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.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)
10g.119677099T>ACA471739656BAG3c.1545T>A (p.Leu515=)
c.1542T>A (p.Leu514=)
10g.119677099T>CCA5716567BAG3c.1545T>C (p.Leu515=)
c.1542T>C (p.Leu514=)
dbSNP ExAC gnomAD v4
10g.119677099T>GCA471739657BAG3c.1545T>G (p.Leu515=)
c.1542T>G (p.Leu514=)
10g.119677099T=CA1940196844BAG3c.1545T= (p.Leu515=)
c.1542T= (p.Leu514=)
10g.119677100G>ACA378297559BAG3c.1546G>A (p.Glu516Lys)
c.1543G>A (p.Glu515Lys)
ClinVar
10g.119677100G>CCA378297560BAG3c.1546G>C (p.Glu516Gln)
c.1543G>C (p.Glu515Gln)
dbSNP
10g.119677100G=CA1940196845BAG3c.1546G= (p.Glu516=)
c.1543G= (p.Glu515=)
10g.119677100G>TCA378297561BAG3c.1546G>T (p.Glu516Ter)
c.1543G>T (p.Glu515Ter)
10g.119677101A>CCA378297562BAG3c.1547A>C (p.Glu516Ala)
c.1544A>C (p.Glu515Ala)
10g.119677101A>GCA378297563BAG3c.1547A>G (p.Glu516Gly)
c.1544A>G (p.Glu515Gly)
10g.119677101A>TCA378297564BAG3c.1547A>T (p.Glu516Val)
c.1544A>T (p.Glu515Val)
10g.119677102A>CCA378297565BAG3c.1548A>C (p.Glu516Asp)
c.1545A>C (p.Glu515Asp)
10g.119677102A>GCA471739659BAG3c.1548A>G (p.Glu516=)
c.1545A>G (p.Glu515=)
10g.119677102A>TCA378297566BAG3c.1548A>T (p.Glu516Asp)
c.1545A>T (p.Glu515Asp)
10g.119677103G>ACA378297567BAG3c.1549G>A (p.Ala517Thr)
c.1546G>A (p.Ala516Thr)
10g.119677103G>CCA378297568BAG3c.1549G>C (p.Ala517Pro)
c.1546G>C (p.Ala516Pro)
10g.119677103G=CA1940196846BAG3c.1549G= (p.Ala517=)
c.1546G= (p.Ala516=)
10g.119677103G>TCA214225324BAG3c.1549G>T (p.Ala517Ser)
c.1546G>T (p.Ala516Ser)
ClinVar dbSNP gnomAD v2 gnomAD v4
10g.119677104C>ACA378297569BAG3c.1550C>A (p.Ala517Glu)
c.1547C>A (p.Ala516Glu)
10g.119677104C>GCA378297570BAG3c.1550C>G (p.Ala517Gly)
c.1547C>G (p.Ala516Gly)
10g.119677104C>TCA378297571BAG3c.1550C>T (p.Ala517Val)
c.1547C>T (p.Ala516Val)
gnomAD v4
10g.119677105A>CCA471739661BAG3c.1551A>C (p.Ala517=)
c.1548A>C (p.Ala516=)
10g.119677105A>GCA471739662BAG3c.1551A>G (p.Ala517=)
c.1548A>G (p.Ala516=)
10g.119677105A>TCA471739663BAG3c.1551A>T (p.Ala517=)
c.1548A>T (p.Ala516=)
10g.119677106G>ACA5716568BAG3c.1552G>A (p.Asp518Asn)
c.1549G>A (p.Asp517Asn)
dbSNP ExAC gnomAD v2 gnomAD v4
10g.119677106G>CCA378297572BAG3c.1552G>C (p.Asp518His)
c.1549G>C (p.Asp517His)
ClinVar gnomAD v4
10g.119677106G=CA1940196847BAG3c.1552G= (p.Asp518=)
c.1549G= (p.Asp517=)
10g.119677106G>TCA378297573BAG3c.1552G>T (p.Asp518Tyr)
c.1549G>T (p.Asp517Tyr)
gnomAD v4
10g.119677107A>CCA378297576BAG3c.1553A>C (p.Asp518Ala)
c.1550A>C (p.Asp517Ala)
10g.119677107A>GCA378297574BAG3c.1553A>G (p.Asp518Gly)
c.1550A>G (p.Asp517Gly)
gnomAD v4
10g.119677107A>TCA378297575BAG3c.1553A>T (p.Asp518Val)
c.1550A>T (p.Asp517Val)
10g.119677108T>ACA5716569BAG3c.1554T>A (p.Asp518Glu)
c.1551T>A (p.Asp517Glu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119677108T>CCA471739666BAG3c.1554T>C (p.Asp518=)
c.1551T>C (p.Asp517=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.119677108T>GCA378297577BAG3c.1554T>G (p.Asp518Glu)
c.1551T>G (p.Asp517Glu)
10g.119677108T=CA1940196848BAG3c.1554T= (p.Asp518=)
c.1551T= (p.Asp517=)
10g.119677109C>ACA378297578BAG3c.1555C>A (p.Gln519Lys)
c.1552C>A (p.Gln518Lys)
10g.119677109C>GCA378297579BAG3c.1555C>G (p.Gln519Glu)
c.1552C>G (p.Gln518Glu)
10g.119677109C>TCA378297580BAG3c.1555C>T (p.Gln519Ter)
c.1552C>T (p.Gln518Ter)
gnomAD v4
10g.119677110A>CCA378297583BAG3c.1556A>C (p.Gln519Pro)
c.1553A>C (p.Gln518Pro)
10g.119677110A>GCA378297581BAG3c.1556A>G (p.Gln519Arg)
c.1553A>G (p.Gln518Arg)
10g.119677110A>TCA378297582BAG3c.1556A>T (p.Gln519Leu)
c.1553A>T (p.Gln518Leu)
10g.119677111G>ACA471739670BAG3c.1557G>A (p.Gln519=)
c.1554G>A (p.Gln518=)
10g.119677111G>CCA378297584BAG3c.1557G>C (p.Gln519His)
c.1554G>C (p.Gln518His)
gnomAD v4
10g.119677111G>TCA378297585BAG3c.1557G>T (p.Gln519His)
c.1554G>T (p.Gln518His)
10g.119677112C>ACA378297586BAG3c.1558C>A (p.Pro520Thr)
c.1555C>A (p.Pro519Thr)
10g.119677112C=CA1940196849BAG3c.1558C= (p.Pro520=)
c.1555C= (p.Pro519=)
10g.119677112C>GCA378297587BAG3c.1558C>G (p.Pro520Ala)
c.1555C>G (p.Pro519Ala)
10g.119677112C>TCA5716570BAG3c.1558C>T (p.Pro520Ser)
c.1555C>T (p.Pro519Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
10g.119677113C>ACA5716571BAG3c.1559C>A (p.Pro520Gln)
c.1556C>A (p.Pro519Gln)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119677113C=CA1940196850BAG3c.1559C= (p.Pro520=)
c.1556C= (p.Pro519=)
10g.119677113C>GCA378297588BAG3c.1559C>G (p.Pro520Arg)
c.1556C>G (p.Pro519Arg)
10g.119677113C>TCA378297589BAG3c.1559C>T (p.Pro520Leu)
c.1556C>T (p.Pro519Leu)
ClinVar
10g.119677114A>CCA471739675BAG3c.1560A>C (p.Pro520=)
c.1557A>C (p.Pro519=)
10g.119677114A>GCA471739673BAG3c.1560A>G (p.Pro520=)
c.1557A>G (p.Pro519=)
10g.119677114A>TCA471739674BAG3c.1560A>T (p.Pro520=)
c.1557A>T (p.Pro519=)
10g.119677115C>ACA378297590BAG3c.1561C>A (p.Leu521Met)
c.1558C>A (p.Leu520Met)
10g.119677115C>GCA378297591BAG3c.1561C>G (p.Leu521Val)
c.1558C>G (p.Leu520Val)
10g.119677115C>TCA471739677BAG3c.1561C>T (p.Leu521=)
c.1558C>T (p.Leu520=)
10g.119677116T>ACA378297592BAG3c.1562T>A (p.Leu521Gln)
c.1559T>A (p.Leu520Gln)
10g.119677116T>CCA378297593BAG3c.1562T>C (p.Leu521Pro)
c.1559T>C (p.Leu520Pro)
10g.119677116T>GCA378297594BAG3c.1562T>G (p.Leu521Arg)
c.1559T>G (p.Leu520Arg)
10g.119677117G>ACA214225340BAG3c.1563G>A (p.Leu521=)
c.1560G>A (p.Leu520=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.119677117G>CCA471739678BAG3c.1563G>C (p.Leu521=)
c.1560G>C (p.Leu520=)
10g.119677117G=CA1940196851BAG3c.1563G= (p.Leu521=)
c.1560G= (p.Leu520=)
10g.119677117G>TCA471739679BAG3c.1563G>T (p.Leu521=)
c.1560G>T (p.Leu520=)
10g.119677118C>ACA378297595BAG3c.1564C>A (p.Gln522Lys)
c.1561C>A (p.Gln521Lys)
10g.119677118C=CA1940196852BAG3c.1564C= (p.Gln522=)
c.1561C= (p.Gln521=)
10g.119677118C>GCA378297597BAG3c.1564C>G (p.Gln522Glu)
c.1561C>G (p.Gln521Glu)
10g.119677118C>TCA378297596BAG3c.1564C>T (p.Gln522Ter)
c.1561C>T (p.Gln521Ter)
ClinVar dbSNP
10g.119677119A=CA1940196853BAG3c.1565A= (p.Gln522=)
c.1562A= (p.Gln521=)
10g.119677119A>CCA378297598BAG3c.1565A>C (p.Gln522Pro)
c.1562A>C (p.Gln521Pro)
10g.119677119A>GCA378297599BAG3c.1565A>G (p.Gln522Arg)
c.1562A>G (p.Gln521Arg)
ClinVar
10g.119677119A>TCA5716572BAG3c.1565A>T (p.Gln522Leu)
c.1562A>T (p.Gln521Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119677120G>ACA471739680BAG3c.1566G>A (p.Gln522=)
c.1563G>A (p.Gln521=)
ClinVar gnomAD v4
10g.119677120G>CCA378297600BAG3c.1566G>C (p.Gln522His)
c.1563G>C (p.Gln521His)
10g.119677120G>TCA378297601BAG3c.1566G>T (p.Gln522His)
c.1563G>T (p.Gln521His)
10g.119677121G>ACA5716573BAG3c.1567G>A (p.Ala523Thr)
c.1564G>A (p.Ala522Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119677121G>CCA378297603BAG3c.1567G>C (p.Ala523Pro)
c.1564G>C (p.Ala522Pro)
10g.119677121G=CA1940196854BAG3c.1567G= (p.Ala523=)
c.1564G= (p.Ala522=)
10g.119677121G>TCA378297602BAG3c.1567G>T (p.Ala523Ser)
c.1564G>T (p.Ala522Ser)
10g.119677122C>ACA378297604BAG3c.1568C>A (p.Ala523Glu)
c.1565C>A (p.Ala522Glu)
10g.119677122C>GCA378297605BAG3c.1568C>G (p.Ala523Gly)
c.1565C>G (p.Ala522Gly)
10g.119677122C>TCA378297606BAG3c.1568C>T (p.Ala523Val)
c.1565C>T (p.Ala522Val)
gnomAD v4
10g.119677123A>CCA471739685BAG3c.1569A>C (p.Ala523=)
c.1566A>C (p.Ala522=)
10g.119677123A>GCA471739686BAG3c.1569A>G (p.Ala523=)
c.1566A>G (p.Ala522=)
10g.119677123A>TCA471739687BAG3c.1569A>T (p.Ala523=)
c.1566A>T (p.Ala522=)
10g.119677124A=CA1940196855BAG3c.1570A= (p.Ile524=)
c.1567A= (p.Ile523=)
10g.119677124A>CCA378297607BAG3c.1570A>C (p.Ile524Leu)
c.1567A>C (p.Ile523Leu)
10g.119677124A>GCA5716574BAG3c.1570A>G (p.Ile524Val)
c.1567A>G (p.Ile523Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
10g.119677124A>TCA378297608BAG3c.1570A>T (p.Ile524Phe)
c.1567A>T (p.Ile523Phe)
ClinVar dbSNP gnomAD v2 gnomAD v4
10g.119677125T>ACA378297609BAG3c.1571T>A (p.Ile524Asn)
c.1568T>A (p.Ile523Asn)
10g.119677125T>CCA5716575BAG3c.1571T>C (p.Ile524Thr)
c.1568T>C (p.Ile523Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119677125T>GCA378297610BAG3c.1571T>G (p.Ile524Ser)
c.1568T>G (p.Ile523Ser)
10g.119677125T=CA1940196856BAG3c.1571T= (p.Ile524=)
c.1568T= (p.Ile523=)
10g.119677126C>ACA471739691BAG3c.1572C>A (p.Ile524=)
c.1569C>A (p.Ile523=)
10g.119677126C>GCA378297611BAG3c.1572C>G (p.Ile524Met)
c.1569C>G (p.Ile523Met)
10g.119677126C>TCA471739692BAG3c.1572C>T (p.Ile524=)
c.1569C>T (p.Ile523=)
gnomAD v4
10g.119677127A=CA1940196857BAG3c.1573A= (p.Met525=)
c.1570A= (p.Met524=)
10g.119677127A>CCA378297612BAG3c.1573A>C (p.Met525Leu)
c.1570A>C (p.Met524Leu)
ClinVar
10g.119677127A>GCA5716576BAG3c.1573A>G (p.Met525Val)
c.1570A>G (p.Met524Val)
dbSNP ExAC gnomAD v2 gnomAD v4
10g.119677127A>TCA378297613BAG3c.1573A>T (p.Met525Leu)
c.1570A>T (p.Met524Leu)
10g.119677128T>ACA378297614BAG3c.1574T>A (p.Met525Lys)
c.1571T>A (p.Met524Lys)
10g.119677128T>CCA378297615BAG3c.1574T>C (p.Met525Thr)
c.1571T>C (p.Met524Thr)
ClinVar dbSNP gnomAD v4
10g.119677128T>GCA378297616BAG3c.1574T>G (p.Met525Arg)
c.1571T>G (p.Met524Arg)
gnomAD v4
10g.119677129G>ACA378297617BAG3c.1575G>A (p.Met525Ile)
c.1572G>A (p.Met524Ile)
dbSNP gnomAD v3 gnomAD v4
10g.119677129G>CCA378297618BAG3c.1575G>C (p.Met525Ile)
c.1572G>C (p.Met524Ile)
10g.119677129G=CA1940196858BAG3c.1575G= (p.Met525=)
c.1572G= (p.Met524=)
10g.119677129G>TCA378297619BAG3c.1575G>T (p.Met525Ile)
c.1572G>T (p.Met524Ile)
10g.119677130G>ACA378297620BAG3c.1576G>A (p.Glu526Lys)
c.1573G>A (p.Glu525Lys)
10g.119677130G>CCA378297622BAG3c.1576G>C (p.Glu526Gln)
c.1573G>C (p.Glu525Gln)
10g.119677130G>TCA378297621BAG3c.1576G>T (p.Glu526Ter)
c.1573G>T (p.Glu525Ter)
10g.119677131A>CCA378297623BAG3c.1577A>C (p.Glu526Ala)
c.1574A>C (p.Glu525Ala)
10g.119677131A>GCA378297625BAG3c.1577A>G (p.Glu526Gly)
c.1574A>G (p.Glu525Gly)
gnomAD v4
10g.119677131A>TCA378297624BAG3c.1577A>T (p.Glu526Val)
c.1574A>T (p.Glu525Val)
10g.119677132G>ACA471739698BAG3c.1578G>A (p.Glu526=)
c.1575G>A (p.Glu525=)
ClinVar dbSNP gnomAD v2 gnomAD v4
10g.119677132G>CCA378297626BAG3c.1578G>C (p.Glu526Asp)
c.1575G>C (p.Glu525Asp)
gnomAD v4
10g.119677132G=CA1940196859BAG3c.1578G= (p.Glu526=)
c.1575G= (p.Glu525=)
10g.119677132G>TCA5716577BAG3c.1578G>T (p.Glu526Asp)
c.1575G>T (p.Glu525Asp)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119677133A>CCA378297627BAG3c.1579A>C (p.Met527Leu)
c.1576A>C (p.Met526Leu)
10g.119677133A>GCA378297628BAG3c.1579A>G (p.Met527Val)
c.1576A>G (p.Met526Val)
10g.119677133A>TCA378297629BAG3c.1579A>T (p.Met527Leu)
c.1576A>T (p.Met526Leu)
10g.119677133dupCA2825001685BAG3c.1579dup (p.Met527AsnfsTer?)
c.1576dup (p.Met526AsnfsTer?)
ClinVar
10g.119677134T>ACA378297630BAG3c.1580T>A (p.Met527Lys)
c.1577T>A (p.Met526Lys)
10g.119677134T>CCA378297631BAG3c.1580T>C (p.Met527Thr)
c.1577T>C (p.Met526Thr)
10g.119677134T>GCA378297632BAG3c.1580T>G (p.Met527Arg)
c.1577T>G (p.Met526Arg)
10g.119677135G>ACA378297633BAG3c.1581G>A (p.Met527Ile)
c.1578G>A (p.Met526Ile)
10g.119677135G>CCA378297634BAG3c.1581G>C (p.Met527Ile)
c.1578G>C (p.Met526Ile)
10g.119677135G>TCA378297635BAG3c.1581G>T (p.Met527Ile)
c.1578G>T (p.Met526Ile)
10g.119677136G>ACA378297636BAG3c.1582G>A (p.Gly528Ser)
c.1579G>A (p.Gly527Ser)
dbSNP
10g.119677136G>CCA5716578BAG3c.1582G>C (p.Gly528Arg)
c.1579G>C (p.Gly527Arg)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.119677136G=CA1940196860BAG3c.1582G= (p.Gly528=)
c.1579G= (p.Gly527=)
10g.119677136G>TCA378297637BAG3c.1582G>T (p.Gly528Cys)
c.1579G>T (p.Gly527Cys)
10g.119677137G>ACA5716579BAG3c.1583G>A (p.Gly528Asp)
c.1580G>A (p.Gly527Asp)
dbSNP ExAC gnomAD v2 gnomAD v4
10g.119677137G>CCA378297638BAG3c.1583G>C (p.Gly528Ala)
c.1580G>C (p.Gly527Ala)
10g.119677137G=CA1940196861BAG3c.1583G= (p.Gly528=)
c.1580G= (p.Gly527=)
10g.119677137G>TCA378297639BAG3c.1583G>T (p.Gly528Val)
c.1580G>T (p.Gly527Val)

Number of alleles fetched