Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.119672256_119677283delCA1139532250BAG3c.509_*1del
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)
10g.119672607T>ACA378295974BAG3c.860T>A (p.Leu287His)
c.686T>A (p.Leu229His)
10g.119672607T>CCA378295976BAG3c.860T>C (p.Leu287Pro)
c.686T>C (p.Leu229Pro)
dbSNP gnomAD v2 gnomAD v4
10g.119672607T>GCA378295977BAG3c.860T>G (p.Leu287Arg)
c.686T>G (p.Leu229Arg)
10g.119672607T=CA1940193520BAG3c.860T= (p.Leu287=)
c.686T= (p.Leu229=)
10g.119672608C>ACA471634719BAG3c.861C>A (p.Leu287=)
c.687C>A (p.Leu229=)
10g.119672608C>GCA471634720BAG3c.861C>G (p.Leu287=)
c.687C>G (p.Leu229=)
10g.119672608C>TCA471634721BAG3c.861C>T (p.Leu287=)
c.687C>T (p.Leu229=)
10g.119672609C>ACA378295984BAG3c.862C>A (p.His288Asn)
c.688C>A (p.His230Asn)
10g.119672609C=CA1940193523BAG3c.862C= (p.His288=)
c.688C= (p.His230=)
10g.119672609C>GCA378295980BAG3c.862C>G (p.His288Asp)
c.688C>G (p.His230Asp)
10g.119672609C>TCA378295982BAG3c.862C>T (p.His288Tyr)
c.688C>T (p.His230Tyr)
dbSNP
10g.119672610A=CA1940193524BAG3c.863A= (p.His288=)
c.689A= (p.His230=)
10g.119672610A>CCA378295986BAG3c.863A>C (p.His288Pro)
c.689A>C (p.His230Pro)
10g.119672610A>GCA378295987BAG3c.863A>G (p.His288Arg)
c.689A>G (p.His230Arg)
10g.119672610A>TCA5716426BAG3c.863A>T (p.His288Leu)
c.689A>T (p.His230Leu)
dbSNP ExAC gnomAD v2 gnomAD v4
10g.119672611C>ACA378295990BAG3c.864C>A (p.His288Gln)
c.690C>A (p.His230Gln)
10g.119672611C=CA1940193525BAG3c.864C= (p.His288=)
c.690C= (p.His230=)
10g.119672611C>GCA378295992BAG3c.864C>G (p.His288Gln)
c.690C>G (p.His230Gln)
10g.119672611C>TCA471634722BAG3c.864C>T (p.His288=)
c.690C>T (p.His230=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.119672612T>ACA378295994BAG3c.865T>A (p.Ser289Thr)
c.691T>A (p.Ser231Thr)
10g.119672612T>CCA378295998BAG3c.865T>C (p.Ser289Pro)
c.691T>C (p.Ser231Pro)
dbSNP gnomAD v2 gnomAD v4
10g.119672612T>GCA378295996BAG3c.865T>G (p.Ser289Ala)
c.691T>G (p.Ser231Ala)
ClinVar dbSNP gnomAD v4
10g.119672612T=CA1940193526BAG3c.865T= (p.Ser289=)
c.691T= (p.Ser231=)
10g.119672613C>ACA378296000BAG3c.866C>A (p.Ser289Tyr)
c.692C>A (p.Ser231Tyr)
10g.119672613C=CA1940193527BAG3c.866C= (p.Ser289=)
c.692C= (p.Ser231=)
10g.119672613C>GCA378296002BAG3c.866C>G (p.Ser289Cys)
c.692C>G (p.Ser231Cys)
10g.119672613C>TCA378296004BAG3c.866C>T (p.Ser289Phe)
c.692C>T (p.Ser231Phe)
dbSNP gnomAD v3 gnomAD v4
10g.119672617dupCA2695212863BAG3c.870dup (p.Ser291LeufsTer28)
c.696dup (p.Ser233LeufsTer27)
c.870dup (p.Ser291LeufsTer27)
10g.119672614C>ACA471634723BAG3c.867C>A (p.Ser289=)
c.693C>A (p.Ser231=)
10g.119672614C=CA1940193530BAG3c.867C= (p.Ser289=)
c.693C= (p.Ser231=)
10g.119672614C>GCA471634724BAG3c.867C>G (p.Ser289=)
c.693C>G (p.Ser231=)
10g.119672614C>TCA471634725BAG3c.867C>T (p.Ser289=)
c.693C>T (p.Ser231=)
dbSNP gnomAD v2 gnomAD v4
10g.119672615C>ACA378296006BAG3c.868C>A (p.Pro290Thr)
c.694C>A (p.Pro232Thr)
10g.119672615C=CA1940193532BAG3c.868C= (p.Pro290=)
c.694C= (p.Pro232=)
10g.119672615C>GCA378296008BAG3c.868C>G (p.Pro290Ala)
c.694C>G (p.Pro232Ala)
ClinVar
10g.119672615C>TCA378296010BAG3c.868C>T (p.Pro290Ser)
c.694C>T (p.Pro232Ser)
dbSNP gnomAD v2 gnomAD v4
10g.119672616C>ACA378296012BAG3c.869C>A (p.Pro290His)
c.695C>A (p.Pro232His)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.119672616C=CA1940193533BAG3c.869C= (p.Pro290=)
c.695C= (p.Pro232=)
10g.119672616C>GCA378296014BAG3c.869C>G (p.Pro290Arg)
c.695C>G (p.Pro232Arg)
10g.119672616C>TCA378296015BAG3c.869C>T (p.Pro290Leu)
c.695C>T (p.Pro232Leu)
dbSNP
10g.119672617C>ACA5716427BAG3c.870C>A (p.Pro290=)
c.696C>A (p.Pro232=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
10g.119672617C=CA1940193535BAG3c.870C= (p.Pro290=)
c.696C= (p.Pro232=)
10g.119672617C>GCA135037BAG3c.870C>G (p.Pro290=)
c.696C>G (p.Pro232=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119672617C>TCA471634727BAG3c.870C>T (p.Pro290=)
c.696C>T (p.Pro232=)
ClinVar
10g.119672618T>ACA378296019BAG3c.871T>A (p.Ser291Thr)
c.697T>A (p.Ser233Thr)
ClinVar
10g.119672618T>CCA378296024BAG3c.871T>C (p.Ser291Pro)
c.697T>C (p.Ser233Pro)
10g.119672618T>GCA378296022BAG3c.871T>G (p.Ser291Ala)
c.697T>G (p.Ser233Ala)
10g.119672618_119672620delinsCCCA2573332533BAG3c.871_873delinsCC (p.Ser291ProfsTer16)
c.697_699delinsCC (p.Ser233ProfsTer15)
c.871_873delinsCC (p.Ser291ProfsTer15)
10g.119672619C>ACA378296026BAG3c.872C>A (p.Ser291Ter)
c.698C>A (p.Ser233Ter)
10g.119672619C=CA1940193536BAG3c.872C= (p.Ser291=)
c.698C= (p.Ser233=)
10g.119672619C>GCA378296027BAG3c.872C>G (p.Ser291Trp)
c.698C>G (p.Ser233Trp)
10g.119672619C>TCA135040BAG3c.872C>T (p.Ser291Leu)
c.698C>T (p.Ser233Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119672620G>ACA471634728BAG3c.873G>A (p.Ser291=)
c.699G>A (p.Ser233=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.119672620G>CCA471634729BAG3c.873G>C (p.Ser291=)
c.699G>C (p.Ser233=)
10g.119672620G=CA1940193538BAG3c.873G= (p.Ser291=)
c.699G= (p.Ser233=)
10g.119672620G>TCA471634730BAG3c.873G>T (p.Ser291=)
c.699G>T (p.Ser233=)
10g.119672621C>ACA378296031BAG3c.874C>A (p.Pro292Thr)
c.700C>A (p.Pro234Thr)
10g.119672621C>GCA378296032BAG3c.874C>G (p.Pro292Ala)
c.700C>G (p.Pro234Ala)
10g.119672621C>TCA378296034BAG3c.874C>T (p.Pro292Ser)
c.700C>T (p.Pro234Ser)
ClinVar
10g.119672622C>ACA378296036BAG3c.875C>A (p.Pro292His)
c.701C>A (p.Pro234His)
10g.119672622C=CA1940193540BAG3c.875C= (p.Pro292=)
c.701C= (p.Pro234=)
10g.119672622C>GCA378296038BAG3c.875C>G (p.Pro292Arg)
c.701C>G (p.Pro234Arg)
ClinVar dbSNP
10g.119672622C>TCA5716428BAG3c.875C>T (p.Pro292Leu)
c.701C>T (p.Pro234Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
10g.119672623C>ACA471634731BAG3c.876C>A (p.Pro292=)
c.702C>A (p.Pro234=)
10g.119672623C>GCA471634732BAG3c.876C>G (p.Pro292=)
c.702C>G (p.Pro234=)
10g.119672623C>TCA471634733BAG3c.876C>T (p.Pro292=)
c.702C>T (p.Pro234=)
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

Number of alleles fetched