Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.119669940A>CCA471634461BAG3c.270A>C (p.Arg90=)
c.96A>C (p.Arg32=)
10g.119669940A>GCA471634462BAG3c.270A>G (p.Arg90=)
c.96A>G (p.Arg32=)
10g.119669940A>TCA471634460BAG3c.270A>T (p.Arg90=)
c.96A>T (p.Arg32=)
10g.119669941C>ACA378294762BAG3c.271C>A (p.Pro91Thr)
c.97C>A (p.Pro33Thr)
10g.119669941C>GCA378294763BAG3c.271C>G (p.Pro91Ala)
c.97C>G (p.Pro33Ala)
10g.119669941C>TCA378294764BAG3c.271C>T (p.Pro91Ser)
c.97C>T (p.Pro33Ser)
ClinVar gnomAD v4
10g.119669941_119669942insACA2789704364BAG3c.271_272insA (p.Pro91HisfsTer11)
c.97_98insA (p.Pro33HisfsTer11)
10g.119669942C>ACA378294765BAG3c.272C>A (p.Pro91Gln)
c.98C>A (p.Pro33Gln)
10g.119669942C=CA1940190928BAG3c.272C= (p.Pro91=)
c.98C= (p.Pro33=)
10g.119669942C>GCA378294766BAG3c.272C>G (p.Pro91Arg)
c.98C>G (p.Pro33Arg)
dbSNP
10g.119669942C>TCA378294767BAG3c.272C>T (p.Pro91Leu)
c.98C>T (p.Pro33Leu)
ClinVar dbSNP gnomAD v4
10g.119669943A>CCA471634465BAG3c.273A>C (p.Pro91=)
c.99A>C (p.Pro33=)
10g.119669943A>GCA471634463BAG3c.273A>G (p.Pro91=)
c.99A>G (p.Pro33=)
ClinVar
10g.119669943A>TCA471634464BAG3c.273A>T (p.Pro91=)
c.99A>T (p.Pro33=)
10g.119669944G>ACA378294768BAG3c.274G>A (p.Gly92Ser)
c.100G>A (p.Gly34Ser)
10g.119669944G>CCA5716279BAG3c.274G>C (p.Gly92Arg)
c.100G>C (p.Gly34Arg)
dbSNP ExAC gnomAD v3 gnomAD v4
10g.119669944G=CA1940190931BAG3c.274G= (p.Gly92=)
c.100G= (p.Gly34=)
10g.119669944G>TCA378294769BAG3c.274G>T (p.Gly92Cys)
c.100G>T (p.Gly34Cys)
10g.119669945G>ACA5716280BAG3c.275G>A (p.Gly92Asp)
c.101G>A (p.Gly34Asp)
dbSNP ExAC gnomAD v2 gnomAD v4
10g.119669945G>CCA378294771BAG3c.275G>C (p.Gly92Ala)
c.101G>C (p.Gly34Ala)
10g.119669945G=CA1940190933BAG3c.275G= (p.Gly92=)
c.101G= (p.Gly34=)
10g.119669945G>TCA378294770BAG3c.275G>T (p.Gly92Val)
c.101G>T (p.Gly34Val)
10g.119669946C>ACA471634466BAG3c.276C>A (p.Gly92=)
c.102C>A (p.Gly34=)
10g.119669946C=CA1940190936BAG3c.276C= (p.Gly92=)
c.102C= (p.Gly34=)
10g.119669946C>GCA471634468BAG3c.276C>G (p.Gly92=)
c.102C>G (p.Gly34=)
10g.119669946C>TCA471634467BAG3c.276C>T (p.Gly92=)
c.102C>T (p.Gly34=)
10g.119669947T>ACA378294772BAG3c.277T>A (p.Tyr93Asn)
c.103T>A (p.Tyr35Asn)
10g.119669947T>CCA214219742BAG3c.277T>C (p.Tyr93His)
c.103T>C (p.Tyr35His)
ClinVar dbSNP gnomAD v2 gnomAD v4
10g.119669947T>GCA378294773BAG3c.277T>G (p.Tyr93Asp)
c.103T>G (p.Tyr35Asp)
ClinVar
10g.119669947T=CA1940190942BAG3c.277T= (p.Tyr93=)
c.103T= (p.Tyr35=)
10g.119669947dupCA891843318BAG3c.277dup (p.Tyr93LeufsTer9)
c.103dup (p.Tyr35LeufsTer9)
ClinVar dbSNP
10g.119669948A>CCA378294774BAG3c.278A>C (p.Tyr93Ser)
c.104A>C (p.Tyr35Ser)
10g.119669948A>GCA378294775BAG3c.278A>G (p.Tyr93Cys)
c.104A>G (p.Tyr35Cys)
gnomAD v4
10g.119669948A>TCA378294776BAG3c.278A>T (p.Tyr93Phe)
c.104A>T (p.Tyr35Phe)
10g.119669949C>ACA378294777BAG3c.279C>A (p.Tyr93Ter)
c.105C>A (p.Tyr35Ter)
10g.119669949C>GCA378294778BAG3c.279C>G (p.Tyr93Ter)
c.105C>G (p.Tyr35Ter)
10g.119669949C>TCA471634469BAG3c.279C>T (p.Tyr93=)
c.105C>T (p.Tyr35=)
10g.119669950_119669954dupCA2740093561BAG3c.280_284dup (p.Ile96PhefsTer?)
c.106_110dup (p.Ile38PhefsTer?)
ClinVar
10g.119669950A=CA1940190945BAG3c.280A= (p.Ile94=)
c.106A= (p.Ile36=)
10g.119669950A>CCA378294779BAG3c.280A>C (p.Ile94Leu)
c.106A>C (p.Ile36Leu)
10g.119669950A>GCA378294780BAG3c.280A>G (p.Ile94Val)
c.106A>G (p.Ile36Val)
ClinVar gnomAD v4
10g.119669950A>TCA181165BAG3c.280A>T (p.Ile94Phe)
c.106A>T (p.Ile36Phe)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119669951T>ACA378294783BAG3c.281T>A (p.Ile94Asn)
c.107T>A (p.Ile36Asn)
10g.119669951T>CCA378294782BAG3c.281T>C (p.Ile94Thr)
c.107T>C (p.Ile36Thr)
10g.119669951T>GCA378294781BAG3c.281T>G (p.Ile94Ser)
c.107T>G (p.Ile36Ser)
10g.119669952T>ACA471634470BAG3c.282T>A (p.Ile94=)
c.108T>A (p.Ile36=)
10g.119669952T>CCA471634471BAG3c.282T>C (p.Ile94=)
c.108T>C (p.Ile36=)
10g.119669952T>GCA378294784BAG3c.282T>G (p.Ile94Met)
c.108T>G (p.Ile36Met)
10g.119669953C>ACA378294785BAG3c.283C>A (p.Pro95Thr)
c.109C>A (p.Pro37Thr)
10g.119669953C=CA1940190951BAG3c.283C= (p.Pro95=)
c.109C= (p.Pro37=)
10g.119669953C>GCA175285BAG3c.283C>G (p.Pro95Ala)
c.109C>G (p.Pro37Ala)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.119669953C>TCA5716281BAG3c.283C>T (p.Pro95Ser)
c.109C>T (p.Pro37Ser)
ClinVar dbSNP ExAC gnomAD v4 COSMIC
10g.119669954C>ACA378294786BAG3c.284C>A (p.Pro95His)
c.110C>A (p.Pro37His)
dbSNP gnomAD v2 gnomAD v4
10g.119669954C=CA1940190956BAG3c.284C= (p.Pro95=)
c.110C= (p.Pro37=)
10g.119669954C>GCA378294787BAG3c.284C>G (p.Pro95Arg)
c.110C>G (p.Pro37Arg)
gnomAD v4
10g.119669954C>TCA351714BAG3c.284C>T (p.Pro95Leu)
c.110C>T (p.Pro37Leu)
ClinVar dbSNP
10g.119669955C>ACA471634472BAG3c.285C>A (p.Pro95=)
c.111C>A (p.Pro37=)
10g.119669955C>GCA471634473BAG3c.285C>G (p.Pro95=)
c.111C>G (p.Pro37=)
10g.119669955C>TCA471634474BAG3c.285C>T (p.Pro95=)
c.111C>T (p.Pro37=)
ClinVar dbSNP gnomAD v4
10g.119669956A=CA1940190960BAG3c.286A= (p.Ile96=)
c.112A= (p.Ile38=)
10g.119669956A>CCA378294788BAG3c.286A>C (p.Ile96Leu)
c.112A>C (p.Ile38Leu)
ClinVar dbSNP gnomAD v2 gnomAD v4
10g.119669956A>GCA378294789BAG3c.286A>G (p.Ile96Val)
c.112A>G (p.Ile38Val)
ClinVar gnomAD v4
10g.119669956A>TCA378294790BAG3c.286A>T (p.Ile96Phe)
c.112A>T (p.Ile38Phe)
10g.119669957T>ACA378294791BAG3c.287T>A (p.Ile96Asn)
c.113T>A (p.Ile38Asn)
10g.119669957T>CCA378294792BAG3c.287T>C (p.Ile96Thr)
c.113T>C (p.Ile38Thr)
10g.119669957T>GCA378294793BAG3c.287T>G (p.Ile96Ser)
c.113T>G (p.Ile38Ser)
10g.119669958T>ACA471634475BAG3c.288T>A (p.Ile96=)
c.114T>A (p.Ile38=)
10g.119669958T>CCA471634476BAG3c.288T>C (p.Ile96=)
c.114T>C (p.Ile38=)
10g.119669958T>GCA378294794BAG3c.288T>G (p.Ile96Met)
c.114T>G (p.Ile38Met)
10g.119669959C>ACA378294795BAG3c.289C>A (p.Pro97Thr)
c.115C>A (p.Pro39Thr)
10g.119669959C=CA1940190964BAG3c.289C= (p.Pro97=)
c.115C= (p.Pro39=)
10g.119669959C>GCA5716283BAG3c.289C>G (p.Pro97Ala)
c.115C>G (p.Pro39Ala)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119669959C>TCA5716282BAG3c.289C>T (p.Pro97Ser)
c.115C>T (p.Pro39Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
10g.119669960C>ACA378294796BAG3c.290C>A (p.Pro97His)
c.116C>A (p.Pro39His)
10g.119669960C>GCA378294797BAG3c.290C>G (p.Pro97Arg)
c.116C>G (p.Pro39Arg)
10g.119669960C>TCA378294798BAG3c.290C>T (p.Pro97Leu)
c.116C>T (p.Pro39Leu)
gnomAD v4
10g.119669961T>ACA471634479BAG3c.291T>A (p.Pro97=)
c.117T>A (p.Pro39=)
10g.119669961T>CCA471634478BAG3c.291T>C (p.Pro97=)
c.117T>C (p.Pro39=)
10g.119669961T>GCA471634477BAG3c.291T>G (p.Pro97=)
c.117T>G (p.Pro39=)
gnomAD v4
10g.119669962G>ACA378294799BAG3c.292G>A (p.Val98Met)
c.118G>A (p.Val40Met)
10g.119669962G>CCA378294800BAG3c.292G>C (p.Val98Leu)
c.118G>C (p.Val40Leu)
10g.119669962G>TCA378294801BAG3c.292G>T (p.Val98Leu)
c.118G>T (p.Val40Leu)
10g.119669963T>ACA378294802BAG3c.293T>A (p.Val98Glu)
c.119T>A (p.Val40Glu)
10g.119669963T>CCA378294803BAG3c.293T>C (p.Val98Ala)
c.119T>C (p.Val40Ala)
10g.119669963T>GCA378294804BAG3c.293T>G (p.Val98Gly)
c.119T>G (p.Val40Gly)
ClinVar
10g.119669964G>ACA471634480BAG3c.294G>A (p.Val98=)
c.120G>A (p.Val40=)
10g.119669964G>CCA471634482BAG3c.294G>C (p.Val98=)
c.120G>C (p.Val40=)
10g.119669964G>TCA471634481BAG3c.294G>T (p.Val98=)
c.120G>T (p.Val40=)
10g.119669965C>ACA378294805BAG3c.295C>A (p.Leu99Ile)
c.121C>A (p.Leu41Ile)
10g.119669965C=CA1940190967BAG3c.295C= (p.Leu99=)
c.121C= (p.Leu41=)
10g.119669965C>GCA378294806BAG3c.295C>G (p.Leu99Val)
c.121C>G (p.Leu41Val)
10g.119669965C>TCA378294807BAG3c.295C>T (p.Leu99Phe)
c.121C>T (p.Leu41Phe)
dbSNP gnomAD v4
10g.119669966T>ACA378294809BAG3c.296T>A (p.Leu99His)
c.122T>A (p.Leu41His)
10g.119669966T>CCA378294810BAG3c.296T>C (p.Leu99Pro)
c.122T>C (p.Leu41Pro)
10g.119669966T>GCA378294808BAG3c.296T>G (p.Leu99Arg)
c.122T>G (p.Leu41Arg)
10g.119669967C>ACA471634483BAG3c.297C>A (p.Leu99=)
c.123C>A (p.Leu41=)
10g.119669967C>GCA471634484BAG3c.297C>G (p.Leu99=)
c.123C>G (p.Leu41=)
10g.119669967C>TCA471634485BAG3c.297C>T (p.Leu99=)
c.123C>T (p.Leu41=)
ClinVar
10g.119669968C>ACA378294811BAG3c.298C>A (p.His100Asn)
c.124C>A (p.His42Asn)
10g.119669968C=CA1940190969BAG3c.298C= (p.His100=)
c.124C= (p.His42=)
10g.119669968C>GCA378294812BAG3c.298C>G (p.His100Asp)
c.124C>G (p.His42Asp)
10g.119669968C>TCA378294813BAG3c.298C>T (p.His100Tyr)
c.124C>T (p.His42Tyr)
dbSNP gnomAD v2 gnomAD v4 COSMIC
10g.119669969A=CA1940190971BAG3c.299A= (p.His100=)
c.125A= (p.His42=)
10g.119669969A>CCA378294814BAG3c.299A>C (p.His100Pro)
c.125A>C (p.His42Pro)
10g.119669969A>GCA378294815BAG3c.299A>G (p.His100Arg)
c.125A>G (p.His42Arg)
ClinVar dbSNP gnomAD v3 gnomAD v4
10g.119669969A>TCA378294816BAG3c.299A>T (p.His100Leu)
c.125A>T (p.His42Leu)
10g.119669970T>ACA378294817BAG3c.300T>A (p.His100Gln)
c.126T>A (p.His42Gln)
10g.119669970T>CCA471634486BAG3c.300T>C (p.His100=)
c.126T>C (p.His42=)
10g.119669970T>GCA378294818BAG3c.300T>G (p.His100Gln)
c.126T>G (p.His42Gln)
10g.119669971G>ACA378294819BAG3c.301G>A (p.Glu101Lys)
c.127G>A (p.Glu43Lys)
10g.119669971G>CCA378294820BAG3c.301G>C (p.Glu101Gln)
c.127G>C (p.Glu43Gln)
10g.119669971G>TCA378294821BAG3c.301G>T (p.Glu101Ter)
c.127G>T (p.Glu43Ter)
10g.119669972A=CA1940190973BAG3c.302A= (p.Glu101=)
c.128A= (p.Glu43=)
10g.119669972A>CCA378294822BAG3c.302A>C (p.Glu101Ala)
c.128A>C (p.Glu43Ala)
gnomAD v4
10g.119669972A>GCA5716284BAG3c.302A>G (p.Glu101Gly)
c.128A>G (p.Glu43Gly)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119669972A>TCA378294823BAG3c.302A>T (p.Glu101Val)
c.128A>T (p.Glu43Val)
10g.119669973A>CCA378294824BAG3c.303A>C (p.Glu101Asp)
c.129A>C (p.Glu43Asp)
10g.119669973A>GCA471634487BAG3c.303A>G (p.Glu101=)
c.129A>G (p.Glu43=)
10g.119669973A>TCA378294825BAG3c.303A>T (p.Glu101Asp)
c.129A>T (p.Glu43Asp)
10g.119669974G>ACA5716285BAG3c.304G>A (p.Gly102Ser)
c.130G>A (p.Gly44Ser)
dbSNP ExAC gnomAD v2 gnomAD v4
10g.119669974G>CCA378294826BAG3c.304G>C (p.Gly102Arg)
c.130G>C (p.Gly44Arg)
10g.119669974G=CA1940190977BAG3c.304G= (p.Gly102=)
c.130G= (p.Gly44=)
10g.119669974G>TCA378294827BAG3c.304G>T (p.Gly102Cys)
c.130G>T (p.Gly44Cys)
10g.119669975G>ACA378294828BAG3c.305G>A (p.Gly102Asp)
c.131G>A (p.Gly44Asp)
ClinVar dbSNP gnomAD v3 gnomAD v4
10g.119669975G>CCA378294829BAG3c.305G>C (p.Gly102Ala)
c.131G>C (p.Gly44Ala)
10g.119669975G=CA1940190980BAG3c.305G= (p.Gly102=)
c.131G= (p.Gly44=)
10g.119669975G>TCA378294830BAG3c.305G>T (p.Gly102Val)
c.131G>T (p.Gly44Val)
10g.119669976C>ACA471634488BAG3c.306C>A (p.Gly102=)
c.132C>A (p.Gly44=)
10g.119669976C=CA1940190985BAG3c.306C= (p.Gly102=)
c.132C= (p.Gly44=)
10g.119669976C>GCA471634489BAG3c.306C>G (p.Gly102=)
c.132C>G (p.Gly44=)
10g.119669976C>TCA5716286BAG3c.306C>T (p.Gly102=)
c.132C>T (p.Gly44=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
10g.119669977G>ACA5716287BAG3c.307G>A (p.Ala103Thr)
c.133G>A (p.Ala45Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119669977G>CCA378294831BAG3c.307G>C (p.Ala103Pro)
c.133G>C (p.Ala45Pro)
10g.119669977G=CA1940190988BAG3c.307G= (p.Ala103=)
c.133G= (p.Ala45=)
10g.119669977G>TCA378294832BAG3c.307G>T (p.Ala103Ser)
c.133G>T (p.Ala45Ser)
gnomAD v4
10g.119669978C>ACA378294833BAG3c.308C>A (p.Ala103Asp)
c.134C>A (p.Ala45Asp)
10g.119669978C>GCA378294834BAG3c.308C>G (p.Ala103Gly)
c.134C>G (p.Ala45Gly)
10g.119669978C>TCA378294835BAG3c.308C>T (p.Ala103Val)
c.134C>T (p.Ala45Val)
10g.119669979T>ACA471634490BAG3c.309T>A (p.Ala103=)
c.135T>A (p.Ala45=)
10g.119669979T>CCA471634491BAG3c.309T>C (p.Ala103=)
c.135T>C (p.Ala45=)
10g.119669979T>GCA471634492BAG3c.309T>G (p.Ala103=)
c.135T>G (p.Ala45=)
gnomAD v4
10g.119669980G>ACA378294837BAG3c.310G>A (p.Glu104Lys)
c.136G>A (p.Glu46Lys)
10g.119669980G>CCA378294838BAG3c.310G>C (p.Glu104Gln)
c.136G>C (p.Glu46Gln)
ClinVar
10g.119669980G>TCA378294836BAG3c.310G>T (p.Glu104Ter)
c.136G>T (p.Glu46Ter)
10g.119669981A>CCA378294839BAG3c.311A>C (p.Glu104Ala)
c.137A>C (p.Glu46Ala)
10g.119669981A>GCA378294841BAG3c.311A>G (p.Glu104Gly)
c.137A>G (p.Glu46Gly)
10g.119669981A>TCA378294840BAG3c.311A>T (p.Glu104Val)
c.137A>T (p.Glu46Val)
COSMIC
10g.119669982G>ACA471634493BAG3c.312G>A (p.Glu104=)
c.138G>A (p.Glu46=)
ClinVar gnomAD v4
10g.119669982G>CCA378294842BAG3c.312G>C (p.Glu104Asp)
c.138G>C (p.Glu46Asp)
10g.119669982G>TCA378294843BAG3c.312G>T (p.Glu104Asp)
c.138G>T (p.Glu46Asp)
10g.119669983A>CCA378294844BAG3c.313A>C (p.Asn105His)
c.139A>C (p.Asn47His)
10g.119669983A>GCA378294845BAG3c.313A>G (p.Asn105Asp)
c.139A>G (p.Asn47Asp)
10g.119669983A>TCA378294846BAG3c.313A>T (p.Asn105Tyr)
c.139A>T (p.Asn47Tyr)
10g.119669984A=CA1940190991BAG3c.314A= (p.Asn105=)
c.140A= (p.Asn47=)
10g.119669984A>CCA378294847BAG3c.314A>C (p.Asn105Thr)
c.140A>C (p.Asn47Thr)
10g.119669984A>GCA378294848BAG3c.314A>G (p.Asn105Ser)
c.140A>G (p.Asn47Ser)
gnomAD v4
10g.119669984A>TCA378294849BAG3c.314A>T (p.Asn105Ile)
c.140A>T (p.Asn47Ile)
dbSNP gnomAD v2 gnomAD v4
10g.119669985C>ACA378294850BAG3c.315C>A (p.Asn105Lys)
c.141C>A (p.Asn47Lys)
10g.119669985C=CA1940190993BAG3c.315C= (p.Asn105=)
c.141C= (p.Asn47=)
10g.119669985C>GCA5716288BAG3c.315C>G (p.Asn105Lys)
c.141C>G (p.Asn47Lys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119669985C>TCA471634494BAG3c.315C>T (p.Asn105=)
c.141C>T (p.Asn47=)
10g.119669986C>ACA471634495BAG3c.316C>A (p.Arg106=)
c.142C>A (p.Arg48=)
gnomAD v4
10g.119669986C=CA1940190997BAG3c.316C= (p.Arg106=)
c.142C= (p.Arg48=)
10g.119669986C>GCA378294851BAG3c.316C>G (p.Arg106Gly)
c.142C>G (p.Arg48Gly)
10g.119669986C>TCA5716289BAG3c.316C>T (p.Arg106Trp)
c.142C>T (p.Arg48Trp)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119669987G>ACA378294854BAG3c.317G>A (p.Arg106Gln)
c.143G>A (p.Arg48Gln)
ClinVar dbSNP gnomAD v4
10g.119669987G>CCA378294853BAG3c.317G>C (p.Arg106Pro)
c.143G>C (p.Arg48Pro)
10g.119669987G=CA1940191002BAG3c.317G= (p.Arg106=)
c.143G= (p.Arg48=)
10g.119669987G>TCA378294852BAG3c.317G>T (p.Arg106Leu)
c.143G>T (p.Arg48Leu)
10g.119669988G>ACA471634496BAG3c.318G>A (p.Arg106=)
c.144G>A (p.Arg48=)
gnomAD v4
10g.119669988G>CCA471634497BAG3c.318G>C (p.Arg106=)
c.144G>C (p.Arg48=)
10g.119669988G=CA1940191004BAG3c.318G= (p.Arg106=)
c.144G= (p.Arg48=)
10g.119669988G>TCA5716290BAG3c.318G>T (p.Arg106=)
c.144G>T (p.Arg48=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119669989C>ACA378294855BAG3c.319C>A (p.Gln107Lys)
c.145C>A (p.Gln49Lys)
10g.119669989C>GCA378294856BAG3c.319C>G (p.Gln107Glu)
c.145C>G (p.Gln49Glu)
10g.119669989C>TCA378294857BAG3c.319C>T (p.Gln107Ter)
c.145C>T (p.Gln49Ter)
10g.119669990A=CA1940191010BAG3c.320A= (p.Gln107=)
c.146A= (p.Gln49=)
10g.119669990A>CCA5716291BAG3c.320A>C (p.Gln107Pro)
c.146A>C (p.Gln49Pro)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119669990A>GCA378294858BAG3c.320A>G (p.Gln107Arg)
c.146A>G (p.Gln49Arg)
10g.119669990A>TCA378294859BAG3c.320A>T (p.Gln107Leu)
c.146A>T (p.Gln49Leu)
10g.119669991G>ACA471634498BAG3c.321G>A (p.Gln107=)
c.147G>A (p.Gln49=)
10g.119669991G>CCA5716292BAG3c.321G>C (p.Gln107His)
c.147G>C (p.Gln49His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119669991G=CA1940191017BAG3c.321G= (p.Gln107=)
c.147G= (p.Gln49=)
10g.119669991G>TCA378294860BAG3c.321G>T (p.Gln107His)
c.147G>T (p.Gln49His)
10g.119669992G>ACA346194BAG3c.322G>A (p.Val108Met)
c.148G>A (p.Val50Met)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119669992G>CCA5716293BAG3c.322G>C (p.Val108Leu)
c.148G>C (p.Val50Leu)
ClinVar dbSNP ExAC gnomAD v2
10g.119669992G=CA1940191024BAG3c.322G= (p.Val108=)
c.148G= (p.Val50=)
10g.119669992G>TCA378294861BAG3c.322G>T (p.Val108Leu)
c.148G>T (p.Val50Leu)
ClinVar dbSNP
10g.119669993T>ACA378294862BAG3c.323T>A (p.Val108Glu)
c.149T>A (p.Val50Glu)
10g.119669993T>CCA378294863BAG3c.323T>C (p.Val108Ala)
c.149T>C (p.Val50Ala)
10g.119669993T>GCA5716294BAG3c.323T>G (p.Val108Gly)
c.149T>G (p.Val50Gly)
dbSNP ExAC gnomAD v2 gnomAD v4
10g.119669993T=CA1940191027BAG3c.323T= (p.Val108=)
c.149T= (p.Val50=)
10g.119669994G>ACA471634499BAG3c.324G>A (p.Val108=)
c.150G>A (p.Val50=)
10g.119669994G>CCA471634501BAG3c.324G>C (p.Val108=)
c.150G>C (p.Val50=)
10g.119669994G>TCA471634500BAG3c.324G>T (p.Val108=)
c.150G>T (p.Val50=)
10g.119669995C>ACA378294864BAG3c.325C>A (p.His109Asn)
c.151C>A (p.His51Asn)
10g.119669995C=CA1940191030BAG3c.325C= (p.His109=)
c.151C= (p.His51=)
10g.119669995C>GCA5716295BAG3c.325C>G (p.His109Asp)
c.151C>G (p.His51Asp)
dbSNP ExAC gnomAD v2
10g.119669995C>TCA214219867BAG3c.325C>T (p.His109Tyr)
c.151C>T (p.His51Tyr)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.119669996A>CCA378294865BAG3c.326A>C (p.His109Pro)
c.152A>C (p.His51Pro)
10g.119669996A>GCA378294866BAG3c.326A>G (p.His109Arg)
c.152A>G (p.His51Arg)
ClinVar
10g.119669996A>TCA378294867BAG3c.326A>T (p.His109Leu)
c.152A>T (p.His51Leu)
10g.119669996_119669997delinsACCA1940191033BAG3c.326_327delinsAC (p.His109=)
c.152_153delinsAC (p.His51=)
10g.119669997C>ACA378294868BAG3c.327C>A (p.His109Gln)
c.153C>A (p.His51Gln)
10g.119669997C>GCA378294869BAG3c.327C>G (p.His109Gln)
c.153C>G (p.His51Gln)
10g.119669997C>TCA471634502BAG3c.327C>T (p.His109=)
c.153C>T (p.His51=)
gnomAD v4
10g.119669999dupCA1139661703BAG3c.329dup (p.His112ProfsTer14)
c.155dup (p.His54ProfsTer14)
ClinVar dbSNP
10g.119669999delCA660663261BAG3c.329del (p.Pro110LeufsTer?)
c.155del (p.Pro52LeufsTer?)
dbSNP
10g.119669998C>ACA5716296BAG3c.328C>A (p.Pro110Thr)
c.154C>A (p.Pro52Thr)
dbSNP ExAC gnomAD v2 gnomAD v4
10g.119669998C=CA1940191043BAG3c.328C= (p.Pro110=)
c.154C= (p.Pro52=)
10g.119669998C>GCA5716297BAG3c.328C>G (p.Pro110Ala)
c.154C>G (p.Pro52Ala)
dbSNP ExAC gnomAD v2 gnomAD v4
10g.119669998C>TCA378294870BAG3c.328C>T (p.Pro110Ser)
c.154C>T (p.Pro52Ser)
dbSNP gnomAD v4
10g.119669999C>ACA378294872BAG3c.329C>A (p.Pro110His)
c.155C>A (p.Pro52His)
10g.119669999C=CA1940191049BAG3c.329C= (p.Pro110=)
c.155C= (p.Pro52=)
10g.119669999C>GCA5716298BAG3c.329C>G (p.Pro110Arg)
c.155C>G (p.Pro52Arg)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
10g.119669999C>TCA378294871BAG3c.329C>T (p.Pro110Leu)
c.155C>T (p.Pro52Leu)
ClinVar dbSNP gnomAD v4
10g.119670000T>ACA471634503BAG3c.330T>A (p.Pro110=)
c.156T>A (p.Pro52=)
10g.119670000T>CCA471634504BAG3c.330T>C (p.Pro110=)
c.156T>C (p.Pro52=)
10g.119670000T>GCA471634505BAG3c.330T>G (p.Pro110=)
c.156T>G (p.Pro52=)
10g.119670001_119670002delCA2573053242BAG3c.331_332del (p.Phe111ProfsTer14)
c.157_158del (p.Phe53ProfsTer14)
ClinVar dbSNP
10g.119670001T>ACA378294873BAG3c.331T>A (p.Phe111Ile)
c.157T>A (p.Phe53Ile)
10g.119670001T>CCA378294874BAG3c.331T>C (p.Phe111Leu)
c.157T>C (p.Phe53Leu)
10g.119670001T>GCA378294875BAG3c.331T>G (p.Phe111Val)
c.157T>G (p.Phe53Val)
10g.119670002T>ACA378294876BAG3c.332T>A (p.Phe111Tyr)
c.158T>A (p.Phe53Tyr)
10g.119670002T>CCA378294877BAG3c.332T>C (p.Phe111Ser)
c.158T>C (p.Phe53Ser)
ClinVar dbSNP gnomAD v4
10g.119670002T>GCA378294878BAG3c.332T>G (p.Phe111Cys)
c.158T>G (p.Phe53Cys)
10g.119670002T=CA1940191051BAG3c.332T= (p.Phe111=)
c.158T= (p.Phe53=)
10g.119670003C>ACA378294879BAG3c.333C>A (p.Phe111Leu)
c.159C>A (p.Phe53Leu)
10g.119670003C=CA1940191054BAG3c.333C= (p.Phe111=)
c.159C= (p.Phe53=)
10g.119670003C>GCA378294880BAG3c.333C>G (p.Phe111Leu)
c.159C>G (p.Phe53Leu)
10g.119670003C>TCA471634506BAG3c.333C>T (p.Phe111=)
c.159C>T (p.Phe53=)
dbSNP gnomAD v2 gnomAD v4
10g.119670004C>ACA378294881BAG3c.334C>A (p.His112Asn)
c.160C>A (p.His54Asn)
10g.119670004C>GCA378294882BAG3c.334C>G (p.His112Asp)
c.160C>G (p.His54Asp)
10g.119670004C>TCA378294883BAG3c.334C>T (p.His112Tyr)
c.160C>T (p.His54Tyr)
10g.119670005A=CA1940191059BAG3c.335A= (p.His112=)
c.161A= (p.His54=)
10g.119670005A>CCA378294884BAG3c.335A>C (p.His112Pro)
c.161A>C (p.His54Pro)
10g.119670005A>GCA5716299BAG3c.335A>G (p.His112Arg)
c.161A>G (p.His54Arg)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
10g.119670005A>TCA378294885BAG3c.335A>T (p.His112Leu)
c.161A>T (p.His54Leu)
gnomAD v4
10g.119670006T>ACA378294886BAG3c.336T>A (p.His112Gln)
c.162T>A (p.His54Gln)
10g.119670006T>CCA471634507BAG3c.336T>C (p.His112=)
c.162T>C (p.His54=)
ClinVar dbSNP gnomAD v2 gnomAD v4
10g.119670006T>GCA378294887BAG3c.336T>G (p.His112Gln)
c.162T>G (p.His54Gln)
10g.119670006T=CA1940191063BAG3c.336T= (p.His112=)
c.162T= (p.His54=)
10g.119670007G>ACA5716300BAG3c.337G>A (p.Val113Ile)
c.163G>A (p.Val55Ile)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119670007G>CCA378294889BAG3c.337G>C (p.Val113Leu)
c.163G>C (p.Val55Leu)
10g.119670007G=CA1940191069BAG3c.337G= (p.Val113=)
c.163G= (p.Val55=)
10g.119670007G>TCA378294888BAG3c.337G>T (p.Val113Phe)
c.163G>T (p.Val55Phe)
10g.119670008T>ACA378294890BAG3c.338T>A (p.Val113Asp)
c.164T>A (p.Val55Asp)
10g.119670008T>CCA378294891BAG3c.338T>C (p.Val113Ala)
c.164T>C (p.Val55Ala)
10g.119670008T>GCA378294892BAG3c.338T>G (p.Val113Gly)
c.164T>G (p.Val55Gly)
dbSNP gnomAD v3 gnomAD v4
10g.119670008T=CA1940191072BAG3c.338T= (p.Val113=)
c.164T= (p.Val55=)
10g.119670008_119670009delinsTCCA1940191073BAG3c.338_339delinsTC (p.Val113=)
c.164_165delinsTC (p.Val55=)
10g.119670009delCA915948731BAG3c.339del (p.Tyr114IlefsTer?)
c.165del (p.Tyr56IlefsTer?)
ClinVar dbSNP
10g.119670009C>ACA214219914BAG3c.339C>A (p.Val113=)
c.165C>A (p.Val55=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.119670009C=CA1940191077BAG3c.339C= (p.Val113=)
c.165C= (p.Val55=)
10g.119670009C>GCA471634508BAG3c.339C>G (p.Val113=)
c.165C>G (p.Val55=)
10g.119670009C>TCA5716301BAG3c.339C>T (p.Val113=)
c.165C>T (p.Val55=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119670010T>ACA378294893BAG3c.340T>A (p.Tyr114Asn)
c.166T>A (p.Tyr56Asn)
10g.119670010T>CCA378294894BAG3c.340T>C (p.Tyr114His)
c.166T>C (p.Tyr56His)
ClinVar dbSNP gnomAD v4
10g.119670010T>GCA378294895BAG3c.340T>G (p.Tyr114Asp)
c.166T>G (p.Tyr56Asp)
10g.119670010T=CA1940191083BAG3c.340T= (p.Tyr114=)
c.166T= (p.Tyr56=)
10g.119670011A=CA1940191087BAG3c.341A= (p.Tyr114=)
c.167A= (p.Tyr56=)
10g.119670011A>CCA378294896BAG3c.341A>C (p.Tyr114Ser)
c.167A>C (p.Tyr56Ser)
10g.119670011A>GCA5716302BAG3c.341A>G (p.Tyr114Cys)
c.167A>G (p.Tyr56Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
10g.119670011A>TCA378294897BAG3c.341A>T (p.Tyr114Phe)
c.167A>T (p.Tyr56Phe)
10g.119670012T>ACA378294899BAG3c.342T>A (p.Tyr114Ter)
c.168T>A (p.Tyr56Ter)
10g.119670012T>CCA471634509BAG3c.342T>C (p.Tyr114=)
c.168T>C (p.Tyr56=)
10g.119670012T>GCA378294898BAG3c.342T>G (p.Tyr114Ter)
c.168T>G (p.Tyr56Ter)
10g.119670013C>ACA378294900BAG3c.343C>A (p.Pro115Thr)
c.169C>A (p.Pro57Thr)
10g.119670013C=CA1940191092BAG3c.343C= (p.Pro115=)
c.169C= (p.Pro57=)
10g.119670013C>GCA378294901BAG3c.343C>G (p.Pro115Ala)
c.169C>G (p.Pro57Ala)
10g.119670013C>TCA5716303BAG3c.343C>T (p.Pro115Ser)
c.169C>T (p.Pro57Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119670021_119670022insTGGATGCAGCGATTCCGAACTGAGGCGGCAGCAGCGGCTCCTCAGAGGTCCCAGTCACCTCTGCGGGGCATGCCAGAAACCACTCAGCCAGATAAACAGCGTGGACAGGTGGCAGCGGCGGCGGCAGCCCAGCCCCCAGCCTCA2580616875BAG3c.351_352insTGGATGCAGCGATTCCGAACTGAGGCGGCAGCAGCGGCTCCTCAGAGGTCCCAGTCACCTCTGCGGGGCATGCCAGAAACCACTCAGCCAGATAAACAGCGTGGACAGGTGGCAGCGGCGGCGGCAGCCCAGCCCCCAGCCT (p.Gly118TrpfsTer55)
c.177_178insTGGATGCAGCGATTCCGAACTGAGGCGGCAGCAGCGGCTCCTCAGAGGTCCCAGTCACCTCTGCGGGGCATGCCAGAAACCACTCAGCCAGATAAACAGCGTGGACAGGTGGCAGCGGCGGCGGCAGCCCAGCCCCCAGCCT (p.Gly60TrpfsTer55)
10g.119670014C>ACA378294902BAG3c.344C>A (p.Pro115His)
c.170C>A (p.Pro57His)
10g.119670014C>GCA378294903BAG3c.344C>G (p.Pro115Arg)
c.170C>G (p.Pro57Arg)
10g.119670014C>TCA378294904BAG3c.344C>T (p.Pro115Leu)
c.170C>T (p.Pro57Leu)
gnomAD v4
10g.119670015C>ACA471634512BAG3c.345C>A (p.Pro115=)
c.171C>A (p.Pro57=)
10g.119670015C>GCA471634511BAG3c.345C>G (p.Pro115=)
c.171C>G (p.Pro57=)
10g.119670015C>TCA471634510BAG3c.345C>T (p.Pro115=)
c.171C>T (p.Pro57=)
10g.119670016C>ACA378294905BAG3c.346C>A (p.Gln116Lys)
c.172C>A (p.Gln58Lys)
10g.119670016C>GCA378294906BAG3c.346C>G (p.Gln116Glu)
c.172C>G (p.Gln58Glu)
10g.119670016C>TCA378294907BAG3c.346C>T (p.Gln116Ter)
c.172C>T (p.Gln58Ter)
ClinVar
10g.119670017A>CCA378294908BAG3c.347A>C (p.Gln116Pro)
c.173A>C (p.Gln58Pro)
10g.119670017A>GCA378294909BAG3c.347A>G (p.Gln116Arg)
c.173A>G (p.Gln58Arg)
10g.119670017A>TCA378294910BAG3c.347A>T (p.Gln116Leu)
c.173A>T (p.Gln58Leu)
10g.119670018G>ACA471634513BAG3c.348G>A (p.Gln116=)
c.174G>A (p.Gln58=)
gnomAD v4
10g.119670018G>CCA5716304BAG3c.348G>C (p.Gln116His)
c.174G>C (p.Gln58His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
10g.119670018G=CA1940191096BAG3c.348G= (p.Gln116=)
c.174G= (p.Gln58=)
10g.119670018G>TCA378294911BAG3c.348G>T (p.Gln116His)
c.174G>T (p.Gln58His)
10g.119670019C>ACA378294912BAG3c.349C>A (p.Pro117Thr)
c.175C>A (p.Pro59Thr)
10g.119670019C>GCA378294913BAG3c.349C>G (p.Pro117Ala)
c.175C>G (p.Pro59Ala)
10g.119670019C>TCA378294914BAG3c.349C>T (p.Pro117Ser)
c.175C>T (p.Pro59Ser)
10g.119670020dupCA16618933BAG3c.350dup (p.Gly118TrpfsTer8)
c.176dup (p.Gly60TrpfsTer8)
ClinVar dbSNP
10g.119670020C>ACA378294915BAG3c.350C>A (p.Pro117His)
c.176C>A (p.Pro59His)
10g.119670020C=CA1940191103BAG3c.350C= (p.Pro117=)
c.176C= (p.Pro59=)
10g.119670020C>GCA214219969BAG3c.350C>G (p.Pro117Arg)
c.176C>G (p.Pro59Arg)
dbSNP
10g.119670020C>TCA5716305BAG3c.350C>T (p.Pro117Leu)
c.176C>T (p.Pro59Leu)
dbSNP ExAC gnomAD v2 gnomAD v4
10g.119670021T>ACA471634514BAG3c.351T>A (p.Pro117=)
c.177T>A (p.Pro59=)
10g.119670021T>CCA471634516BAG3c.351T>C (p.Pro117=)
c.177T>C (p.Pro59=)
dbSNP
10g.119670021T>GCA471634515BAG3c.351T>G (p.Pro117=)
c.177T>G (p.Pro59=)
10g.119670021T=CA1940191107BAG3c.351T= (p.Pro117=)
c.177T= (p.Pro59=)
10g.119670022G>ACA378294916BAG3c.352G>A (p.Gly118Arg)
c.178G>A (p.Gly60Arg)
10g.119670022G>CCA378294917BAG3c.352G>C (p.Gly118Arg)
c.178G>C (p.Gly60Arg)
10g.119670022G>TCA378294918BAG3c.352G>T (p.Gly118Trp)
c.178G>T (p.Gly60Trp)
10g.119670023G>ACA378294919BAG3c.353G>A (p.Gly118Glu)
c.179G>A (p.Gly60Glu)
10g.119670023G>CCA378294920BAG3c.353G>C (p.Gly118Ala)
c.179G>C (p.Gly60Ala)
10g.119670023G>TCA378294921BAG3c.353G>T (p.Gly118Val)
c.179G>T (p.Gly60Val)
10g.119670024G>ACA471634517BAG3c.354G>A (p.Gly118=)
c.180G>A (p.Gly60=)
gnomAD v4
10g.119670024G>CCA471634518BAG3c.354G>C (p.Gly118=)
c.180G>C (p.Gly60=)
10g.119670024G>TCA471634519BAG3c.354G>T (p.Gly118=)
c.180G>T (p.Gly60=)
10g.119670025A=CA1940191111BAG3c.355A= (p.Met119=)
c.181A= (p.Met61=)
10g.119670025A>CCA378294923BAG3c.355A>C (p.Met119Leu)
c.181A>C (p.Met61Leu)
10g.119670025A>GCA378294924BAG3c.355A>G (p.Met119Val)
c.181A>G (p.Met61Val)
ClinVar dbSNP gnomAD v2 gnomAD v4
10g.119670025A>TCA378294922BAG3c.355A>T (p.Met119Leu)
c.181A>T (p.Met61Leu)
10g.119670026T>ACA378294925BAG3c.356T>A (p.Met119Lys)
c.182T>A (p.Met61Lys)
10g.119670026T>CCA378294926BAG3c.356T>C (p.Met119Thr)
c.182T>C (p.Met61Thr)
10g.119670026T>GCA378294927BAG3c.356T>G (p.Met119Arg)
c.182T>G (p.Met61Arg)
gnomAD v4
10g.119670027G>ACA378294928BAG3c.357G>A (p.Met119Ile)
c.183G>A (p.Met61Ile)
10g.119670027G>CCA378294929BAG3c.357G>C (p.Met119Ile)
c.183G>C (p.Met61Ile)
10g.119670027G>TCA378294930BAG3c.357G>T (p.Met119Ile)
c.183G>T (p.Met61Ile)
10g.119670028C>ACA378294931BAG3c.358C>A (p.Gln120Lys)
c.184C>A (p.Gln62Lys)
10g.119670028C>GCA378294933BAG3c.358C>G (p.Gln120Glu)
c.184C>G (p.Gln62Glu)
10g.119670028C>TCA378294932BAG3c.358C>T (p.Gln120Ter)
c.184C>T (p.Gln62Ter)
ClinVar
10g.119670029A=CA1940191114BAG3c.359A= (p.Gln120=)
c.185A= (p.Gln62=)
10g.119670029A>CCA378294934BAG3c.359A>C (p.Gln120Pro)
c.185A>C (p.Gln62Pro)
10g.119670029A>GCA378294935BAG3c.359A>G (p.Gln120Arg)
c.185A>G (p.Gln62Arg)
ClinVar
10g.119670029A>TCA378294936BAG3c.359A>T (p.Gln120Leu)
c.185A>T (p.Gln62Leu)
ClinVar dbSNP gnomAD v4
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)

Number of alleles fetched