Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.119672256_119677283delCA1139532250BAG3c.509_*1del
10g.119674392_119683124delCA2580082473 ClinVar
10g.119675031_119678711delCA2580082474 ClinVar
10g.119676642_119677262delCA2573145588BAG3c.1088_1708del (p.Glu363_Pro569del)
c.1085_1705del (p.Glu362_Pro568del)
ClinVar dbSNP
10g.119676994_119677004delCA2825001684BAG3c.1440_1450del (p.Arg480SerfsTer12)
c.1437_1447del (p.Arg479SerfsTer12)
ClinVar
10g.119676998_119676999delCA2695212842BAG3c.1444_1445del (p.Asp482ArgfsTer13)
c.1441_1442del (p.Asp481ArgfsTer13)
10g.119676998G>ACA378297329BAG3c.1444G>A (p.Asp482Asn)
c.1441G>A (p.Asp481Asn)
10g.119676998G>CCA378297330BAG3c.1444G>C (p.Asp482His)
c.1441G>C (p.Asp481His)
COSMIC
10g.119676998G>TCA378297331BAG3c.1444G>T (p.Asp482Tyr)
c.1441G>T (p.Asp481Tyr)
10g.119676999A>CCA378297332BAG3c.1445A>C (p.Asp482Ala)
c.1442A>C (p.Asp481Ala)
10g.119676999A>GCA378297334BAG3c.1445A>G (p.Asp482Gly)
c.1442A>G (p.Asp481Gly)
10g.119676999A>TCA378297333BAG3c.1445A>T (p.Asp482Val)
c.1442A>T (p.Asp481Val)
10g.119676999dupCA2740093566BAG3c.1445dup (p.Asp482GlufsTer14)
c.1442dup (p.Asp481GlufsTer14)
ClinVar
10g.119677000C>ACA378297335BAG3c.1446C>A (p.Asp482Glu)
c.1443C>A (p.Asp481Glu)
10g.119677000C=CA1940196801BAG3c.1446C= (p.Asp482=)
c.1443C= (p.Asp481=)
10g.119677000C>GCA5716553BAG3c.1446C>G (p.Asp482Glu)
c.1443C>G (p.Asp481Glu)
dbSNP ExAC gnomAD v2 gnomAD v4
10g.119677000C>TCA5716552BAG3c.1446C>T (p.Asp482=)
c.1443C>T (p.Asp481=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119677001G>ACA5716554BAG3c.1447G>A (p.Gly483Ser)
c.1444G>A (p.Gly482Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119677001G>CCA378297336BAG3c.1447G>C (p.Gly483Arg)
c.1444G>C (p.Gly482Arg)
10g.119677001G=CA1940196802BAG3c.1447G= (p.Gly483=)
c.1444G= (p.Gly482=)
10g.119677001G>TCA378297337BAG3c.1447G>T (p.Gly483Cys)
c.1444G>T (p.Gly482Cys)
10g.119677002G>ACA378297338BAG3c.1448G>A (p.Gly483Asp)
c.1445G>A (p.Gly482Asp)
10g.119677002G>CCA378297339BAG3c.1448G>C (p.Gly483Ala)
c.1445G>C (p.Gly482Ala)
10g.119677002G>TCA378297340BAG3c.1448G>T (p.Gly483Val)
c.1445G>T (p.Gly482Val)
10g.119677003T>ACA471739456BAG3c.1449T>A (p.Gly483=)
c.1446T>A (p.Gly482=)
10g.119677003T>CCA471739458BAG3c.1449T>C (p.Gly483=)
c.1446T>C (p.Gly482=)
dbSNP
10g.119677003T>GCA471739459BAG3c.1449T>G (p.Gly483=)
c.1446T>G (p.Gly482=)
ClinVar dbSNP
10g.119677003T=CA1940196803BAG3c.1449T= (p.Gly483=)
c.1446T= (p.Gly482=)
10g.119677004G>ACA378297341BAG3c.1450G>A (p.Val484Ile)
c.1447G>A (p.Val483Ile)
ClinVar dbSNP gnomAD v3 gnomAD v4
10g.119677004G>CCA378297342BAG3c.1450G>C (p.Val484Leu)
c.1447G>C (p.Val483Leu)
10g.119677004G=CA1940196804BAG3c.1450G= (p.Val484=)
c.1447G= (p.Val483=)
10g.119677004G>TCA378297343BAG3c.1450G>T (p.Val484Phe)
c.1447G>T (p.Val483Phe)
10g.119677005T>ACA378297344BAG3c.1451T>A (p.Val484Asp)
c.1448T>A (p.Val483Asp)
ClinVar dbSNP
10g.119677005T>CCA378297345BAG3c.1451T>C (p.Val484Ala)
c.1448T>C (p.Val483Ala)
10g.119677005T>GCA378297346BAG3c.1451T>G (p.Val484Gly)
c.1448T>G (p.Val483Gly)
10g.119677006C>ACA471739462BAG3c.1452C>A (p.Val484=)
c.1449C>A (p.Val483=)
ClinVar dbSNP
10g.119677006C=CA1940196805BAG3c.1452C= (p.Val484=)
c.1449C= (p.Val483=)
10g.119677006C>GCA471739464BAG3c.1452C>G (p.Val484=)
c.1449C>G (p.Val483=)
gnomAD v4
10g.119677006C>TCA471739465BAG3c.1452C>T (p.Val484=)
c.1449C>T (p.Val483=)
dbSNP gnomAD v4
10g.119677007A>CCA471739466BAG3c.1453A>C (p.Arg485=)
c.1450A>C (p.Arg484=)
10g.119677007A>GCA378297347BAG3c.1453A>G (p.Arg485Gly)
c.1450A>G (p.Arg484Gly)
ClinVar dbSNP
10g.119677007A>TCA378297348BAG3c.1453A>T (p.Arg485Trp)
c.1450A>T (p.Arg484Trp)
10g.119677008G>ACA378297349BAG3c.1454G>A (p.Arg485Lys)
c.1451G>A (p.Arg484Lys)
10g.119677008G>CCA378297350BAG3c.1454G>C (p.Arg485Thr)
c.1451G>C (p.Arg484Thr)
10g.119677008G>TCA378297351BAG3c.1454G>T (p.Arg485Met)
c.1451G>T (p.Arg484Met)
10g.119677009G>ACA214225269BAG3c.1455G>A (p.Arg485=)
c.1452G>A (p.Arg484=)
ClinVar dbSNP gnomAD v4
10g.119677009G>CCA378297352BAG3c.1455G>C (p.Arg485Ser)
c.1452G>C (p.Arg484Ser)
10g.119677009G=CA1940196806BAG3c.1455G= (p.Arg485=)
c.1452G= (p.Arg484=)
10g.119677009G>TCA378297353BAG3c.1455G>T (p.Arg485Ser)
c.1452G>T (p.Arg484Ser)
10g.119677010A>CCA378297354BAG3c.1456A>C (p.Lys486Gln)
c.1453A>C (p.Lys485Gln)
10g.119677010A>GCA378297355BAG3c.1456A>G (p.Lys486Glu)
c.1453A>G (p.Lys485Glu)
10g.119677010A>TCA378297356BAG3c.1456A>T (p.Lys486Ter)
c.1453A>T (p.Lys485Ter)
10g.119677011A=CA1940196807BAG3c.1457A= (p.Lys486=)
c.1454A= (p.Lys485=)
10g.119677011A>CCA378297357BAG3c.1457A>C (p.Lys486Thr)
c.1454A>C (p.Lys485Thr)
10g.119677011A>GCA5716555BAG3c.1457A>G (p.Lys486Arg)
c.1454A>G (p.Lys485Arg)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119677011A>TCA378297358BAG3c.1457A>T (p.Lys486Met)
c.1454A>T (p.Lys485Met)
10g.119677012G>ACA471739468BAG3c.1458G>A (p.Lys486=)
c.1455G>A (p.Lys485=)
dbSNP gnomAD v3 gnomAD v4
10g.119677012G>CCA378297359BAG3c.1458G>C (p.Lys486Asn)
c.1455G>C (p.Lys485Asn)
gnomAD v4
10g.119677012G=CA1940196808BAG3c.1458G= (p.Lys486=)
c.1455G= (p.Lys485=)
10g.119677012G>TCA378297360BAG3c.1458G>T (p.Lys486Asn)
c.1455G>T (p.Lys485Asn)
dbSNP
10g.119677013G>ACA378297361BAG3c.1459G>A (p.Val487Ile)
c.1456G>A (p.Val486Ile)
10g.119677013G>CCA378297363BAG3c.1459G>C (p.Val487Leu)
c.1456G>C (p.Val486Leu)
10g.119677013G>TCA378297362BAG3c.1459G>T (p.Val487Phe)
c.1456G>T (p.Val486Phe)
10g.119677014T>ACA378297364BAG3c.1460T>A (p.Val487Asp)
c.1457T>A (p.Val486Asp)
10g.119677014T>CCA378297365BAG3c.1460T>C (p.Val487Ala)
c.1457T>C (p.Val486Ala)
10g.119677014T>GCA378297366BAG3c.1460T>G (p.Val487Gly)
c.1457T>G (p.Val486Gly)
10g.119677015T>ACA471739470BAG3c.1461T>A (p.Val487=)
c.1458T>A (p.Val486=)
gnomAD v4
10g.119677015T>CCA471739471BAG3c.1461T>C (p.Val487=)
c.1458T>C (p.Val486=)
10g.119677015T>GCA471739472BAG3c.1461T>G (p.Val487=)
c.1458T>G (p.Val486=)
10g.119677016C>ACA378297367BAG3c.1462C>A (p.Gln488Lys)
c.1459C>A (p.Gln487Lys)
10g.119677016C>GCA378297368BAG3c.1462C>G (p.Gln488Glu)
c.1459C>G (p.Gln487Glu)
10g.119677016C>TCA378297369BAG3c.1462C>T (p.Gln488Ter)
c.1459C>T (p.Gln487Ter)
10g.119677017A>CCA378297370BAG3c.1463A>C (p.Gln488Pro)
c.1460A>C (p.Gln487Pro)
10g.119677017A>GCA378297371BAG3c.1463A>G (p.Gln488Arg)
c.1460A>G (p.Gln487Arg)
10g.119677017A>TCA378297372BAG3c.1463A>T (p.Gln488Leu)
c.1460A>T (p.Gln487Leu)
10g.119677018G>ACA471739475BAG3c.1464G>A (p.Gln488=)
c.1461G>A (p.Gln487=)
10g.119677018G>CCA378297373BAG3c.1464G>C (p.Gln488His)
c.1461G>C (p.Gln487His)
gnomAD v4
10g.119677018G>TCA378297374BAG3c.1464G>T (p.Gln488His)
c.1461G>T (p.Gln487His)
10g.119677019A>CCA378297377BAG3c.1465A>C (p.Thr489Pro)
c.1462A>C (p.Thr488Pro)
10g.119677019A>GCA378297376BAG3c.1465A>G (p.Thr489Ala)
c.1462A>G (p.Thr488Ala)
10g.119677019A>TCA378297375BAG3c.1465A>T (p.Thr489Ser)
c.1462A>T (p.Thr488Ser)
10g.119677020C>ACA378297378BAG3c.1466C>A (p.Thr489Asn)
c.1463C>A (p.Thr488Asn)
10g.119677020C>GCA378297379BAG3c.1466C>G (p.Thr489Ser)
c.1463C>G (p.Thr488Ser)
10g.119677020C>TCA378297380BAG3c.1466C>T (p.Thr489Ile)
c.1463C>T (p.Thr488Ile)
10g.119677021C>ACA471739476BAG3c.1467C>A (p.Thr489=)
c.1464C>A (p.Thr488=)
10g.119677021C=CA1940196809BAG3c.1467C= (p.Thr489=)
c.1464C= (p.Thr488=)
10g.119677021C>GCA471739477BAG3c.1467C>G (p.Thr489=)
c.1464C>G (p.Thr488=)
10g.119677021C>TCA471739478BAG3c.1467C>T (p.Thr489=)
c.1464C>T (p.Thr488=)
dbSNP
10g.119677022A=CA1940196810BAG3c.1468A= (p.Ile490=)
c.1465A= (p.Ile489=)
10g.119677022A>CCA378297381BAG3c.1468A>C (p.Ile490Leu)
c.1465A>C (p.Ile489Leu)
10g.119677022A>GCA308239BAG3c.1468A>G (p.Ile490Val)
c.1465A>G (p.Ile489Val)
dbSNP ExAC gnomAD v2 gnomAD v4
10g.119677022A>TCA378297382BAG3c.1468A>T (p.Ile490Phe)
c.1465A>T (p.Ile489Phe)
10g.119677023T>ACA378297383BAG3c.1469T>A (p.Ile490Asn)
c.1466T>A (p.Ile489Asn)
10g.119677023T>CCA378297384BAG3c.1469T>C (p.Ile490Thr)
c.1466T>C (p.Ile489Thr)
ClinVar dbSNP gnomAD v3 gnomAD v4
10g.119677023T>GCA378297385BAG3c.1469T>G (p.Ile490Ser)
c.1466T>G (p.Ile489Ser)
10g.119677023T=CA1940196811BAG3c.1469T= (p.Ile490=)
c.1466T= (p.Ile489=)
10g.119677024C>ACA471739482BAG3c.1470C>A (p.Ile490=)
c.1467C>A (p.Ile489=)
10g.119677024C=CA1940196812BAG3c.1470C= (p.Ile490=)
c.1467C= (p.Ile489=)
10g.119677024C>GCA378297386BAG3c.1470C>G (p.Ile490Met)
c.1467C>G (p.Ile489Met)
gnomAD v4
10g.119677024C>TCA214225279BAG3c.1470C>T (p.Ile490=)
c.1467C>T (p.Ile489=)
ClinVar dbSNP
10g.119677025T>ACA378297387BAG3c.1471T>A (p.Leu491Met)
c.1468T>A (p.Leu490Met)
10g.119677025T>CCA471739484BAG3c.1471T>C (p.Leu491=)
c.1468T>C (p.Leu490=)
10g.119677025T>GCA378297388BAG3c.1471T>G (p.Leu491Val)
c.1468T>G (p.Leu490Val)
ClinVar
10g.119677026T>ACA378297389BAG3c.1472T>A (p.Leu491Ter)
c.1469T>A (p.Leu490Ter)
10g.119677026T>CCA378297391BAG3c.1472T>C (p.Leu491Ser)
c.1469T>C (p.Leu490Ser)
10g.119677026T>GCA378297390BAG3c.1472T>G (p.Leu491Trp)
c.1469T>G (p.Leu490Trp)
10g.119677027G>ACA5716556BAG3c.1473G>A (p.Leu491=)
c.1470G>A (p.Leu490=)
dbSNP ExAC gnomAD v4
10g.119677027G>CCA378297393BAG3c.1473G>C (p.Leu491Phe)
c.1470G>C (p.Leu490Phe)
gnomAD v4 COSMIC
10g.119677027G=CA1940196813BAG3c.1473G= (p.Leu491=)
c.1470G= (p.Leu490=)
10g.119677027G>TCA378297392BAG3c.1473G>T (p.Leu491Phe)
c.1470G>T (p.Leu490Phe)
10g.119677028G>ACA378297394BAG3c.1474G>A (p.Glu492Lys)
c.1471G>A (p.Glu491Lys)
10g.119677028G>CCA378297395BAG3c.1474G>C (p.Glu492Gln)
c.1471G>C (p.Glu491Gln)
10g.119677028G>TCA378297396BAG3c.1474G>T (p.Glu492Ter)
c.1471G>T (p.Glu491Ter)
10g.119677029A>CCA378297397BAG3c.1475A>C (p.Glu492Ala)
c.1472A>C (p.Glu491Ala)
10g.119677029A>GCA378297398BAG3c.1475A>G (p.Glu492Gly)
c.1472A>G (p.Glu491Gly)
10g.119677029A>TCA378297399BAG3c.1475A>T (p.Glu492Val)
c.1472A>T (p.Glu491Val)
10g.119677030A=CA1940196814BAG3c.1476A= (p.Glu492=)
c.1473A= (p.Glu491=)
10g.119677030A>CCA378297400BAG3c.1476A>C (p.Glu492Asp)
c.1473A>C (p.Glu491Asp)
10g.119677030A>GCA471739488BAG3c.1476A>G (p.Glu492=)
c.1473A>G (p.Glu491=)
dbSNP gnomAD v2 gnomAD v4
10g.119677030A>TCA378297401BAG3c.1476A>T (p.Glu492Asp)
c.1473A>T (p.Glu491Asp)
10g.119677031A=CA1940196815BAG3c.1477A= (p.Lys493=)
c.1474A= (p.Lys492=)
10g.119677031A>CCA378297402BAG3c.1477A>C (p.Lys493Gln)
c.1474A>C (p.Lys492Gln)
10g.119677031A>GCA378297403BAG3c.1477A>G (p.Lys493Glu)
c.1474A>G (p.Lys492Glu)
ClinVar dbSNP gnomAD v3 gnomAD v4
10g.119677031A>TCA378297404BAG3c.1477A>T (p.Lys493Ter)
c.1474A>T (p.Lys492Ter)
10g.119677032A>CCA378297405BAG3c.1478A>C (p.Lys493Thr)
c.1475A>C (p.Lys492Thr)
10g.119677032A>GCA378297406BAG3c.1478A>G (p.Lys493Arg)
c.1475A>G (p.Lys492Arg)
10g.119677032A>TCA378297407BAG3c.1478A>T (p.Lys493Ile)
c.1475A>T (p.Lys492Ile)
10g.119677033A>CCA378297408BAG3c.1479A>C (p.Lys493Asn)
c.1476A>C (p.Lys492Asn)
10g.119677033A>GCA471739490BAG3c.1479A>G (p.Lys493=)
c.1476A>G (p.Lys492=)
10g.119677033A>TCA378297409BAG3c.1479A>T (p.Lys493Asn)
c.1476A>T (p.Lys492Asn)
10g.119677034C>ACA378297410BAG3c.1480C>A (p.Leu494Ile)
c.1477C>A (p.Leu493Ile)
10g.119677034C=CA1940196816BAG3c.1480C= (p.Leu494=)
c.1477C= (p.Leu493=)
10g.119677034C>GCA378297411BAG3c.1480C>G (p.Leu494Val)
c.1477C>G (p.Leu493Val)
10g.119677034C>TCA378297412BAG3c.1480C>T (p.Leu494Phe)
c.1477C>T (p.Leu493Phe)
ClinVar dbSNP gnomAD v2 gnomAD v4
10g.119677035T>ACA378297413BAG3c.1481T>A (p.Leu494His)
c.1478T>A (p.Leu493His)
10g.119677035T>CCA378297414BAG3c.1481T>C (p.Leu494Pro)
c.1478T>C (p.Leu493Pro)
ClinVar
10g.119677035T>GCA378297415BAG3c.1481T>G (p.Leu494Arg)
c.1478T>G (p.Leu493Arg)
10g.119677036delCA471739494BAG3c.1482del (p.Glu495AsnfsTer?)
c.1479del (p.Glu494AsnfsTer?)
COSMIC COSMIC
10g.119677036T>ACA471739495BAG3c.1482T>A (p.Leu494=)
c.1479T>A (p.Leu493=)
10g.119677036T>CCA471739496BAG3c.1482T>C (p.Leu494=)
c.1479T>C (p.Leu493=)
10g.119677036T>GCA471739497BAG3c.1482T>G (p.Leu494=)
c.1479T>G (p.Leu493=)
10g.119677037G>ACA378297416BAG3c.1483G>A (p.Glu495Lys)
c.1480G>A (p.Glu494Lys)
10g.119677037G>CCA378297417BAG3c.1483G>C (p.Glu495Gln)
c.1480G>C (p.Glu494Gln)
10g.119677037G>TCA378297418BAG3c.1483G>T (p.Glu495Ter)
c.1480G>T (p.Glu494Ter)
10g.119677037dupCA2789707798BAG3c.1483dup (p.Glu495GlyfsTer6)
c.1480dup (p.Glu494GlyfsTer6)
10g.119677038A>CCA378297419BAG3c.1484A>C (p.Glu495Ala)
c.1481A>C (p.Glu494Ala)
10g.119677038A>GCA378297420BAG3c.1484A>G (p.Glu495Gly)
c.1481A>G (p.Glu494Gly)
10g.119677038A>TCA378297421BAG3c.1484A>T (p.Glu495Val)
c.1481A>T (p.Glu494Val)
10g.119677039A=CA1940196817BAG3c.1485A= (p.Glu495=)
c.1482A= (p.Glu494=)
10g.119677039A>CCA378297422BAG3c.1485A>C (p.Glu495Asp)
c.1482A>C (p.Glu494Asp)
10g.119677039A>GCA5716557BAG3c.1485A>G (p.Glu495=)
c.1482A>G (p.Glu494=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
10g.119677039A>TCA378297423BAG3c.1485A>T (p.Glu495Asp)
c.1482A>T (p.Glu494Asp)
10g.119677040C>ACA378297424BAG3c.1486C>A (p.Gln496Lys)
c.1483C>A (p.Gln495Lys)
10g.119677040C>GCA378297425BAG3c.1486C>G (p.Gln496Glu)
c.1483C>G (p.Gln495Glu)
10g.119677040C>TCA378297426BAG3c.1486C>T (p.Gln496Ter)
c.1483C>T (p.Gln495Ter)
10g.119677041A>CCA378297427BAG3c.1487A>C (p.Gln496Pro)
c.1484A>C (p.Gln495Pro)
10g.119677041A>GCA378297428BAG3c.1487A>G (p.Gln496Arg)
c.1484A>G (p.Gln495Arg)
10g.119677041A>TCA378297429BAG3c.1487A>T (p.Gln496Leu)
c.1484A>T (p.Gln495Leu)
10g.119677042G>ACA471739502BAG3c.1488G>A (p.Gln496=)
c.1485G>A (p.Gln495=)
10g.119677042G>CCA378297430BAG3c.1488G>C (p.Gln496His)
c.1485G>C (p.Gln495His)
10g.119677042G>TCA378297431BAG3c.1488G>T (p.Gln496His)
c.1485G>T (p.Gln495His)
10g.119677043A>CCA378297432BAG3c.1489A>C (p.Lys497Gln)
c.1486A>C (p.Lys496Gln)
ClinVar
10g.119677043A>GCA378297433BAG3c.1489A>G (p.Lys497Glu)
c.1486A>G (p.Lys496Glu)
10g.119677043A>TCA378297434BAG3c.1489A>T (p.Lys497Ter)
c.1486A>T (p.Lys496Ter)
10g.119677045delCA2740093567BAG3c.1491del (p.Ala498ProfsTer?)
c.1488del (p.Ala497ProfsTer?)
ClinVar
10g.119677044A>CCA378297437BAG3c.1490A>C (p.Lys497Thr)
c.1487A>C (p.Lys496Thr)
10g.119677044A>GCA378297435BAG3c.1490A>G (p.Lys497Arg)
c.1487A>G (p.Lys496Arg)
gnomAD v4
10g.119677044A>TCA378297436BAG3c.1490A>T (p.Lys497Ile)
c.1487A>T (p.Lys496Ile)
10g.119677045A>CCA378297438BAG3c.1491A>C (p.Lys497Asn)
c.1488A>C (p.Lys496Asn)
10g.119677045A>GCA471739504BAG3c.1491A>G (p.Lys497=)
c.1488A>G (p.Lys496=)
ClinVar dbSNP gnomAD v4
10g.119677045A>TCA378297439BAG3c.1491A>T (p.Lys497Asn)
c.1488A>T (p.Lys496Asn)
gnomAD v4
10g.119677046G>ACA378297440BAG3c.1492G>A (p.Ala498Thr)
c.1489G>A (p.Ala497Thr)
10g.119677046G>CCA378297441BAG3c.1492G>C (p.Ala498Pro)
c.1489G>C (p.Ala497Pro)
10g.119677046G>TCA378297442BAG3c.1492G>T (p.Ala498Ser)
c.1489G>T (p.Ala497Ser)
ClinVar gnomAD v4
10g.119677047C>ACA378297443BAG3c.1493C>A (p.Ala498Asp)
c.1490C>A (p.Ala497Asp)
10g.119677047C=CA1940196818BAG3c.1493C= (p.Ala498=)
c.1490C= (p.Ala497=)
10g.119677047C>GCA378297444BAG3c.1493C>G (p.Ala498Gly)
c.1490C>G (p.Ala497Gly)
10g.119677047C>TCA378297445BAG3c.1493C>T (p.Ala498Val)
c.1490C>T (p.Ala497Val)
dbSNP
10g.119677047_119677048insGGGAGACCA2548133862BAG3c.1493_1494insGGGAGAC (p.Ile499GlyfsTer4)
c.1490_1491insGGGAGAC (p.Ile498GlyfsTer4)
10g.119677050_119677060delCA2740093568BAG3c.1496_1506del (p.Ile499ArgfsTer7)
c.1493_1503del (p.Ile498ArgfsTer7)
ClinVar
10g.119677048C>ACA471739506BAG3c.1494C>A (p.Ala498=)
c.1491C>A (p.Ala497=)
dbSNP
10g.119677048C=CA1940196819BAG3c.1494C= (p.Ala498=)
c.1491C= (p.Ala497=)
10g.119677048C>GCA471739507BAG3c.1494C>G (p.Ala498=)
c.1491C>G (p.Ala497=)
10g.119677048C>TCA471739508BAG3c.1494C>T (p.Ala498=)
c.1491C>T (p.Ala497=)
ClinVar gnomAD v4
10g.119677049A>CCA378297446BAG3c.1495A>C (p.Ile499Leu)
c.1492A>C (p.Ile498Leu)
10g.119677049A>GCA378297447BAG3c.1495A>G (p.Ile499Val)
c.1492A>G (p.Ile498Val)
10g.119677049A>TCA378297448BAG3c.1495A>T (p.Ile499Phe)
c.1492A>T (p.Ile498Phe)
10g.119677049_119677050insAATAAATTGGCCTAACAGCGACAACAGTTTTGTCTCTCGAAATTCGTCACACATAACTAACACTTATGAAACATCTTAGAATACTCATCCTGACAATCGTCCTGAGCAGCGTTGCAGGCCCA2559022289BAG3c.1495_1496insAATAAATTGGCCTAACAGCGACAACAGTTTTGTCTCTCGAAATTCGTCACACATAACTAACACTTATGAAACATCTTAGAATACTCATCCTGACAATCGTCCTGAGCAGCGTTGCAGGCC (p.Ile499LysfsTer2)
c.1492_1493insAATAAATTGGCCTAACAGCGACAACAGTTTTGTCTCTCGAAATTCGTCACACATAACTAACACTTATGAAACATCTTAGAATACTCATCCTGACAATCGTCCTGAGCAGCGTTGCAGGCC (p.Ile498LysfsTer2)
10g.119677050T>ACA378297450BAG3c.1496T>A (p.Ile499Asn)
c.1493T>A (p.Ile498Asn)
ClinVar gnomAD v4
10g.119677050T>CCA378297451BAG3c.1496T>C (p.Ile499Thr)
c.1493T>C (p.Ile498Thr)
ClinVar dbSNP gnomAD v2 gnomAD v4
10g.119677050T>GCA378297449BAG3c.1496T>G (p.Ile499Ser)
c.1493T>G (p.Ile498Ser)
10g.119677050T=CA1940196820BAG3c.1496T= (p.Ile499=)
c.1493T= (p.Ile498=)
10g.119677051T>ACA471739510BAG3c.1497T>A (p.Ile499=)
c.1494T>A (p.Ile498=)
10g.119677051T>CCA471739511BAG3c.1497T>C (p.Ile499=)
c.1494T>C (p.Ile498=)
dbSNP
10g.119677051T>GCA378297452BAG3c.1497T>G (p.Ile499Met)
c.1494T>G (p.Ile498Met)
10g.119677051T=CA1940196821BAG3c.1497T= (p.Ile499=)
c.1494T= (p.Ile498=)
10g.119677052G>ACA378297453BAG3c.1498G>A (p.Asp500Asn)
c.1495G>A (p.Asp499Asn)
10g.119677052G>CCA5716558BAG3c.1498G>C (p.Asp500His)
c.1495G>C (p.Asp499His)
dbSNP ExAC gnomAD v2 gnomAD v4
10g.119677052G=CA1940196822BAG3c.1498G= (p.Asp500=)
c.1495G= (p.Asp499=)
10g.119677052G>TCA378297454BAG3c.1498G>T (p.Asp500Tyr)
c.1495G>T (p.Asp499Tyr)
ClinVar gnomAD v4
10g.119677053A>CCA378297455BAG3c.1499A>C (p.Asp500Ala)
c.1496A>C (p.Asp499Ala)
10g.119677053A>GCA378297456BAG3c.1499A>G (p.Asp500Gly)
c.1496A>G (p.Asp499Gly)
10g.119677053A>TCA378297457BAG3c.1499A>T (p.Asp500Val)
c.1496A>T (p.Asp499Val)
ClinVar dbSNP
10g.119677054T>ACA378297458BAG3c.1500T>A (p.Asp500Glu)
c.1497T>A (p.Asp499Glu)
gnomAD v4
10g.119677054T>CCA471739515BAG3c.1500T>C (p.Asp500=)
c.1497T>C (p.Asp499=)
10g.119677054T>GCA378297459BAG3c.1500T>G (p.Asp500Glu)
c.1497T>G (p.Asp499Glu)
10g.119677055G>ACA378297460BAG3c.1501G>A (p.Val501Ile)
c.1498G>A (p.Val500Ile)
dbSNP
10g.119677055G>CCA378297461BAG3c.1501G>C (p.Val501Leu)
c.1498G>C (p.Val500Leu)
10g.119677055G=CA1940196823BAG3c.1501G= (p.Val501=)
c.1498G= (p.Val500=)
10g.119677055G>TCA378297462BAG3c.1501G>T (p.Val501Phe)
c.1498G>T (p.Val500Phe)
10g.119677056T>ACA378297463BAG3c.1502T>A (p.Val501Asp)
c.1499T>A (p.Val500Asp)
dbSNP
10g.119677056T>CCA378297464BAG3c.1502T>C (p.Val501Ala)
c.1499T>C (p.Val500Ala)
10g.119677056T>GCA378297465BAG3c.1502T>G (p.Val501Gly)
c.1499T>G (p.Val500Gly)
10g.119677056T=CA1940196824BAG3c.1502T= (p.Val501=)
c.1499T= (p.Val500=)
10g.119677057C>ACA5716559BAG3c.1503C>A (p.Val501=)
c.1500C>A (p.Val500=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119677057C=CA1940196825BAG3c.1503C= (p.Val501=)
c.1500C= (p.Val500=)
10g.119677057C>GCA471739517BAG3c.1503C>G (p.Val501=)
c.1500C>G (p.Val500=)
10g.119677057C>TCA10635036BAG3c.1503C>T (p.Val501=)
c.1500C>T (p.Val500=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.119677058C>ACA378297466BAG3c.1504C>A (p.Pro502Thr)
c.1501C>A (p.Pro501Thr)
10g.119677058C=CA1940196826BAG3c.1504C= (p.Pro502=)
c.1501C= (p.Pro501=)
10g.119677058C>GCA378297467BAG3c.1504C>G (p.Pro502Ala)
c.1501C>G (p.Pro501Ala)
ClinVar dbSNP gnomAD v4
10g.119677058C>TCA378297468BAG3c.1504C>T (p.Pro502Ser)
c.1501C>T (p.Pro501Ser)
ClinVar gnomAD v4
10g.119677065_119677075delCA2580082443BAG3c.1511_1521del (p.Gln504LeufsTer2)
c.1508_1518del (p.Gln503LeufsTer2)
ClinVar
10g.119677059C>ACA378297469BAG3c.1505C>A (p.Pro502Gln)
c.1502C>A (p.Pro501Gln)
10g.119677059C=CA1940196827BAG3c.1505C= (p.Pro502=)
c.1502C= (p.Pro501=)
10g.119677059C>GCA5716560BAG3c.1505C>G (p.Pro502Arg)
c.1502C>G (p.Pro501Arg)
dbSNP ExAC gnomAD v2 gnomAD v4
10g.119677059C>TCA378297470BAG3c.1505C>T (p.Pro502Leu)
c.1502C>T (p.Pro501Leu)
10g.119677060A>CCA471739518BAG3c.1506A>C (p.Pro502=)
c.1503A>C (p.Pro501=)
10g.119677060A>GCA471739519BAG3c.1506A>G (p.Pro502=)
c.1503A>G (p.Pro501=)
10g.119677060A>TCA471739520BAG3c.1506A>T (p.Pro502=)
c.1503A>T (p.Pro501=)
10g.119677061G>ACA378297471BAG3c.1507G>A (p.Gly503Ser)
c.1504G>A (p.Gly502Ser)
ClinVar
10g.119677061G>CCA378297472BAG3c.1507G>C (p.Gly503Arg)
c.1504G>C (p.Gly502Arg)
10g.119677061G>TCA378297473BAG3c.1507G>T (p.Gly503Cys)
c.1504G>T (p.Gly502Cys)
10g.119677062G>ACA378297474BAG3c.1508G>A (p.Gly503Asp)
c.1505G>A (p.Gly502Asp)
dbSNP
10g.119677062G>CCA378297475BAG3c.1508G>C (p.Gly503Ala)
c.1505G>C (p.Gly502Ala)
10g.119677062G=CA1940196828BAG3c.1508G= (p.Gly503=)
c.1505G= (p.Gly502=)
10g.119677062G>TCA378297476BAG3c.1508G>T (p.Gly503Val)
c.1505G>T (p.Gly502Val)
gnomAD v4
10g.119677063T>ACA471739524BAG3c.1509T>A (p.Gly503=)
c.1506T>A (p.Gly502=)
10g.119677063T>CCA471739525BAG3c.1509T>C (p.Gly503=)
c.1506T>C (p.Gly502=)
10g.119677063T>GCA471739526BAG3c.1509T>G (p.Gly503=)
c.1506T>G (p.Gly502=)
gnomAD v4
10g.119677064C>ACA378297479BAG3c.1510C>A (p.Gln504Lys)
c.1507C>A (p.Gln503Lys)
10g.119677064C>GCA378297478BAG3c.1510C>G (p.Gln504Glu)
c.1507C>G (p.Gln503Glu)
10g.119677064C>TCA378297477BAG3c.1510C>T (p.Gln504Ter)
c.1507C>T (p.Gln503Ter)
10g.119677065A=CA1940196829BAG3c.1511A= (p.Gln504=)
c.1508A= (p.Gln503=)
10g.119677065A>CCA378297480BAG3c.1511A>C (p.Gln504Pro)
c.1508A>C (p.Gln503Pro)
dbSNP gnomAD v2
10g.119677065A>GCA378297481BAG3c.1511A>G (p.Gln504Arg)
c.1508A>G (p.Gln503Arg)
10g.119677065A>TCA378297482BAG3c.1511A>T (p.Gln504Leu)
c.1508A>T (p.Gln503Leu)
10g.119677066A=CA1940196830BAG3c.1512A= (p.Gln504=)
c.1509A= (p.Gln503=)
10g.119677066A>CCA378297483BAG3c.1512A>C (p.Gln504His)
c.1509A>C (p.Gln503His)
10g.119677066A>GCA471739527BAG3c.1512A>G (p.Gln504=)
c.1509A>G (p.Gln503=)
dbSNP gnomAD v3 gnomAD v4
10g.119677066A>TCA378297484BAG3c.1512A>T (p.Gln504His)
c.1509A>T (p.Gln503His)
10g.119677067G>ACA378297487BAG3c.1513G>A (p.Val505Ile)
c.1510G>A (p.Val504Ile)
10g.119677067G>CCA378297486BAG3c.1513G>C (p.Val505Leu)
c.1510G>C (p.Val504Leu)
10g.119677067G>TCA378297485BAG3c.1513G>T (p.Val505Phe)
c.1510G>T (p.Val504Phe)
10g.119677068T>ACA378297488BAG3c.1514T>A (p.Val505Asp)
c.1511T>A (p.Val504Asp)
10g.119677068T>CCA378297489BAG3c.1514T>C (p.Val505Ala)
c.1511T>C (p.Val504Ala)
10g.119677068T>GCA378297490BAG3c.1514T>G (p.Val505Gly)
c.1511T>G (p.Val504Gly)
10g.119677069C>ACA471739529BAG3c.1515C>A (p.Val505=)
c.1512C>A (p.Val504=)
10g.119677069C=CA1940196831BAG3c.1515C= (p.Val505=)
c.1512C= (p.Val504=)
10g.119677069C>GCA471739530BAG3c.1515C>G (p.Val505=)
c.1512C>G (p.Val504=)
dbSNP gnomAD v2 gnomAD v4
10g.119677069C>TCA471739531BAG3c.1515C>T (p.Val505=)
c.1512C>T (p.Val504=)
10g.119677070C>ACA378297491BAG3c.1516C>A (p.Gln506Lys)
c.1513C>A (p.Gln505Lys)
10g.119677070C>GCA378297492BAG3c.1516C>G (p.Gln506Glu)
c.1513C>G (p.Gln505Glu)
ClinVar gnomAD v4
10g.119677070C>TCA378297493BAG3c.1516C>T (p.Gln506Ter)
c.1513C>T (p.Gln505Ter)
10g.119677071A>CCA378297494BAG3c.1517A>C (p.Gln506Pro)
c.1514A>C (p.Gln505Pro)
10g.119677071A>GCA378297496BAG3c.1517A>G (p.Gln506Arg)
c.1514A>G (p.Gln505Arg)
gnomAD v4
10g.119677071A>TCA378297495BAG3c.1517A>T (p.Gln506Leu)
c.1514A>T (p.Gln505Leu)
10g.119677072G>ACA471739533BAG3c.1518G>A (p.Gln506=)
c.1515G>A (p.Gln505=)
gnomAD v4
10g.119677072G>CCA378297497BAG3c.1518G>C (p.Gln506His)
c.1515G>C (p.Gln505His)
10g.119677072G>TCA378297498BAG3c.1518G>T (p.Gln506His)
c.1515G>T (p.Gln505His)
10g.119677073delCA2573145591BAG3c.1519del (p.Val507SerfsTer?)
c.1516del (p.Val506SerfsTer?)
ClinVar dbSNP
10g.119677073G>ACA378297499BAG3c.1519G>A (p.Val507Ile)
c.1516G>A (p.Val506Ile)
gnomAD v4
10g.119677073G>CCA378297500BAG3c.1519G>C (p.Val507Leu)
c.1516G>C (p.Val506Leu)
10g.119677073G>TCA378297501BAG3c.1519G>T (p.Val507Phe)
c.1516G>T (p.Val506Phe)
10g.119677074T>ACA378297502BAG3c.1520T>A (p.Val507Asp)
c.1517T>A (p.Val506Asp)
10g.119677074T>CCA378297503BAG3c.1520T>C (p.Val507Ala)
c.1517T>C (p.Val506Ala)
dbSNP
10g.119677074T>GCA378297504BAG3c.1520T>G (p.Val507Gly)
c.1517T>G (p.Val506Gly)
10g.119677074T=CA1940196832BAG3c.1520T= (p.Val507=)
c.1517T= (p.Val506=)
10g.119677075C>ACA471739534BAG3c.1521C>A (p.Val507=)
c.1518C>A (p.Val506=)
10g.119677075C>GCA471739535BAG3c.1521C>G (p.Val507=)
c.1518C>G (p.Val506=)
10g.119677075C>TCA471739536BAG3c.1521C>T (p.Val507=)
c.1518C>T (p.Val506=)
10g.119677076T>ACA378297505BAG3c.1522T>A (p.Tyr508Asn)
c.1519T>A (p.Tyr507Asn)
10g.119677076T>CCA378297506BAG3c.1522T>C (p.Tyr508His)
c.1519T>C (p.Tyr507His)
10g.119677076T>GCA378297507BAG3c.1522T>G (p.Tyr508Asp)
c.1519T>G (p.Tyr507Asp)
10g.119677077A=CA1940196833BAG3c.1523A= (p.Tyr508=)
c.1520A= (p.Tyr507=)
10g.119677077A>CCA378297509BAG3c.1523A>C (p.Tyr508Ser)
c.1520A>C (p.Tyr507Ser)
10g.119677077A>GCA5716561BAG3c.1523A>G (p.Tyr508Cys)
c.1520A>G (p.Tyr507Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119677077A>TCA378297508BAG3c.1523A>T (p.Tyr508Phe)
c.1520A>T (p.Tyr507Phe)
10g.119677078T>ACA378297510BAG3c.1524T>A (p.Tyr508Ter)
c.1521T>A (p.Tyr507Ter)
10g.119677078T>CCA471739540BAG3c.1524T>C (p.Tyr508=)
c.1521T>C (p.Tyr507=)
dbSNP
10g.119677078T>GCA378297511BAG3c.1524T>G (p.Tyr508Ter)
c.1521T>G (p.Tyr507Ter)
10g.119677079G>ACA378297512BAG3c.1525G>A (p.Glu509Lys)
c.1522G>A (p.Glu508Lys)
10g.119677079G>CCA378297513BAG3c.1525G>C (p.Glu509Gln)
c.1522G>C (p.Glu508Gln)
10g.119677079G>TCA378297514BAG3c.1525G>T (p.Glu509Ter)
c.1522G>T (p.Glu508Ter)
10g.119677080A>CCA378297515BAG3c.1526A>C (p.Glu509Ala)
c.1523A>C (p.Glu508Ala)
10g.119677080A>GCA378297516BAG3c.1526A>G (p.Glu509Gly)
c.1523A>G (p.Glu508Gly)
10g.119677080A>TCA378297517BAG3c.1526A>T (p.Glu509Val)
c.1523A>T (p.Glu508Val)
10g.119677081A=CA1940196835BAG3c.1527A= (p.Glu509=)
c.1524A= (p.Glu508=)
10g.119677081A>CCA378297518BAG3c.1527A>C (p.Glu509Asp)
c.1524A>C (p.Glu508Asp)
10g.119677081A>GCA471739636BAG3c.1527A>G (p.Glu509=)
c.1524A>G (p.Glu508=)
ClinVar dbSNP gnomAD v4
10g.119677081A>TCA378297519BAG3c.1527A>T (p.Glu509Asp)
c.1524A>T (p.Glu508Asp)
10g.119677081_119677087delinsACTCCAGCA1940196834BAG3c.1527_1533delinsACTCCAG (p.Glu509=)
c.1524_1530delinsACTCCAG (p.Glu508=)
10g.119677082C>ACA378297520BAG3c.1528C>A (p.Leu510Ile)
c.1525C>A (p.Leu509Ile)
10g.119677082C=CA1940196836BAG3c.1528C= (p.Leu510=)
c.1525C= (p.Leu509=)
10g.119677082C>GCA378297521BAG3c.1528C>G (p.Leu510Val)
c.1525C>G (p.Leu509Val)
10g.119677082C>TCA5716562BAG3c.1528C>T (p.Leu510Phe)
c.1525C>T (p.Leu509Phe)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
10g.119677083_119677088delCA596578108BAG3c.1529_1534del (p.Leu510_Gln511del)
c.1526_1531del (p.Leu509_Gln510del)
dbSNP gnomAD v2 gnomAD v4
10g.119677083T>ACA378297522BAG3c.1529T>A (p.Leu510His)
c.1526T>A (p.Leu509His)
10g.119677083T>CCA378297523BAG3c.1529T>C (p.Leu510Pro)
c.1526T>C (p.Leu509Pro)
10g.119677083T>GCA378297524BAG3c.1529T>G (p.Leu510Arg)
c.1526T>G (p.Leu509Arg)
10g.119677084C>ACA471739640BAG3c.1530C>A (p.Leu510=)
c.1527C>A (p.Leu509=)
10g.119677084C>GCA471739642BAG3c.1530C>G (p.Leu510=)
c.1527C>G (p.Leu509=)
gnomAD v4 COSMIC
10g.119677084C>TCA471739641BAG3c.1530C>T (p.Leu510=)
c.1527C>T (p.Leu509=)
ClinVar
10g.119677085C>ACA378297525BAG3c.1531C>A (p.Gln511Lys)
c.1528C>A (p.Gln510Lys)
ClinVar dbSNP gnomAD v4
10g.119677085C=CA1940196837BAG3c.1531C= (p.Gln511=)
c.1528C= (p.Gln510=)
10g.119677085C>GCA5716563BAG3c.1531C>G (p.Gln511Glu)
c.1528C>G (p.Gln510Glu)
dbSNP ExAC gnomAD v2 gnomAD v4
10g.119677085C>TCA378297526BAG3c.1531C>T (p.Gln511Ter)
c.1528C>T (p.Gln510Ter)
ClinVar dbSNP
10g.119677086A>CCA378297527BAG3c.1532A>C (p.Gln511Pro)
c.1529A>C (p.Gln510Pro)
10g.119677086A>GCA378297528BAG3c.1532A>G (p.Gln511Arg)
c.1529A>G (p.Gln510Arg)
10g.119677086A>TCA378297529BAG3c.1532A>T (p.Gln511Leu)
c.1529A>T (p.Gln510Leu)
gnomAD v4
10g.119677087G>ACA5716564BAG3c.1533G>A (p.Gln511=)
c.1530G>A (p.Gln510=)
dbSNP ExAC gnomAD v2 gnomAD v4
10g.119677087G>CCA378297530BAG3c.1533G>C (p.Gln511His)
c.1530G>C (p.Gln510His)
gnomAD v4
10g.119677087G=CA1940196838BAG3c.1533G= (p.Gln511=)
c.1530G= (p.Gln510=)
10g.119677087G>TCA378297531BAG3c.1533G>T (p.Gln511His)
c.1530G>T (p.Gln510His)
10g.119677088C>ACA378297532BAG3c.1534C>A (p.Pro512Thr)
c.1531C>A (p.Pro511Thr)
10g.119677088C=CA1940196839BAG3c.1534C= (p.Pro512=)
c.1531C= (p.Pro511=)
10g.119677088C>GCA378297533BAG3c.1534C>G (p.Pro512Ala)
c.1531C>G (p.Pro511Ala)
10g.119677088C>TCA5716565BAG3c.1534C>T (p.Pro512Ser)
c.1531C>T (p.Pro511Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119677089C>ACA378297534BAG3c.1535C>A (p.Pro512His)
c.1532C>A (p.Pro511His)
10g.119677089C>GCA378297535BAG3c.1535C>G (p.Pro512Arg)
c.1532C>G (p.Pro511Arg)
10g.119677089C>TCA378297536BAG3c.1535C>T (p.Pro512Leu)
c.1532C>T (p.Pro511Leu)
10g.119677090C>ACA471739646BAG3c.1536C>A (p.Pro512=)
c.1533C>A (p.Pro511=)
10g.119677090C=CA1940196840BAG3c.1536C= (p.Pro512=)
c.1533C= (p.Pro511=)
10g.119677090C>GCA471739647BAG3c.1536C>G (p.Pro512=)
c.1533C>G (p.Pro511=)
10g.119677090C>TCA471739648BAG3c.1536C>T (p.Pro512=)
c.1533C>T (p.Pro511=)
ClinVar dbSNP gnomAD v4
10g.119677091A=CA1940196841BAG3c.1537A= (p.Ser513=)
c.1534A= (p.Ser512=)
10g.119677091A>CCA378297539BAG3c.1537A>C (p.Ser513Arg)
c.1534A>C (p.Ser512Arg)
10g.119677091A>GCA378297537BAG3c.1537A>G (p.Ser513Gly)
c.1534A>G (p.Ser512Gly)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.119677091A>TCA378297538BAG3c.1537A>T (p.Ser513Cys)
c.1534A>T (p.Ser512Cys)
10g.119677092G>ACA378297540BAG3c.1538G>A (p.Ser513Asn)
c.1535G>A (p.Ser512Asn)
10g.119677092G>CCA378297541BAG3c.1538G>C (p.Ser513Thr)
c.1535G>C (p.Ser512Thr)
ClinVar
10g.119677092G>TCA378297542BAG3c.1538G>T (p.Ser513Ile)
c.1535G>T (p.Ser512Ile)
10g.119677093C>ACA378297543BAG3c.1539C>A (p.Ser513Arg)
c.1536C>A (p.Ser512Arg)
10g.119677093C=CA1940196842BAG3c.1539C= (p.Ser513=)
c.1536C= (p.Ser512=)
10g.119677093C>GCA378297544BAG3c.1539C>G (p.Ser513Arg)
c.1536C>G (p.Ser512Arg)
gnomAD v4
10g.119677093C>TCA5716566BAG3c.1539C>T (p.Ser513=)
c.1536C>T (p.Ser512=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
10g.119677094A>CCA378297547BAG3c.1540A>C (p.Asn514His)
c.1537A>C (p.Asn513His)
10g.119677094A>GCA378297545BAG3c.1540A>G (p.Asn514Asp)
c.1537A>G (p.Asn513Asp)
10g.119677094A>TCA378297546BAG3c.1540A>T (p.Asn514Tyr)
c.1537A>T (p.Asn513Tyr)
10g.119677095A=CA1940196843BAG3c.1541A= (p.Asn514=)
c.1538A= (p.Asn513=)
10g.119677095A>CCA378297548BAG3c.1541A>C (p.Asn514Thr)
c.1538A>C (p.Asn513Thr)
10g.119677095A>GCA378297549BAG3c.1541A>G (p.Asn514Ser)
c.1538A>G (p.Asn513Ser)
ClinVar dbSNP
10g.119677095A>TCA378297550BAG3c.1541A>T (p.Asn514Ile)
c.1538A>T (p.Asn513Ile)
dbSNP gnomAD v3 gnomAD v4
10g.119677096C>ACA378297551BAG3c.1542C>A (p.Asn514Lys)
c.1539C>A (p.Asn513Lys)
10g.119677096C>GCA378297552BAG3c.1542C>G (p.Asn514Lys)
c.1539C>G (p.Asn513Lys)
gnomAD v4
10g.119677096C>TCA471739654BAG3c.1542C>T (p.Asn514=)
c.1539C>T (p.Asn513=)
ClinVar
10g.119677097C>ACA378297555BAG3c.1543C>A (p.Leu515Ile)
c.1540C>A (p.Leu514Ile)
10g.119677097C>GCA378297553BAG3c.1543C>G (p.Leu515Val)
c.1540C>G (p.Leu514Val)
10g.119677097C>TCA378297554BAG3c.1543C>T (p.Leu515Phe)
c.1540C>T (p.Leu514Phe)
ClinVar gnomAD v4
10g.119677098T>ACA378297556BAG3c.1544T>A (p.Leu515His)
c.1541T>A (p.Leu514His)
gnomAD v4
10g.119677098T>CCA378297557BAG3c.1544T>C (p.Leu515Pro)
c.1541T>C (p.Leu514Pro)
gnomAD v4
10g.119677098T>GCA378297558BAG3c.1544T>G (p.Leu515Arg)
c.1541T>G (p.Leu514Arg)

Number of alleles fetched