Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.119651773_119651781delinsAGACCGGCTCA1940184282BAG3c.98_106delinsAGACCGGCT (p.Gln33=)
10g.119651775_119651782delCA273668BAG3c.100_107del (p.Thr34AlafsTer21)
ClinVar dbSNP
10g.119651775A>CCA378294176BAG3c.100A>C (p.Thr34Pro)
10g.119651775A>GCA378294177BAG3c.100A>G (p.Thr34Ala)
10g.119651775A>TCA378294178BAG3c.100A>T (p.Thr34Ser)
10g.119651776C>ACA378294181BAG3c.101C>A (p.Thr34Asn)
10g.119651776C=CA1940184283BAG3c.101C= (p.Thr34=)
10g.119651776C>GCA378294180BAG3c.101C>G (p.Thr34Ser)
10g.119651776C>TCA378294179BAG3c.101C>T (p.Thr34Ile)
ClinVar dbSNP gnomAD v3 gnomAD v4
10g.119651777C>ACA471634057BAG3c.102C>A (p.Thr34=)
10g.119651777C=CA1940184284BAG3c.102C= (p.Thr34=)
10g.119651777C>GCA5716216BAG3c.102C>G (p.Thr34=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119651777C>TCA471634059BAG3c.102C>T (p.Thr34=)
gnomAD v4
10g.119651778G>ACA5716217BAG3c.103G>A (p.Gly35Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119651778G>CCA378294182BAG3c.103G>C (p.Gly35Arg)
10g.119651778G=CA1940184285BAG3c.103G= (p.Gly35=)
10g.119651778G>TCA378294183BAG3c.103G>T (p.Gly35Cys)
ClinVar dbSNP gnomAD v4
10g.119651779G>ACA378294184BAG3c.104G>A (p.Gly35Asp)
ClinVar gnomAD v4
10g.119651779G>CCA378294185BAG3c.104G>C (p.Gly35Ala)
gnomAD v4
10g.119651779G>TCA378294186BAG3c.104G>T (p.Gly35Val)
10g.119651780C>ACA471634065BAG3c.105C>A (p.Gly35=)
10g.119651780C=CA1940184286BAG3c.105C= (p.Gly35=)
10g.119651780C>GCA16605609BAG3c.105C>G (p.Gly35=)
ClinVar dbSNP
10g.119651780C>TCA471634068BAG3c.105C>T (p.Gly35=)
10g.119651781T>ACA378294187BAG3c.106T>A (p.Trp36Arg)
10g.119651781T>CCA378294188BAG3c.106T>C (p.Trp36Arg)
10g.119651781T>GCA378294189BAG3c.106T>G (p.Trp36Gly)
10g.119651781T=CA1940184287BAG3c.106T= (p.Trp36=)
10g.119651782G>ACA378294190BAG3c.107G>A (p.Trp36Ter)
gnomAD v4
10g.119651782G>CCA378294191BAG3c.107G>C (p.Trp36Ser)
10g.119651782G>TCA378294192BAG3c.107G>T (p.Trp36Leu)
10g.119651783dupCA214208143BAG3c.108dup (p.Pro37AlafsTer21)
dbSNP
10g.119651783G>ACA378294193BAG3c.108G>A (p.Trp36Ter)
ClinVar dbSNP gnomAD v4
10g.119651783G>CCA378294195BAG3c.108G>C (p.Trp36Cys)
10g.119651783G=CA1940184288BAG3c.108G= (p.Trp36=)
10g.119651783G>TCA378294194BAG3c.108G>T (p.Trp36Cys)
10g.119651784C>ACA378294196BAG3c.109C>A (p.Pro37Thr)
gnomAD v4
10g.119651784C=CA1940184289BAG3c.109C= (p.Pro37=)
10g.119651784C>GCA378294197BAG3c.109C>G (p.Pro37Ala)
gnomAD v4
10g.119651784C>TCA5716218BAG3c.109C>T (p.Pro37Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119651785C>ACA378294198BAG3c.110C>A (p.Pro37His)
10g.119651785C=CA1940184291BAG3c.110C= (p.Pro37=)
10g.119651785C>GCA378294199BAG3c.110C>G (p.Pro37Arg)
10g.119651785C>TCA5716219BAG3c.110C>T (p.Pro37Leu)
dbSNP ExAC gnomAD v2 gnomAD v4
10g.119651785_119651788delinsCCTTCA1940184290BAG3c.110_113delinsCCTT (p.Pro37=)
10g.119651786C>ACA471634088BAG3c.111C>A (p.Pro37=)
10g.119651786C=CA1940184292BAG3c.111C= (p.Pro37=)
10g.119651786C>GCA471634090BAG3c.111C>G (p.Pro37=)
ClinVar dbSNP gnomAD v4
10g.119651786C>TCA135013BAG3c.111C>T (p.Pro37=)
ClinVar dbSNP gnomAD v4
10g.119651790_119651792delCA16618931BAG3c.115_117del (p.Phe39del)
ClinVar dbSNP

Number of alleles fetched