Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.119672256_119677283delCA1139532250BAG3c.509_*1del
10g.119672624A>CCA378296040BAG3c.877A>C (p.Ile293Leu)
c.703A>C (p.Ile235Leu)
10g.119672624A>GCA378296042BAG3c.877A>G (p.Ile293Val)
c.703A>G (p.Ile235Val)
10g.119672624A>TCA378296044BAG3c.877A>T (p.Ile293Phe)
c.703A>T (p.Ile235Phe)
10g.119672625T>ACA378296051BAG3c.878T>A (p.Ile293Asn)
c.704T>A (p.Ile235Asn)
10g.119672625T>CCA378296047BAG3c.878T>C (p.Ile293Thr)
c.704T>C (p.Ile235Thr)
10g.119672625T>GCA378296050BAG3c.878T>G (p.Ile293Ser)
c.704T>G (p.Ile235Ser)
10g.119672626C>ACA471634735BAG3c.879C>A (p.Ile293=)
c.705C>A (p.Ile235=)
10g.119672626C>GCA378296054BAG3c.879C>G (p.Ile293Met)
c.705C>G (p.Ile235Met)
10g.119672626C>TCA471634734BAG3c.879C>T (p.Ile293=)
c.705C>T (p.Ile235=)
10g.119672627C>ACA308230BAG3c.880C>A (p.Arg294Ser)
c.706C>A (p.Arg236Ser)
ClinVar dbSNP
10g.119672627C=CA1940193542BAG3c.880C= (p.Arg294=)
c.706C= (p.Arg236=)
10g.119672627C>GCA378296057BAG3c.880C>G (p.Arg294Gly)
c.706C>G (p.Arg236Gly)
gnomAD v4
10g.119672627C>TCA5716429BAG3c.880C>T (p.Arg294Cys)
c.706C>T (p.Arg236Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
10g.119672628G>ACA5716430BAG3c.881G>A (p.Arg294His)
c.707G>A (p.Arg236His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
10g.119672628G>CCA378296061BAG3c.881G>C (p.Arg294Pro)
c.707G>C (p.Arg236Pro)
10g.119672628G=CA1940193548BAG3c.881G= (p.Arg294=)
c.707G= (p.Arg236=)
10g.119672628G>TCA378296063BAG3c.881G>T (p.Arg294Leu)
c.707G>T (p.Arg236Leu)
gnomAD v4
10g.119672629T>ACA471634736BAG3c.882T>A (p.Arg294=)
c.708T>A (p.Arg236=)
10g.119672629T>CCA471634737BAG3c.882T>C (p.Arg294=)
c.708T>C (p.Arg236=)
10g.119672629T>GCA471634738BAG3c.882T>G (p.Arg294=)
c.708T>G (p.Arg236=)
10g.119672630G>ACA378296065BAG3c.883G>A (p.Val295Met)
c.709G>A (p.Val237Met)
dbSNP gnomAD v4
10g.119672630G>CCA378296067BAG3c.883G>C (p.Val295Leu)
c.709G>C (p.Val237Leu)
10g.119672630G=CA1940193551BAG3c.883G= (p.Val295=)
c.709G= (p.Val237=)
10g.119672630G>TCA378296069BAG3c.883G>T (p.Val295Leu)
c.709G>T (p.Val237Leu)
10g.119672631T>ACA378296075BAG3c.884T>A (p.Val295Glu)
c.710T>A (p.Val237Glu)
10g.119672631T>CCA378296073BAG3c.884T>C (p.Val295Ala)
c.710T>C (p.Val237Ala)
gnomAD v4
10g.119672631T>GCA378296071BAG3c.884T>G (p.Val295Gly)
c.710T>G (p.Val237Gly)
ClinVar gnomAD v4
10g.119672632G>ACA214222156BAG3c.885G>A (p.Val295=)
c.711G>A (p.Val237=)
ClinVar dbSNP
10g.119672632G>CCA471634740BAG3c.885G>C (p.Val295=)
c.711G>C (p.Val237=)
10g.119672632G=CA1940193552BAG3c.885G= (p.Val295=)
c.711G= (p.Val237=)
10g.119672632G>TCA471634739BAG3c.885G>T (p.Val295=)
c.711G>T (p.Val237=)
gnomAD v4
10g.119672632_119672634delinsGCACA1940193553BAG3c.885_887delinsGCA (p.Val295=)
c.711_713delinsGCA (p.Val237=)
10g.119672633C>ACA378296077BAG3c.886C>A (p.His296Asn)
c.712C>A (p.His238Asn)
10g.119672633C=CA1940193555BAG3c.886C= (p.His296=)
c.712C= (p.His238=)
10g.119672633C>GCA378296081BAG3c.886C>G (p.His296Asp)
c.712C>G (p.His238Asp)
10g.119672633C>TCA378296079BAG3c.886C>T (p.His296Tyr)
c.712C>T (p.His238Tyr)
ClinVar dbSNP gnomAD v2 gnomAD v4
10g.119672636_119672637delCA1940193554BAG3c.889_890del (p.Thr297ArgfsTer21)
c.715_716del (p.Thr239ArgfsTer20)
c.889_890del (p.Thr297ArgfsTer20)
ClinVar dbSNP
10g.119672634A>CCA378296083BAG3c.887A>C (p.His296Pro)
c.713A>C (p.His238Pro)
10g.119672634A>GCA378296085BAG3c.887A>G (p.His296Arg)
c.713A>G (p.His238Arg)
10g.119672634A>TCA378296086BAG3c.887A>T (p.His296Leu)
c.713A>T (p.His238Leu)
10g.119672635C>ACA378296089BAG3c.888C>A (p.His296Gln)
c.714C>A (p.His238Gln)
ClinVar dbSNP
10g.119672635C=CA1940193557BAG3c.888C= (p.His296=)
c.714C= (p.His238=)
10g.119672635C>GCA378296091BAG3c.888C>G (p.His296Gln)
c.714C>G (p.His238Gln)
10g.119672635C>TCA175300BAG3c.888C>T (p.His296=)
c.714C>T (p.His238=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
10g.119672636A=CA1940193561BAG3c.889A= (p.Thr297=)
c.715A= (p.Thr239=)
10g.119672636A>CCA378296094BAG3c.889A>C (p.Thr297Pro)
c.715A>C (p.Thr239Pro)
10g.119672636A>GCA308233BAG3c.889A>G (p.Thr297Ala)
c.715A>G (p.Thr239Ala)
ClinVar dbSNP
10g.119672636A>TCA378296097BAG3c.889A>T (p.Thr297Ser)
c.715A>T (p.Thr239Ser)
10g.119672637C>ACA378296099BAG3c.890C>A (p.Thr297Asn)
c.716C>A (p.Thr239Asn)
10g.119672637C>GCA378296101BAG3c.890C>G (p.Thr297Ser)
c.716C>G (p.Thr239Ser)
10g.119672637C>TCA378296103BAG3c.890C>T (p.Thr297Ile)
c.716C>T (p.Thr239Ile)
ClinVar dbSNP
10g.119672638C>ACA471634741BAG3c.891C>A (p.Thr297=)
c.717C>A (p.Thr239=)
dbSNP gnomAD v3 gnomAD v4
10g.119672638C=CA1940193562BAG3c.891C= (p.Thr297=)
c.717C= (p.Thr239=)
10g.119672638C>GCA5716431BAG3c.891C>G (p.Thr297=)
c.717C>G (p.Thr239=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119672638C>TCA5716432BAG3c.891C>T (p.Thr297=)
c.717C>T (p.Thr239=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119672639G>ACA243297BAG3c.892G>A (p.Val298Met)
c.718G>A (p.Val240Met)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119672639G>CCA378296107BAG3c.892G>C (p.Val298Leu)
c.718G>C (p.Val240Leu)
10g.119672639G=CA1940193565BAG3c.892G= (p.Val298=)
c.718G= (p.Val240=)
10g.119672639G>TCA378296109BAG3c.892G>T (p.Val298Leu)
c.718G>T (p.Val240Leu)
10g.119672640T>ACA378296111BAG3c.893T>A (p.Val298Glu)
c.719T>A (p.Val240Glu)
gnomAD v4
10g.119672640T>CCA378296112BAG3c.893T>C (p.Val298Ala)
c.719T>C (p.Val240Ala)
10g.119672640T>GCA378296114BAG3c.893T>G (p.Val298Gly)
c.719T>G (p.Val240Gly)
10g.119672641G>ACA471634742BAG3c.894G>A (p.Val298=)
c.720G>A (p.Val240=)
gnomAD v4
10g.119672641G>CCA471634743BAG3c.894G>C (p.Val298=)
c.720G>C (p.Val240=)
10g.119672641G>TCA471634744BAG3c.894G>T (p.Val298=)
c.720G>T (p.Val240=)
10g.119672642G>ACA378296116BAG3c.895G>A (p.Val299Ile)
c.721G>A (p.Val241Ile)
10g.119672642G>CCA378296118BAG3c.895G>C (p.Val299Leu)
c.721G>C (p.Val241Leu)
10g.119672642G>TCA378296120BAG3c.895G>T (p.Val299Phe)
c.721G>T (p.Val241Phe)
ClinVar
10g.119672643T>ACA378296122BAG3c.896T>A (p.Val299Asp)
c.722T>A (p.Val241Asp)
ClinVar dbSNP gnomAD v2 gnomAD v4
10g.119672643T>CCA378296124BAG3c.896T>C (p.Val299Ala)
c.722T>C (p.Val241Ala)
10g.119672643T>GCA378296126BAG3c.896T>G (p.Val299Gly)
c.722T>G (p.Val241Gly)
10g.119672643T=CA1940193566BAG3c.896T= (p.Val299=)
c.722T= (p.Val241=)
10g.119672644C>ACA471634745BAG3c.897C>A (p.Val299=)
c.723C>A (p.Val241=)
gnomAD v4
10g.119672644C=CA1940193567BAG3c.897C= (p.Val299=)
c.723C= (p.Val241=)
10g.119672644C>GCA471634746BAG3c.897C>G (p.Val299=)
c.723C>G (p.Val241=)
10g.119672644C>TCA5716433BAG3c.897C>T (p.Val299=)
c.723C>T (p.Val241=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
10g.119672645G>ACA308215BAG3c.898G>A (p.Asp300Asn)
c.724G>A (p.Asp242Asn)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119672645G>CCA378296130BAG3c.898G>C (p.Asp300His)
c.724G>C (p.Asp242His)
10g.119672645G=CA1940193572BAG3c.898G= (p.Asp300=)
c.724G= (p.Asp242=)
10g.119672645G>TCA378296131BAG3c.898G>T (p.Asp300Tyr)
c.724G>T (p.Asp242Tyr)
10g.119672646A>CCA378296135BAG3c.899A>C (p.Asp300Ala)
c.725A>C (p.Asp242Ala)
10g.119672646A>GCA378296137BAG3c.899A>G (p.Asp300Gly)
c.725A>G (p.Asp242Gly)
10g.119672646A>TCA378296139BAG3c.899A>T (p.Asp300Val)
c.725A>T (p.Asp242Val)
10g.119672647C>ACA378296140BAG3c.900C>A (p.Asp300Glu)
c.726C>A (p.Asp242Glu)
10g.119672647C=CA1940193573BAG3c.900C= (p.Asp300=)
c.726C= (p.Asp242=)
10g.119672647C>GCA378296142BAG3c.900C>G (p.Asp300Glu)
c.726C>G (p.Asp242Glu)
10g.119672647C>TCA471634747BAG3c.900C>T (p.Asp300=)
c.726C>T (p.Asp242=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.119672648A=CA1940193574BAG3c.901A= (p.Arg301=)
c.727A= (p.Arg243=)
10g.119672648A>CCA471634748BAG3c.901A>C (p.Arg301=)
c.727A>C (p.Arg243=)
10g.119672648A>GCA378296144BAG3c.901A>G (p.Arg301Gly)
c.727A>G (p.Arg243Gly)
dbSNP gnomAD v4
10g.119672648A>TCA378296146BAG3c.901A>T (p.Arg301Trp)
c.727A>T (p.Arg243Trp)
10g.119672648_119672649delCA923726207BAG3c.901_902del (p.Arg301AlafsTer17)
c.727_728del (p.Arg243AlafsTer16)
c.901_902del (p.Arg301AlafsTer16)
ClinVar
10g.119672649G>ACA378296148BAG3c.902G>A (p.Arg301Lys)
c.728G>A (p.Arg243Lys)
10g.119672649G>CCA378296150BAG3c.902G>C (p.Arg301Thr)
c.728G>C (p.Arg243Thr)
10g.119672649G>TCA378296152BAG3c.902G>T (p.Arg301Met)
c.728G>T (p.Arg243Met)
10g.119672650delCA1139532243BAG3c.903del (p.Arg301SerfsTer6)
c.729del (p.Arg243SerfsTer5)
c.903del (p.Arg301SerfsTer5)
dbSNP
10g.119672650G>ACA471634749BAG3c.903G>A (p.Arg301=)
c.729G>A (p.Arg243=)
gnomAD v4
10g.119672650G>CCA378296154BAG3c.903G>C (p.Arg301Ser)
c.729G>C (p.Arg243Ser)
10g.119672650G>TCA378296156BAG3c.903G>T (p.Arg301Ser)
c.729G>T (p.Arg243Ser)
10g.119672651C>ACA378296158BAG3c.904C>A (p.Pro302Thr)
c.730C>A (p.Pro244Thr)
10g.119672651C=CA1940193576BAG3c.904C= (p.Pro302=)
c.730C= (p.Pro244=)
10g.119672651C>GCA5716434BAG3c.904C>G (p.Pro302Ala)
c.730C>G (p.Pro244Ala)
dbSNP ExAC gnomAD v3 gnomAD v4
10g.119672651C>TCA378296159BAG3c.904C>T (p.Pro302Ser)
c.730C>T (p.Pro244Ser)
10g.119672652C>ACA378296162BAG3c.905C>A (p.Pro302His)
c.731C>A (p.Pro244His)
10g.119672652C=CA1940193577BAG3c.905C= (p.Pro302=)
c.731C= (p.Pro244=)
10g.119672652C>GCA378296163BAG3c.905C>G (p.Pro302Arg)
c.731C>G (p.Pro244Arg)
10g.119672652C>TCA214222209BAG3c.905C>T (p.Pro302Leu)
c.731C>T (p.Pro244Leu)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.119672653T>ACA471634752BAG3c.906T>A (p.Pro302=)
c.732T>A (p.Pro244=)
10g.119672653T>CCA471634750BAG3c.906T>C (p.Pro302=)
c.732T>C (p.Pro244=)
10g.119672653T>GCA471634751BAG3c.906T>G (p.Pro302=)
c.732T>G (p.Pro244=)
10g.119672654C>ACA378296166BAG3c.907C>A (p.Gln303Lys)
c.733C>A (p.Gln245Lys)
dbSNP gnomAD v2
10g.119672654C=CA1940193578BAG3c.907C= (p.Gln303=)
c.733C= (p.Gln245=)
10g.119672654C>GCA378296168BAG3c.907C>G (p.Gln303Glu)
c.733C>G (p.Gln245Glu)
ClinVar
10g.119672654C>TCA378296169BAG3c.907C>T (p.Gln303Ter)
c.733C>T (p.Gln245Ter)
ClinVar
10g.119672655A=CA1940193579BAG3c.908A= (p.Gln303=)
c.734A= (p.Gln245=)
10g.119672655A>CCA378296172BAG3c.908A>C (p.Gln303Pro)
c.734A>C (p.Gln245Pro)
10g.119672655A>GCA378296174BAG3c.908A>G (p.Gln303Arg)
c.734A>G (p.Gln245Arg)
dbSNP
10g.119672655A>TCA378296176BAG3c.908A>T (p.Gln303Leu)
c.734A>T (p.Gln245Leu)
10g.119672656G>ACA471634753BAG3c.909G>A (p.Gln303=)
c.735G>A (p.Gln245=)
10g.119672656G>CCA378296178BAG3c.909G>C (p.Gln303His)
c.735G>C (p.Gln245His)
ClinVar dbSNP
10g.119672656G=CA1940193580BAG3c.909G= (p.Gln303=)
c.735G= (p.Gln245=)
10g.119672656G>TCA378296180BAG3c.909G>T (p.Gln303His)
c.735G>T (p.Gln245His)
10g.119672657G>ACA352059BAG3c.909+1G>A (n.909+1G>A)
c.735+1G>A (n.735+1G>A)
ClinVar dbSNP
10g.119672657G>CCA378296184BAG3c.909+1G>C (n.909+1G>C)
c.735+1G>C (n.735+1G>C)
ClinVar
10g.119672657G=CA1940193583BAG3c.909+1G= (n.909+1G=)
c.735+1G= (n.735+1G=)
10g.119672657G>TCA378296182BAG3c.909+1G>T (n.909+1G>T)
c.735+1G>T (n.735+1G>T)
10g.119672658T>ACA378296189BAG3c.909+2T>A (n.909+2T>A)
c.735+2T>A (n.735+2T>A)
10g.119672658T>CCA378296187BAG3c.909+2T>C (n.909+2T>C)
c.735+2T>C (n.735+2T>C)
10g.119672658T>GCA378296191BAG3c.909+2T>G (n.909+2T>G)
c.735+2T>G (n.735+2T>G)
10g.119672660C>ACA933134000BAG3c.909+4C>A (n.909+4C>A)
c.735+4C>A (n.735+4C>A)
ClinVar dbSNP
10g.119672660C=CA1940193586BAG3c.909+4C= (n.909+4C=)
c.735+4C= (n.735+4C=)
10g.119672660C>GCA1940193587BAG3c.909+4C>G (n.909+4C>G)
c.735+4C>G (n.735+4C>G)
ClinVar dbSNP
10g.119672660C>TCA5716435BAG3c.909+4C>T (n.909+4C>T)
c.735+4C>T (n.735+4C>T)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119672661G>ACA214222234BAG3c.909+5G>A (n.909+5G>A)
c.735+5G>A (n.735+5G>A)
ClinVar dbSNP gnomAD v4
10g.119672661G=CA1940193588BAG3c.909+5G= (n.909+5G=)
c.735+5G= (n.735+5G=)
10g.119672661G>TCA2611160111BAG3c.909+5G>T (n.909+5G>T)
c.735+5G>T (n.735+5G>T)
gnomAD v4
10g.119672662G>CCA2741134749BAG3c.909+6G>C (n.909+6G>C)
c.735+6G>C (n.735+6G>C)
10g.119672665A>GCA2611160112BAG3c.909+9A>G (n.909+9A>G)
c.735+9A>G (n.735+9A>G)
gnomAD v4
10g.119672666delCA2574457210BAG3c.909+10del (n.909+10del)
c.735+10del (n.735+10del)
10g.119672667T>ACA2740093562BAG3c.909+11T>A (n.909+11T>A)
c.735+11T>A (n.735+11T>A)
ClinVar
10g.119672669A=CA1940193589BAG3c.909+13A= (n.909+13A=)
c.735+13A= (n.735+13A=)
10g.119672669_119672672delCA2611160113BAG3c.909+13_909+16del (n.909+13_909+16del)
c.735+13_735+16del (n.735+13_735+16del)
gnomAD v4
10g.119672670_119672671dupCA5716436BAG3c.909+14_909+15dup (n.909+14_909+15dup)
c.735+14_735+15dup (n.735+14_735+15dup)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119672672C=CA1940193590BAG3c.909+16C= (n.909+16C=)
c.735+16C= (n.735+16C=)
10g.119672672C>TCA5716437BAG3c.909+16C>T (n.909+16C>T)
c.735+16C>T (n.735+16C>T)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119672673G>ACA5716438BAG3c.909+17G>A (n.909+17G>A)
c.735+17G>A (n.735+17G>A)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119672673G=CA1940193592BAG3c.909+17G= (n.909+17G=)
c.735+17G= (n.735+17G=)
10g.119672673G>TCA2574457212BAG3c.909+17G>T (n.909+17G>T)
c.735+17G>T (n.735+17G>T)
10g.119672675C=CA1940193593BAG3c.909+19C= (n.909+19C=)
c.735+19C= (n.735+19C=)
10g.119672675C>TCA596326300BAG3c.909+19C>T (n.909+19C>T)
c.735+19C>T (n.735+19C>T)
dbSNP gnomAD v2 gnomAD v4 COSMIC
10g.119672677G>ACA2611160114BAG3c.909+21G>A (n.909+21G>A)
c.735+21G>A (n.735+21G>A)
gnomAD v4
10g.119672677G>TCA2611160115BAG3c.909+21G>T (n.909+21G>T)
c.735+21G>T (n.735+21G>T)
gnomAD v4
10g.119672679A=CA1940193594BAG3c.909+23A= (n.909+23A=)
c.735+23A= (n.735+23A=)
10g.119672679A>CCA2611160116BAG3c.909+23A>C (n.909+23A>C)
c.735+23A>C (n.735+23A>C)
gnomAD v4
10g.119672679A>GCA214222238BAG3c.909+23A>G (n.909+23A>G)
c.735+23A>G (n.735+23A>G)
dbSNP gnomAD v3 gnomAD v4
10g.119672680G>TCA2611160117BAG3c.909+24G>T (n.909+24G>T)
c.735+24G>T (n.735+24G>T)
gnomAD v4
10g.119672684G>TCA2611160118BAG3c.909+28G>T (n.909+28G>T)
c.735+28G>T (n.735+28G>T)
gnomAD v4
10g.119672685G>TCA2611160119BAG3c.909+29G>T (n.909+29G>T)
c.735+29G>T (n.735+29G>T)
gnomAD v4
10g.119672686T>CCA596326301BAG3c.909+30T>C (n.909+30T>C)
c.735+30T>C (n.735+30T>C)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.119672686T>GCA5716439BAG3c.909+30T>G (n.909+30T>G)
c.735+30T>G (n.735+30T>G)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119672686T=CA1940193595BAG3c.909+30T= (n.909+30T=)
c.735+30T= (n.735+30T=)
10g.119672689T>CCA596326303BAG3c.909+33T>C (n.909+33T>C)
c.735+33T>C (n.735+33T>C)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.119672689T=CA1940193596BAG3c.909+33T= (n.909+33T=)
c.735+33T= (n.735+33T=)
10g.119672691G>ACA2611160120BAG3c.909+35G>A (n.909+35G>A)
c.735+35G>A (n.735+35G>A)
gnomAD v4
10g.119672693G>ACA5716440BAG3c.909+37G>A (n.909+37G>A)
c.735+37G>A (n.735+37G>A)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119672693G=CA1940193597BAG3c.909+37G= (n.909+37G=)
c.735+37G= (n.735+37G=)
10g.119672693G>TCA2611160121BAG3c.909+37G>T (n.909+37G>T)
c.735+37G>T (n.735+37G>T)
gnomAD v4
10g.119672694G>ACA2611160122BAG3c.909+38G>A (n.909+38G>A)
c.735+38G>A (n.735+38G>A)
gnomAD v4
10g.119672694G>CCA2611160124BAG3c.909+38G>C (n.909+38G>C)
c.735+38G>C (n.735+38G>C)
gnomAD v4
10g.119672694G>TCA2611160123BAG3c.909+38G>T (n.909+38G>T)
c.735+38G>T (n.735+38G>T)
gnomAD v4
10g.119672695dupCA2611160125BAG3c.909+39dup (n.909+39dup)
c.735+39dup (n.735+39dup)
gnomAD v4
10g.119672696A=CA1940193601BAG3c.909+40A= (n.909+40A=)
c.735+40A= (n.735+40A=)
10g.119672696A>GCA5716441BAG3c.909+40A>G (n.909+40A>G)
c.735+40A>G (n.735+40A>G)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119672698G>ACA214222246BAG3c.909+42G>A (n.909+42G>A)
c.735+42G>A (n.735+42G>A)
dbSNP gnomAD v4
10g.119672698G=CA1940193602BAG3c.909+42G= (n.909+42G=)
c.735+42G= (n.735+42G=)
10g.119672700C>ACA2611160126BAG3c.909+44C>A (n.909+44C>A)
c.735+44C>A (n.735+44C>A)
gnomAD v4
10g.119672700C>GCA2611160127BAG3c.909+44C>G (n.909+44C>G)
c.735+44C>G (n.735+44C>G)
gnomAD v4
10g.119672702C>TCA2611160128BAG3c.909+46C>T (n.909+46C>T)
c.735+46C>T (n.735+46C>T)
gnomAD v4
10g.119672704A>GCA2611160129BAG3c.909+48A>G (n.909+48A>G)
c.735+48A>G (n.735+48A>G)
gnomAD v4
10g.119672705G=CA1940193603BAG3c.909+49G= (n.909+49G=)
c.735+49G= (n.735+49G=)
10g.119672705G>TCA5716442BAG3c.909+49G>T (n.909+49G>T)
c.735+49G>T (n.735+49G>T)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119672706G>TCA2611160130BAG3c.909+50G>T (n.909+50G>T)
c.735+50G>T (n.735+50G>T)
gnomAD v4
10g.119672707G>ACA2574457220BAG3c.909+51G>A (n.909+51G>A)
c.735+51G>A (n.735+51G>A)
dbSNP
10g.119672707G=CA1940193604BAG3c.909+51G= (n.909+51G=)
c.735+51G= (n.735+51G=)
10g.119672707G>TCA214222251BAG3c.909+51G>T (n.909+51G>T)
c.735+51G>T (n.735+51G>T)
dbSNP gnomAD v4
10g.119672708G>ACA653727879BAG3c.909+52G>A (n.909+52G>A)
c.735+52G>A (n.735+52G>A)
COSMIC
10g.119672708G>CCA2611160131BAG3c.909+52G>C (n.909+52G>C)
c.735+52G>C (n.735+52G>C)
gnomAD v4
10g.119672708G=CA1940193605BAG3c.909+52G= (n.909+52G=)
c.735+52G= (n.735+52G=)
10g.119672708G>TCA596326306BAG3c.909+52G>T (n.909+52G>T)
c.735+52G>T (n.735+52G>T)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.119672709T>GCA1940193607BAG3c.909+53T>G (n.909+53T>G)
c.735+53T>G (n.735+53T>G)
dbSNP
10g.119672709T=CA1940193606BAG3c.909+53T= (n.909+53T=)
c.735+53T= (n.735+53T=)
10g.119672710G>CCA2611160132BAG3c.909+54G>C (n.909+54G>C)
c.735+54G>C (n.735+54G>C)
gnomAD v4
10g.119672710G>TCA2611160133BAG3c.909+54G>T (n.909+54G>T)
c.735+54G>T (n.735+54G>T)
gnomAD v4
10g.119672711C>TCA2611160134BAG3c.909+55C>T (n.909+55C>T)
c.735+55C>T (n.735+55C>T)
gnomAD v4
10g.119672713G>ACA2611160135BAG3c.909+57G>A (n.909+57G>A)
c.735+57G>A (n.735+57G>A)
gnomAD v4
10g.119672714G>TCA2611160136BAG3c.909+58G>T (n.909+58G>T)
c.735+58G>T (n.735+58G>T)
gnomAD v4
10g.119672715A>CCA2611160137BAG3c.909+59A>C (n.909+59A>C)
c.735+59A>C (n.735+59A>C)
gnomAD v4
10g.119672716G>ACA660665600BAG3c.909+60G>A (n.909+60G>A)
c.735+60G>A (n.735+60G>A)
dbSNP
10g.119672716G=CA1940193608BAG3c.909+60G= (n.909+60G=)
c.735+60G= (n.735+60G=)
10g.119672717C>TCA2611160138BAG3c.909+61C>T (n.909+61C>T)
c.735+61C>T (n.735+61C>T)
gnomAD v4
10g.119672719C>TCA2611160139BAG3c.909+63C>T (n.909+63C>T)
c.735+63C>T (n.735+63C>T)
gnomAD v4
10g.119672720T>GCA2574457222BAG3c.909+64T>G (n.909+64T>G)
c.735+64T>G (n.735+64T>G)
gnomAD v4
10g.119672721G>ACA596326308BAG3c.909+65G>A (n.909+65G>A)
c.735+65G>A (n.735+65G>A)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.119672721G=CA1940193609BAG3c.909+65G= (n.909+65G=)
c.735+65G= (n.735+65G=)
10g.119672724G>ACA2789704664BAG3c.909+68G>A (n.909+68G>A)
c.735+68G>A (n.735+68G>A)
10g.119672724G>CCA214222254BAG3c.909+68G>C (n.909+68G>C)
c.735+68G>C (n.735+68G>C)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.119672724G=CA1940193610BAG3c.909+68G= (n.909+68G=)
c.735+68G= (n.735+68G=)
10g.119672724G>TCA2611160140BAG3c.909+68G>T (n.909+68G>T)
c.735+68G>T (n.735+68G>T)
gnomAD v4

Number of alleles fetched