Chr Mutation (hg38) CAid Gene Transcript Linkouts
4g.186288460C>ACA358945837F11,F11-AS1c.1724C>A (p.Ser575Ter)
c.324C>A
c.1562C>A (p.Ser521Ter)
n.243C>A
n.1034G>T
c.1727C>A (p.Ser576Ter)
c.1631C>A (p.Ser544Ter)
c.1457C>A (p.Ser486Ter)
c.1679C>A (p.Ser560Ter)
 ClinVar dbSNP gnomAD v2 gnomAD v4
4g.186288460C=CA1519939799F11,F11-AS1c.1724C= (p.Ser575=)
c.324C=
c.1562C= (p.Ser521=)
n.243C=
n.1034G=
c.1727C= (p.Ser576=)
c.1631C= (p.Ser544=)
c.1457C= (p.Ser486=)
c.1679C= (p.Ser560=)
4g.186288460C>GCA358945839F11,F11-AS1c.1724C>G (p.Ser575Trp)
c.324C>G
c.1562C>G (p.Ser521Trp)
n.243C>G
n.1034G>C
c.1727C>G (p.Ser576Trp)
c.1631C>G (p.Ser544Trp)
c.1457C>G (p.Ser486Trp)
c.1679C>G (p.Ser560Trp)
4g.186288460C>TCA219128F11,F11-AS1c.1724C>T (p.Ser575Leu)
c.324C>T
c.1562C>T (p.Ser521Leu)
n.243C>T
n.1034G>A
c.1727C>T (p.Ser576Leu)
c.1631C>T (p.Ser544Leu)
c.1457C>T (p.Ser486Leu)
c.1679C>T (p.Ser560Leu)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
4g.186288461G>ACA3164107F11,F11-AS1c.1725G>A (p.Ser575=)
c.325G>A
c.1563G>A (p.Ser521=)
n.244G>A
n.1033C>T
c.1728G>A (p.Ser576=)
c.1632G>A (p.Ser544=)
c.1458G>A (p.Ser486=)
c.1680G>A (p.Ser560=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.186288461G>CCA442641340F11,F11-AS1c.1725G>C (p.Ser575=)
c.325G>C
c.1563G>C (p.Ser521=)
n.244G>C
n.1033C>G
c.1728G>C (p.Ser576=)
c.1632G>C (p.Ser544=)
c.1458G>C (p.Ser486=)
c.1680G>C (p.Ser560=)
 ClinVar
4g.186288461G=CA1519939800F11,F11-AS1c.1725G= (p.Ser575=)
c.325G=
c.1563G= (p.Ser521=)
n.244G=
n.1033C=
c.1728G= (p.Ser576=)
c.1632G= (p.Ser544=)
c.1458G= (p.Ser486=)
c.1680G= (p.Ser560=)
4g.186288461G>TCA442641339F11,F11-AS1c.1725G>T (p.Ser575=)
c.325G>T
c.1563G>T (p.Ser521=)
n.244G>T
n.1033C>A
c.1728G>T (p.Ser576=)
c.1632G>T (p.Ser544=)
c.1458G>T (p.Ser486=)
c.1680G>T (p.Ser560=)
 COSMIC
4g.186288462G>ACA358945843F11,F11-AS1c.1726G>A (p.Gly576Arg)
c.326G>A
c.1564G>A (p.Gly522Arg)
n.245G>A
n.1032C>T
c.1729G>A (p.Gly577Arg)
c.1633G>A (p.Gly545Arg)
c.1459G>A (p.Gly487Arg)
c.1681G>A (p.Gly561Arg)
4g.186288462G>CCA358945846F11,F11-AS1c.1726G>C (p.Gly576Arg)
c.326G>C
c.1564G>C (p.Gly522Arg)
n.245G>C
n.1032C>G
c.1729G>C (p.Gly577Arg)
c.1633G>C (p.Gly545Arg)
c.1459G>C (p.Gly487Arg)
c.1681G>C (p.Gly561Arg)
4g.186288462G>TCA358945844F11,F11-AS1c.1726G>T (p.Gly576Ter)
c.326G>T
c.1564G>T (p.Gly522Ter)
n.245G>T
n.1032C>A
c.1729G>T (p.Gly577Ter)
c.1633G>T (p.Gly545Ter)
c.1459G>T (p.Gly487Ter)
c.1681G>T (p.Gly561Ter)
 ClinVar
4g.186288463G>ACA3164108F11,F11-AS1c.1727G>A (p.Gly576Glu)
c.327G>A
c.1565G>A (p.Gly522Glu)
n.246G>A
n.1031C>T
c.1730G>A (p.Gly577Glu)
c.1634G>A (p.Gly545Glu)
c.1460G>A (p.Gly487Glu)
c.1682G>A (p.Gly561Glu)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.186288463G>CCA358945850F11,F11-AS1c.1727G>C (p.Gly576Ala)
c.327G>C
c.1565G>C (p.Gly522Ala)
n.246G>C
n.1031C>G
c.1730G>C (p.Gly577Ala)
c.1634G>C (p.Gly545Ala)
c.1460G>C (p.Gly487Ala)
c.1682G>C (p.Gly561Ala)
 gnomAD v4
4g.186288463G=CA1519939801F11,F11-AS1c.1727G= (p.Gly576=)
c.327G=
c.1565G= (p.Gly522=)
n.246G=
n.1031C=
c.1730G= (p.Gly577=)
c.1634G= (p.Gly545=)
c.1460G= (p.Gly487=)
c.1682G= (p.Gly561=)
4g.186288463G>TCA358945851F11,F11-AS1c.1727G>T (p.Gly576Val)
c.327G>T
c.1565G>T (p.Gly522Val)
n.246G>T
n.1031C>A
c.1730G>T (p.Gly577Val)
c.1634G>T (p.Gly545Val)
c.1460G>T (p.Gly487Val)
c.1682G>T (p.Gly561Val)
4g.186288464A=CA1519939802F11,F11-AS1c.1728A= (p.Gly576=)
c.328A=
c.1566A= (p.Gly522=)
n.247A=
n.1030T=
c.1731A= (p.Gly577=)
c.1635A= (p.Gly545=)
c.1461A= (p.Gly487=)
c.1683A= (p.Gly561=)
4g.186288464A>CCA442641341F11,F11-AS1c.1728A>C (p.Gly576=)
c.328A>C
c.1566A>C (p.Gly522=)
n.247A>C
n.1030T>G
c.1731A>C (p.Gly577=)
c.1635A>C (p.Gly545=)
c.1461A>C (p.Gly487=)
c.1683A>C (p.Gly561=)
4g.186288464A>GCA442641342F11,F11-AS1c.1728A>G (p.Gly576=)
c.328A>G
c.1566A>G (p.Gly522=)
n.247A>G
n.1030T>C
c.1731A>G (p.Gly577=)
c.1635A>G (p.Gly545=)
c.1461A>G (p.Gly487=)
c.1683A>G (p.Gly561=)
4g.186288464A>TCA3164109F11,F11-AS1c.1728A>T (p.Gly576=)
c.328A>T
c.1566A>T (p.Gly522=)
n.247A>T
n.1030T>A
c.1731A>T (p.Gly577=)
c.1635A>T (p.Gly545=)
c.1461A>T (p.Gly487=)
c.1683A>T (p.Gly561=)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.186288465G>ACA112106166F11,F11-AS1c.1729G>A (p.Gly577Ser)
c.329G>A
c.1567G>A (p.Gly523Ser)
n.248G>A
n.1029C>T
c.1732G>A (p.Gly578Ser)
c.1636G>A (p.Gly546Ser)
c.1462G>A (p.Gly488Ser)
c.1684G>A (p.Gly562Ser)
 dbSNP
4g.186288465G>CCA358945854F11,F11-AS1c.1729G>C (p.Gly577Arg)
c.329G>C
c.1567G>C (p.Gly523Arg)
n.248G>C
n.1029C>G
c.1732G>C (p.Gly578Arg)
c.1636G>C (p.Gly546Arg)
c.1462G>C (p.Gly488Arg)
c.1684G>C (p.Gly562Arg)
4g.186288465G=CA1519939803F11,F11-AS1c.1729G= (p.Gly577=)
c.329G=
c.1567G= (p.Gly523=)
n.248G=
n.1029C=
c.1732G= (p.Gly578=)
c.1636G= (p.Gly546=)
c.1462G= (p.Gly488=)
c.1684G= (p.Gly562=)
4g.186288465G>TCA358945856F11,F11-AS1c.1729G>T (p.Gly577Cys)
c.329G>T
c.1567G>T (p.Gly523Cys)
n.248G>T
n.1029C>A
c.1732G>T (p.Gly578Cys)
c.1636G>T (p.Gly546Cys)
c.1462G>T (p.Gly488Cys)
c.1684G>T (p.Gly562Cys)
4g.186288466G>ACA358945857F11,F11-AS1c.1730G>A (p.Gly577Asp)
c.330G>A
c.1568G>A (p.Gly523Asp)
n.249G>A
n.1028C>T
c.1733G>A (p.Gly578Asp)
c.1637G>A (p.Gly546Asp)
c.1463G>A (p.Gly488Asp)
c.1685G>A (p.Gly562Asp)
 gnomAD v4
4g.186288466G>CCA358945859F11,F11-AS1c.1730G>C (p.Gly577Ala)
c.330G>C
c.1568G>C (p.Gly523Ala)
n.249G>C
n.1028C>G
c.1733G>C (p.Gly578Ala)
c.1637G>C (p.Gly546Ala)
c.1463G>C (p.Gly488Ala)
c.1685G>C (p.Gly562Ala)
4g.186288466G>TCA358945860F11,F11-AS1c.1730G>T (p.Gly577Val)
c.330G>T
c.1568G>T (p.Gly523Val)
n.249G>T
n.1028C>A
c.1733G>T (p.Gly578Val)
c.1637G>T (p.Gly546Val)
c.1463G>T (p.Gly488Val)
c.1685G>T (p.Gly562Val)
4g.186288467C>ACA442641343F11,F11-AS1c.1731C>A (p.Gly577=)
c.331C>A
c.1569C>A (p.Gly523=)
n.250C>A
n.1027G>T
c.1734C>A (p.Gly578=)
c.1638C>A (p.Gly546=)
c.1464C>A (p.Gly488=)
c.1686C>A (p.Gly562=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.186288467C=CA1519939804F11,F11-AS1c.1731C= (p.Gly577=)
c.331C=
c.1569C= (p.Gly523=)
n.250C=
n.1027G=
c.1734C= (p.Gly578=)
c.1638C= (p.Gly546=)
c.1464C= (p.Gly488=)
c.1686C= (p.Gly562=)
4g.186288467C>GCA442641344F11,F11-AS1c.1731C>G (p.Gly577=)
c.331C>G
c.1569C>G (p.Gly523=)
n.250C>G
n.1027G>C
c.1734C>G (p.Gly578=)
c.1638C>G (p.Gly546=)
c.1464C>G (p.Gly488=)
c.1686C>G (p.Gly562=)
4g.186288467C>TCA3164110F11,F11-AS1c.1731C>T (p.Gly577=)
c.331C>T
c.1569C>T (p.Gly523=)
n.250C>T
n.1027G>A
c.1734C>T (p.Gly578=)
c.1638C>T (p.Gly546=)
c.1464C>T (p.Gly488=)
c.1686C>T (p.Gly562=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.186288468C>ACA358945865F11,F11-AS1c.1732C>A (p.Pro578Thr)
c.332C>A
c.1570C>A (p.Pro524Thr)
n.251C>A
n.1026G>T
c.1735C>A (p.Pro579Thr)
c.1639C>A (p.Pro547Thr)
c.1465C>A (p.Pro489Thr)
c.1687C>A (p.Pro563Thr)
4g.186288468C>GCA358945866F11,F11-AS1c.1732C>G (p.Pro578Ala)
c.332C>G
c.1570C>G (p.Pro524Ala)
n.251C>G
n.1026G>C
c.1735C>G (p.Pro579Ala)
c.1639C>G (p.Pro547Ala)
c.1465C>G (p.Pro489Ala)
c.1687C>G (p.Pro563Ala)
4g.186288468C>TCA358945863F11,F11-AS1c.1732C>T (p.Pro578Ser)
c.332C>T
c.1570C>T (p.Pro524Ser)
n.251C>T
n.1026G>A
c.1735C>T (p.Pro579Ser)
c.1639C>T (p.Pro547Ser)
c.1465C>T (p.Pro489Ser)
c.1687C>T (p.Pro563Ser)
4g.186288469C>ACA358945867F11,F11-AS1c.1733C>A (p.Pro578His)
c.333C>A
c.1571C>A (p.Pro524His)
n.252C>A
n.1025G>T
c.1736C>A (p.Pro579His)
c.1640C>A (p.Pro547His)
c.1466C>A (p.Pro489His)
c.1688C>A (p.Pro563His)
4g.186288469C>GCA358945870F11,F11-AS1c.1733C>G (p.Pro578Arg)
c.333C>G
c.1571C>G (p.Pro524Arg)
n.252C>G
n.1025G>C
c.1736C>G (p.Pro579Arg)
c.1640C>G (p.Pro547Arg)
c.1466C>G (p.Pro489Arg)
c.1688C>G (p.Pro563Arg)
4g.186288469C>TCA358945869F11,F11-AS1c.1733C>T (p.Pro578Leu)
c.333C>T
c.1571C>T (p.Pro524Leu)
n.252C>T
n.1025G>A
c.1736C>T (p.Pro579Leu)
c.1640C>T (p.Pro547Leu)
c.1466C>T (p.Pro489Leu)
c.1688C>T (p.Pro563Leu)
4g.186288470T>ACA442641345F11,F11-AS1c.1734T>A (p.Pro578=)
c.334T>A
c.1572T>A (p.Pro524=)
n.253T>A
n.1024A>T
c.1737T>A (p.Pro579=)
c.1641T>A (p.Pro547=)
c.1467T>A (p.Pro489=)
c.1689T>A (p.Pro563=)
4g.186288470T>CCA442641346F11,F11-AS1c.1734T>C (p.Pro578=)
c.334T>C
c.1572T>C (p.Pro524=)
n.253T>C
n.1024A>G
c.1737T>C (p.Pro579=)
c.1641T>C (p.Pro547=)
c.1467T>C (p.Pro489=)
c.1689T>C (p.Pro563=)
4g.186288470T>GCA442641347F11,F11-AS1c.1734T>G (p.Pro578=)
c.334T>G
c.1572T>G (p.Pro524=)
n.253T>G
n.1024A>C
c.1737T>G (p.Pro579=)
c.1641T>G (p.Pro547=)
c.1467T>G (p.Pro489=)
c.1689T>G (p.Pro563=)
4g.186288471C>ACA358945872F11,F11-AS1c.1735C>A (p.Leu579Met)
c.335C>A
c.1573C>A (p.Leu525Met)
n.254C>A
n.1023G>T
c.1738C>A (p.Leu580Met)
c.1642C>A (p.Leu548Met)
c.1468C>A (p.Leu490Met)
c.1690C>A (p.Leu564Met)
4g.186288471C>GCA358945874F11,F11-AS1c.1735C>G (p.Leu579Val)
c.335C>G
c.1573C>G (p.Leu525Val)
n.254C>G
n.1023G>C
c.1738C>G (p.Leu580Val)
c.1642C>G (p.Leu548Val)
c.1468C>G (p.Leu490Val)
c.1690C>G (p.Leu564Val)
4g.186288471C>TCA442641348F11,F11-AS1c.1735C>T (p.Leu579=)
c.335C>T
c.1573C>T (p.Leu525=)
n.254C>T
n.1023G>A
c.1738C>T (p.Leu580=)
c.1642C>T (p.Leu548=)
c.1468C>T (p.Leu490=)
c.1690C>T (p.Leu564=)
 ClinVar COSMIC COSMIC
4g.186288472T>ACA358945876F11,F11-AS1c.1736T>A (p.Leu579Gln)
c.336T>A
c.1574T>A (p.Leu525Gln)
n.255T>A
n.1022A>T
c.1739T>A (p.Leu580Gln)
c.1643T>A (p.Leu548Gln)
c.1469T>A (p.Leu490Gln)
c.1691T>A (p.Leu564Gln)
4g.186288472T>CCA358945878F11,F11-AS1c.1736T>C (p.Leu579Pro)
c.336T>C
c.1574T>C (p.Leu525Pro)
n.255T>C
n.1022A>G
c.1739T>C (p.Leu580Pro)
c.1643T>C (p.Leu548Pro)
c.1469T>C (p.Leu490Pro)
c.1691T>C (p.Leu564Pro)
 COSMIC COSMIC
4g.186288472T>GCA358945879F11,F11-AS1c.1736T>G (p.Leu579Arg)
c.336T>G
c.1574T>G (p.Leu525Arg)
n.255T>G
n.1022A>C
c.1739T>G (p.Leu580Arg)
c.1643T>G (p.Leu548Arg)
c.1469T>G (p.Leu490Arg)
c.1691T>G (p.Leu564Arg)
4g.186288473G>ACA442641349F11,F11-AS1c.1737G>A (p.Leu579=)
c.337G>A
c.1575G>A (p.Leu525=)
n.256G>A
n.1021C>T
c.1740G>A (p.Leu580=)
c.1644G>A (p.Leu548=)
c.1470G>A (p.Leu490=)
c.1692G>A (p.Leu564=)
 gnomAD v4
4g.186288473G>CCA442641350F11,F11-AS1c.1737G>C (p.Leu579=)
c.337G>C
c.1575G>C (p.Leu525=)
n.256G>C
n.1021C>G
c.1740G>C (p.Leu580=)
c.1644G>C (p.Leu548=)
c.1470G>C (p.Leu490=)
c.1692G>C (p.Leu564=)
4g.186288473G>TCA442641351F11,F11-AS1c.1737G>T (p.Leu579=)
c.337G>T
c.1575G>T (p.Leu525=)
n.256G>T
n.1021C>A
c.1740G>T (p.Leu580=)
c.1644G>T (p.Leu548=)
c.1470G>T (p.Leu490=)
c.1692G>T (p.Leu564=)
4g.186288474T>ACA358945881F11,F11-AS1c.1738T>A (p.Ser580Thr)
c.338T>A
c.1576T>A (p.Ser526Thr)
n.257T>A
n.1020A>T
c.1741T>A (p.Ser581Thr)
c.1645T>A (p.Ser549Thr)
c.1471T>A (p.Ser491Thr)
c.1693T>A (p.Ser565Thr)
4g.186288474T>CCA358945883F11,F11-AS1c.1738T>C (p.Ser580Pro)
c.338T>C
c.1576T>C (p.Ser526Pro)
n.257T>C
n.1020A>G
c.1741T>C (p.Ser581Pro)
c.1645T>C (p.Ser549Pro)
c.1471T>C (p.Ser491Pro)
c.1693T>C (p.Ser565Pro)

Number of alleles fetched