Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.119670030G>ACA471634520BAG3c.360G>A (p.Gln120=)
c.186G>A (p.Gln62=)
10g.119670030G>CCA378294937BAG3c.360G>C (p.Gln120His)
c.186G>C (p.Gln62His)
10g.119670030G>TCA378294938BAG3c.360G>T (p.Gln120His)
c.186G>T (p.Gln62His)
10g.119670031C>ACA471634521BAG3c.361C>A (p.Arg121=)
c.187C>A (p.Arg63=)
10g.119670031C>GCA378294940BAG3c.361C>G (p.Arg121Gly)
c.187C>G (p.Arg63Gly)
10g.119670031C>TCA378294939BAG3c.361C>T (p.Arg121Ter)
c.187C>T (p.Arg63Ter)
ClinVar dbSNP gnomAD v4
10g.119670032G>ACA10576775BAG3c.362G>A (p.Arg121Gln)
c.188G>A (p.Arg63Gln)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
10g.119670032G>CCA378294942BAG3c.362G>C (p.Arg121Pro)
c.188G>C (p.Arg63Pro)
10g.119670032G=CA1940191118BAG3c.362G= (p.Arg121=)
c.188G= (p.Arg63=)
10g.119670032G>TCA378294941BAG3c.362G>T (p.Arg121Leu)
c.188G>T (p.Arg63Leu)
10g.119670033A>CCA471634522BAG3c.363A>C (p.Arg121=)
c.189A>C (p.Arg63=)
10g.119670033A>GCA471634523BAG3c.363A>G (p.Arg121=)
c.189A>G (p.Arg63=)
10g.119670033A>TCA471634524BAG3c.363A>T (p.Arg121=)
c.189A>T (p.Arg63=)
10g.119670034T>ACA378294943BAG3c.364T>A (p.Phe122Ile)
c.190T>A (p.Phe64Ile)
10g.119670034T>CCA378294944BAG3c.364T>C (p.Phe122Leu)
c.190T>C (p.Phe64Leu)
10g.119670034T>GCA378294945BAG3c.364T>G (p.Phe122Val)
c.190T>G (p.Phe64Val)
10g.119670035T>ACA378294946BAG3c.365T>A (p.Phe122Tyr)
c.191T>A (p.Phe64Tyr)
10g.119670035T>CCA378294947BAG3c.365T>C (p.Phe122Ser)
c.191T>C (p.Phe64Ser)
10g.119670035T>GCA378294948BAG3c.365T>G (p.Phe122Cys)
c.191T>G (p.Phe64Cys)
10g.119670036C>ACA378294949BAG3c.366C>A (p.Phe122Leu)
c.192C>A (p.Phe64Leu)
gnomAD v4
10g.119670036C>GCA378294950BAG3c.366C>G (p.Phe122Leu)
c.192C>G (p.Phe64Leu)
10g.119670036C>TCA471634525BAG3c.366C>T (p.Phe122=)
c.192C>T (p.Phe64=)
10g.119670037C>ACA471634526BAG3c.367C>A (p.Arg123=)
c.193C>A (p.Arg65=)
10g.119670037C=CA1940191121BAG3c.367C= (p.Arg123=)
c.193C= (p.Arg65=)
10g.119670037C>GCA378294951BAG3c.367C>G (p.Arg123Gly)
c.193C>G (p.Arg65Gly)
10g.119670037C>TCA259790BAG3c.367C>T (p.Arg123Ter)
c.193C>T (p.Arg65Ter)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
10g.119670038G>ACA237043BAG3c.368G>A (p.Arg123Gln)
c.194G>A (p.Arg65Gln)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119670038G>CCA378294952BAG3c.368G>C (p.Arg123Pro)
c.194G>C (p.Arg65Pro)
10g.119670038G=CA1940191125BAG3c.368G= (p.Arg123=)
c.194G= (p.Arg65=)
10g.119670038G>TCA378294953BAG3c.368G>T (p.Arg123Leu)
c.194G>T (p.Arg65Leu)
10g.119670039A>CCA471634527BAG3c.369A>C (p.Arg123=)
c.195A>C (p.Arg65=)
10g.119670039A>GCA471634528BAG3c.369A>G (p.Arg123=)
c.195A>G (p.Arg65=)
gnomAD v4
10g.119670039A>TCA471634529BAG3c.369A>T (p.Arg123=)
c.195A>T (p.Arg65=)
10g.119670040A>CCA378294954BAG3c.370A>C (p.Thr124Pro)
c.196A>C (p.Thr66Pro)
10g.119670040A>GCA378294955BAG3c.370A>G (p.Thr124Ala)
c.196A>G (p.Thr66Ala)
10g.119670040A>TCA378294956BAG3c.370A>T (p.Thr124Ser)
c.196A>T (p.Thr66Ser)
10g.119670041C>ACA378294957BAG3c.371C>A (p.Thr124Asn)
c.197C>A (p.Thr66Asn)
10g.119670041C>GCA378294959BAG3c.371C>G (p.Thr124Ser)
c.197C>G (p.Thr66Ser)
10g.119670041C>TCA378294958BAG3c.371C>T (p.Thr124Ile)
c.197C>T (p.Thr66Ile)
10g.119670042T>ACA471634531BAG3c.372T>A (p.Thr124=)
c.198T>A (p.Thr66=)
10g.119670042T>CCA471634530BAG3c.372T>C (p.Thr124=)
c.198T>C (p.Thr66=)
10g.119670042T>GCA5716306BAG3c.372T>G (p.Thr124=)
c.198T>G (p.Thr66=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119670042T=CA1940191129BAG3c.372T= (p.Thr124=)
c.198T= (p.Thr66=)
10g.119670043G>ACA378294960BAG3c.373G>A (p.Glu125Lys)
c.199G>A (p.Glu67Lys)
10g.119670043G>CCA378294961BAG3c.373G>C (p.Glu125Gln)
c.199G>C (p.Glu67Gln)
10g.119670043G>TCA378294962BAG3c.373G>T (p.Glu125Ter)
c.199G>T (p.Glu67Ter)
10g.119670044A>CCA378294963BAG3c.374A>C (p.Glu125Ala)
c.200A>C (p.Glu67Ala)
10g.119670044A>GCA378294964BAG3c.374A>G (p.Glu125Gly)
c.200A>G (p.Glu67Gly)
10g.119670044A>TCA378294965BAG3c.374A>T (p.Glu125Val)
c.200A>T (p.Glu67Val)
10g.119670045G>ACA471634532BAG3c.375G>A (p.Glu125=)
c.201G>A (p.Glu67=)

Number of alleles fetched