-916G= (n.-21-916G=)
c.96+230G= (n.96+230G=)
n.473G=
c.100G= (p.Val34=)
17g.7676152C>GCA397845718TP53c.217G>C (p.Val73Leu)
c.-21-916G>C (n.-21-916G>C)
c.96+230G>C (n.96+230G>C)
n.473G>C
c.100G>C (p.Val34Leu)
 dbSNP gnomAD v4 COSMIC
17g.7676152C>TCA000075TP53c.217G>A (p.Val73Met)
c.-21-916G>A (n.-21-916G>A)
c.96+230G>A (n.96+230G>A)
n.473G>A
c.100G>A (p.Val34Met)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
17g.7676152_7676153delinsCGCA2245934651TP53c.216_217delinsCG (p.Pro72=)
c.-21-917_-21-916delinsCG (n.-21-917_-21-916delinsCG)
c.96+229_96+230delinsCG (n.96+229_96+230delinsCG)
n.472_473delinsCG
c.99_100delinsCG (p.Pro33=)
17g.7676152_7676154delinsTGCCA913187840TP53c.215_217delinsGCA (p.Pro72_Val73delinsArgMet)
c.-21-918_-21-916delinsGCA (n.-21-918_-21-916delinsGCA)
c.96+228_96+230delinsGCA (n.96+228_96+230delinsGCA)
n.471_473delinsGCA
c.98_100delinsGCA (p.Pro33_Val34delinsArgMet)
 ClinVar
17g.7676153G>ACA000074TP53c.216C>T (p.Pro72=)
c.-21-917C>T (n.-21-917C>T)
c.96+229C>T (n.96+229C>T)
n.472C>T
c.99C>T (p.Pro33=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.7676153G>CCA287489091TP53c.216C>G (p.Pro72=)
c.-21-917C>G (n.-21-917C>G)
c.96+229C>G (n.96+229C>G)
n.472C>G
c.99C>G (p.Pro33=)
 ClinVar dbSNP gnomAD v4
17g.7676153G=CA2245934701TP53c.216C= (p.Pro72=)
c.-21-917C= (n.-21-917C=)
c.96+229C= (n.96+229C=)
n.472C=
c.99C= (p.Pro33=)
17g.7676153G>TCA497925989TP53c.216C>A (p.Pro72=)
c.-21-917C>A (n.-21-917C>A)
c.96+229C>A (n.96+229C>A)
n.472C>A
c.99C>A (p.Pro33=)
 gnomAD v4
17g.7676153_7676154delinsACA645589371TP53c.215_216delinsT (p.Pro72LeufsTer?)
c.-21-918_-21-917delinsT (n.-21-918_-21-917delinsT)
c.96+228_96+229delinsT (n.96+228_96+229delinsT)
n.471_472delinsT
c.98_99delinsT (p.Pro33LeufsTer?)
 COSMIC
17g.7676153_7676154delinsACCA10583683TP53c.215_216delinsGT (p.Pro72Arg)
c.-21-918_-21-917delinsGT (n.-21-918_-21-917delinsGT)
c.96+228_96+229delinsGT (n.96+228_96+229delinsGT)
n.471_472delinsGT
c.98_99delinsGT (p.Pro33Arg)
 ClinVar dbSNP
17g.7676153_7676154delinsGGCA2245934705TP53c.215_216delinsCC (p.Pro72=)
c.-21-918_-21-917delinsCC (n.-21-918_-21-917delinsCC)
c.96+228_96+229delinsCC (n.96+228_96+229delinsCC)
n.471_472delinsCC
c.98_99delinsCC (p.Pro33=)
17g.7676153_7676155delinsCCCA645589370TP53c.214_216delinsGG (p.Pro72GlyfsTer?)
c.-21-919_-21-917delinsGG (n.-21-919_-21-917delinsGG)
c.96+227_96+229delinsGG (n.96+227_96+229delinsGG)
n.470_472delinsGG
c.97_99delinsGG (p.Pro33GlyfsTer?)
 COSMIC
17g.7676158dupCA000073TP53c.216dup (p.Val73ArgfsTer?)
c.-21-917dup (n.-21-917dup)
c.96+229dup (n.96+229dup)
n.472dup
c.99dup (p.Val34ArgfsTer?)
 ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7676158delCA497925988TP53c.216del (p.Val73TrpfsTer?)
c.-21-917del (n.-21-917del)
c.96+229del (n.96+229del)
n.472del
c.99del (p.Val34TrpfsTer?)
 ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7676153_7676154insCCA497925990TP53c.215_216insG (p.Val73ArgfsTer?)
c.-21-918_-21-917insG (n.-21-918_-21-917insG)
c.96+228_96+229insG (n.96+228_96+229insG)
n.471_472insG
c.98_99insG (p.Val34ArgfsTer?)
 dbSNP
17g.7676154G>ACA397845758TP53c.215C>T (p.Pro72Leu)
c.-21-918C>T (n.-21-918C>T)
c.96+228C>T (n.96+228C>T)
n.471C>T
c.98C>T (p.Pro33Leu)
 ClinVar dbSNP gnomAD v4
17g.7676154G>CCA000072TP53c.215C>G (p.Pro72Arg)
c.-21-918C>G (n.-21-918C>G)
c.96+228C>G (n.96+228C>G)
n.471C>G
c.98C>G (p.Pro33Arg)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.7676154G=CA178298TP53c.215C= (p.Pro72=)
c.-21-918C= (n.-21-918C=)
c.96+228C= (n.96+228C=)
n.471C=
c.98C= (p.Pro33=)
17g.7676154G>TCA000071TP53c.215C>A (p.Pro72His)
c.-21-918C>A (n.-21-918C>A)
c.96+228C>A (n.96+228C>A)
n.471C>A
c.98C>A (p.Pro33His)
 ClinVar dbSNP gnomAD v4 COSMIC
17g.7676154_7676155delinsCACA000069TP53c.214_215delinsTG (p.Pro72Cys)
c.-21-919_-21-918delinsTG (n.-21-919_-21-918delinsTG)
c.96+227_96+228delinsTG (n.96+227_96+228delinsTG)
n.470_471delinsTG
c.97_98delinsTG (p.Pro33Cys)
 ClinVar dbSNP
17g.7676154_7676155delinsCCCA2580095108TP53c.214_215delinsGG (p.Pro72Gly)
c.-21-919_-21-918delinsGG (n.-21-919_-21-918delinsGG)
c.96+227_96+228delinsGG (n.96+227_96+228delinsGG)
n.470_471delinsGG
c.97_98delinsGG (p.Pro33Gly)
 ClinVar
17g.7676154_7676155delinsGGCA2245934737TP53c.214_215delinsCC (p.Pro72=)
c.-21-919_-21-918delinsCC (n.-21-919_-21-918delinsCC)
c.96+227_96+228delinsCC (n.96+227_96+228delinsCC)
n.470_471delinsCC
c.97_98delinsCC (p.Pro33=)
17g.7676154_7676160delinsCCTCA891842284TP53c.209_215delinsAGG (p.Ala70GlufsTer?)
c.-21-924_-21-918delinsAGG (n.-21-924_-21-918delinsAGG)
c.96+222_96+228delinsAGG (n.96+222_96+228delinsAGG)
n.465_471delinsAGG
c.92_98delinsAGG (p.Ala31GlufsTer?)
17g.7676154_7676155insCCA645369692TP53c.214_215insG (p.Pro72ArgfsTer?)
c.-21-919_-21-918insG (n.-21-919_-21-918insG)
c.96+227_96+228insG (n.96+227_96+228insG)
n.470_471insG
c.97_98insG (p.Pro33ArgfsTer?)
 ClinVar dbSNP
17g.7676155G>ACA003069TP53c.214C>T (p.Pro72Ser)
c.-21-919C>T (n.-21-919C>T)
c.96+227C>T (n.96+227C>T)
n.470C>T
c.97C>T (p.Pro33Ser)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7676155G>CCA000070TP53c.214C>G (p.Pro72Ala)
c.-21-919C>G (n.-21-919C>G)
c.96+227C>G (n.96+227C>G)
n.470C>G
c.97C>G (p.Pro33Ala)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7676155G=CA2245934766TP53c.214C= (p.Pro72=)
c.-21-919C= (n.-21-919C=)
c.96+227C= (n.96+227C=)
n.470C=
c.97C= (p.Pro33=)
17g.7676155G>TCA003071TP53c.214C>A (p.Pro72Thr)
c.-21-919C>A (n.-21-919C>A)
c.96+227C>A (n.96+227C>A)
n.470C>A
c.97C>A (p.Pro33Thr)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.7676156G>ACA497925991TP53c.213C>T (p.Pro71=)
c.-21-920C>T (n.-21-920C>T)
c.96+226C>T (n.96+226C>T)
n.469C>T
c.96C>T (p.Pro32=)
 ClinVar dbSNP
17g.7676156G>CCA497925992TP53c.213C>G (p.Pro71=)
c.-21-920C>G (n.-21-920C>G)
c.96+226C>G (n.96+226C>G)
n.469C>G
c.96C>G (p.Pro32=)
17g.7676156G=CA2245934780TP53c.213C= (p.Pro71=)
c.-21-920C= (n.-21-920C=)
c.96+226C= (n.96+226C=)
n.469C=
c.96C= (p.Pro32=)
17g.7676156G>TCA497925993TP53c.213C>A (p.Pro71=)
c.-21-920C>A (n.-21-920C>A)
c.96+226C>A (n.96+226C>A)
n.469C>A
c.96C>A (p.Pro32=)
 dbSNP
17g.7676162_7676182delCA645589372TP53c.193_213del (p.Arg65_Pro71del)
c.-21-940_-21-920del (n.-21-940_-21-920del)
c.96+206_96+226del (n.96+206_96+226del)
n.449_469del
c.76_96del (p.Arg26_Pro32del)
 COSMIC
17g.7676157G>ACA397845812TP53c.212C>T (p.Pro71Leu)
c.-21-921C>T (n.-21-921C>T)
c.96+225C>T (n.96+225C>T)
n.468C>T
c.95C>T (p.Pro32Leu)
 dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7676157G>CCA10583684TP53c.212C>G (p.Pro71Arg)
c.-21-921C>G (n.-21-921C>G)
c.96+225C>G (n.96+225C>G)
n.468C>G
c.95C>G (p.Pro32Arg)
 ClinVar dbSNP
17g.7676157G=CA2245934796TP53c.212C= (p.Pro71=)
c.-21-921C= (n.-21-921C=)
c.96+225C= (n.96+225C=)
n.468C=
c.95C= (p.Pro32=)
17g.7676157G>TCA397845819TP53c.212C>A (p.Pro71His)
c.-21-921C>A (n.-21-921C>A)
c.96+225C>A (n.96+225C>A)
n.468C>A
c.95C>A (p.Pro32His)
17g.7676158G>ACA397845838TP53c.211C>T (p.Pro71Ser)
c.-21-922C>T (n.-21-922C>T)
c.96+224C>T (n.96+224C>T)
n.467C>T
c.94C>T (p.Pro32Ser)
 ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7676158G>CCA397845842TP53c.211C>G (p.Pro71Ala)
c.-21-922C>G (n.-21-922C>G)
c.96+224C>G (n.96+224C>G)
n.467C>G
c.94C>G (p.Pro32Ala)
 ClinVar dbSNP
17g.7676158G=CA2245934811TP53c.211C= (p.Pro71=)
c.-21-922C= (n.-21-922C=)
c.96+224C= (n.96+224C=)
n.467C=
c.94C= (p.Pro32=)
17g.7676158G>TCA397845843TP53c.211C>A (p.Pro71Thr)
c.-21-922C>A (n.-21-922C>A)
c.96+224C>A (n.96+224C>A)
n.467C>A
c.94C>A (p.Pro32Thr)
17g.7676159_7676160delCA645589373TP53c.210_211del (p.Pro72ArgfsTer?)
c.-21-923_-21-922del (n.-21-923_-21-922del)
c.96+223_96+224del (n.96+223_96+224del)
n.466_467del
c.93_94del (p.Pro33ArgfsTer?)
 COSMIC COSMIC COSMIC
17g.7676159A=CA2245934844TP53c.210T= (p.Ala70=)
c.-21-923T= (n.-21-923T=)
c.96+223T= (n.96+223T=)
n.466T=
c.93T= (p.Ala31=)
17g.7676159A>CCA497925994TP53c.210T>G (p.Ala70=)
c.-21-923T>G (n.-21-923T>G)
c.96+223T>G (n.96+223T>G)
n.466T>G
c.93T>G (p.Ala31=)
 COSMIC
17g.7676159A>GCA000068TP53c.210T>C (p.Ala70=)
c.-21-923T>C (n.-21-923T>C)
c.96+223T>C (n.96+223T>C)
n.466T>C
c.93T>C (p.Ala31=)
 ClinVar dbSNP gnomAD v4
17g.7676159A>TCA16616004TP53c.210T>A (p.Ala70=)
c.-21-923T>A (n.-21-923T>A)
c.96+223T>A (n.96+223T>A)
n.466T>A
c.93T>A (p.Ala31=)
 ClinVar dbSNP gnomAD v4
17g.7676162_7676164delCA658820767TP53c.208_210del (p.Ala70del)
c.-21-925_-21-923del (n.-21-925_-21-923del)
c.96+221_96+223del (n.96+221_96+223del)
n.464_466del
c.91_93del (p.Ala31del)
17g.7676160G>ACA397845860TP53c.209C>T (p.Ala70Val)
c.-21-924C>T (n.-21-924C>T)
c.96+222C>T (n.96+222C>T)
n.465C>T
c.92C>T (p.Ala31Val)
 ClinVar dbSNP
17g.7676160G>CCA397845851TP53c.209C>G (p.Ala70Gly)
c.-21-924C>G (n.-21-924C>G)
c.96+222C>G (n.96+222C>G)
n.465C>G
c.92C>G (p.Ala31Gly)
 dbSNP
17g.7676160G=CA2245934862TP53c.209C= (p.Ala70=)
c.-21-924C= (n.-21-924C=)
c.96+222C= (n.96+222C=)
n.465C=
c.92C= (p.Ala31=)
17g.7676160G>TCA397845855TP53c.209C>A (p.Ala70Asp)
c.-21-924C>A (n.-21-924C>A)
c.96+222C>A (n.96+222C>A)
n.465C>A
c.92C>A (p.Ala31Asp)
 dbSNP
17g.7676161C>ACA397845864TP53c.208G>T (p.Ala70Ser)
c.-21-925G>T (n.-21-925G>T)
c.96+221G>T (n.96+221G>T)
n.464G>T
c.91G>T (p.Ala31Ser)
 dbSNP
17g.7676161C>GCA397845865TP53c.208G>C (p.Ala70Pro)
c.-21-925G>C (n.-21-925G>C)
c.96+221G>C (n.96+221G>C)
n.464G>C
c.91G>C (p.Ala31Pro)
 dbSNP
17g.7676161C>TCA397845866TP53c.208G>A (p.Ala70Thr)
c.-21-925G>A (n.-21-925G>A)
c.96+221G>A (n.96+221G>A)
n.464G>A
c.91G>A (p.Ala31Thr)
 dbSNP COSMIC
17g.7676162delCA2635874979TP53c.207del (p.Ala70LeufsTer?)
c.-21-926del (n.-21-926del)
c.96+220del (n.96+220del)
n.463del
c.90del (p.Ala31LeufsTer?)
 gnomAD v4
17g.7676162A=CA2245934871TP53c.207T= (p.Ala69=)
c.-21-926T= (n.-21-926T=)
c.96+220T= (n.96+220T=)
n.463T=
c.90T= (p.Ala30=)
17g.7676162A>CCA497925995TP53c.207T>G (p.Ala69=)
c.-21-926T>G (n.-21-926T>G)
c.96+220T>G (n.96+220T>G)
n.463T>G
c.90T>G (p.Ala30=)
17g.7676162A>GCA003098TP53c.207T>C (p.Ala69=)
c.-21-926T>C (n.-21-926T>C)
c.96+220T>C (n.96+220T>C)
n.463T>C
c.90T>C (p.Ala30=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7676162A>TCA497925996TP53c.207T>A (p.Ala69=)
c.-21-926T>A (n.-21-926T>A)
c.96+220T>A (n.96+220T>A)
n.463T>A
c.90T>A (p.Ala30=)
 dbSNP
17g.7676163G>ACA287489112TP53c.206C>T (p.Ala69Val)
c.-21-927C>T (n.-21-927C>T)
c.96+219C>T (n.96+219C>T)
n.462C>T
c.89C>T (p.Ala30Val)
 ClinVar dbSNP gnomAD v4 COSMIC
17g.7676163G>CCA10580956TP53c.206C>G (p.Ala69Gly)
c.-21-927C>G (n.-21-927C>G)
c.96+219C>G (n.96+219C>G)
n.462C>G
c.89C>G (p.Ala30Gly)
 ClinVar dbSNP COSMIC
17g.7676163G=CA2245934893TP53c.206C= (p.Ala69=)
c.-21-927C= (n.-21-927C=)
c.96+219C= (n.96+219C=)
n.462C=
c.89C= (p.Ala30=)
17g.7676163G>TCA397845889TP53c.206C>A (p.Ala69Asp)
c.-21-927C>A (n.-21-927C>A)
c.96+219C>A (n.96+219C>A)
n.462C>A
c.89C>A (p.Ala30Asp)
 dbSNP
17g.7676163_7676164delCA645589374TP53c.205_206del (p.Ala69CysfsTer?)
c.-21-928_-21-927del (n.-21-928_-21-927del)
c.96+218_96+219del (n.96+218_96+219del)
n.461_462del
c.88_89del (p.Ala30CysfsTer?)
 COSMIC
17g.7676164C>ACA397845894TP53c.205G>T (p.Ala69Ser)
c.-21-928G>T (n.-21-928G>T)
c.96+218G>T (n.96+218G>T)
n.461G>T
c.88G>T (p.Ala30Ser)
 dbSNP
17g.7676164C=CA2245934909TP53c.205G= (p.Ala69=)
c.-21-928G= (n.-21-928G=)
c.96+218G= (n.96+218G=)
n.461G=
c.88G= (p.Ala30=)
17g.7676164C>GCA397845901TP53c.205G>C (p.Ala69Pro)
c.-21-928G>C (n.-21-928G>C)
c.96+218G>C (n.96+218G>C)
n.461G>C
c.88G>C (p.Ala30Pro)
 ClinVar dbSNP gnomAD v4
17g.7676164C>TCA397845904TP53c.205G>A (p.Ala69Thr)
c.-21-928G>A (n.-21-928G>A)
c.96+218G>A (n.96+218G>A)
n.461G>A
c.88G>A (p.Ala30Thr)
 ClinVar dbSNP gnomAD v4
17g.7676165delCA497925997TP53c.205del (p.Ala69LeufsTer?)
c.-21-928del (n.-21-928del)
c.96+218del (n.96+218del)
n.461del
c.88del (p.Ala30LeufsTer?)
 ClinVar dbSNP COSMIC
17g.7676165C>ACA397845922TP53c.204G>T (p.Glu68Asp)
c.-21-929G>T (n.-21-929G>T)
c.96+217G>T (n.96+217G>T)
n.460G>T
c.87G>T (p.Glu29Asp)
 dbSNP
17g.7676165C=CA2245934918TP53c.204G= (p.Glu68=)
c.-21-929G= (n.-21-929G=)
c.96+217G= (n.96+217G=)
n.460G=
c.87G= (p.Glu29=)
17g.7676165C>GCA397845918TP53c.204G>C (p.Glu68Asp)
c.-21-929G>C (n.-21-929G>C)
c.96+217G>C (n.96+217G>C)
n.460G>C
c.87G>C (p.Glu29Asp)
 dbSNP
17g.7676165C>TCA000067TP53c.204G>A (p.Glu68=)
c.-21-929G>A (n.-21-929G>A)
c.96+217G>A (n.96+217G>A)
n.460G>A
c.87G>A (p.Glu29=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
17g.7676166T>ACA397845932TP53c.203A>T (p.Glu68Val)
c.-21-930A>T (n.-21-930A>T)
c.96+216A>T (n.96+216A>T)
n.459A>T
c.86A>T (p.Glu29Val)
 dbSNP
17g.7676166T>CCA397845936TP53c.203A>G (p.Glu68Gly)
c.-21-930A>G (n.-21-930A>G)
c.96+216A>G (n.96+216A>G)
n.459A>G
c.86A>G (p.Glu29Gly)
 dbSNP COSMIC
17g.7676166T>GCA397845940TP53c.203A>C (p.Glu68Ala)
c.-21-930A>C (n.-21-930A>C)
c.96+216A>C (n.96+216A>C)
n.459A>C
c.86A>C (p.Glu29Ala)
17g.7676171_7676178delCA645589375TP53c.196_203del (p.Met66GlyfsTer?)
c.-21-937_-21-930del (n.-21-937_-21-930del)
c.96+209_96+216del (n.96+209_96+216del)
n.452_459del
c.79_86del (p.Met27GlyfsTer?)
 COSMIC
17g.7676167delCA497925998TP53c.202del (p.Glu68ArgfsTer?)
c.-21-931del (n.-21-931del)
c.96+215del (n.96+215del)
n.458del
c.85del (p.Glu29ArgfsTer?)
 COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7676167C>ACA353535TP53c.202G>T (p.Glu68Ter)
c.-21-931G>T (n.-21-931G>T)
c.96+215G>T (n.96+215G>T)
n.458G>T
c.85G>T (p.Glu29Ter)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7676167C=CA2245934936TP53c.202G= (p.Glu68=)
c.-21-931G= (n.-21-931G=)
c.96+215G= (n.96+215G=)
n.458G=
c.85G= (p.Glu29=)
17g.7676167C>GCA397845956TP53c.202G>C (p.Glu68Gln)
c.-21-931G>C (n.-21-931G>C)
c.96+215G>C (n.96+215G>C)
n.458G>C
c.85G>C (p.Glu29Gln)
 ClinVar dbSNP COSMIC
17g.7676167C>TCA397845957TP53c.202G>A (p.Glu68Lys)
c.-21-931G>A (n.-21-931G>A)
c.96+215G>A (n.96+215G>A)
n.458G>A
c.85G>A (p.Glu29Lys)
 dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7676168T>ACA497926000TP53c.201A>T (p.Pro67=)
c.-21-932A>T (n.-21-932A>T)
c.96+214A>T (n.96+214A>T)
n.457A>T
c.84A>T (p.Pro28=)
17g.7676168T>CCA000066TP53c.201A>G (p.Pro67=)
c.-21-932A>G (n.-21-932A>G)
c.96+214A>G (n.96+214A>G)
n.457A>G
c.84A>G (p.Pro28=)
 ClinVar dbSNP COSMIC
17g.7676168T>GCA497925999TP53c.201A>C (p.Pro67=)
c.-21-932A>C (n.-21-932A>C)
c.96+214A>C (n.96+214A>C)
n.457A>C
c.84A>C (p.Pro28=)
17g.7676168T=CA2245934952TP53c.201A= (p.Pro67=)
c.-21-932A= (n.-21-932A=)
c.96+214A= (n.96+214A=)
n.457A=
c.84A= (p.Pro28=)
17g.7676168_7676169delCA645589376TP53c.200_201del (p.Pro67ArgfsTer?)
c.-21-933_-21-932del (n.-21-933_-21-932del)
c.96+213_96+214del (n.96+213_96+214del)
n.456_457del
c.83_84del (p.Pro28ArgfsTer?)
 COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7676169G>ACA397845965TP53c.200C>T (p.Pro67Leu)
c.-21-933C>T (n.-21-933C>T)
c.96+213C>T (n.96+213C>T)
n.456C>T
c.83C>T (p.Pro28Leu)
 dbSNP COSMIC
17g.7676169G>CCA397845968TP53c.200C>G (p.Pro67Arg)
c.-21-933C>G (n.-21-933C>G)
c.96+213C>G (n.96+213C>G)
n.456C>G
c.83C>G (p.Pro28Arg)
 dbSNP COSMIC
17g.7676169G=CA2245934966TP53c.200C= (p.Pro67=)
c.-21-933C= (n.-21-933C=)
c.96+213C= (n.96+213C=)
n.456C=
c.83C= (p.Pro28=)
17g.7676169G>TCA397845972TP53c.200C>A (p.Pro67Gln)
c.-21-933C>A (n.-21-933C>A)
c.96+213C>A (n.96+213C>A)
n.456C>A
c.83C>A (p.Pro28Gln)
 ClinVar dbSNP
17g.7676170dupCA645589377TP53c.200dup (p.Glu68ArgfsTer?)
c.-21-933dup (n.-21-933dup)
c.96+213dup (n.96+213dup)
n.456dup
c.83dup (p.Glu29ArgfsTer?)
 COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7676170delCA497926001TP53c.200del (p.Pro67GlnfsTer?)
c.-21-933del (n.-21-933del)
c.96+213del (n.96+213del)
n.456del
c.83del (p.Pro28GlnfsTer?)
 ClinVar COSMIC
17g.7676170G>ACA397845977TP53c.199C>T (p.Pro67Ser)
c.-21-934C>T (n.-21-934C>T)
c.96+212C>T (n.96+212C>T)
n.455C>T
c.82C>T (p.Pro28Ser)
 ClinVar dbSNP COSMIC
17g.7676170G>CCA397845985TP53c.199C>G (p.Pro67Ala)
c.-21-934C>G (n.-21-934C>G)
c.96+212C>G (n.96+212C>G)
n.455C>G
c.82C>G (p.Pro28Ala)
 ClinVar dbSNP
17g.7676170G=CA2245934977TP53c.199C= (p.Pro67=)
c.-21-934C= (n.-21-934C=)
c.96+212C= (n.96+212C=)
n.455C=
c.82C= (p.Pro28=)
17g.7676170G>TCA397845998TP53c.199C>A (p.Pro67Thr)
c.-21-934C>A (n.-21-934C>A)
c.96+212C>A (n.96+212C>A)
n.455C>A
c.82C>A (p.Pro28Thr)
 dbSNP
17g.7676170_7676171delinsGCCA2245934976TP53c.198_199delinsGC (p.Met66=)
c.-21-935_-21-934delinsGC (n.-21-935_-21-934delinsGC)
c.96+211_96+212delinsGC (n.96+211_96+212delinsGC)
n.454_455delinsGC
c.81_82delinsGC (p.Met27=)
17g.7676171delCA287489129TP53c.198del (p.Met66IlefsTer?)
c.-21-935del (n.-21-935del)
c.96+211del (n.96+211del)
n.454del
c.81del (p.Met27IlefsTer?)
 dbSNP
17g.7676171C>ACA397846013TP53c.198G>T (p.Met66Ile)
c.-21-935G>T (n.-21-935G>T)
c.96+211G>T (n.96+211G>T)
n.454G>T
c.81G>T (p.Met27Ile)
 dbSNP
17g.7676171C=CA2245934987TP53c.198G= (p.Met66=)
c.-21-935G= (n.-21-935G=)
c.96+211G= (n.96+211G=)
n.454G=
c.81G= (p.Met27=)
17g.7676171C>GCA397846016TP53c.198G>C (p.Met66Ile)
c.-21-935G>C (n.-21-935G>C)
c.96+211G>C (n.96+211G>C)
n.454G>C
c.81G>C (p.Met27Ile)
 dbSNP
17g.7676171C>TCA397846006TP53c.198G>A (p.Met66Ile)
c.-21-935G>A (n.-21-935G>A)
c.96+211G>A (n.96+211G>A)
n.454G>A
c.81G>A (p.Met27Ile)
 ClinVar dbSNP COSMIC
17g.7676172A=CA2245935006TP53c.197T= (p.Met66=)
c.-21-936T= (n.-21-936T=)
c.96+210T= (n.96+210T=)
n.453T=
c.80T= (p.Met27=)
17g.7676172A>CCA397846032TP53c.197T>G (p.Met66Arg)
c.-21-936T>G (n.-21-936T>G)
c.96+210T>G (n.96+210T>G)
n.453T>G
c.80T>G (p.Met27Arg)
 ClinVar dbSNP COSMIC
17g.7676172A>GCA397846021TP53c.197T>C (p.Met66Thr)
c.-21-936T>C (n.-21-936T>C)
c.96+210T>C (n.96+210T>C)
n.453T>C
c.80T>C (p.Met27Thr)
 ClinVar dbSNP
17g.7676172A>TCA397846037TP53c.197T>A (p.Met66Lys)
c.-21-936T>A (n.-21-936T>A)
c.96+210T>A (n.96+210T>A)
n.453T>A
c.80T>A (p.Met27Lys)
 dbSNP
17g.7676172_7676173insATTCTGGGCA645589378TP53c.196_197insCCCAGAAT (p.Met66ThrfsTer?)
c.-21-937_-21-936insCCCAGAAT (n.-21-937_-21-936insCCCAGAAT)
c.96+209_96+210insCCCAGAAT (n.96+209_96+210insCCCAGAAT)
n.452_453insCCCAGAAT
c.79_80insCCCAGAAT (p.Met27ThrfsTer?)
 COSMIC COSMIC COSMIC
17g.7676173T>ACA397846045TP53c.196A>T (p.Met66Leu)
c.-21-937A>T (n.-21-937A>T)
c.96+209A>T (n.96+209A>T)
n.452A>T
c.79A>T (p.Met27Leu)
 dbSNP
17g.7676173T>CCA397846060TP53c.196A>G (p.Met66Val)
c.-21-937A>G (n.-21-937A>G)
c.96+209A>G (n.96+209A>G)
n.452A>G
c.79A>G (p.Met27Val)
 ClinVar dbSNP gnomAD v3 gnomAD v4
17g.7676173T>GCA397846047TP53c.196A>C (p.Met66Leu)
c.-21-937A>C (n.-21-937A>C)
c.96+209A>C (n.96+209A>C)
n.452A>C
c.79A>C (p.Met27Leu)
 dbSNP
17g.7676173T=CA2245935022TP53c.196A= (p.Met66=)
c.-21-937A= (n.-21-937A=)
c.96+209A= (n.96+209A=)
n.452A=
c.79A= (p.Met27=)
17g.7676174dupCA645589379TP53c.196dup (p.Met66AsnfsTer?)
c.-21-937dup (n.-21-937dup)
c.96+209dup (n.96+209dup)
n.452dup
c.79dup (p.Met27AsnfsTer?)
 ClinVar dbSNP COSMIC
17g.7676173_7676174insACA497926002TP53c.195_196insT (p.Met66TyrfsTer?)
c.-21-938_-21-937insT (n.-21-938_-21-937insT)
c.96+208_96+209insT (n.96+208_96+209insT)
n.451_452insT
c.78_79insT (p.Met27TyrfsTer?)
17g.7676174T>ACA397846063TP53c.195A>T (p.Arg65Ser)
c.-21-938A>T (n.-21-938A>T)
c.96+208A>T (n.96+208A>T)
n.451A>T
c.78A>T (p.Arg26Ser)
 dbSNP
17g.7676174T>CCA497926003TP53c.195A>G (p.Arg65=)
c.-21-938A>G (n.-21-938A>G)
c.96+208A>G (n.96+208A>G)
n.451A>G
c.78A>G (p.Arg26=)
 ClinVar dbSNP
17g.7676174T>GCA397846065TP53c.195A>C (p.Arg65Ser)
c.-21-938A>C (n.-21-938A>C)
c.96+208A>C (n.96+208A>C)
n.451A>C
c.78A>C (p.Arg26Ser)
 dbSNP
17g.7676174T=CA2245935027TP53c.195A= (p.Arg65=)
c.-21-938A= (n.-21-938A=)
c.96+208A= (n.96+208A=)
n.451A=
c.78A= (p.Arg26=)
17g.7676175C>ACA397846071TP53c.194G>T (p.Arg65Ile)
c.-21-939G>T (n.-21-939G>T)
c.96+207G>T (n.96+207G>T)
n.450G>T
c.77G>T (p.Arg26Ile)
 dbSNP
17g.7676175C=CA2245935032TP53c.194G= (p.Arg65=)
c.-21-939G= (n.-21-939G=)
c.96+207G= (n.96+207G=)
n.450G=
c.77G= (p.Arg26=)
17g.7676175C>GCA16615958TP53c.194G>C (p.Arg65Thr)
c.-21-939G>C (n.-21-939G>C)
c.96+207G>C (n.96+207G>C)
n.450G>C
c.77G>C (p.Arg26Thr)
 ClinVar dbSNP
17g.7676175C>TCA397846082TP53c.194G>A (p.Arg65Lys)
c.-21-939G>A (n.-21-939G>A)
c.96+207G>A (n.96+207G>A)
n.450G>A
c.77G>A (p.Arg26Lys)
 dbSNP
17g.7676175_7676176insGCA645589380TP53c.193_194insC (p.Arg65ThrfsTer?)
c.-21-940_-21-939insC (n.-21-940_-21-939insC)
c.96+206_96+207insC (n.96+206_96+207insC)
n.449_450insC
c.76_77insC (p.Arg26ThrfsTer?)
 COSMIC COSMIC COSMIC
17g.7676176T>ACA397846088TP53c.193A>T (p.Arg65Ter)
c.-21-940A>T (n.-21-940A>T)
c.96+206A>T (n.96+206A>T)
n.449A>T
c.76A>T (p.Arg26Ter)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7676176T>CCA397846091TP53c.193A>G (p.Arg65Gly)
c.-21-940A>G (n.-21-940A>G)
c.96+206A>G (n.96+206A>G)
n.449A>G
c.76A>G (p.Arg26Gly)
 ClinVar dbSNP
17g.7676176T>GCA497926004TP53c.193A>C (p.Arg65=)
c.-21-940A>C (n.-21-940A>C)
c.96+206A>C (n.96+206A>C)
n.449A>C
c.76A>C (p.Arg26=)
 ClinVar dbSNP
17g.7676176T=CA2245935060TP53c.193A= (p.Arg65=)
c.-21-940A= (n.-21-940A=)
c.96+206A= (n.96+206A=)
n.449A=
c.76A= (p.Arg26=)
17g.7676176dupCA645589381TP53c.193dup (p.Arg65LysfsTer?)
c.-21-940dup (n.-21-940dup)
c.96+206dup (n.96+206dup)
n.449dup
c.76dup (p.Arg26LysfsTer?)
 COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7676176_7676177insCCA497926008TP53c.192_193insG (p.Arg65GlufsTer?)
c.-21-941_-21-940insG (n.-21-941_-21-940insG)
c.96+205_96+206insG (n.96+205_96+206insG)
n.448_449insG
c.75_76insG (p.Arg26GlufsTer?)
17g.7676177G>ACA497926007TP53c.192C>T (p.Pro64=)
c.-21-941C>T (n.-21-941C>T)
c.96+205C>T (n.96+205C>T)
n.448C>T
c.75C>T (p.Pro25=)
 ClinVar dbSNP gnomAD v4
17g.7676177G>CCA497926006TP53c.192C>G (p.Pro64=)
c.-21-941C>G (n.-21-941C>G)
c.96+205C>G (n.96+205C>G)
n.448C>G
c.75C>G (p.Pro25=)
 ClinVar dbSNP
17g.7676177G=CA2245935083TP53c.192C= (p.Pro64=)
c.-21-941C= (n.-21-941C=)
c.96+205C= (n.96+205C=)
n.448C=
c.75C= (p.Pro25=)
17g.7676177G>TCA497926005TP53c.192C>A (p.Pro64=)
c.-21-941C>A (n.-21-941C>A)
c.96+205C>A (n.96+205C>A)
n.448C>A
c.75C>A (p.Pro25=)
 dbSNP
17g.7676179dupCA645589383TP53c.192dup (p.Arg65GlnfsTer?)
c.-21-941dup (n.-21-941dup)
c.96+205dup (n.96+205dup)
n.448dup
c.75dup (p.Arg26GlnfsTer?)
 COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7676179delCA645589382TP53c.192del (p.Arg65GlufsTer?)
c.-21-941del (n.-21-941del)
c.96+205del (n.96+205del)
n.448del
c.75del (p.Arg26GlufsTer?)
 COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7676178_7676179delCA2695223138TP53c.191_192del (p.Pro64GlnfsTer?)
c.-21-942_-21-941del (n.-21-942_-21-941del)
c.96+204_96+205del (n.96+204_96+205del)
n.447_448del
c.74_75del (p.Pro25GlnfsTer?)
17g.7676181_7676233delCA1139768370TP53c.140_192del (p.Pro47GlnfsTer?)
c.-21-993_-21-941del (n.-21-993_-21-941del)
c.96+153_96+205del (n.96+153_96+205del)
n.396_448del
c.23_75del (p.Pro8GlnfsTer?)
17g.7676177_7676178insCCA497926009TP53c.191_192insG (p.Arg65GlnfsTer?)
c.-21-942_-21-941insG (n.-21-942_-21-941insG)
c.96+204_96+205insG (n.96+204_96+205insG)
n.447_448insG
c.74_75insG (p.Arg26GlnfsTer?)
17g.7676178G>ACA397846114TP53c.191C>T (p.Pro64Leu)
c.-21-942C>T (n.-21-942C>T)
c.96+204C>T (n.96+204C>T)
n.447C>T
c.74C>T (p.Pro25Leu)
 dbSNP
17g.7676178G>CCA397846118TP53c.191C>G (p.Pro64Arg)
c.-21-942C>G (n.-21-942C>G)
c.96+204C>G (n.96+204C>G)
n.447C>G
c.74C>G (p.Pro25Arg)
 dbSNP
17g.7676178G>TCA397846119TP53c.191C>A (p.Pro64His)
c.-21-942C>A (n.-21-942C>A)
c.96+204C>A (n.96+204C>A)
n.447C>A
c.74C>A (p.Pro25His)
 dbSNP
17g.7676179G>ACA397846122TP53c.190C>T (p.Pro64Ser)
c.-21-943C>T (n.-21-943C>T)
c.96+203C>T (n.96+203C>T)
n.446C>T
c.73C>T (p.Pro25Ser)
 ClinVar
17g.7676179G>CCA397846123TP53c.190C>G (p.Pro64Ala)
c.-21-943C>G (n.-21-943C>G)
c.96+203C>G (n.96+203C>G)
n.446C>G
c.73C>G (p.Pro25Ala)
17g.7676179G>TCA397846125TP53c.190C>A (p.Pro64Thr)
c.-21-943C>A (n.-21-943C>A)
c.96+203C>A (n.96+203C>A)
n.446C>A
c.73C>A (p.Pro25Thr)
 gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7676180A>CCA497926010TP53c.189T>G (p.Ala63=)
c.-21-944T>G (n.-21-944T>G)
c.96+202T>G (n.96+202T>G)
n.445T>G
c.72T>G (p.Ala24=)
17g.7676180A>GCA497926011TP53c.189T>C (p.Ala63=)
c.-21-944T>C (n.-21-944T>C)
c.96+202T>C (n.96+202T>C)
n.445T>C
c.72T>C (p.Ala24=)
 ClinVar dbSNP
17g.7676180A>TCA497926012TP53c.189T>A (p.Ala63=)
c.-21-944T>A (n.-21-944T>A)
c.96+202T>A (n.96+202T>A)
n.445T>A
c.72T>A (p.Ala24=)
 dbSNP
17g.7676180delinsTCTCA2695223139TP53c.189delinsAGA (p.Pro64AspfsTer?)
c.-21-944delinsAGA (n.-21-944delinsAGA)
c.96+202delinsAGA (n.96+202delinsAGA)
n.445delinsAGA
c.72delinsAGA (p.Pro25AspfsTer?)
17g.7676181_7676220delCA645589384TP53c.150_189del (p.Glu51ProfsTer?)
c.-21-983_-21-944del (n.-21-983_-21-944del)
c.96+163_96+202del (n.96+163_96+202del)
n.406_445del
c.33_72del (p.Glu12ProfsTer?)
 COSMIC
17g.7676181G>ACA000063TP53c.188C>T (p.Ala63Val)
c.-21-945C>T (n.-21-945C>T)
c.96+201C>T (n.96+201C>T)
n.444C>T
c.71C>T (p.Ala24Val)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
17g.7676181G>CCA10580957TP53c.188C>G (p.Ala63Gly)
c.-21-945C>G (n.-21-945C>G)
c.96+201C>G (n.96+201C>G)
n.444C>G
c.71C>G (p.Ala24Gly)
 ClinVar dbSNP gnomAD v2 gnomAD v4
17g.7676181G=CA2245935091TP53c.188C= (p.Ala63=)
c.-21-945C= (n.-21-945C=)
c.96+201C= (n.96+201C=)
n.444C=
c.71C= (p.Ala24=)
17g.7676181G>TCA397846132TP53c.188C>A (p.Ala63Asp)
c.-21-945C>A (n.-21-945C>A)
c.96+201C>A (n.96+201C>A)
n.444C>A
c.71C>A (p.Ala24Asp)
 dbSNP
17g.7676182C>ACA397846140TP53c.187G>T (p.Ala63Ser)
c.-21-946G>T (n.-21-946G>T)
c.96+200G>T (n.96+200G>T)
n.443G>T
c.70G>T (p.Ala24Ser)
 dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7676182C=CA2245935102TP53c.187G= (p.Ala63=)
c.-21-946G= (n.-21-946G=)
c.96+200G= (n.96+200G=)
n.443G=
c.70G= (p.Ala24=)
17g.7676182C>GCA397846142TP53c.187G>C (p.Ala63Pro)
c.-21-946G>C (n.-21-946G>C)
c.96+200G>C (n.96+200G>C)
n.443G>C
c.70G>C (p.Ala24Pro)
 dbSNP
17g.7676182C>TCA10580958TP53c.187G>A (p.Ala63Thr)
c.-21-946G>A (n.-21-946G>A)
c.96+200G>A (n.96+200G>A)
n.443G>A
c.70G>A (p.Ala24Thr)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7676183T>ACA397846150TP53c.186A>T (p.Glu62Asp)
c.-21-947A>T (n.-21-947A>T)
c.96+199A>T (n.96+199A>T)
n.442A>T
c.69A>T (p.Glu23Asp)
 dbSNP
17g.7676183T>CCA497926014TP53c.186A>G (p.Glu62=)
c.-21-947A>G (n.-21-947A>G)
c.96+199A>G (n.96+199A>G)
n.442A>G
c.69A>G (p.Glu23=)
 dbSNP COSMIC
17g.7676183T>GCA397846152TP53c.186A>C (p.Glu62Asp)
c.-21-947A>C (n.-21-947A>C)
c.96+199A>C (n.96+199A>C)
n.442A>C
c.69A>C (p.Glu23Asp)
 COSMIC
17g.7676184delCA497926013TP53c.186del (p.Ala63LeufsTer?)
c.-21-947del (n.-21-947del)
c.96+199del (n.96+199del)
n.442del
c.69del (p.Ala24LeufsTer?)
 COSMIC
17g.7676184T>ACA397846156TP53c.185A>T (p.Glu62Val)
c.-21-948A>T (n.-21-948A>T)
c.96+198A>T (n.96+198A>T)
n.441A>T
c.68A>T (p.Glu23Val)
 dbSNP
17g.7676184T>CCA397846161TP53c.185A>G (p.Glu62Gly)
c.-21-948A>G (n.-21-948A>G)
c.96+198A>G (n.96+198A>G)
n.441A>G
c.68A>G (p.Glu23Gly)
 dbSNP
17g.7676184T>GCA397846174TP53c.185A>C (p.Glu62Ala)
c.-21-948A>C (n.-21-948A>C)
c.96+198A>C (n.96+198A>C)
n.441A>C
c.68A>C (p.Glu23Ala)
 ClinVar dbSNP
17g.7676185_7676201dupCA645589385TP53c.169_185dup (p.Ala63ThrfsTer?)
c.-21-964_-21-948dup (n.-21-964_-21-948dup)
c.96+182_96+198dup (n.96+182_96+198dup)
n.425_441dup
c.52_68dup (p.Ala24ThrfsTer?)
 COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7676185_7676201delCA645589386TP53c.169_185del (p.Asp57SerfsTer?)
c.-21-964_-21-948del (n.-21-964_-21-948del)
c.96+182_96+198del (n.96+182_96+198del)
n.425_441del
c.52_68del (p.Asp18SerfsTer?)
 COSMIC
17g.7676185C>ACA397846175TP53c.184G>T (p.Glu62Ter)
c.-21-949G>T (n.-21-949G>T)
c.96+197G>T (n.96+197G>T)
n.440G>T
c.67G>T (p.Glu23Ter)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC
17g.7676185C=CA2245935118TP53c.184G= (p.Glu62=)
c.-21-949G= (n.-21-949G=)
c.96+197G= (n.96+197G=)
n.440G=
c.67G= (p.Glu23=)
17g.7676185C>GCA397846176TP53c.184G>C (p.Glu62Gln)
c.-21-949G>C (n.-21-949G>C)
c.96+197G>C (n.96+197G>C)
n.440G>C
c.67G>C (p.Glu23Gln)
 dbSNP
17g.7676185C>TCA397846178TP53c.184G>A (p.Glu62Lys)
c.-21-949G>A (n.-21-949G>A)
c.96+197G>A (n.96+197G>A)
n.440G>A
c.67G>A (p.Glu23Lys)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7676186delCA2733133702TP53c.183del (p.Asp61GlufsTer?)
c.-21-950del (n.-21-950del)
c.96+196del (n.96+196del)
n.439del
c.66del (p.Asp22GlufsTer?)
 dbSNP
17g.7676186A=CA2245935143TP53c.183T= (p.Asp61=)
c.-21-950T= (n.-21-950T=)
c.96+196T= (n.96+196T=)
n.439T=
c.66T= (p.Asp22=)
17g.7676186A>CCA397846181TP53c.183T>G (p.Asp61Glu)
c.-21-950T>G (n.-21-950T>G)
c.96+196T>G (n.96+196T>G)
n.439T>G
c.66T>G (p.Asp22Glu)
 dbSNP
17g.7676186A>GCA497926015TP53c.183T>C (p.Asp61=)
c.-21-950T>C (n.-21-950T>C)
c.96+196T>C (n.96+196T>C)
n.439T>C
c.66T>C (p.Asp22=)
 ClinVar dbSNP
17g.7676186A>TCA397846186TP53c.183T>A (p.Asp61Glu)
c.-21-950T>A (n.-21-950T>A)
c.96+196T>A (n.96+196T>A)
n.439T>A
c.66T>A (p.Asp22Glu)
 ClinVar dbSNP gnomAD v4
17g.7676195_7676196insTATCTGGACCTCA645589387TP53c.183_184insAAGGTCCAGAT (p.Glu62LysfsTer?)
c.-21-950_-21-949insAAGGTCCAGAT (n.-21-950_-21-949insAAGGTCCAGAT)
c.96+196_96+197insAAGGTCCAGAT (n.96+196_96+197insAAGGTCCAGAT)
n.439_440insAAGGTCCAGAT
c.66_67insAAGGTCCAGAT (p.Glu23LysfsTer?)
 COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7676187delCA645589389TP53c.182del (p.Asp61ValfsTer?)
c.-21-951del (n.-21-951del)
c.96+195del (n.96+195del)
n.438del
c.65del (p.Asp22ValfsTer?)
 COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7676187T>ACA397846191TP53c.182A>T (p.Asp61Val)
c.-21-951A>T (n.-21-951A>T)
c.96+195A>T (n.96+195A>T)
n.438A>T
c.65A>T (p.Asp22Val)
 ClinVar dbSNP
17g.7676187T>CCA397846192TP53c.182A>G (p.Asp61Gly)
c.-21-951A>G (n.-21-951A>G)
c.96+195A>G (n.96+195A>G)
n.438A>G
c.65A>G (p.Asp22Gly)
 ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC
17g.7676187T>GCA397846193TP53c.182A>C (p.Asp61Ala)
c.-21-951A>C (n.-21-951A>C)
c.96+195A>C (n.96+195A>C)
n.438A>C
c.65A>C (p.Asp22Ala)
17g.7676187T=CA2245935150TP53c.182A= (p.Asp61=)
c.-21-951A= (n.-21-951A=)
c.96+195A= (n.96+195A=)
n.438A=
c.65A= (p.Asp22=)
17g.7676188_7676189delCA645589388TP53c.181_182del (p.Asp61Ter)
c.-21-952_-21-951del (n.-21-952_-21-951del)
c.96+194_96+195del (n.96+194_96+195del)
n.437_438del
c.64_65del (p.Asp22Ter)
 COSMIC COSMIC COSMIC
17g.7676188C>ACA397846194TP53c.181G>T (p.Asp61Tyr)
c.-21-952G>T (n.-21-952G>T)
c.96+194G>T (n.96+194G>T)
n.437G>T
c.64G>T (p.Asp22Tyr)
 ClinVar dbSNP
17g.7676188C>GCA397846204TP53c.181G>C (p.Asp61His)
c.-21-952G>C (n.-21-952G>C)
c.96+194G>C (n.96+194G>C)
n.437G>C
c.64G>C (p.Asp22His)
 dbSNP
17g.7676188C>TCA397846209TP53c.181G>A (p.Asp61Asn)
c.-21-952G>A (n.-21-952G>A)
c.96+194G>A (n.96+194G>A)
n.437G>A
c.64G>A (p.Asp22Asn)
 dbSNP COSMIC
17g.7676189_7676211dupCA2635875042TP53c.159_181dup (p.Asp61GlyfsTer?)
c.-21-974_-21-952dup (n.-21-974_-21-952dup)
c.96+172_96+194dup (n.96+172_96+194dup)
n.415_437dup
c.42_64dup (p.Asp22GlyfsTer?)
 gnomAD v4
17g.7676189T>ACA497926016TP53c.180A>T (p.Pro60=)
c.-21-953A>T (n.-21-953A>T)
c.96+193A>T (n.96+193A>T)
n.436A>T
c.63A>T (p.Pro21=)
 COSMIC
17g.7676189T>CCA497926017TP53c.180A>G (p.Pro60=)
c.-21-953A>G (n.-21-953A>G)
c.96+193A>G (n.96+193A>G)
n.436A>G
c.63A>G (p.Pro21=)
 ClinVar
17g.7676189T>GCA000062TP53c.180A>C (p.Pro60=)
c.-21-953A>C (n.-21-953A>C)
c.96+193A>C (n.96+193A>C)
n.436A>C
c.63A>C (p.Pro21=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.7676189T=CA2245935158TP53c.180A= (p.Pro60=)
c.-21-953A= (n.-21-953A=)
c.96+193A= (n.96+193A=)
n.436A=
c.63A= (p.Pro21=)
17g.7676190G>ACA397846216TP53c.179C>T (p.Pro60Leu)
c.-21-954C>T (n.-21-954C>T)
c.96+192C>T (n.96+192C>T)
n.435C>T
c.62C>T (p.Pro21Leu)
 ClinVar dbSNP COSMIC
17g.7676190G>CCA397846222TP53c.179C>G (p.Pro60Arg)
c.-21-954C>G (n.-21-954C>G)
c.96+192C>G (n.96+192C>G)
n.435C>G
c.62C>G (p.Pro21Arg)
 dbSNP COSMIC
17g.7676190G=CA2245935169TP53c.179C= (p.Pro60=)
c.-21-954C= (n.-21-954C=)
c.96+192C= (n.96+192C=)
n.435C=
c.62C= (p.Pro21=)
17g.7676190G>TCA397846223TP53c.179C>A (p.Pro60Gln)
c.-21-954C>A (n.-21-954C>A)
c.96+192C>A (n.96+192C>A)
n.435C>A
c.62C>A (p.Pro21Gln)
 COSMIC
17g.7676191delCA497926018TP53c.179del (p.Pro60GlnfsTer?)
c.-21-954del (n.-21-954del)
c.96+192del (n.96+192del)
n.435del
c.62del (p.Pro21GlnfsTer?)
 COSMIC COSMIC COSMIC
17g.7676191G>ACA397846224TP53c.178C>T (p.Pro60Ser)
c.-21-955C>T (n.-21-955C>T)
c.96+191C>T (n.96+191C>T)
n.434C>T
c.61C>T (p.Pro21Ser)
 dbSNP COSMIC
17g.7676191G>CCA397846226TP53c.178C>G (p.Pro60Ala)
c.-21-955C>G (n.-21-955C>G)
c.96+191C>G (n.96+191C>G)
n.434C>G
c.61C>G (p.Pro21Ala)
 dbSNP COSMIC
17g.7676191G>TCA397846228TP53c.178C>A (p.Pro60Thr)
c.-21-955C>A (n.-21-955C>A)
c.96+191C>A (n.96+191C>A)
n.434C>A
c.61C>A (p.Pro21Thr)
 dbSNP COSMIC
17g.7676192A>CCA497926021TP53c.177T>G (p.Gly59=)
c.-21-956T>G (n.-21-956T>G)
c.96+190T>G (n.96+190T>G)
n.433T>G
c.60T>G (p.Gly20=)
 dbSNP
17g.7676192A>GCA497926020TP53c.177T>C (p.Gly59=)
c.-21-956T>C (n.-21-956T>C)
c.96+190T>C (n.96+190T>C)
n.433T>C
c.60T>C (p.Gly20=)
 dbSNP
17g.7676192A>TCA497926019TP53c.177T>A (p.Gly59=)
c.-21-956T>A (n.-21-956T>A)
c.96+190T>A (n.96+190T>A)
n.433T>A
c.60T>A (p.Gly20=)
 ClinVar dbSNP
17g.7676192_7676193delinsACCA2245935173TP53c.176_177delinsGT (p.Gly59=)
c.-21-957_-21-956delinsGT (n.-21-957_-21-956delinsGT)
c.96+189_96+190delinsGT (n.96+189_96+190delinsGT)
n.432_433delinsGT
c.59_60delinsGT (p.Gly20=)
17g.7676193C>ACA397846241TP53c.176G>T (p.Gly59Val)
c.-21-957G>T (n.-21-957G>T)
c.96+189G>T (n.96+189G>T)
n.432G>T
c.59G>T (p.Gly20Val)
 dbSNP
17g.7676193C=CA2245935181TP53c.176G= (p.Gly59=)
c.-21-957G= (n.-21-957G=)
c.96+189G= (n.96+189G=)
n.432G=
c.59G= (p.Gly20=)
17g.7676193C>GCA397846232TP53c.176G>C (p.Gly59Ala)
c.-21-957G>C (n.-21-957G>C)
c.96+189G>C (n.96+189G>C)
n.432G>C
c.59G>C (p.Gly20Ala)
 ClinVar dbSNP
17g.7676193C>TCA397846235TP53c.176G>A (p.Gly59Asp)
c.-21-957G>A (n.-21-957G>A)
c.96+189G>A (n.96+189G>A)
n.432G>A
c.59G>A (p.Gly20Asp)
 ClinVar dbSNP COSMIC
17g.7676193_7676194delinsTTCA645589391TP53c.175_176delinsAA (p.Gly59Asn)
c.-21-958_-21-957delinsAA (n.-21-958_-21-957delinsAA)
c.96+188_96+189delinsAA (n.96+188_96+189delinsAA)
n.431_432delinsAA
c.58_59delinsAA (p.Gly20Asn)
 COSMIC
17g.7676194delCA913191063TP53c.176del (p.Gly59ValfsTer?)
c.-21-957del (n.-21-957del)
c.96+189del (n.96+189del)
n.432del
c.59del (p.Gly20ValfsTer?)
 ClinVar dbSNP
17g.7676194_7676218delCA645589390TP53c.152_176del (p.Glu51ValfsTer?)
c.-21-981_-21-957del (n.-21-981_-21-957del)
c.96+165_96+189del (n.96+165_96+189del)
n.408_432del
c.35_59del (p.Glu12ValfsTer?)
 COSMIC
17g.7676194C>ACA397846253TP53c.175G>T (p.Gly59Cys)
c.-21-958G>T (n.-21-958G>T)
c.96+188G>T (n.96+188G>T)
n.431G>T
c.58G>T (p.Gly20Cys)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
17g.7676194C=CA2245935189TP53c.175G= (p.Gly59=)
c.-21-958G= (n.-21-958G=)
c.96+188G= (n.96+188G=)
n.431G=
c.58G= (p.Gly20=)
17g.7676194C>GCA397846263TP53c.175G>C (p.Gly59Arg)
c.-21-958G>C (n.-21-958G>C)
c.96+188G>C (n.96+188G>C)
n.431G>C
c.58G>C (p.Gly20Arg)
 ClinVar dbSNP
17g.7676194C>TCA397846266TP53c.175G>A (p.Gly59Ser)
c.-21-958G>A (n.-21-958G>A)
c.96+188G>A (n.96+188G>A)
n.431G>A
c.58G>A (p.Gly20Ser)
 ClinVar
17g.7676195delCA645589392TP53c.174del (p.Gly59ValfsTer?)
c.-21-959del (n.-21-959del)
c.96+187del (n.96+187del)
n.430del
c.57del (p.Gly20ValfsTer?)
 COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7676195T>ACA497926022TP53c.174A>T (p.Pro58=)
c.-21-959A>T (n.-21-959A>T)
c.96+187A>T (n.96+187A>T)
n.430A>T
c.57A>T (p.Pro19=)
17g.7676195T>CCA16616006TP53c.174A>G (p.Pro58=)
c.-21-959A>G (n.-21-959A>G)
c.96+187A>G (n.96+187A>G)
n.430A>G
c.57A>G (p.Pro19=)
 ClinVar dbSNP
17g.7676195T>GCA497926023TP53c.174A>C (p.Pro58=)
c.-21-959A>C (n.-21-959A>C)
c.96+187A>C (n.96+187A>C)
n.430A>C
c.57A>C (p.Pro19=)
17g.7676195T=CA2245935204TP53c.174A= (p.Pro58=)
c.-21-959A= (n.-21-959A=)
c.96+187A= (n.96+187A=)
n.430A=
c.57A= (p.Pro19=)
17g.7676196G>ACA397846274TP53c.173C>T (p.Pro58Leu)
c.-21-960C>T (n.-21-960C>T)
c.96+186C>T (n.96+186C>T)
n.429C>T
c.56C>T (p.Pro19Leu)
 dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7676196G>CCA000061TP53c.173C>G (p.Pro58Arg)
c.-21-960C>G (n.-21-960C>G)
c.96+186C>G (n.96+186C>G)
n.429C>G
c.56C>G (p.Pro19Arg)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
17g.7676196G=CA2245935224TP53c.173C= (p.Pro58=)
c.-21-960C= (n.-21-960C=)
c.96+186C= (n.96+186C=)
n.429C=
c.56C= (p.Pro19=)
17g.7676196G>TCA397846279TP53c.173C>A (p.Pro58Gln)
c.-21-960C>A (n.-21-960C>A)
c.96+186C>A (n.96+186C>A)
n.429C>A
c.56C>A (p.Pro19Gln)
 dbSNP COSMIC COSMIC COSMIC COSMIC
17g.7676198delCA497926024TP53c.173del (p.Pro58GlnfsTer?)
c.-21-960del (n.-21-960del)
c.96+186del (n.96+186del)
n.429del
c.56del (p.Pro19GlnfsTer?)
 ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7676197G>ACA397846284TP53c.172C>T (p.Pro58Ser)
c.-21-961C>T (n.-21-961C>T)
c.96+185C>T (n.96+185C>T)
n.428C>T
c.55C>T (p.Pro19Ser)
 dbSNP
17g.7676197G>CCA397846288TP53c.172C>G (p.Pro58Ala)
c.-21-961C>G (n.-21-961C>G)
c.96+185C>G (n.96+185C>G)
n.428C>G
c.55C>G (p.Pro19Ala)
 ClinVar dbSNP
17g.7676197G=CA2245935252TP53c.172C= (p.Pro58=)
c.-21-961C= (n.-21-961C=)
c.96+185C= (n.96+185C=)
n.428C=
c.55C= (p.Pro19=)
17g.7676197G>TCA397846289TP53c.172C>A (p.Pro58Thr)
c.-21-961C>A (n.-21-961C>A)
c.96+185C>A (n.96+185C>A)
n.428C>A
c.55C>A (p.Pro19Thr)
 ClinVar dbSNP
17g.7676197_7676200dupCA645589393TP53c.169_172dup (p.Pro58ArgfsTer6)
c.-21-964_-21-961dup (n.-21-964_-21-961dup)
c.96+182_96+185dup (n.96+182_96+185dup)
n.425_428dup
c.52_55dup (p.Pro19ArgfsTer6)
 COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7676198G>ACA497926025TP53c.171C>T (p.Asp57=)
c.-21-962C>T (n.-21-962C>T)
c.96+184C>T (n.96+184C>T)
n.427C>T
c.54C>T (p.Asp18=)
 ClinVar dbSNP
17g.7676198G>CCA397846290TP53c.171C>G (p.Asp57Glu)
c.-21-962C>G (n.-21-962C>G)
c.96+184C>G (n.96+184C>G)
n.427C>G
c.54C>G (p.Asp18Glu)
 dbSNP
17g.7676198G=CA2245935268TP53c.171C= (p.Asp57=)
c.-21-962C= (n.-21-962C=)
c.96+184C= (n.96+184C=)
n.427C=
c.54C= (p.Asp18=)
17g.7676198G>TCA000060TP53c.171C>A (p.Asp57Glu)
c.-21-962C>A (n.-21-962C>A)
c.96+184C>A (n.96+184C>A)
n.427C>A
c.54C>A (p.Asp18Glu)
 ClinVar dbSNP gnomAD v3 gnomAD v4
17g.7676199T>ACA397846310TP53c.170A>T (p.Asp57Val)
c.-21-963A>T (n.-21-963A>T)
c.96+183A>T (n.96+183A>T)
n.426A>T
c.53A>T (p.Asp18Val)
 ClinVar
17g.7676199T>CCA397846305TP53c.170A>G (p.Asp57Gly)
c.-21-963A>G (n.-21-963A>G)
c.96+183A>G (n.96+183A>G)
n.426A>G
c.53A>G (p.Asp18Gly)
 ClinVar dbSNP gnomAD v2 gnomAD v4
17g.7676199T>GCA397846304TP53c.170A>C (p.Asp57Ala)
c.-21-963A>C (n.-21-963A>C)
c.96+183A>C (n.96+183A>C)
n.426A>C
c.53A>C (p.Asp18Ala)
 ClinVar dbSNP
17g.7676199T=CA2245935273TP53c.170A= (p.Asp57=)
c.-21-963A= (n.-21-963A=)
c.96+183A= (n.96+183A=)
n.426A=
c.53A= (p.Asp18=)
17g.7676200_7676213delCA891842285TP53c.157_170del (p.Trp53ProfsTer5)
c.-21-976_-21-963del (n.-21-976_-21-963del)
c.96+170_96+183del (n.96+170_96+183del)
n.413_426del
c.40_53del (p.Trp14ProfsTer5)
17g.7676200C>ACA397846323TP53c.169G>T (p.Asp57Tyr)
c.-21-964G>T (n.-21-964G>T)
c.96+182G>T (n.96+182G>T)
n.425G>T
c.52G>T (p.Asp18Tyr)
 dbSNP
17g.7676200C>GCA397846331TP53c.169G>C (p.Asp57His)
c.-21-964G>C (n.-21-964G>C)
c.96+182G>C (n.96+182G>C)
n.425G>C
c.52G>C (p.Asp18His)
 dbSNP
17g.7676200C>TCA397846329TP53c.169G>A (p.Asp57Asn)
c.-21-964G>A (n.-21-964G>A)
c.96+182G>A (n.96+182G>A)
n.425G>A
c.52G>A (p.Asp18Asn)
 dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7676201T>ACA397846348TP53c.168A>T (p.Glu56Asp)
c.-21-965A>T (n.-21-965A>T)
c.96+181A>T (n.96+181A>T)
n.424A>T
c.51A>T (p.Glu17Asp)
 dbSNP
17g.7676201T>CCA003148TP53c.168A>G (p.Glu56=)
c.-21-965A>G (n.-21-965A>G)
c.96+181A>G (n.96+181A>G)
n.424A>G
c.51A>G (p.Glu17=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
17g.7676201T>GCA397846370TP53c.168A>C (p.Glu56Asp)
c.-21-965A>C (n.-21-965A>C)
c.96+181A>C (n.96+181A>C)
n.424A>C
c.51A>C (p.Glu17Asp)
17g.7676201T=CA2245935282TP53c.168A= (p.Glu56=)
c.-21-965A= (n.-21-965A=)
c.96+181A= (n.96+181A=)
n.424A=
c.51A= (p.Glu17=)
17g.7676202delCA2580095112TP53c.168del (p.Asp57ThrfsTer?)
c.-21-965del (n.-21-965del)
c.96+181del (n.96+181del)
n.424del
c.51del (p.Asp18ThrfsTer?)
 ClinVar
17g.7676202T>ACA397846381TP53c.167A>T (p.Glu56Val)
c.-21-966A>T (n.-21-966A>T)
c.96+180A>T (n.96+180A>T)
n.423A>T
c.50A>T (p.Glu17Val)
 dbSNP COSMIC
17g.7676202T>CCA397846383TP53c.167A>G (p.Glu56Gly)
c.-21-966A>G (n.-21-966A>G)
c.96+180A>G (n.96+180A>G)
n.423A>G
c.50A>G (p.Glu17Gly)
 dbSNP
17g.7676202T>GCA397846387TP53c.167A>C (p.Glu56Ala)
c.-21-966A>C (n.-21-966A>C)
c.96+180A>C (n.96+180A>C)
n.423A>C
c.50A>C (p.Glu17Ala)
17g.7676204_7676205insTCTGGACCTGGGTCTCACA645589394TP53c.167_168insGACCCAGGTCCAGATGA (p.Asp57ThrfsTer?)
c.-21-966_-21-965insGACCCAGGTCCAGATGA (n.-21-966_-21-965insGACCCAGGTCCAGATGA)
c.96+180_96+181insGACCCAGGTCCAGATGA (n.96+180_96+181insGACCCAGGTCCAGATGA)
n.423_424insGACCCAGGTCCAGATGA
c.50_51insGACCCAGGTCCAGATGA (p.Asp18ThrfsTer?)
 COSMIC COSMIC

Number of alleles fetched