Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.80105787G>ACA502177532GAAc.585G>A (p.Leu195=)
17g.80105787G>CCA401362178GAAc.585G>C (p.Leu195Phe)
17g.80105787G>TCA401362180GAAc.585G>T (p.Leu195Phe)
17g.80105787_80105788delCA2840238209GAAc.585_586del (p.Glu196AspfsTer?)
17g.80105788delCA2965194656GAAc.586del (p.Glu196ArgfsTer25)
c.586del (p.Glu196ArgfsTer?)
17g.80105788G>ACA401362183GAAc.586G>A (p.Glu196Lys)
17g.80105788G>CCA401362184GAAc.586G>C (p.Glu196Gln)
dbSNP gnomAD v2 gnomAD v4
17g.80105788G=CA2277811237GAAc.586G= (p.Glu196=)
dbSNP
17g.80105788G>TCA401362187GAAc.586G>T (p.Glu196Ter)
gnomAD v4
17g.80105790_80105791delCA2965194662GAAc.588_589del (p.Glu196AspfsTer?)
17g.80105789delCA2580095298GAAc.587del (p.Glu196GlyfsTer25)
c.587del (p.Glu196GlyfsTer?)
ClinVar dbSNP
17g.80105789A=CA3227603051GAAc.587A= (p.Glu196=)
dbSNP
17g.80105789A>CCA401362189GAAc.587A>C (p.Glu196Ala)
17g.80105789A>GCA401362191GAAc.587A>G (p.Glu196Gly)
17g.80105789A>TCA401362192GAAc.587A>T (p.Glu196Val)
17g.80105790G>ACA502177537GAAc.588G>A (p.Glu196=)
17g.80105790G>CCA401362194GAAc.588G>C (p.Glu196Asp)
17g.80105790G>TCA401362196GAAc.588G>T (p.Glu196Asp)
17g.80105791A>CCA401362201GAAc.589A>C (p.Thr197Pro)
17g.80105791A>GCA401362200GAAc.589A>G (p.Thr197Ala)
17g.80105791A>TCA401362198GAAc.589A>T (p.Thr197Ser)
17g.80105792C>ACA8814936GAAc.590C>A (p.Thr197Asn)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
17g.80105792C=CA2277811238GAAc.590C= (p.Thr197=)
dbSNP
17g.80105792C>GCA401362205GAAc.590C>G (p.Thr197Ser)
17g.80105792C>TCA401362206GAAc.590C>T (p.Thr197Ile)
ClinVar dbSNP
17g.80105795dupCA2965194681GAAc.593dup (p.His199AlafsTer?)
17g.80105795delCA2640277686GAAc.593del (p.Pro198ArgfsTer23)
c.593del (p.Pro198ArgfsTer?)
gnomAD v4
17g.80105794_80105795delCA2965194717GAAc.592_593del (p.Pro198AlafsTer?)
17g.80105793C>ACA502177543GAAc.591C>A (p.Thr197=)
17g.80105793C=CA3227603085GAAc.591C= (p.Thr197=)
dbSNP
17g.80105793C>GCA502177545GAAc.591C>G (p.Thr197=)
17g.80105793C>TCA502177547GAAc.591C>T (p.Thr197=)
dbSNP gnomAD v4
17g.80105794C>ACA294888175GAAc.592C>A (p.Pro198Thr)
dbSNP
17g.80105794C=CA2277811239GAAc.592C= (p.Pro198=)
dbSNP
17g.80105794C>GCA401362209GAAc.592C>G (p.Pro198Ala)
dbSNP gnomAD v4
17g.80105794C>TCA401362210GAAc.592C>T (p.Pro198Ser)
ClinVar
17g.80105795C>ACA401362212GAAc.593C>A (p.Pro198Gln)
ClinVar dbSNP
17g.80105795C=CA2277811240GAAc.593C= (p.Pro198=)
dbSNP
17g.80105795C>GCA401362214GAAc.593C>G (p.Pro198Arg)
dbSNP gnomAD v3 gnomAD v4
17g.80105795C>TCA8814937GAAc.593C>T (p.Pro198Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.80105796delCA2965194761GAAc.594del (p.His199MetfsTer22)
c.594del (p.His199MetfsTer?)
17g.80105796G>ACA502177552GAAc.594G>A (p.Pro198=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.80105796G>CCA502177553GAAc.594G>C (p.Pro198=)
ClinVar dbSNP gnomAD v4
17g.80105796G=CA2277811241GAAc.594G= (p.Pro198=)
dbSNP
17g.80105796G>TCA502177555GAAc.594G>T (p.Pro198=)
ClinVar dbSNP gnomAD v4
17g.80105797C>ACA401362217GAAc.595C>A (p.His199Asn)
17g.80105797C=CA3227603104GAAc.595C= (p.His199=)
dbSNP
17g.80105797C>GCA401362219GAAc.595C>G (p.His199Asp)
17g.80105797C>TCA401362222GAAc.595C>T (p.His199Tyr)
dbSNP gnomAD v4 COSMIC
17g.80105797_80105798delCA2965194790GAAc.595_596del (p.His199CysfsTer?)

Number of alleles fetched