Chr Mutation (hg38) CAid Gene Transcript Linkouts
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=)
10g.119670045G>CCA378294966BAG3c.375G>C (p.Glu125Asp)
c.201G>C (p.Glu67Asp)
10g.119670045G>TCA378294967BAG3c.375G>T (p.Glu125Asp)
c.201G>T (p.Glu67Asp)
ClinVar dbSNP gnomAD v4
10g.119670046G>ACA378294968BAG3c.376G>A (p.Ala126Thr)
c.202G>A (p.Ala68Thr)
10g.119670046G>CCA378294969BAG3c.376G>C (p.Ala126Pro)
c.202G>C (p.Ala68Pro)
10g.119670046G>TCA378294970BAG3c.376G>T (p.Ala126Ser)
c.202G>T (p.Ala68Ser)
gnomAD v4
10g.119670047C>ACA378294971BAG3c.377C>A (p.Ala126Glu)
c.203C>A (p.Ala68Glu)
10g.119670047C=CA1940191132BAG3c.377C= (p.Ala126=)
c.203C= (p.Ala68=)
10g.119670047C>GCA378294973BAG3c.377C>G (p.Ala126Gly)
c.203C>G (p.Ala68Gly)
10g.119670047C>TCA378294972BAG3c.377C>T (p.Ala126Val)
c.203C>T (p.Ala68Val)
ClinVar dbSNP gnomAD v3 gnomAD v4
10g.119670048G>ACA5716307BAG3c.378G>A (p.Ala126=)
c.204G>A (p.Ala68=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC

Number of alleles fetched