Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.119651771_119651772delCA2580082464BAG3c.96_97del (p.Gln33AspfsTer24)
ClinVar
10g.119651771G>ACA471634035BAG3c.96G>A (p.Pro32=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.119651771G>CCA471634037BAG3c.96G>C (p.Pro32=)
10g.119651771G=CA1940184281BAG3c.96G= (p.Pro32=)
10g.119651771G>TCA5716215BAG3c.96G>T (p.Pro32=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119651772C>ACA378294168BAG3c.97C>A (p.Gln33Lys)
gnomAD v4
10g.119651772C>GCA378294170BAG3c.97C>G (p.Gln33Glu)
10g.119651772C>TCA378294169BAG3c.97C>T (p.Gln33Ter)
10g.119651773A>CCA378294171BAG3c.98A>C (p.Gln33Pro)
10g.119651773A>GCA378294172BAG3c.98A>G (p.Gln33Arg)
gnomAD v4
10g.119651773A>TCA378294173BAG3c.98A>T (p.Gln33Leu)
10g.119651773_119651781delinsAGACCGGCTCA1940184282BAG3c.98_106delinsAGACCGGCT (p.Gln33=)
10g.119651774G>ACA471634049BAG3c.99G>A (p.Gln33=)
ClinVar
10g.119651774G>CCA378294174BAG3c.99G>C (p.Gln33His)
ClinVar dbSNP
10g.119651774G>TCA378294175BAG3c.99G>T (p.Gln33His)
gnomAD v4
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)

Number of alleles fetched