Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.119672256_119677283delCA1139532250BAG3c.509_*1del
10g.119672293_119672298dupCA2611160105BAG3c.546_551dup (p.Ser184_Ser185insSerSer)
c.372_377dup (p.Ser126_Ser127insSerSer)
gnomAD v4
10g.119672285T>ACA378295296BAG3c.538T>A (p.Ser180Thr)
c.364T>A (p.Ser122Thr)
10g.119672285T>CCA378295297BAG3c.538T>C (p.Ser180Pro)
c.364T>C (p.Ser122Pro)
ClinVar dbSNP gnomAD v3 gnomAD v4
10g.119672285T>GCA378295298BAG3c.538T>G (p.Ser180Ala)
c.364T>G (p.Ser122Ala)
ClinVar
10g.119672285_119672307delCA2611160106BAG3c.538_560del (p.Ser180ProfsTer?)
c.364_386del (p.Ser122ProfsTer?)
gnomAD v4
10g.119672286C>ACA378295299BAG3c.539C>A (p.Ser180Ter)
c.365C>A (p.Ser122Ter)
10g.119672286C>GCA378295300BAG3c.539C>G (p.Ser180Ter)
c.365C>G (p.Ser122Ter)
10g.119672286C>TCA378295301BAG3c.539C>T (p.Ser180Leu)
c.365C>T (p.Ser122Leu)
gnomAD v4
10g.119672287A=CA1940193063BAG3c.540A= (p.Ser180=)
c.366A= (p.Ser122=)
10g.119672287A>CCA471739165BAG3c.540A>C (p.Ser180=)
c.366A>C (p.Ser122=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.119672287A>GCA471739166BAG3c.540A>G (p.Ser180=)
c.366A>G (p.Ser122=)
gnomAD v4
10g.119672287A>TCA471739167BAG3c.540A>T (p.Ser180=)
c.366A>T (p.Ser122=)
dbSNP
10g.119672288T>ACA378295302BAG3c.541T>A (p.Ser181Thr)
c.367T>A (p.Ser123Thr)
10g.119672288T>CCA378295303BAG3c.541T>C (p.Ser181Pro)
c.367T>C (p.Ser123Pro)
10g.119672288T>GCA378295304BAG3c.541T>G (p.Ser181Ala)
c.367T>G (p.Ser123Ala)
10g.119672288_119672289delinsAACA2580082420BAG3c.541_542delinsAA (p.Ser181Asn)
c.367_368delinsAA (p.Ser123Asn)
ClinVar
10g.119672289C>ACA378295305BAG3c.542C>A (p.Ser181Tyr)
c.368C>A (p.Ser123Tyr)
10g.119672289C=CA1940193067BAG3c.542C= (p.Ser181=)
c.368C= (p.Ser123=)
10g.119672289C>GCA378295307BAG3c.542C>G (p.Ser181Cys)
c.368C>G (p.Ser123Cys)
10g.119672289C>TCA378295306BAG3c.542C>T (p.Ser181Phe)
c.368C>T (p.Ser123Phe)
ClinVar dbSNP gnomAD v3 gnomAD v4
10g.119672290C>ACA471739168BAG3c.543C>A (p.Ser181=)
c.369C>A (p.Ser123=)
10g.119672290C=CA1940193070BAG3c.543C= (p.Ser181=)
c.369C= (p.Ser123=)
10g.119672290C>GCA471739169BAG3c.543C>G (p.Ser181=)
c.369C>G (p.Ser123=)
10g.119672290C>TCA471739170BAG3c.543C>T (p.Ser181=)
c.369C>T (p.Ser123=)
dbSNP gnomAD v2 gnomAD v4
10g.119672291T>ACA378295308BAG3c.544T>A (p.Ser182Thr)
c.370T>A (p.Ser124Thr)
10g.119672291T>CCA378295309BAG3c.544T>C (p.Ser182Pro)
c.370T>C (p.Ser124Pro)
dbSNP gnomAD v2 gnomAD v4
10g.119672291T>GCA378295310BAG3c.544T>G (p.Ser182Ala)
c.370T>G (p.Ser124Ala)
10g.119672291T=CA1940193075BAG3c.544T= (p.Ser182=)
c.370T= (p.Ser124=)
10g.119672292C>ACA378295311BAG3c.545C>A (p.Ser182Ter)
c.371C>A (p.Ser124Ter)
10g.119672292C=CA1940193081BAG3c.545C= (p.Ser182=)
c.371C= (p.Ser124=)
10g.119672292C>GCA378295312BAG3c.545C>G (p.Ser182Ter)
c.371C>G (p.Ser124Ter)
10g.119672292C>TCA378295313BAG3c.545C>T (p.Ser182Leu)
c.371C>T (p.Ser124Leu)
ClinVar dbSNP gnomAD v4
10g.119672293A>CCA471739171BAG3c.546A>C (p.Ser182=)
c.372A>C (p.Ser124=)
10g.119672293A>GCA471739173BAG3c.546A>G (p.Ser182=)
c.372A>G (p.Ser124=)
10g.119672293A>TCA471739172BAG3c.546A>T (p.Ser182=)
c.372A>T (p.Ser124=)
10g.119672293_119672296delinsATCCCA1940193084BAG3c.546_549delinsATCC (p.Ser182=)
c.372_375delinsATCC (p.Ser124=)
10g.119672294T>ACA378295314BAG3c.547T>A (p.Ser183Thr)
c.373T>A (p.Ser125Thr)
10g.119672294T>CCA5716365BAG3c.547T>C (p.Ser183Pro)
c.373T>C (p.Ser125Pro)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
10g.119672294T>GCA378295315BAG3c.547T>G (p.Ser183Ala)
c.373T>G (p.Ser125Ala)
10g.119672294T=CA1940193089BAG3c.547T= (p.Ser183=)
c.373T= (p.Ser125=)
10g.119672296_119672301dupCA5716364BAG3c.549_554dup (p.Ser185_Ala186insSerSer)
c.375_380dup (p.Ser127_Ala128insSerSer)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119672299_119672301delCA16612847BAG3c.552_554del (p.Ser185del)
c.378_380del (p.Ser127del)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.119672296_119672301delCA2611160107BAG3c.549_554del (p.Ser184_Ser185del)
c.375_380del (p.Ser126_Ser127del)
gnomAD v4
10g.119672295C>ACA378295316BAG3c.548C>A (p.Ser183Tyr)
c.374C>A (p.Ser125Tyr)
10g.119672295C=CA1940193095BAG3c.548C= (p.Ser183=)
c.374C= (p.Ser125=)
10g.119672295C>GCA378295317BAG3c.548C>G (p.Ser183Cys)
c.374C>G (p.Ser125Cys)
10g.119672295C>TCA378295318BAG3c.548C>T (p.Ser183Phe)
c.374C>T (p.Ser125Phe)
dbSNP gnomAD v2
10g.119672296C>ACA471739174BAG3c.549C>A (p.Ser183=)
c.375C>A (p.Ser125=)
10g.119672296C=CA1940193116BAG3c.549C= (p.Ser183=)
c.375C= (p.Ser125=)
10g.119672296C>GCA295670BAG3c.549C>G (p.Ser183=)
c.375C>G (p.Ser125=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119672296C>TCA471739175BAG3c.549C>T (p.Ser183=)
c.375C>T (p.Ser125=)
10g.119672297T>ACA378295319BAG3c.550T>A (p.Ser184Thr)
c.376T>A (p.Ser126Thr)
ClinVar
10g.119672297T>CCA378295320BAG3c.550T>C (p.Ser184Pro)
c.376T>C (p.Ser126Pro)
gnomAD v4
10g.119672297T>GCA378295321BAG3c.550T>G (p.Ser184Ala)
c.376T>G (p.Ser126Ala)
ClinVar dbSNP gnomAD v3 gnomAD v4
10g.119672297T=CA1940193123BAG3c.550T= (p.Ser184=)
c.376T= (p.Ser126=)
10g.119672298C>ACA378295322BAG3c.551C>A (p.Ser184Tyr)
c.377C>A (p.Ser126Tyr)
10g.119672298C=CA1940193125BAG3c.551C= (p.Ser184=)
c.377C= (p.Ser126=)
10g.119672298C>GCA378295323BAG3c.551C>G (p.Ser184Cys)
c.377C>G (p.Ser126Cys)
10g.119672298C>TCA378295324BAG3c.551C>T (p.Ser184Phe)
c.377C>T (p.Ser126Phe)
ClinVar dbSNP gnomAD v2 gnomAD v4
10g.119672299C>ACA471739176BAG3c.552C>A (p.Ser184=)
c.378C>A (p.Ser126=)
10g.119672299C>GCA471739177BAG3c.552C>G (p.Ser184=)
c.378C>G (p.Ser126=)
10g.119672299C>TCA471739178BAG3c.552C>T (p.Ser184=)
c.378C>T (p.Ser126=)
gnomAD v4
10g.119672300T>ACA378295325BAG3c.553T>A (p.Ser185Thr)
c.379T>A (p.Ser127Thr)
10g.119672300T>CCA378295326BAG3c.553T>C (p.Ser185Pro)
c.379T>C (p.Ser127Pro)
10g.119672300T>GCA378295327BAG3c.553T>G (p.Ser185Ala)
c.379T>G (p.Ser127Ala)
10g.119672301C>ACA378295328BAG3c.554C>A (p.Ser185Ter)
c.380C>A (p.Ser127Ter)
10g.119672301C=CA1940193128BAG3c.554C= (p.Ser185=)
c.380C= (p.Ser127=)
10g.119672301C>GCA378295329BAG3c.554C>G (p.Ser185Trp)
c.380C>G (p.Ser127Trp)
10g.119672301C>TCA346197BAG3c.554C>T (p.Ser185Leu)
c.380C>T (p.Ser127Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119672302G>ACA471739181BAG3c.555G>A (p.Ser185=)
c.381G>A (p.Ser127=)
ClinVar dbSNP gnomAD v2 gnomAD v4
10g.119672302G>CCA471739180BAG3c.555G>C (p.Ser185=)
c.381G>C (p.Ser127=)
10g.119672302G=CA1940193129BAG3c.555G= (p.Ser185=)
c.381G= (p.Ser127=)
10g.119672302G>TCA471739179BAG3c.555G>T (p.Ser185=)
c.381G>T (p.Ser127=)
10g.119672303G>ACA378295331BAG3c.556G>A (p.Ala186Thr)
c.382G>A (p.Ala128Thr)
10g.119672303G>CCA378295332BAG3c.556G>C (p.Ala186Pro)
c.382G>C (p.Ala128Pro)
ClinVar dbSNP
10g.119672303G>TCA378295330BAG3c.556G>T (p.Ala186Ser)
c.382G>T (p.Ala128Ser)
10g.119672304C>ACA378295334BAG3c.557C>A (p.Ala186Asp)
c.383C>A (p.Ala128Asp)
10g.119672304C=CA1940193131BAG3c.557C= (p.Ala186=)
c.383C= (p.Ala128=)
10g.119672304C>GCA378295333BAG3c.557C>G (p.Ala186Gly)
c.383C>G (p.Ala128Gly)
10g.119672304C>TCA5716366BAG3c.557C>T (p.Ala186Val)
c.383C>T (p.Ala128Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
10g.119672304_119672328delinsCCAGCCTGCCTTCCTCCGGCAGGAGCA1940193130BAG3c.557_581delinsCCAGCCTGCCTTCCTCCGGCAGGAG (p.Ala186=)
c.383_407delinsCCAGCCTGCCTTCCTCCGGCAGGAG (p.Ala128=)
10g.119672305C>ACA471739182BAG3c.558C>A (p.Ala186=)
c.384C>A (p.Ala128=)
10g.119672305C=CA1940193133BAG3c.558C= (p.Ala186=)
c.384C= (p.Ala128=)
10g.119672305C>GCA471739183BAG3c.558C>G (p.Ala186=)
c.384C>G (p.Ala128=)
10g.119672305C>TCA471739184BAG3c.558C>T (p.Ala186=)
c.384C>T (p.Ala128=)
dbSNP gnomAD v2 gnomAD v4
10g.119672312_119672335delCA1940193132BAG3c.565_588del (p.Pro189_Leu196del)
c.391_414del (p.Pro131_Leu138del)
ClinVar dbSNP
10g.119672306A>CCA378295335BAG3c.559A>C (p.Ser187Arg)
c.385A>C (p.Ser129Arg)
10g.119672306A>GCA378295336BAG3c.559A>G (p.Ser187Gly)
c.385A>G (p.Ser129Gly)
10g.119672306A>TCA378295337BAG3c.559A>T (p.Ser187Cys)
c.385A>T (p.Ser129Cys)
10g.119672307G>ACA378295338BAG3c.560G>A (p.Ser187Asn)
c.386G>A (p.Ser129Asn)
10g.119672307G>CCA378295339BAG3c.560G>C (p.Ser187Thr)
c.386G>C (p.Ser129Thr)
10g.119672307G=CA1940193134BAG3c.560G= (p.Ser187=)
c.386G= (p.Ser129=)
10g.119672307G>TCA378295340BAG3c.560G>T (p.Ser187Ile)
c.386G>T (p.Ser129Ile)
dbSNP gnomAD v2 gnomAD v4
10g.119672308C>ACA378295341BAG3c.561C>A (p.Ser187Arg)
c.387C>A (p.Ser129Arg)
10g.119672308C>GCA378295342BAG3c.561C>G (p.Ser187Arg)
c.387C>G (p.Ser129Arg)
gnomAD v4
10g.119672308C>TCA471739185BAG3c.561C>T (p.Ser187=)
c.387C>T (p.Ser129=)
ClinVar
10g.119672309C>ACA378295343BAG3c.562C>A (p.Leu188Met)
c.388C>A (p.Leu130Met)
10g.119672309C>GCA378295344BAG3c.562C>G (p.Leu188Val)
c.388C>G (p.Leu130Val)
gnomAD v4
10g.119672309C>TCA471739186BAG3c.562C>T (p.Leu188=)
c.388C>T (p.Leu130=)
10g.119672310T>ACA378295346BAG3c.563T>A (p.Leu188Gln)
c.389T>A (p.Leu130Gln)
10g.119672310T>CCA378295347BAG3c.563T>C (p.Leu188Pro)
c.389T>C (p.Leu130Pro)
10g.119672310T>GCA378295345BAG3c.563T>G (p.Leu188Arg)
c.389T>G (p.Leu130Arg)
10g.119672311G>ACA471739187BAG3c.564G>A (p.Leu188=)
c.390G>A (p.Leu130=)
ClinVar gnomAD v4
10g.119672311G>CCA471739188BAG3c.564G>C (p.Leu188=)
c.390G>C (p.Leu130=)
10g.119672311G=CA1940193135BAG3c.564G= (p.Leu188=)
c.390G= (p.Leu130=)
10g.119672311G>TCA10631054BAG3c.564G>T (p.Leu188=)
c.390G>T (p.Leu130=)
ClinVar dbSNP gnomAD v3 gnomAD v4
10g.119672312C>ACA378295348BAG3c.565C>A (p.Pro189Thr)
c.391C>A (p.Pro131Thr)
10g.119672312C=CA1940193137BAG3c.565C= (p.Pro189=)
c.391C= (p.Pro131=)
10g.119672312C>GCA378295349BAG3c.565C>G (p.Pro189Ala)
c.391C>G (p.Pro131Ala)
10g.119672312C>TCA378295350BAG3c.565C>T (p.Pro189Ser)
c.391C>T (p.Pro131Ser)
dbSNP gnomAD v3 gnomAD v4
10g.119672312_119672327delCA2611160108BAG3c.565_580del (p.Pro189AlafsTer17)
c.391_406del (p.Pro131AlafsTer17)
gnomAD v4
10g.119672313C>ACA378295353BAG3c.566C>A (p.Pro189His)
c.392C>A (p.Pro131His)
10g.119672313C>GCA378295352BAG3c.566C>G (p.Pro189Arg)
c.392C>G (p.Pro131Arg)
10g.119672313C>TCA378295351BAG3c.566C>T (p.Pro189Leu)
c.392C>T (p.Pro131Leu)
gnomAD v4
10g.119672314T>ACA471739189BAG3c.567T>A (p.Pro189=)
c.393T>A (p.Pro131=)
10g.119672314T>CCA471739190BAG3c.567T>C (p.Pro189=)
c.393T>C (p.Pro131=)
10g.119672314T>GCA471739191BAG3c.567T>G (p.Pro189=)
c.393T>G (p.Pro131=)
10g.119672314_119672324delinsTTCCTCCGGCACA1940193140BAG3c.567_577delinsTTCCTCCGGCA (p.Pro189=)
c.393_403delinsTTCCTCCGGCA (p.Pro131=)
10g.119672315T>ACA378295354BAG3c.568T>A (p.Ser190Thr)
c.394T>A (p.Ser132Thr)
10g.119672315T>CCA378295355BAG3c.568T>C (p.Ser190Pro)
c.394T>C (p.Ser132Pro)
10g.119672315T>GCA378295356BAG3c.568T>G (p.Ser190Ala)
c.394T>G (p.Ser132Ala)
10g.119672315_119672324delCA1139661705BAG3c.568_577del (p.Ser190GlyfsTer18)
c.394_403del (p.Ser132GlyfsTer18)
ClinVar dbSNP
10g.119672316C>ACA378295357BAG3c.569C>A (p.Ser190Tyr)
c.395C>A (p.Ser132Tyr)
10g.119672316C=CA1940193146BAG3c.569C= (p.Ser190=)
c.395C= (p.Ser132=)
10g.119672316C>GCA378295358BAG3c.569C>G (p.Ser190Cys)
c.395C>G (p.Ser132Cys)
10g.119672316C>TCA16606637BAG3c.569C>T (p.Ser190Phe)
c.395C>T (p.Ser132Phe)
ClinVar dbSNP
10g.119672317C>ACA471739192BAG3c.570C>A (p.Ser190=)
c.396C>A (p.Ser132=)
10g.119672317C=CA1940193153BAG3c.570C= (p.Ser190=)
c.396C= (p.Ser132=)
10g.119672317C>GCA471739193BAG3c.570C>G (p.Ser190=)
c.396C>G (p.Ser132=)
dbSNP gnomAD v2 gnomAD v4
10g.119672317C>TCA471739194BAG3c.570C>T (p.Ser190=)
c.396C>T (p.Ser132=)
10g.119672318T>ACA378295361BAG3c.571T>A (p.Ser191Thr)
c.397T>A (p.Ser133Thr)
10g.119672318T>CCA378295360BAG3c.571T>C (p.Ser191Pro)
c.397T>C (p.Ser133Pro)
10g.119672318T>GCA378295359BAG3c.571T>G (p.Ser191Ala)
c.397T>G (p.Ser133Ala)
10g.119672319C>ACA378295362BAG3c.572C>A (p.Ser191Tyr)
c.398C>A (p.Ser133Tyr)
10g.119672319C>GCA378295363BAG3c.572C>G (p.Ser191Cys)
c.398C>G (p.Ser133Cys)
10g.119672319C>TCA378295364BAG3c.572C>T (p.Ser191Phe)
c.398C>T (p.Ser133Phe)
10g.119672320C>ACA471739195BAG3c.573C>A (p.Ser191=)
c.399C>A (p.Ser133=)
10g.119672320C=CA1940193157BAG3c.573C= (p.Ser191=)
c.399C= (p.Ser133=)
10g.119672320C>GCA471739196BAG3c.573C>G (p.Ser191=)
c.399C>G (p.Ser133=)
10g.119672320C>TCA5716367BAG3c.573C>T (p.Ser191=)
c.399C>T (p.Ser133=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
10g.119672320_119672321insTCTCA1940193164BAG3c.573_574insTCT (p.Ser191_Gly192insSer)
c.399_400insTCT (p.Ser133_Gly134insSer)
dbSNP
10g.119672321G>ACA5716368BAG3c.574G>A (p.Gly192Ser)
c.400G>A (p.Gly134Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119672321G>CCA378295365BAG3c.574G>C (p.Gly192Arg)
c.400G>C (p.Gly134Arg)
10g.119672321G=CA1940193165BAG3c.574G= (p.Gly192=)
c.400G= (p.Gly134=)
10g.119672321G>TCA5716369BAG3c.574G>T (p.Gly192Cys)
c.400G>T (p.Gly134Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
10g.119672322G>ACA378295366BAG3c.575G>A (p.Gly192Asp)
c.401G>A (p.Gly134Asp)
10g.119672322G>CCA378295367BAG3c.575G>C (p.Gly192Ala)
c.401G>C (p.Gly134Ala)
10g.119672322G>TCA378295368BAG3c.575G>T (p.Gly192Val)
c.401G>T (p.Gly134Val)
10g.119672323C>ACA471739197BAG3c.576C>A (p.Gly192=)
c.402C>A (p.Gly134=)
10g.119672323C=CA1940193170BAG3c.576C= (p.Gly192=)
c.402C= (p.Gly134=)
10g.119672323C>GCA471739199BAG3c.576C>G (p.Gly192=)
c.402C>G (p.Gly134=)
dbSNP gnomAD v2 gnomAD v4
10g.119672323C>TCA471739198BAG3c.576C>T (p.Gly192=)
c.402C>T (p.Gly134=)
ClinVar dbSNP
10g.119672324A>CCA471739200BAG3c.577A>C (p.Arg193=)
c.403A>C (p.Arg135=)
10g.119672324A>GCA378295369BAG3c.577A>G (p.Arg193Gly)
c.403A>G (p.Arg135Gly)
ClinVar
10g.119672324A>TCA378295370BAG3c.577A>T (p.Arg193Trp)
c.403A>T (p.Arg135Trp)
10g.119672325G>ACA5716370BAG3c.578G>A (p.Arg193Lys)
c.404G>A (p.Arg135Lys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
10g.119672325G>CCA378295372BAG3c.578G>C (p.Arg193Thr)
c.404G>C (p.Arg135Thr)
10g.119672325G=CA1940193177BAG3c.578G= (p.Arg193=)
c.404G= (p.Arg135=)
10g.119672325G>TCA378295371BAG3c.578G>T (p.Arg193Met)
c.404G>T (p.Arg135Met)
dbSNP gnomAD v2 gnomAD v4
10g.119672326G>ACA471739201BAG3c.579G>A (p.Arg193=)
c.405G>A (p.Arg135=)
10g.119672326G>CCA378295373BAG3c.579G>C (p.Arg193Ser)
c.405G>C (p.Arg135Ser)
10g.119672326G>TCA378295374BAG3c.579G>T (p.Arg193Ser)
c.405G>T (p.Arg135Ser)
10g.119672326_119672327delinsGACA1940193180BAG3c.579_580delinsGA (p.Arg193=)
c.405_406delinsGA (p.Arg135=)
10g.119672327delCA16618934BAG3c.580del (p.Ser194AlafsTer17)
c.406del (p.Ser136AlafsTer17)
ClinVar dbSNP
10g.119672327A=CA1940193184BAG3c.580A= (p.Ser194=)
c.406A= (p.Ser136=)
10g.119672327A>CCA378295375BAG3c.580A>C (p.Ser194Arg)
c.406A>C (p.Ser136Arg)
10g.119672327A>GCA378295376BAG3c.580A>G (p.Ser194Gly)
c.406A>G (p.Ser136Gly)
ClinVar dbSNP gnomAD v3 gnomAD v4
10g.119672327A>TCA378295377BAG3c.580A>T (p.Ser194Cys)
c.406A>T (p.Ser136Cys)
10g.119672328G>ACA378295380BAG3c.581G>A (p.Ser194Asn)
c.407G>A (p.Ser136Asn)
10g.119672328G>CCA378295378BAG3c.581G>C (p.Ser194Thr)
c.407G>C (p.Ser136Thr)
10g.119672328G>TCA378295379BAG3c.581G>T (p.Ser194Ile)
c.407G>T (p.Ser136Ile)
10g.119672329C>ACA378295381BAG3c.582C>A (p.Ser194Arg)
c.408C>A (p.Ser136Arg)
10g.119672329C=CA1940193187BAG3c.582C= (p.Ser194=)
c.408C= (p.Ser136=)
10g.119672329C>GCA214221693BAG3c.582C>G (p.Ser194Arg)
c.408C>G (p.Ser136Arg)
ClinVar dbSNP
10g.119672329C>TCA471739202BAG3c.582C>T (p.Ser194=)
c.408C>T (p.Ser136=)
10g.119672330A=CA1940193189BAG3c.583A= (p.Ser195=)
c.409A= (p.Ser137=)
10g.119672330A>CCA378295382BAG3c.583A>C (p.Ser195Arg)
c.409A>C (p.Ser137Arg)
10g.119672330A>GCA5716371BAG3c.583A>G (p.Ser195Gly)
c.409A>G (p.Ser137Gly)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
10g.119672330A>TCA378295383BAG3c.583A>T (p.Ser195Cys)
c.409A>T (p.Ser137Cys)
10g.119672331G>ACA5716372BAG3c.584G>A (p.Ser195Asn)
c.410G>A (p.Ser137Asn)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119672331G>CCA378295385BAG3c.584G>C (p.Ser195Thr)
c.410G>C (p.Ser137Thr)
10g.119672331G=CA1940193192BAG3c.584G= (p.Ser195=)
c.410G= (p.Ser137=)
10g.119672331G>TCA378295384BAG3c.584G>T (p.Ser195Ile)
c.410G>T (p.Ser137Ile)
10g.119672332C>ACA378295386BAG3c.585C>A (p.Ser195Arg)
c.411C>A (p.Ser137Arg)
10g.119672332C=CA1940193197BAG3c.585C= (p.Ser195=)
c.411C= (p.Ser137=)
10g.119672332C>GCA378295387BAG3c.585C>G (p.Ser195Arg)
c.411C>G (p.Ser137Arg)
10g.119672332C>TCA471739203BAG3c.585C>T (p.Ser195=)
c.411C>T (p.Ser137=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.119672333C>ACA378295388BAG3c.586C>A (p.Leu196Met)
c.412C>A (p.Leu138Met)
10g.119672333C=CA1940193199BAG3c.586C= (p.Leu196=)
c.412C= (p.Leu138=)
10g.119672333C>GCA214221700BAG3c.586C>G (p.Leu196Val)
c.412C>G (p.Leu138Val)
dbSNP gnomAD v4
10g.119672333C>TCA471739204BAG3c.586C>T (p.Leu196=)
c.412C>T (p.Leu138=)
10g.119672334T>ACA378295389BAG3c.587T>A (p.Leu196Gln)
c.413T>A (p.Leu138Gln)
10g.119672334T>CCA378295390BAG3c.587T>C (p.Leu196Pro)
c.413T>C (p.Leu138Pro)
10g.119672334T>GCA378295391BAG3c.587T>G (p.Leu196Arg)
c.413T>G (p.Leu138Arg)
10g.119672335G>ACA471739205BAG3c.588G>A (p.Leu196=)
c.414G>A (p.Leu138=)
10g.119672335G>CCA471739207BAG3c.588G>C (p.Leu196=)
c.414G>C (p.Leu138=)
10g.119672335G>TCA471739206BAG3c.588G>T (p.Leu196=)
c.414G>T (p.Leu138=)
10g.119672336G>ACA5716373BAG3c.589G>A (p.Gly197Ser)
c.415G>A (p.Gly139Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119672336G>CCA378295392BAG3c.589G>C (p.Gly197Arg)
c.415G>C (p.Gly139Arg)
10g.119672336G=CA1940193202BAG3c.589G= (p.Gly197=)
c.415G= (p.Gly139=)
10g.119672336G>TCA378295393BAG3c.589G>T (p.Gly197Cys)
c.415G>T (p.Gly139Cys)
COSMIC
10g.119672337G>ACA5716374BAG3c.590G>A (p.Gly197Asp)
c.416G>A (p.Gly139Asp)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
10g.119672337G>CCA378295394BAG3c.590G>C (p.Gly197Ala)
c.416G>C (p.Gly139Ala)
10g.119672337G=CA1940193204BAG3c.590G= (p.Gly197=)
c.416G= (p.Gly139=)
10g.119672337G>TCA378295395BAG3c.590G>T (p.Gly197Val)
c.416G>T (p.Gly139Val)
10g.119672338C>ACA471739208BAG3c.591C>A (p.Gly197=)
c.417C>A (p.Gly139=)
10g.119672338C=CA1940193208BAG3c.591C= (p.Gly197=)
c.417C= (p.Gly139=)
10g.119672338C>GCA471739209BAG3c.591C>G (p.Gly197=)
c.417C>G (p.Gly139=)
10g.119672338C>TCA471739210BAG3c.591C>T (p.Gly197=)
c.417C>T (p.Gly139=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.119672339A>CCA378295396BAG3c.592A>C (p.Ser198Arg)
c.418A>C (p.Ser140Arg)
10g.119672339A>GCA378295397BAG3c.592A>G (p.Ser198Gly)
c.418A>G (p.Ser140Gly)
10g.119672339A>TCA378295398BAG3c.592A>T (p.Ser198Cys)
c.418A>T (p.Ser140Cys)
ClinVar
10g.119672340G>ACA378295401BAG3c.593G>A (p.Ser198Asn)
c.419G>A (p.Ser140Asn)
10g.119672340G>CCA378295399BAG3c.593G>C (p.Ser198Thr)
c.419G>C (p.Ser140Thr)
10g.119672340G>TCA378295400BAG3c.593G>T (p.Ser198Ile)
c.419G>T (p.Ser140Ile)
10g.119672341T>ACA378295402BAG3c.594T>A (p.Ser198Arg)
c.420T>A (p.Ser140Arg)
10g.119672341T>CCA471739211BAG3c.594T>C (p.Ser198=)
c.420T>C (p.Ser140=)
10g.119672341T>GCA378295403BAG3c.594T>G (p.Ser198Arg)
c.420T>G (p.Ser140Arg)
10g.119672342C>ACA378295404BAG3c.595C>A (p.His199Asn)
c.421C>A (p.His141Asn)
10g.119672342C=CA1940193212BAG3c.595C= (p.His199=)
c.421C= (p.His141=)
10g.119672342C>GCA378295405BAG3c.595C>G (p.His199Asp)
c.421C>G (p.His141Asp)
10g.119672342C>TCA5716375BAG3c.595C>T (p.His199Tyr)
c.421C>T (p.His141Tyr)
dbSNP ExAC gnomAD v2 gnomAD v4
10g.119672343A>CCA378295406BAG3c.596A>C (p.His199Pro)
c.422A>C (p.His141Pro)
10g.119672343A>GCA378295407BAG3c.596A>G (p.His199Arg)
c.422A>G (p.His141Arg)
10g.119672343A>TCA378295408BAG3c.596A>T (p.His199Leu)
c.422A>T (p.His141Leu)
10g.119672344C>ACA378295409BAG3c.597C>A (p.His199Gln)
c.423C>A (p.His141Gln)
10g.119672344C=CA1940193216BAG3c.597C= (p.His199=)
c.423C= (p.His141=)
10g.119672344C>GCA378295410BAG3c.597C>G (p.His199Gln)
c.423C>G (p.His141Gln)
10g.119672344C>TCA5716376BAG3c.597C>T (p.His199=)
c.423C>T (p.His141=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119672345C>ACA378295413BAG3c.598C>A (p.Gln200Lys)
c.424C>A (p.Gln142Lys)
10g.119672345C>GCA378295412BAG3c.598C>G (p.Gln200Glu)
c.424C>G (p.Gln142Glu)
10g.119672345C>TCA378295411BAG3c.598C>T (p.Gln200Ter)
c.424C>T (p.Gln142Ter)
ClinVar dbSNP COSMIC
10g.119672346A=CA1940193218BAG3c.599A= (p.Gln200=)
c.425A= (p.Gln142=)
10g.119672346A>CCA378295414BAG3c.599A>C (p.Gln200Pro)
c.425A>C (p.Gln142Pro)
dbSNP gnomAD v2 gnomAD v4
10g.119672346A>GCA378295415BAG3c.599A>G (p.Gln200Arg)
c.425A>G (p.Gln142Arg)
dbSNP gnomAD v4
10g.119672346A>TCA378295416BAG3c.599A>T (p.Gln200Leu)
c.425A>T (p.Gln142Leu)
10g.119672347G>ACA471739744BAG3c.600G>A (p.Gln200=)
c.426G>A (p.Gln142=)
10g.119672347G>CCA5716377BAG3c.600G>C (p.Gln200His)
c.426G>C (p.Gln142His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
10g.119672347G=CA1940193219BAG3c.600G= (p.Gln200=)
c.426G= (p.Gln142=)
10g.119672347G>TCA378295417BAG3c.600G>T (p.Gln200His)
c.426G>T (p.Gln142His)
10g.119672348C>ACA378295418BAG3c.601C>A (p.Leu201Ile)
c.427C>A (p.Leu143Ile)
10g.119672348C>GCA378295419BAG3c.601C>G (p.Leu201Val)
c.427C>G (p.Leu143Val)
dbSNP gnomAD v4
10g.119672348C>TCA378295420BAG3c.601C>T (p.Leu201Phe)
c.427C>T (p.Leu143Phe)
gnomAD v4
10g.119672349T>ACA378295421BAG3c.602T>A (p.Leu201His)
c.428T>A (p.Leu143His)
10g.119672349T>CCA214221721BAG3c.602T>C (p.Leu201Pro)
c.428T>C (p.Leu143Pro)
dbSNP
10g.119672349T>GCA378295422BAG3c.602T>G (p.Leu201Arg)
c.428T>G (p.Leu143Arg)
dbSNP
10g.119672349T=CA1940193223BAG3c.602T= (p.Leu201=)
c.428T= (p.Leu143=)
10g.119672350C>ACA471739745BAG3c.603C>A (p.Leu201=)
c.429C>A (p.Leu143=)
10g.119672350C=CA1940193225BAG3c.603C= (p.Leu201=)
c.429C= (p.Leu143=)
10g.119672350C>GCA471739746BAG3c.603C>G (p.Leu201=)
c.429C>G (p.Leu143=)
dbSNP
10g.119672350C>TCA471739747BAG3c.603C>T (p.Leu201=)
c.429C>T (p.Leu143=)
10g.119672351C>ACA378295425BAG3c.604C>A (p.Pro202Thr)
c.430C>A (p.Pro144Thr)
10g.119672351C>GCA378295424BAG3c.604C>G (p.Pro202Ala)
c.430C>G (p.Pro144Ala)
10g.119672351C>TCA378295423BAG3c.604C>T (p.Pro202Ser)
c.430C>T (p.Pro144Ser)
10g.119672352C>ACA378295426BAG3c.605C>A (p.Pro202Gln)
c.431C>A (p.Pro144Gln)
10g.119672352C=CA1940193229BAG3c.605C= (p.Pro202=)
c.431C= (p.Pro144=)
10g.119672352C>GCA378295427BAG3c.605C>G (p.Pro202Arg)
c.431C>G (p.Pro144Arg)
10g.119672352C>TCA5716378BAG3c.605C>T (p.Pro202Leu)
c.431C>T (p.Pro144Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119672353G>ACA5716379BAG3c.606G>A (p.Pro202=)
c.432G>A (p.Pro144=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119672353G>CCA471739748BAG3c.606G>C (p.Pro202=)
c.432G>C (p.Pro144=)
dbSNP gnomAD v2 gnomAD v4
10g.119672353G=CA1940193232BAG3c.606G= (p.Pro202=)
c.432G= (p.Pro144=)
10g.119672353G>TCA282473BAG3c.606G>T (p.Pro202=)
c.432G>T (p.Pro144=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119672354C>ACA214221736BAG3c.607C>A (p.Arg203=)
c.433C>A (p.Arg145=)
ClinVar dbSNP gnomAD v3 gnomAD v4
10g.119672354C=CA1940193237BAG3c.607C= (p.Arg203=)
c.433C= (p.Arg145=)
10g.119672354C>GCA378295428BAG3c.607C>G (p.Arg203Gly)
c.433C>G (p.Arg145Gly)
gnomAD v4
10g.119672354C>TCA378295429BAG3c.607C>T (p.Arg203Trp)
c.433C>T (p.Arg145Trp)
ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC
10g.119672354dupCA16612935BAG3c.607dup (p.Arg203ProfsTer?)
c.433dup (p.Arg145ProfsTer?)
ClinVar dbSNP
10g.119672355G>ACA16605610BAG3c.608G>A (p.Arg203Gln)
c.434G>A (p.Arg145Gln)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.119672355G>CCA378295430BAG3c.608G>C (p.Arg203Pro)
c.434G>C (p.Arg145Pro)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.119672355G=CA1940193244BAG3c.608G= (p.Arg203=)
c.434G= (p.Arg145=)
10g.119672355G>TCA378295431BAG3c.608G>T (p.Arg203Leu)
c.434G>T (p.Arg145Leu)
gnomAD v4
10g.119672359delCA2573145589BAG3c.612del (p.Tyr205ThrfsTer6)
c.438del (p.Tyr147ThrfsTer6)
ClinVar dbSNP
10g.119672356G>ACA471739750BAG3c.609G>A (p.Arg203=)
c.435G>A (p.Arg145=)
10g.119672356G>CCA471739751BAG3c.609G>C (p.Arg203=)
c.435G>C (p.Arg145=)
ClinVar dbSNP
10g.119672356G=CA1940193246BAG3c.609G= (p.Arg203=)
c.435G= (p.Arg145=)
10g.119672356G>TCA471739749BAG3c.609G>T (p.Arg203=)
c.435G>T (p.Arg145=)
10g.119672357G>ACA378295432BAG3c.610G>A (p.Gly204Arg)
c.436G>A (p.Gly146Arg)
ClinVar dbSNP gnomAD v2 gnomAD v4
10g.119672357G>CCA378295433BAG3c.610G>C (p.Gly204Arg)
c.436G>C (p.Gly146Arg)
10g.119672357G=CA1940193249BAG3c.610G= (p.Gly204=)
c.436G= (p.Gly146=)
10g.119672357G>TCA378295434BAG3c.610G>T (p.Gly204Trp)
c.436G>T (p.Gly146Trp)
10g.119672358G>ACA378295435BAG3c.611G>A (p.Gly204Glu)
c.437G>A (p.Gly146Glu)
10g.119672358G>CCA378295436BAG3c.611G>C (p.Gly204Ala)
c.437G>C (p.Gly146Ala)
10g.119672358G=CA1940193250BAG3c.611G= (p.Gly204=)
c.437G= (p.Gly146=)
10g.119672358G>TCA5716380BAG3c.611G>T (p.Gly204Val)
c.437G>T (p.Gly146Val)
dbSNP ExAC gnomAD v2 gnomAD v4
10g.119672359G>ACA471739754BAG3c.612G>A (p.Gly204=)
c.438G>A (p.Gly146=)
ClinVar dbSNP
10g.119672359G>CCA471739753BAG3c.612G>C (p.Gly204=)
c.438G>C (p.Gly146=)
10g.119672359G>TCA471739752BAG3c.612G>T (p.Gly204=)
c.438G>T (p.Gly146=)
10g.119672359_119672360delinsGTCA1940193252BAG3c.612_613delinsGT (p.Gly204=)
c.438_439delinsGT (p.Gly146=)
10g.119672360delCA915948733BAG3c.613del (p.Tyr205ThrfsTer6)
c.439del (p.Tyr147ThrfsTer6)
10g.119672360T>ACA378295438BAG3c.613T>A (p.Tyr205Asn)
c.439T>A (p.Tyr147Asn)
10g.119672360T>CCA5716381BAG3c.613T>C (p.Tyr205His)
c.439T>C (p.Tyr147His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119672360T>GCA378295437BAG3c.613T>G (p.Tyr205Asp)
c.439T>G (p.Tyr147Asp)
dbSNP
10g.119672360T=CA1940193258BAG3c.613T= (p.Tyr205=)
c.439T= (p.Tyr147=)
10g.119672361A=CA1940193267BAG3c.614A= (p.Tyr205=)
c.440A= (p.Tyr147=)
10g.119672361A>CCA378295439BAG3c.614A>C (p.Tyr205Ser)
c.440A>C (p.Tyr147Ser)
10g.119672361A>GCA378295440BAG3c.614A>G (p.Tyr205Cys)
c.440A>G (p.Tyr147Cys)
gnomAD v4 COSMIC
10g.119672361A>TCA5716382BAG3c.614A>T (p.Tyr205Phe)
c.440A>T (p.Tyr147Phe)
dbSNP ExAC gnomAD v3 gnomAD v4
10g.119672362C>ACA378295441BAG3c.615C>A (p.Tyr205Ter)
c.441C>A (p.Tyr147Ter)
10g.119672362C=CA1940193269BAG3c.615C= (p.Tyr205=)
c.441C= (p.Tyr147=)
10g.119672362C>GCA378295442BAG3c.615C>G (p.Tyr205Ter)
c.441C>G (p.Tyr147Ter)
10g.119672362C>TCA214221744BAG3c.615C>T (p.Tyr205=)
c.441C>T (p.Tyr147=)
dbSNP
10g.119672363A=CA1940193279BAG3c.616A= (p.Ile206=)
c.442A= (p.Ile148=)
10g.119672363A>CCA5716383BAG3c.616A>C (p.Ile206Leu)
c.442A>C (p.Ile148Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119672363A>GCA237049BAG3c.616A>G (p.Ile206Val)
c.442A>G (p.Ile148Val)
ClinVar dbSNP gnomAD v4
10g.119672363A>TCA378295443BAG3c.616A>T (p.Ile206Phe)
c.442A>T (p.Ile148Phe)
gnomAD v4
10g.119672364T>ACA378295444BAG3c.617T>A (p.Ile206Asn)
c.443T>A (p.Ile148Asn)
10g.119672364T>CCA378295445BAG3c.617T>C (p.Ile206Thr)
c.443T>C (p.Ile148Thr)
10g.119672364T>GCA378295446BAG3c.617T>G (p.Ile206Ser)
c.443T>G (p.Ile148Ser)
10g.119672365C>ACA471739755BAG3c.618C>A (p.Ile206=)
c.444C>A (p.Ile148=)
10g.119672365C=CA1940193285BAG3c.618C= (p.Ile206=)
c.444C= (p.Ile148=)
10g.119672365C>GCA378295447BAG3c.618C>G (p.Ile206Met)
c.444C>G (p.Ile148Met)
ClinVar dbSNP
10g.119672365C>TCA471739756BAG3c.618C>T (p.Ile206=)
c.444C>T (p.Ile148=)
10g.119672366T>ACA378295448BAG3c.619T>A (p.Ser207Thr)
c.445T>A (p.Ser149Thr)
10g.119672366T>CCA378295449BAG3c.619T>C (p.Ser207Pro)
c.445T>C (p.Ser149Pro)
10g.119672366T>GCA378295450BAG3c.619T>G (p.Ser207Ala)
c.445T>G (p.Ser149Ala)
10g.119672367C>ACA378295451BAG3c.620C>A (p.Ser207Tyr)
c.446C>A (p.Ser149Tyr)
dbSNP
10g.119672367C=CA1940193289BAG3c.620C= (p.Ser207=)
c.446C= (p.Ser149=)
10g.119672367C>GCA378295452BAG3c.620C>G (p.Ser207Cys)
c.446C>G (p.Ser149Cys)
10g.119672367C>TCA5716384BAG3c.620C>T (p.Ser207Phe)
c.446C>T (p.Ser149Phe)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119672368C>ACA471739757BAG3c.621C>A (p.Ser207=)
c.447C>A (p.Ser149=)
10g.119672368C>GCA471739758BAG3c.621C>G (p.Ser207=)
c.447C>G (p.Ser149=)
10g.119672368C>TCA471739759BAG3c.621C>T (p.Ser207=)
c.447C>T (p.Ser149=)
10g.119672369A=CA1940193295BAG3c.622A= (p.Ile208=)
c.448A= (p.Ile150=)
10g.119672369A>CCA214221754BAG3c.622A>C (p.Ile208Leu)
c.448A>C (p.Ile150Leu)
ClinVar dbSNP
10g.119672369A>GCA378295453BAG3c.622A>G (p.Ile208Val)
c.448A>G (p.Ile150Val)
ClinVar dbSNP gnomAD v3 gnomAD v4
10g.119672369A>TCA378295454BAG3c.622A>T (p.Ile208Phe)
c.448A>T (p.Ile150Phe)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.119672370T>ACA378295455BAG3c.623T>A (p.Ile208Asn)
c.449T>A (p.Ile150Asn)
gnomAD v4
10g.119672370T>CCA378295456BAG3c.623T>C (p.Ile208Thr)
c.449T>C (p.Ile150Thr)
ClinVar dbSNP
10g.119672370T>GCA378295457BAG3c.623T>G (p.Ile208Ser)
c.449T>G (p.Ile150Ser)
10g.119672370T=CA1940193300BAG3c.623T= (p.Ile208=)
c.449T= (p.Ile150=)
10g.119672371T>ACA471739760BAG3c.624T>A (p.Ile208=)
c.450T>A (p.Ile150=)
10g.119672371T>CCA471739761BAG3c.624T>C (p.Ile208=)
c.450T>C (p.Ile150=)
10g.119672371T>GCA378295458BAG3c.624T>G (p.Ile208Met)
c.450T>G (p.Ile150Met)
COSMIC
10g.119672372C>ACA378295461BAG3c.625C>A (p.Pro209Thr)
c.451C>A (p.Pro151Thr)
10g.119672372C=CA1940193303BAG3c.625C= (p.Pro209=)
c.451C= (p.Pro151=)
10g.119672372C>GCA378295460BAG3c.625C>G (p.Pro209Ala)
c.451C>G (p.Pro151Ala)
ClinVar dbSNP
10g.119672372C>TCA378295459BAG3c.625C>T (p.Pro209Ser)
c.451C>T (p.Pro151Ser)
ClinVar dbSNP
10g.119672372_119672373delinsTTCA645568596BAG3c.625_626delinsTT (p.Pro209Leu)
c.451_452delinsTT (p.Pro151Leu)
COSMIC
10g.119672373C>ACA170913BAG3c.626C>A (p.Pro209Gln)
c.452C>A (p.Pro151Gln)
ClinVar dbSNP
10g.119672373C=CA1940193308BAG3c.626C= (p.Pro209=)
c.452C= (p.Pro151=)
10g.119672373C>GCA378295462BAG3c.626C>G (p.Pro209Arg)
c.452C>G (p.Pro151Arg)
10g.119672373C>TCA308228BAG3c.626C>T (p.Pro209Leu)
c.452C>T (p.Pro151Leu)
ClinVar dbSNP COSMIC
10g.119672374G>ACA5716385BAG3c.627G>A (p.Pro209=)
c.453G>A (p.Pro151=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119672374G>CCA471739762BAG3c.627G>C (p.Pro209=)
c.453G>C (p.Pro151=)
ClinVar dbSNP
10g.119672374G=CA1940193313BAG3c.627G= (p.Pro209=)
c.453G= (p.Pro151=)
10g.119672374G>TCA471739763BAG3c.627G>T (p.Pro209=)
c.453G>T (p.Pro151=)
dbSNP gnomAD v2 gnomAD v4
10g.119672375G>ACA378295463BAG3c.628G>A (p.Val210Met)
c.454G>A (p.Val152Met)
10g.119672375G>CCA378295464BAG3c.628G>C (p.Val210Leu)
c.454G>C (p.Val152Leu)
ClinVar gnomAD v4
10g.119672375G>TCA378295465BAG3c.628G>T (p.Val210Leu)
c.454G>T (p.Val152Leu)
ClinVar dbSNP
10g.119672376T>ACA378295466BAG3c.629T>A (p.Val210Glu)
c.455T>A (p.Val152Glu)
10g.119672376T>CCA378295467BAG3c.629T>C (p.Val210Ala)
c.455T>C (p.Val152Ala)
gnomAD v4
10g.119672376T>GCA378295468BAG3c.629T>G (p.Val210Gly)
c.455T>G (p.Val152Gly)
10g.119672377G>ACA471739766BAG3c.630G>A (p.Val210=)
c.456G>A (p.Val152=)
10g.119672377G>CCA471739764BAG3c.630G>C (p.Val210=)
c.456G>C (p.Val152=)
10g.119672377G>TCA471739765BAG3c.630G>T (p.Val210=)
c.456G>T (p.Val152=)
10g.119672378A>CCA378295469BAG3c.631A>C (p.Ile211Leu)
c.457A>C (p.Ile153Leu)
10g.119672378A>GCA378295470BAG3c.631A>G (p.Ile211Val)
c.457A>G (p.Ile153Val)
ClinVar
10g.119672378A>TCA378295471BAG3c.631A>T (p.Ile211Leu)
c.457A>T (p.Ile153Leu)
ClinVar
10g.119672379T>ACA378295474BAG3c.632T>A (p.Ile211Lys)
c.458T>A (p.Ile153Lys)
10g.119672379T>CCA378295472BAG3c.632T>C (p.Ile211Thr)
c.458T>C (p.Ile153Thr)
10g.119672379T>GCA378295473BAG3c.632T>G (p.Ile211Arg)
c.458T>G (p.Ile153Arg)
10g.119672380A>CCA471739768BAG3c.633A>C (p.Ile211=)
c.459A>C (p.Ile153=)
10g.119672380A>GCA378295475BAG3c.633A>G (p.Ile211Met)
c.459A>G (p.Ile153Met)
10g.119672380A>TCA471739767BAG3c.633A>T (p.Ile211=)
c.459A>T (p.Ile153=)
10g.119672381C>ACA378295476BAG3c.634C>A (p.His212Asn)
c.460C>A (p.His154Asn)
ClinVar dbSNP gnomAD v4
10g.119672381C=CA1940193322BAG3c.634C= (p.His212=)
c.460C= (p.His154=)
10g.119672381C>GCA378295477BAG3c.634C>G (p.His212Asp)
c.460C>G (p.His154Asp)
10g.119672381C>TCA5716386BAG3c.634C>T (p.His212Tyr)
c.460C>T (p.His154Tyr)
dbSNP ExAC gnomAD v2
10g.119672382A>CCA378295478BAG3c.635A>C (p.His212Pro)
c.461A>C (p.His154Pro)
10g.119672382A>GCA378295479BAG3c.635A>G (p.His212Arg)
c.461A>G (p.His154Arg)
10g.119672382A>TCA378295480BAG3c.635A>T (p.His212Leu)
c.461A>T (p.His154Leu)
10g.119672383C>ACA378295481BAG3c.636C>A (p.His212Gln)
c.462C>A (p.His154Gln)
10g.119672383C=CA1940193327BAG3c.636C= (p.His212=)
c.462C= (p.His154=)
10g.119672383C>GCA378295482BAG3c.636C>G (p.His212Gln)
c.462C>G (p.His154Gln)
dbSNP gnomAD v3 gnomAD v4 COSMIC
10g.119672383C>TCA5716387BAG3c.636C>T (p.His212=)
c.462C>T (p.His154=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119672384G>ACA378295483BAG3c.637G>A (p.Glu213Lys)
c.463G>A (p.Glu155Lys)
ClinVar dbSNP gnomAD v2 gnomAD v4
10g.119672384G>CCA378295484BAG3c.637G>C (p.Glu213Gln)
c.463G>C (p.Glu155Gln)
10g.119672384G=CA1940193333BAG3c.637G= (p.Glu213=)
c.463G= (p.Glu155=)
10g.119672384G>TCA378295485BAG3c.637G>T (p.Glu213Ter)
c.463G>T (p.Glu155Ter)
10g.119672385A>CCA378295487BAG3c.638A>C (p.Glu213Ala)
c.464A>C (p.Glu155Ala)
10g.119672385A>GCA378295488BAG3c.638A>G (p.Glu213Gly)
c.464A>G (p.Glu155Gly)
10g.119672385A>TCA378295486BAG3c.638A>T (p.Glu213Val)
c.464A>T (p.Glu155Val)
10g.119672388_119672414delCA2580082424BAG3c.641_667del (p.Gln214_Gln222del)
c.467_493del (p.Gln156_Gln164del)
ClinVar

Number of alleles fetched