Chr Mutation (hg38) CAid Gene Transcript Linkouts
6g.7579597delCA2573131738DSPc.3407del (p.Lys1136ArgfsTer23)
6g.7579597A>CCA362683976DSPc.3407A>C (p.Lys1136Thr)
6g.7579597A>GCA362683977DSPc.3407A>G (p.Lys1136Arg)
6g.7579597A>TCA362683978DSPc.3407A>T (p.Lys1136Met)
6g.7579598G>ACA448714079DSPc.3408G>A (p.Lys1136=)
ClinVar dbSNP gnomAD v2 gnomAD v4
6g.7579598G>CCA362683980DSPc.3408G>C (p.Lys1136Asn)
6g.7579598G=CA1608614258DSPc.3408G= (p.Lys1136=)
6g.7579598G>TCA362683979DSPc.3408G>T (p.Lys1136Asn)
6g.7579598_7579599delinsAGCA913187624DSPc.3408_3409delinsAG (p.Asn1137Asp)
ClinVar dbSNP
6g.7579598_7579599delinsGACA1608614261DSPc.3408_3409delinsGA (p.Lys1136=)
6g.7579599A=CA1608614266DSPc.3409A= (p.Asn1137=)
6g.7579599A>CCA362683981DSPc.3409A>C (p.Asn1137His)
6g.7579599A>GCA362683982DSPc.3409A>G (p.Asn1137Asp)
ClinVar dbSNP gnomAD v2 gnomAD v4
6g.7579599A>TCA362683983DSPc.3409A>T (p.Asn1137Tyr)
6g.7579600A>CCA362683984DSPc.3410A>C (p.Asn1137Thr)
6g.7579600A>GCA362683985DSPc.3410A>G (p.Asn1137Ser)
6g.7579600A>TCA362683986DSPc.3410A>T (p.Asn1137Ile)
6g.7579601T>ACA362683987DSPc.3411T>A (p.Asn1137Lys)
6g.7579601T>CCA448714084DSPc.3411T>C (p.Asn1137=)
6g.7579601T>GCA362683988DSPc.3411T>G (p.Asn1137Lys)
6g.7579602G>ACA362683989DSPc.3412G>A (p.Asp1138Asn)
6g.7579602G>CCA362683990DSPc.3412G>C (p.Asp1138His)
6g.7579602G>TCA362683991DSPc.3412G>T (p.Asp1138Tyr)
6g.7579603A=CA1608614271DSPc.3413A= (p.Asp1138=)
6g.7579603A>CCA362683992DSPc.3413A>C (p.Asp1138Ala)
6g.7579603A>GCA362683993DSPc.3413A>G (p.Asp1138Gly)
dbSNP gnomAD v2
6g.7579603A>TCA362683994DSPc.3413A>T (p.Asp1138Val)
6g.7579604C>ACA362683995DSPc.3414C>A (p.Asp1138Glu)
6g.7579604C=CA1608614281DSPc.3414C= (p.Asp1138=)
6g.7579604C>GCA362683996DSPc.3414C>G (p.Asp1138Glu)
6g.7579604C>TCA038078DSPc.3414C>T (p.Asp1138=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.7579604_7579607delinsCTATCA1608614282DSPc.3414_3417delinsCTAT (p.Asp1138=)
6g.7579605T>ACA362683997DSPc.3415T>A (p.Tyr1139Asn)
6g.7579605T>CCA362683999DSPc.3415T>C (p.Tyr1139His)
6g.7579605T>GCA362683998DSPc.3415T>G (p.Tyr1139Asp)
COSMIC
6g.7579605dupCA2677226030DSPc.3415dup (p.Tyr1139LeufsTer2)
gnomAD v4
6g.7579605_7579607delinsGCA16618323DSPc.3415_3417delinsG (p.Tyr1139GlyfsTer10)
ClinVar dbSNP
6g.7579606A=CA1608614291DSPc.3416A= (p.Tyr1139=)
6g.7579606A>CCA362684000DSPc.3416A>C (p.Tyr1139Ser)
6g.7579606A>GCA362684002DSPc.3416A>G (p.Tyr1139Cys)
dbSNP gnomAD v3 gnomAD v4
6g.7579606A>TCA362684001DSPc.3416A>T (p.Tyr1139Phe)
6g.7579607T>ACA362684003DSPc.3417T>A (p.Tyr1139Ter)
6g.7579607T>CCA448714088DSPc.3417T>C (p.Tyr1139=)
6g.7579607T>GCA362684004DSPc.3417T>G (p.Tyr1139Ter)
6g.7579608G>ACA362684005DSPc.3418G>A (p.Asp1140Asn)
6g.7579608G>CCA362684006DSPc.3418G>C (p.Asp1140His)
6g.7579608G>TCA362684007DSPc.3418G>T (p.Asp1140Tyr)
gnomAD v4
6g.7579608_7579609delinsGACA1608614295DSPc.3418_3419delinsGA (p.Asp1140=)
6g.7579609delCA005795DSPc.3419del (p.Asp1140AlafsTer19)
ClinVar dbSNP
6g.7579609A>CCA362684010DSPc.3419A>C (p.Asp1140Ala)

Number of alleles fetched