Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.119672256_119677283delCA1139532250BAG3c.509_*1del
10g.119672506T>ACA378295747BAG3c.759T>A (p.Asp253Glu)
c.585T>A (p.Asp195Glu)
10g.119672506T>CCA471740052BAG3c.759T>C (p.Asp253=)
c.585T>C (p.Asp195=)
10g.119672506T>GCA378295748BAG3c.759T>G (p.Asp253Glu)
c.585T>G (p.Asp195Glu)
10g.119672507G>ACA378295751BAG3c.760G>A (p.Asp254Asn)
c.586G>A (p.Asp196Asn)
10g.119672507G>CCA378295749BAG3c.760G>C (p.Asp254His)
c.586G>C (p.Asp196His)
10g.119672507G>TCA378295750BAG3c.760G>T (p.Asp254Tyr)
c.586G>T (p.Asp196Tyr)
10g.119672508A>CCA378295752BAG3c.761A>C (p.Asp254Ala)
c.587A>C (p.Asp196Ala)
10g.119672508A>GCA378295753BAG3c.761A>G (p.Asp254Gly)
c.587A>G (p.Asp196Gly)
 ClinVar dbSNP
10g.119672508A>TCA378295754BAG3c.761A>T (p.Asp254Val)
c.587A>T (p.Asp196Val)
 gnomAD v4
10g.119672509C>ACA378295755BAG3c.762C>A (p.Asp254Glu)
c.588C>A (p.Asp196Glu)
10g.119672509C>GCA378295756BAG3c.762C>G (p.Asp254Glu)
c.588C>G (p.Asp196Glu)
10g.119672509C>TCA471740060BAG3c.762C>T (p.Asp254=)
c.588C>T (p.Asp196=)
10g.119672510T>ACA378295757BAG3c.763T>A (p.Trp255Arg)
c.589T>A (p.Trp197Arg)
10g.119672510T>CCA378295759BAG3c.763T>C (p.Trp255Arg)
c.589T>C (p.Trp197Arg)
10g.119672510T>GCA378295758BAG3c.763T>G (p.Trp255Gly)
c.589T>G (p.Trp197Gly)
10g.119672511G>ACA378295760BAG3c.764G>A (p.Trp255Ter)
c.590G>A (p.Trp197Ter)
 ClinVar
10g.119672511G>CCA378295761BAG3c.764G>C (p.Trp255Ser)
c.590G>C (p.Trp197Ser)
10g.119672511G>TCA378295762BAG3c.764G>T (p.Trp255Leu)
c.590G>T (p.Trp197Leu)
10g.119672512G>ACA378295763BAG3c.765G>A (p.Trp255Ter)
c.591G>A (p.Trp197Ter)
 ClinVar dbSNP
10g.119672512G>CCA378295764BAG3c.765G>C (p.Trp255Cys)
c.591G>C (p.Trp197Cys)
10g.119672512G=CA1940193429BAG3c.765G= (p.Trp255=)
c.591G= (p.Trp197=)
10g.119672512G>TCA378295765BAG3c.765G>T (p.Trp255Cys)
c.591G>T (p.Trp197Cys)
10g.119672513G>ACA378295766BAG3c.766G>A (p.Glu256Lys)
c.592G>A (p.Glu198Lys)
10g.119672513G>CCA378295767BAG3c.766G>C (p.Glu256Gln)
c.592G>C (p.Glu198Gln)
10g.119672513G>TCA378295768BAG3c.766G>T (p.Glu256Ter)
c.592G>T (p.Glu198Ter)
 ClinVar dbSNP
10g.119672514A>CCA378295769BAG3c.767A>C (p.Glu256Ala)
c.593A>C (p.Glu198Ala)
10g.119672514A>GCA378295770BAG3c.767A>G (p.Glu256Gly)
c.593A>G (p.Glu198Gly)
10g.119672514A>TCA378295771BAG3c.767A>T (p.Glu256Val)
c.593A>T (p.Glu198Val)
10g.119672515G>ACA471740075BAG3c.768G>A (p.Glu256=)
c.594G>A (p.Glu198=)
 ClinVar dbSNP
10g.119672515G>CCA378295773BAG3c.768G>C (p.Glu256Asp)
c.594G>C (p.Glu198Asp)
10g.119672515G>TCA378295772BAG3c.768G>T (p.Glu256Asp)
c.594G>T (p.Glu198Asp)
10g.119672520_119672525delCA2611160109BAG3c.773_778del (p.Arg258_Pro259del)
c.599_604del (p.Arg200_Pro201del)
 gnomAD v4
10g.119672516C>ACA378295774BAG3c.769C>A (p.Pro257Thr)
c.595C>A (p.Pro199Thr)
10g.119672516C>GCA378295776BAG3c.769C>G (p.Pro257Ala)
c.595C>G (p.Pro199Ala)
10g.119672516C>TCA378295775BAG3c.769C>T (p.Pro257Ser)
c.595C>T (p.Pro199Ser)
 gnomAD v4
10g.119672517C>ACA378295777BAG3c.770C>A (p.Pro257His)
c.596C>A (p.Pro199His)
10g.119672517C=CA1940193431BAG3c.770C= (p.Pro257=)
c.596C= (p.Pro199=)
10g.119672517C>GCA378295778BAG3c.770C>G (p.Pro257Arg)
c.596C>G (p.Pro199Arg)
10g.119672517C>TCA5716406BAG3c.770C>T (p.Pro257Leu)
c.596C>T (p.Pro199Leu)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119672518C>ACA471740082BAG3c.771C>A (p.Pro257=)
c.597C>A (p.Pro199=)
10g.119672518C=CA1940193432BAG3c.771C= (p.Pro257=)
c.597C= (p.Pro199=)
10g.119672518C>GCA5716407BAG3c.771C>G (p.Pro257=)
c.597C>G (p.Pro199=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
10g.119672518C>TCA175294BAG3c.771C>T (p.Pro257=)
c.597C>T (p.Pro199=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119672519C>ACA471740089BAG3c.772C>A (p.Arg258=)
c.598C>A (p.Arg200=)
10g.119672519C=CA1940193433BAG3c.772C= (p.Arg258=)
c.598C= (p.Arg200=)
10g.119672519C>GCA378295779BAG3c.772C>G (p.Arg258Gly)
c.598C>G (p.Arg200Gly)
10g.119672519C>TCA135025BAG3c.772C>T (p.Arg258Trp)
c.598C>T (p.Arg200Trp)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
10g.119672520G>ACA5716408BAG3c.773G>A (p.Arg258Gln)
c.599G>A (p.Arg200Gln)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
10g.119672520G>CCA378295780BAG3c.773G>C (p.Arg258Pro)
c.599G>C (p.Arg200Pro)
10g.119672520G=CA1940193434BAG3c.773G= (p.Arg258=)
c.599G= (p.Arg200=)
10g.119672520G>TCA378295781BAG3c.773G>T (p.Arg258Leu)
c.599G>T (p.Arg200Leu)
10g.119672521G>ACA471740099BAG3c.774G>A (p.Arg258=)
c.600G>A (p.Arg200=)
10g.119672521G>CCA471740097BAG3c.774G>C (p.Arg258=)
c.600G>C (p.Arg200=)
10g.119672521G>TCA471740093BAG3c.774G>T (p.Arg258=)
c.600G>T (p.Arg200=)
10g.119672522C>ACA378295782BAG3c.775C>A (p.Pro259Thr)
c.601C>A (p.Pro201Thr)
10g.119672522C=CA1940193435BAG3c.775C= (p.Pro259=)
c.601C= (p.Pro201=)
10g.119672522C>GCA378295783BAG3c.775C>G (p.Pro259Ala)
c.601C>G (p.Pro201Ala)
10g.119672522C>TCA214221961BAG3c.775C>T (p.Pro259Ser)
c.601C>T (p.Pro201Ser)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.119672523C>ACA378295784BAG3c.776C>A (p.Pro259His)
c.602C>A (p.Pro201His)
10g.119672523C=CA1940193438BAG3c.776C= (p.Pro259=)
c.602C= (p.Pro201=)
10g.119672523C>GCA378295785BAG3c.776C>G (p.Pro259Arg)
c.602C>G (p.Pro201Arg)
10g.119672523C>TCA5716409BAG3c.776C>T (p.Pro259Leu)
c.602C>T (p.Pro201Leu)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
10g.119672524C>ACA471740108BAG3c.777C>A (p.Pro259=)
c.603C>A (p.Pro201=)
10g.119672524C=CA1940193441BAG3c.777C= (p.Pro259=)
c.603C= (p.Pro201=)
10g.119672524C>GCA471740110BAG3c.777C>G (p.Pro259=)
c.603C>G (p.Pro201=)
10g.119672524C>TCA471740113BAG3c.777C>T (p.Pro259=)
c.603C>T (p.Pro201=)
 ClinVar dbSNP
10g.119672525C>ACA378295786BAG3c.778C>A (p.Leu260Met)
c.604C>A (p.Leu202Met)
10g.119672525C=CA1940193443BAG3c.778C= (p.Leu260=)
c.604C= (p.Leu202=)
10g.119672525C>GCA378295787BAG3c.778C>G (p.Leu260Val)
c.604C>G (p.Leu202Val)
10g.119672525C>TCA471740116BAG3c.778C>T (p.Leu260=)
c.604C>T (p.Leu202=)
 dbSNP
10g.119672526T>ACA378295788BAG3c.779T>A (p.Leu260Gln)
c.605T>A (p.Leu202Gln)
10g.119672526T>CCA378295789BAG3c.779T>C (p.Leu260Pro)
c.605T>C (p.Leu202Pro)
 gnomAD v4
10g.119672526T>GCA378295790BAG3c.779T>G (p.Leu260Arg)
c.605T>G (p.Leu202Arg)
10g.119672526_119672541delinsTGCGGGCGGCATCCCCCA1940193445BAG3c.779_794delinsTGCGGGCGGCATCCCC (p.Leu260=)
c.605_620delinsTGCGGGCGGCATCCCC (p.Leu202=)
10g.119672527G>ACA471740121BAG3c.780G>A (p.Leu260=)
c.606G>A (p.Leu202=)
 ClinVar
10g.119672527G>CCA471740126BAG3c.780G>C (p.Leu260=)
c.606G>C (p.Leu202=)
10g.119672527G>TCA471740125BAG3c.780G>T (p.Leu260=)
c.606G>T (p.Leu202=)
10g.119672528_119672533delCA2611160110BAG3c.781_786del (p.Arg261_Ala262del)
c.607_612del (p.Arg203_Ala204del)
 gnomAD v4
10g.119672528_119672542delCA1940193446BAG3c.781_795del (p.Arg261_Pro265del)
c.607_621del (p.Arg203_Pro207del)
 ClinVar dbSNP gnomAD v3 gnomAD v4
10g.119672528C>ACA471740127BAG3c.781C>A (p.Arg261=)
c.607C>A (p.Arg203=)
 gnomAD v4
10g.119672528C=CA1940193448BAG3c.781C= (p.Arg261=)
c.607C= (p.Arg203=)
10g.119672528C>GCA378295791BAG3c.781C>G (p.Arg261Gly)
c.607C>G (p.Arg203Gly)
 gnomAD v4
10g.119672528C>TCA175297BAG3c.781C>T (p.Arg261Trp)
c.607C>T (p.Arg203Trp)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
10g.119672529G>ACA5716410BAG3c.782G>A (p.Arg261Gln)
c.608G>A (p.Arg203Gln)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
10g.119672529G>CCA378295792BAG3c.782G>C (p.Arg261Pro)
c.608G>C (p.Arg203Pro)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.119672529G=CA1940193449BAG3c.782G= (p.Arg261=)
c.608G= (p.Arg203=)
10g.119672529G>TCA378295793BAG3c.782G>T (p.Arg261Leu)
c.608G>T (p.Arg203Leu)
10g.119672530G>ACA471740130BAG3c.783G>A (p.Arg261=)
c.609G>A (p.Arg203=)
 gnomAD v4
10g.119672530G>CCA471740133BAG3c.783G>C (p.Arg261=)
c.609G>C (p.Arg203=)
10g.119672530G>TCA471740135BAG3c.783G>T (p.Arg261=)
c.609G>T (p.Arg203=)
10g.119672531G>ACA10581155BAG3c.784G>A (p.Ala262Thr)
c.610G>A (p.Ala204Thr)
 ClinVar dbSNP gnomAD v4
10g.119672531G>CCA378295795BAG3c.784G>C (p.Ala262Pro)
c.610G>C (p.Ala204Pro)
10g.119672531G=CA1940193450BAG3c.784G= (p.Ala262=)
c.610G= (p.Ala204=)
10g.119672531G>TCA378295794BAG3c.784G>T (p.Ala262Ser)
c.610G>T (p.Ala204Ser)
 gnomAD v4
10g.119672532C>ACA378295796BAG3c.785C>A (p.Ala262Glu)
c.611C>A (p.Ala204Glu)
10g.119672532C=CA1940193451BAG3c.785C= (p.Ala262=)
c.611C= (p.Ala204=)
10g.119672532C>GCA378295797BAG3c.785C>G (p.Ala262Gly)
c.611C>G (p.Ala204Gly)
10g.119672532C>TCA135031BAG3c.785C>T (p.Ala262Val)
c.611C>T (p.Ala204Val)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119672533G>ACA5716411BAG3c.786G>A (p.Ala262=)
c.612G>A (p.Ala204=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119672533G>CCA471740140BAG3c.786G>C (p.Ala262=)
c.612G>C (p.Ala204=)
10g.119672533G=CA1940193452BAG3c.786G= (p.Ala262=)
c.612G= (p.Ala204=)
10g.119672533G>TCA471740141BAG3c.786G>T (p.Ala262=)
c.612G>T (p.Ala204=)
10g.119672534G>ACA5716412BAG3c.787G>A (p.Ala263Thr)
c.613G>A (p.Ala205Thr)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
10g.119672534G>CCA378295798BAG3c.787G>C (p.Ala263Pro)
c.613G>C (p.Ala205Pro)
10g.119672534G=CA1940193454BAG3c.787G= (p.Ala263=)
c.613G= (p.Ala205=)
10g.119672534G>TCA378295799BAG3c.787G>T (p.Ala263Ser)
c.613G>T (p.Ala205Ser)
10g.119672535C>ACA378295800BAG3c.788C>A (p.Ala263Glu)
c.614C>A (p.Ala205Glu)
10g.119672535C=CA1940193455BAG3c.788C= (p.Ala263=)
c.614C= (p.Ala205=)
10g.119672535C>GCA378295801BAG3c.788C>G (p.Ala263Gly)
c.614C>G (p.Ala205Gly)
 gnomAD v4
10g.119672535C>TCA16605990BAG3c.788C>T (p.Ala263Val)
c.614C>T (p.Ala205Val)
 ClinVar dbSNP gnomAD v4
10g.119672536A>CCA471740146BAG3c.789A>C (p.Ala263=)
c.615A>C (p.Ala205=)
10g.119672536A>GCA471740148BAG3c.789A>G (p.Ala263=)
c.615A>G (p.Ala205=)
10g.119672536A>TCA471740144BAG3c.789A>T (p.Ala263=)
c.615A>T (p.Ala205=)
 ClinVar dbSNP gnomAD v4
10g.119672537T>ACA378295802BAG3c.790T>A (p.Ser264Thr)
c.616T>A (p.Ser206Thr)
10g.119672537T>CCA378295803BAG3c.790T>C (p.Ser264Pro)
c.616T>C (p.Ser206Pro)
10g.119672537T>GCA378295804BAG3c.790T>G (p.Ser264Ala)
c.616T>G (p.Ser206Ala)
10g.119672538C>ACA378295807BAG3c.791C>A (p.Ser264Tyr)
c.617C>A (p.Ser206Tyr)
10g.119672538C>GCA378295805BAG3c.791C>G (p.Ser264Cys)
c.617C>G (p.Ser206Cys)
10g.119672538C>TCA378295806BAG3c.791C>T (p.Ser264Phe)
c.617C>T (p.Ser206Phe)
10g.119672539C>ACA471740154BAG3c.792C>A (p.Ser264=)
c.618C>A (p.Ser206=)
10g.119672539C=CA1940193456BAG3c.792C= (p.Ser264=)
c.618C= (p.Ser206=)
10g.119672539C>GCA471740156BAG3c.792C>G (p.Ser264=)
c.618C>G (p.Ser206=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.119672539C>TCA471740157BAG3c.792C>T (p.Ser264=)
c.618C>T (p.Ser206=)
 ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC
10g.119672540C>ACA378295808BAG3c.793C>A (p.Pro265Thr)
c.619C>A (p.Pro207Thr)
10g.119672540C>GCA378295809BAG3c.793C>G (p.Pro265Ala)
c.619C>G (p.Pro207Ala)
10g.119672540C>TCA378295810BAG3c.793C>T (p.Pro265Ser)
c.619C>T (p.Pro207Ser)
10g.119672541C>ACA378295811BAG3c.794C>A (p.Pro265Gln)
c.620C>A (p.Pro207Gln)
10g.119672541C=CA1940193457BAG3c.794C= (p.Pro265=)
c.620C= (p.Pro207=)
10g.119672541C>GCA378295812BAG3c.794C>G (p.Pro265Arg)
c.620C>G (p.Pro207Arg)
10g.119672541C>TCA5716413BAG3c.794C>T (p.Pro265Leu)
c.620C>T (p.Pro207Leu)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
10g.119672542G>ACA5716414BAG3c.795G>A (p.Pro265=)
c.621G>A (p.Pro207=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119672542G>CCA471740160BAG3c.795G>C (p.Pro265=)
c.621G>C (p.Pro207=)
10g.119672542G=CA1940193458BAG3c.795G= (p.Pro265=)
c.621G= (p.Pro207=)
10g.119672542G>TCA471740162BAG3c.795G>T (p.Pro265=)
c.621G>T (p.Pro207=)
10g.119672543T>ACA378295813BAG3c.796T>A (p.Phe266Ile)
c.622T>A (p.Phe208Ile)
10g.119672543T>CCA378295814BAG3c.796T>C (p.Phe266Leu)
c.622T>C (p.Phe208Leu)
10g.119672543T>GCA378295815BAG3c.796T>G (p.Phe266Val)
c.622T>G (p.Phe208Val)
10g.119672544T>ACA378295816BAG3c.797T>A (p.Phe266Tyr)
c.623T>A (p.Phe208Tyr)
10g.119672544T>CCA378295817BAG3c.797T>C (p.Phe266Ser)
c.623T>C (p.Phe208Ser)
10g.119672544T>GCA378295818BAG3c.797T>G (p.Phe266Cys)
c.623T>G (p.Phe208Cys)
10g.119672545C>ACA378295820BAG3c.798C>A (p.Phe266Leu)
c.624C>A (p.Phe208Leu)
10g.119672545C>GCA378295819BAG3c.798C>G (p.Phe266Leu)
c.624C>G (p.Phe208Leu)
 gnomAD v4
10g.119672545C>TCA471740165BAG3c.798C>T (p.Phe266=)
c.624C>T (p.Phe208=)
 ClinVar
10g.119672546A>CCA471740166BAG3c.799A>C (p.Arg267=)
c.625A>C (p.Arg209=)
10g.119672546A>GCA378295821BAG3c.799A>G (p.Arg267Gly)
c.625A>G (p.Arg209Gly)
10g.119672546A>TCA378295822BAG3c.799A>T (p.Arg267Trp)
c.625A>T (p.Arg209Trp)
10g.119672547G>ACA378295823BAG3c.800G>A (p.Arg267Lys)
c.626G>A (p.Arg209Lys)
10g.119672547G>CCA378295825BAG3c.800G>C (p.Arg267Thr)
c.626G>C (p.Arg209Thr)
10g.119672547G>TCA378295824BAG3c.800G>T (p.Arg267Met)
c.626G>T (p.Arg209Met)
10g.119672548G>ACA471740170BAG3c.801G>A (p.Arg267=)
c.627G>A (p.Arg209=)
10g.119672548G>CCA378295826BAG3c.801G>C (p.Arg267Ser)
c.627G>C (p.Arg209Ser)
10g.119672548G>TCA378295827BAG3c.801G>T (p.Arg267Ser)
c.627G>T (p.Arg209Ser)
 ClinVar dbSNP
10g.119672548_119672549insCCCA2506671054BAG3c.801_802insCC (p.Ser268ProfsTer?)
c.627_628insCC (p.Ser210ProfsTer?)
10g.119672549T>ACA378295828BAG3c.802T>A (p.Ser268Thr)
c.628T>A (p.Ser210Thr)
10g.119672549T>CCA5716415BAG3c.802T>C (p.Ser268Pro)
c.628T>C (p.Ser210Pro)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
10g.119672549T>GCA378295829BAG3c.802T>G (p.Ser268Ala)
c.628T>G (p.Ser210Ala)
10g.119672549T=CA1940193459BAG3c.802T= (p.Ser268=)
c.628T= (p.Ser210=)
10g.119672550C>ACA378295830BAG3c.803C>A (p.Ser268Ter)
c.629C>A (p.Ser210Ter)
 ClinVar
10g.119672550C>GCA378295831BAG3c.803C>G (p.Ser268Ter)
c.629C>G (p.Ser210Ter)
10g.119672550C>TCA378295832BAG3c.803C>T (p.Ser268Leu)
c.629C>T (p.Ser210Leu)
10g.119672551A>CCA471740175BAG3c.804A>C (p.Ser268=)
c.630A>C (p.Ser210=)
10g.119672551A>GCA471740176BAG3c.804A>G (p.Ser268=)
c.630A>G (p.Ser210=)
 gnomAD v4
10g.119672551A>TCA471740177BAG3c.804A>T (p.Ser268=)
c.630A>T (p.Ser210=)
 ClinVar
10g.119672551_119672552delCA2562834606BAG3c.804_805del (p.Ser269CysfsTer?)
c.630_631del (p.Ser211CysfsTer?)
10g.119672552T>ACA378295833BAG3c.805T>A (p.Ser269Thr)
c.631T>A (p.Ser211Thr)
10g.119672552T>CCA378295834BAG3c.805T>C (p.Ser269Pro)
c.631T>C (p.Ser211Pro)
10g.119672552T>GCA378295835BAG3c.805T>G (p.Ser269Ala)
c.631T>G (p.Ser211Ala)
 gnomAD v4
10g.119672553C>ACA378295838BAG3c.806C>A (p.Ser269Tyr)
c.632C>A (p.Ser211Tyr)
10g.119672553C>GCA378295837BAG3c.806C>G (p.Ser269Cys)
c.632C>G (p.Ser211Cys)
10g.119672553C>TCA378295836BAG3c.806C>T (p.Ser269Phe)
c.632C>T (p.Ser211Phe)
 ClinVar COSMIC
10g.119672554T>ACA471740182BAG3c.807T>A (p.Ser269=)
c.633T>A (p.Ser211=)
 gnomAD v4
10g.119672554T>CCA471740183BAG3c.807T>C (p.Ser269=)
c.633T>C (p.Ser211=)
10g.119672554T>GCA471740185BAG3c.807T>G (p.Ser269=)
c.633T>G (p.Ser211=)
10g.119672555G>ACA378295839BAG3c.808G>A (p.Val270Ile)
c.634G>A (p.Val212Ile)
10g.119672555G>CCA378295840BAG3c.808G>C (p.Val270Leu)
c.634G>C (p.Val212Leu)
10g.119672555G>TCA378295841BAG3c.808G>T (p.Val270Phe)
c.634G>T (p.Val212Phe)
10g.119672556T>ACA378295842BAG3c.809T>A (p.Val270Asp)
c.635T>A (p.Val212Asp)
10g.119672556T>CCA378295843BAG3c.809T>C (p.Val270Ala)
c.635T>C (p.Val212Ala)
10g.119672556T>GCA378295844BAG3c.809T>G (p.Val270Gly)
c.635T>G (p.Val212Gly)
10g.119672557C>ACA471740191BAG3c.810C>A (p.Val270=)
c.636C>A (p.Val212=)
10g.119672557C>GCA471740192BAG3c.810C>G (p.Val270=)
c.636C>G (p.Val212=)
10g.119672557C>TCA471740190BAG3c.810C>T (p.Val270=)
c.636C>T (p.Val212=)
10g.119672558C>ACA378295845BAG3c.811C>A (p.Gln271Lys)
c.637C>A (p.Gln213Lys)
10g.119672558C>GCA378295846BAG3c.811C>G (p.Gln271Glu)
c.637C>G (p.Gln213Glu)
10g.119672558C>TCA378295847BAG3c.811C>T (p.Gln271Ter)
c.637C>T (p.Gln213Ter)
 ClinVar dbSNP
10g.119672559A>CCA378295848BAG3c.812A>C (p.Gln271Pro)
c.638A>C (p.Gln213Pro)
10g.119672559A>GCA378295849BAG3c.812A>G (p.Gln271Arg)
c.638A>G (p.Gln213Arg)
 gnomAD v4
10g.119672559A>TCA378295850BAG3c.812A>T (p.Gln271Leu)
c.638A>T (p.Gln213Leu)
10g.119672560G>ACA471740199BAG3c.813G>A (p.Gln271=)
c.639G>A (p.Gln213=)
10g.119672560G>CCA378295852BAG3c.813G>C (p.Gln271His)
c.639G>C (p.Gln213His)
10g.119672560G>TCA378295851BAG3c.813G>T (p.Gln271His)
c.639G>T (p.Gln213His)
10g.119672561G>ACA378295853BAG3c.814G>A (p.Gly272Ser)
c.640G>A (p.Gly214Ser)
 gnomAD v4
10g.119672561G>CCA378295854BAG3c.814G>C (p.Gly272Arg)
c.640G>C (p.Gly214Arg)
10g.119672561G>TCA378295855BAG3c.814G>T (p.Gly272Cys)
c.640G>T (p.Gly214Cys)
10g.119672562G>ACA378295856BAG3c.815G>A (p.Gly272Asp)
c.641G>A (p.Gly214Asp)
 ClinVar dbSNP gnomAD v4
10g.119672562G>CCA378295857BAG3c.815G>C (p.Gly272Ala)
c.641G>C (p.Gly214Ala)
10g.119672562G=CA1940193460BAG3c.815G= (p.Gly272=)
c.641G= (p.Gly214=)
10g.119672562G>TCA378295858BAG3c.815G>T (p.Gly272Val)
c.641G>T (p.Gly214Val)
 ClinVar dbSNP gnomAD v4
10g.119672563T>ACA471740205BAG3c.816T>A (p.Gly272=)
c.642T>A (p.Gly214=)
10g.119672563T>CCA471740206BAG3c.816T>C (p.Gly272=)
c.642T>C (p.Gly214=)
10g.119672563T>GCA471740207BAG3c.816T>G (p.Gly272=)
c.642T>G (p.Gly214=)
10g.119672564G>ACA378295861BAG3c.817G>A (p.Ala273Thr)
c.643G>A (p.Ala215Thr)
 gnomAD v4
10g.119672564G>CCA378295860BAG3c.817G>C (p.Ala273Pro)
c.643G>C (p.Ala215Pro)
10g.119672564G>TCA378295859BAG3c.817G>T (p.Ala273Ser)
c.643G>T (p.Ala215Ser)
10g.119672565C>ACA378295862BAG3c.818C>A (p.Ala273Glu)
c.644C>A (p.Ala215Glu)
10g.119672565C=CA1940193461BAG3c.818C= (p.Ala273=)
c.644C= (p.Ala215=)
10g.119672565C>GCA378295863BAG3c.818C>G (p.Ala273Gly)
c.644C>G (p.Ala215Gly)
10g.119672565C>TCA378295864BAG3c.818C>T (p.Ala273Val)
c.644C>T (p.Ala215Val)
 ClinVar dbSNP gnomAD v3 gnomAD v4
10g.119672566A=CA1940193462BAG3c.819A= (p.Ala273=)
c.645A= (p.Ala215=)
10g.119672566A>CCA471740211BAG3c.819A>C (p.Ala273=)
c.645A>C (p.Ala215=)
10g.119672566A>GCA471740213BAG3c.819A>G (p.Ala273=)
c.645A>G (p.Ala215=)
 ClinVar dbSNP
10g.119672566A>TCA471740214BAG3c.819A>T (p.Ala273=)
c.645A>T (p.Ala215=)
 COSMIC
10g.119672567T>ACA378295865BAG3c.820T>A (p.Ser274Thr)
c.646T>A (p.Ser216Thr)
10g.119672567T>CCA378295866BAG3c.820T>C (p.Ser274Pro)
c.646T>C (p.Ser216Pro)
10g.119672567T>GCA378295867BAG3c.820T>G (p.Ser274Ala)
c.646T>G (p.Ser216Ala)
10g.119672568C>ACA378295868BAG3c.821C>A (p.Ser274Ter)
c.647C>A (p.Ser216Ter)
 dbSNP gnomAD v4
10g.119672568C=CA1940193463BAG3c.821C= (p.Ser274=)
c.647C= (p.Ser216=)
10g.119672568C>GCA378295869BAG3c.821C>G (p.Ser274Trp)
c.647C>G (p.Ser216Trp)
10g.119672568C>TCA135034BAG3c.821C>T (p.Ser274Leu)
c.647C>T (p.Ser216Leu)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119672569G>ACA5716416BAG3c.822G>A (p.Ser274=)
c.648G>A (p.Ser216=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119672569G>CCA471740216BAG3c.822G>C (p.Ser274=)
c.648G>C (p.Ser216=)
 ClinVar dbSNP
10g.119672569G=CA1940193465BAG3c.822G= (p.Ser274=)
c.648G= (p.Ser216=)
10g.119672569G>TCA471740217BAG3c.822G>T (p.Ser274=)
c.648G>T (p.Ser216=)
 ClinVar dbSNP gnomAD v4
10g.119672570A=CA1940193466BAG3c.823A= (p.Ser275=)
c.649A= (p.Ser217=)
10g.119672570A>CCA378295870BAG3c.823A>C (p.Ser275Arg)
c.649A>C (p.Ser217Arg)
 dbSNP
10g.119672570A>GCA378295871BAG3c.823A>G (p.Ser275Gly)
c.649A>G (p.Ser217Gly)
10g.119672570A>TCA378295872BAG3c.823A>T (p.Ser275Cys)
c.649A>T (p.Ser217Cys)
10g.119672571delCA2499220173BAG3c.824del (p.Ser275ThrfsTer?)
c.650del (p.Ser217ThrfsTer?)
 ClinVar dbSNP
10g.119672571G>ACA378295873BAG3c.824G>A (p.Ser275Asn)
c.650G>A (p.Ser217Asn)
10g.119672571G>CCA378295874BAG3c.824G>C (p.Ser275Thr)
c.650G>C (p.Ser217Thr)
10g.119672571G>TCA378295875BAG3c.824G>T (p.Ser275Ile)
c.650G>T (p.Ser217Ile)
 COSMIC
10g.119672572C>ACA378295876BAG3c.825C>A (p.Ser275Arg)
c.651C>A (p.Ser217Arg)
10g.119672572C>GCA378295877BAG3c.825C>G (p.Ser275Arg)
c.651C>G (p.Ser217Arg)
10g.119672572C>TCA471740223BAG3c.825C>T (p.Ser275=)
c.651C>T (p.Ser217=)
 gnomAD v4
10g.119672573C>ACA471740224BAG3c.826C>A (p.Arg276=)
c.652C>A (p.Arg218=)
10g.119672573C=CA1940193467BAG3c.826C= (p.Arg276=)
c.652C= (p.Arg218=)
10g.119672573C>GCA378295878BAG3c.826C>G (p.Arg276Gly)
c.652C>G (p.Arg218Gly)
10g.119672573C>TCA5716417BAG3c.826C>T (p.Arg276Trp)
c.652C>T (p.Arg218Trp)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119672574G>ACA5716418BAG3c.827G>A (p.Arg276Gln)
c.653G>A (p.Arg218Gln)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119672574G>CCA378295880BAG3c.827G>C (p.Arg276Pro)
c.653G>C (p.Arg218Pro)
10g.119672574G=CA1940193469BAG3c.827G= (p.Arg276=)
c.653G= (p.Arg218=)
10g.119672574G>TCA378295879BAG3c.827G>T (p.Arg276Leu)
c.653G>T (p.Arg218Leu)
10g.119672575G>ACA5716419BAG3c.828G>A (p.Arg276=)
c.654G>A (p.Arg218=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119672575G>CCA471740232BAG3c.828G>C (p.Arg276=)
c.654G>C (p.Arg218=)
10g.119672575G=CA1940193474BAG3c.828G= (p.Arg276=)
c.654G= (p.Arg218=)
10g.119672575G>TCA471740233BAG3c.828G>T (p.Arg276=)
c.654G>T (p.Arg218=)
10g.119672576G>ACA378295883BAG3c.829G>A (p.Glu277Lys)
c.655G>A (p.Glu219Lys)
10g.119672576G>CCA378295881BAG3c.829G>C (p.Glu277Gln)
c.655G>C (p.Glu219Gln)
10g.119672576G>TCA378295882BAG3c.829G>T (p.Glu277Ter)
c.655G>T (p.Glu219Ter)
10g.119672577A=CA1940193476BAG3c.830A= (p.Glu277=)
c.656A= (p.Glu219=)
10g.119672577A>CCA378295884BAG3c.830A>C (p.Glu277Ala)
c.656A>C (p.Glu219Ala)
10g.119672577A>GCA378295885BAG3c.830A>G (p.Glu277Gly)
c.656A>G (p.Glu219Gly)
10g.119672577A>TCA5716420BAG3c.830A>T (p.Glu277Val)
c.656A>T (p.Glu219Val)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119672578G>ACA471740240BAG3c.831G>A (p.Glu277=)
c.657G>A (p.Glu219=)
10g.119672578G>CCA378295886BAG3c.831G>C (p.Glu277Asp)
c.657G>C (p.Glu219Asp)
10g.119672578G>TCA378295887BAG3c.831G>T (p.Glu277Asp)
c.657G>T (p.Glu219Asp)
10g.119672579G>ACA378295888BAG3c.832G>A (p.Gly278Ser)
c.658G>A (p.Gly220Ser)
10g.119672579G>CCA378295889BAG3c.832G>C (p.Gly278Arg)
c.658G>C (p.Gly220Arg)
10g.119672579G>TCA378295890BAG3c.832G>T (p.Gly278Cys)
c.658G>T (p.Gly220Cys)
10g.119672580G>ACA5716421BAG3c.833G>A (p.Gly278Asp)
c.659G>A (p.Gly220Asp)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119672580G>CCA378295891BAG3c.833G>C (p.Gly278Ala)
c.659G>C (p.Gly220Ala)
10g.119672580G=CA1940193479BAG3c.833G= (p.Gly278=)
c.659G= (p.Gly220=)
10g.119672580G>TCA378295892BAG3c.833G>T (p.Gly278Val)
c.659G>T (p.Gly220Val)
 ClinVar
10g.119672581C>ACA471740246BAG3c.834C>A (p.Gly278=)
c.660C>A (p.Gly220=)
10g.119672581C>GCA471740247BAG3c.834C>G (p.Gly278=)
c.660C>G (p.Gly220=)
 ClinVar dbSNP gnomAD v4
10g.119672581C>TCA471740248BAG3c.834C>T (p.Gly278=)
c.660C>T (p.Gly220=)
10g.119672582T>ACA378295893BAG3c.835T>A (p.Ser279Thr)
c.661T>A (p.Ser221Thr)
10g.119672582T>CCA378295895BAG3c.835T>C (p.Ser279Pro)
c.661T>C (p.Ser221Pro)
 gnomAD v4
10g.119672582T>GCA378295894BAG3c.835T>G (p.Ser279Ala)
c.661T>G (p.Ser221Ala)
10g.119672583C>ACA214222103BAG3c.836C>A (p.Ser279Ter)
c.662C>A (p.Ser221Ter)
 ClinVar dbSNP
10g.119672583C=CA1940193483BAG3c.836C= (p.Ser279=)
c.662C= (p.Ser221=)
10g.119672583C>GCA378295896BAG3c.836C>G (p.Ser279Ter)
c.662C>G (p.Ser221Ter)
10g.119672583C>TCA5716422BAG3c.836C>T (p.Ser279Leu)
c.662C>T (p.Ser221Leu)
 ClinVar dbSNP ExAC gnomAD v3 gnomAD v4
10g.119672584A=CA1940193486BAG3c.837A= (p.Ser279=)
c.663A= (p.Ser221=)
10g.119672584A>CCA5716423BAG3c.837A>C (p.Ser279=)
c.663A>C (p.Ser221=)
 dbSNP ExAC gnomAD v2 gnomAD v4
10g.119672584A>GCA471740253BAG3c.837A>G (p.Ser279=)
c.663A>G (p.Ser221=)
10g.119672584A>TCA471740254BAG3c.837A>T (p.Ser279=)
c.663A>T (p.Ser221=)
10g.119672585C>ACA378295897BAG3c.838C>A (p.Pro280Thr)
c.664C>A (p.Pro222Thr)
10g.119672585C=CA1940193489BAG3c.838C= (p.Pro280=)
c.664C= (p.Pro222=)
10g.119672585C>GCA378295898BAG3c.838C>G (p.Pro280Ala)
c.664C>G (p.Pro222Ala)
10g.119672585C>TCA378295899BAG3c.838C>T (p.Pro280Ser)
c.664C>T (p.Pro222Ser)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.119672586C>ACA378295900BAG3c.839C>A (p.Pro280Gln)
c.665C>A (p.Pro222Gln)
10g.119672586C>GCA378295901BAG3c.839C>G (p.Pro280Arg)
c.665C>G (p.Pro222Arg)
10g.119672586C>TCA378295902BAG3c.839C>T (p.Pro280Leu)
c.665C>T (p.Pro222Leu)
10g.119672587A>CCA471740258BAG3c.840A>C (p.Pro280=)
c.666A>C (p.Pro222=)
10g.119672587A>GCA471740260BAG3c.840A>G (p.Pro280=)
c.666A>G (p.Pro222=)
10g.119672587A>TCA471740261BAG3c.840A>T (p.Pro280=)
c.666A>T (p.Pro222=)
10g.119672588G>ACA378295904BAG3c.841G>A (p.Ala281Thr)
c.667G>A (p.Ala223Thr)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.119672588G>CCA378295905BAG3c.841G>C (p.Ala281Pro)
c.667G>C (p.Ala223Pro)
10g.119672588G=CA1940193493BAG3c.841G= (p.Ala281=)
c.667G= (p.Ala223=)
10g.119672588G>TCA378295903BAG3c.841G>T (p.Ala281Ser)
c.667G>T (p.Ala223Ser)
 gnomAD v4
10g.119672589C>ACA378295906BAG3c.842C>A (p.Ala281Asp)
c.668C>A (p.Ala223Asp)
10g.119672589C>GCA378295907BAG3c.842C>G (p.Ala281Gly)
c.668C>G (p.Ala223Gly)
10g.119672589C>TCA378295908BAG3c.842C>T (p.Ala281Val)
c.668C>T (p.Ala223Val)
 gnomAD v4
10g.119672590C>ACA471740267BAG3c.843C>A (p.Ala281=)
c.669C>A (p.Ala223=)
10g.119672590C=CA1940193495BAG3c.843C= (p.Ala281=)
c.669C= (p.Ala223=)
10g.119672590C>GCA471740268BAG3c.843C>G (p.Ala281=)
c.669C>G (p.Ala223=)
 ClinVar
10g.119672590C>TCA214222112BAG3c.843C>T (p.Ala281=)
c.669C>T (p.Ala223=)
 ClinVar dbSNP gnomAD v4
10g.119672591A=CA1940193499BAG3c.844A= (p.Arg282=)
c.670A= (p.Arg224=)
10g.119672591A>CCA471740274BAG3c.844A>C (p.Arg282=)
c.670A>C (p.Arg224=)
10g.119672591A>GCA378295909BAG3c.844A>G (p.Arg282Gly)
c.670A>G (p.Arg224Gly)
 ClinVar dbSNP gnomAD v3 gnomAD v4
10g.119672591A>TCA378295910BAG3c.844A>T (p.Arg282Trp)
c.670A>T (p.Arg224Trp)
10g.119672592G>ACA378295911BAG3c.845G>A (p.Arg282Lys)
c.671G>A (p.Arg224Lys)
 COSMIC
10g.119672592G>CCA378295912BAG3c.845G>C (p.Arg282Thr)
c.671G>C (p.Arg224Thr)
10g.119672592G>TCA378295913BAG3c.845G>T (p.Arg282Met)
c.671G>T (p.Arg224Met)
10g.119672593G>ACA471740278BAG3c.846G>A (p.Arg282=)
c.672G>A (p.Arg224=)
 ClinVar
10g.119672593G>CCA378295914BAG3c.846G>C (p.Arg282Ser)
c.672G>C (p.Arg224Ser)
10g.119672593G>TCA378295915BAG3c.846G>T (p.Arg282Ser)
c.672G>T (p.Arg224Ser)
10g.119672594A>CCA378295916BAG3c.847A>C (p.Ser283Arg)
c.673A>C (p.Ser225Arg)
10g.119672594A>GCA378295918BAG3c.847A>G (p.Ser283Gly)
c.673A>G (p.Ser225Gly)
10g.119672594A>TCA378295919BAG3c.847A>T (p.Ser283Cys)
c.673A>T (p.Ser225Cys)
10g.119672595G>ACA378295924BAG3c.848G>A (p.Ser283Asn)
c.674G>A (p.Ser225Asn)
10g.119672595G>CCA378295923BAG3c.848G>C (p.Ser283Thr)
c.674G>C (p.Ser225Thr)
10g.119672595G>TCA378295921BAG3c.848G>T (p.Ser283Ile)
c.674G>T (p.Ser225Ile)
10g.119672596C>ACA378295926BAG3c.849C>A (p.Ser283Arg)
c.675C>A (p.Ser225Arg)
10g.119672596C>GCA378295928BAG3c.849C>G (p.Ser283Arg)
c.675C>G (p.Ser225Arg)
10g.119672596C>TCA471740287BAG3c.849C>T (p.Ser283=)
c.675C>T (p.Ser225=)
 gnomAD v4
10g.119672597A=CA1940193504BAG3c.850A= (p.Ser284=)
c.676A= (p.Ser226=)
10g.119672597A>CCA378295930BAG3c.850A>C (p.Ser284Arg)
c.676A>C (p.Ser226Arg)
 dbSNP gnomAD v2 gnomAD v4
10g.119672597A>GCA214222113BAG3c.850A>G (p.Ser284Gly)
c.676A>G (p.Ser226Gly)
 dbSNP gnomAD v3 gnomAD v4
10g.119672597A>TCA378295933BAG3c.850A>T (p.Ser284Cys)
c.676A>T (p.Ser226Cys)
10g.119672598G>ACA378295935BAG3c.851G>A (p.Ser284Asn)
c.677G>A (p.Ser226Asn)
10g.119672598G>CCA378295937BAG3c.851G>C (p.Ser284Thr)
c.677G>C (p.Ser226Thr)
10g.119672598G=CA1940193505BAG3c.851G= (p.Ser284=)
c.677G= (p.Ser226=)
10g.119672598G>TCA378295938BAG3c.851G>T (p.Ser284Ile)
c.677G>T (p.Ser226Ile)
 ClinVar gnomAD v4
10g.119672599C>ACA378295940BAG3c.852C>A (p.Ser284Arg)
c.678C>A (p.Ser226Arg)
10g.119672599C>GCA378295942BAG3c.852C>G (p.Ser284Arg)
c.678C>G (p.Ser226Arg)
10g.119672599C>TCA471740292BAG3c.852C>T (p.Ser284=)
c.678C>T (p.Ser226=)
 gnomAD v4
10g.119672602_119672606dupCA16042687BAG3c.855_859dup (p.Leu287ArgfsTer22)
c.681_685dup (p.Leu229ArgfsTer21)
c.855_859dup (p.Leu287ArgfsTer21)
 ClinVar dbSNP
10g.119672600A>CCA378295945BAG3c.853A>C (p.Thr285Pro)
c.679A>C (p.Thr227Pro)
10g.119672600A>GCA378295947BAG3c.853A>G (p.Thr285Ala)
c.679A>G (p.Thr227Ala)
 ClinVar
10g.119672600A>TCA378295949BAG3c.853A>T (p.Thr285Ser)
c.679A>T (p.Thr227Ser)
10g.119672601C>ACA378295954BAG3c.854C>A (p.Thr285Lys)
c.680C>A (p.Thr227Lys)
 gnomAD v4
10g.119672601C=CA1940193510BAG3c.854C= (p.Thr285=)
c.680C= (p.Thr227=)
10g.119672601C>GCA378295952BAG3c.854C>G (p.Thr285Arg)
c.680C>G (p.Thr227Arg)
10g.119672601C>TCA5716424BAG3c.854C>T (p.Thr285Met)
c.680C>T (p.Thr227Met)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
10g.119672602G>ACA308212BAG3c.855G>A (p.Thr285=)
c.681G>A (p.Thr227=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
10g.119672602G>CCA471634716BAG3c.855G>C (p.Thr285=)
c.681G>C (p.Thr227=)
10g.119672602G=CA1940193514BAG3c.855G= (p.Thr285=)
c.681G= (p.Thr227=)
10g.119672602G>TCA471634715BAG3c.855G>T (p.Thr285=)
c.681G>T (p.Thr227=)
10g.119672603C>ACA378295959BAG3c.856C>A (p.Pro286Thr)
c.682C>A (p.Pro228Thr)
10g.119672603C>GCA378295958BAG3c.856C>G (p.Pro286Ala)
c.682C>G (p.Pro228Ala)
10g.119672603C>TCA378295961BAG3c.856C>T (p.Pro286Ser)
c.682C>T (p.Pro228Ser)
10g.119672604C>ACA378295963BAG3c.857C>A (p.Pro286Gln)
c.683C>A (p.Pro228Gln)
10g.119672604C>GCA378295965BAG3c.857C>G (p.Pro286Arg)
c.683C>G (p.Pro228Arg)
10g.119672604C>TCA378295964BAG3c.857C>T (p.Pro286Leu)
c.683C>T (p.Pro228Leu)
 gnomAD v4
10g.119672605A=CA1940193519BAG3c.858A= (p.Pro286=)
c.684A= (p.Pro228=)
10g.119672605A>CCA471634717BAG3c.858A>C (p.Pro286=)
c.684A>C (p.Pro228=)
10g.119672605A>GCA5716425BAG3c.858A>G (p.Pro286=)
c.684A>G (p.Pro228=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
10g.119672605A>TCA471634718BAG3c.858A>T (p.Pro286=)
c.684A>T (p.Pro228=)
10g.119672606C>ACA378295968BAG3c.859C>A (p.Leu287Ile)
c.685C>A (p.Leu229Ile)
10g.119672606C>GCA378295970BAG3c.859C>G (p.Leu287Val)
c.685C>G (p.Leu229Val)
10g.119672606C>TCA378295972BAG3c.859C>T (p.Leu287Phe)
c.685C>T (p.Leu229Phe)

Number of alleles fetched