Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
18 | g.57674878G>A | CA402560775 | ATP8B1 | c.1775C>T (p.Ala592Val) c.1640C>T c.1661C>T (p.Ala554Val) c.1055C>T (p.Ala352Val) c.1625C>T (p.Ala542Val) | gnomAD v4 |
18 | g.57674878G>C | CA402560779 | ATP8B1 | c.1775C>G (p.Ala592Gly) c.1640C>G c.1661C>G (p.Ala554Gly) c.1055C>G (p.Ala352Gly) c.1625C>G (p.Ala542Gly) | |
18 | g.57674878G>T | CA402560777 | ATP8B1 | c.1775C>A (p.Ala592Asp) c.1640C>A c.1661C>A (p.Ala554Asp) c.1055C>A (p.Ala352Asp) c.1625C>A (p.Ala542Asp) | |
18 | g.57674879C>A | CA402560783 | ATP8B1 | c.1774G>T (p.Ala592Ser) c.1639G>T c.1660G>T (p.Ala554Ser) c.1054G>T (p.Ala352Ser) c.1624G>T (p.Ala542Ser) | |
18 | g.57674879C>G | CA402560786 | ATP8B1 | c.1774G>C (p.Ala592Pro) c.1639G>C c.1660G>C (p.Ala554Pro) c.1054G>C (p.Ala352Pro) c.1624G>C (p.Ala542Pro) | |
18 | g.57674879C>T | CA402560791 | ATP8B1 | c.1774G>A (p.Ala592Thr) c.1639G>A c.1660G>A (p.Ala554Thr) c.1054G>A (p.Ala352Thr) c.1624G>A (p.Ala542Thr) | |
18 | g.57674880A>C | CA504021204 | ATP8B1 | c.1773T>G (p.Leu591=) c.1638T>G c.1659T>G (p.Leu553=) c.1053T>G (p.Leu351=) c.1623T>G (p.Leu541=) | |
18 | g.57674880A>G | CA504021202 | ATP8B1 | c.1773T>C (p.Leu591=) c.1638T>C c.1659T>C (p.Leu553=) c.1053T>C (p.Leu351=) c.1623T>C (p.Leu541=) | |
18 | g.57674880A>T | CA504021203 | ATP8B1 | c.1773T>A (p.Leu591=) c.1638T>A c.1659T>A (p.Leu553=) c.1053T>A (p.Leu351=) c.1623T>A (p.Leu541=) | |
18 | g.57674881A>C | CA402560795 | ATP8B1 | c.1772T>G (p.Leu591Arg) c.1637T>G c.1658T>G (p.Leu553Arg) c.1052T>G (p.Leu351Arg) c.1622T>G (p.Leu541Arg) | |
18 | g.57674881A>G | CA402560798 | ATP8B1 | c.1772T>C (p.Leu591Pro) c.1637T>C c.1658T>C (p.Leu553Pro) c.1052T>C (p.Leu351Pro) c.1622T>C (p.Leu541Pro) | |
18 | g.57674881A>T | CA402560800 | ATP8B1 | c.1772T>A (p.Leu591His) c.1637T>A c.1658T>A (p.Leu553His) c.1052T>A (p.Leu351His) c.1622T>A (p.Leu541His) | |
18 | g.57674882G>A | CA402560805 | ATP8B1 | c.1771C>T (p.Leu591Phe) c.1636C>T c.1657C>T (p.Leu553Phe) c.1051C>T (p.Leu351Phe) c.1621C>T (p.Leu541Phe) | |
18 | g.57674882G>C | CA402560816 | ATP8B1 | c.1771C>G (p.Leu591Val) c.1636C>G c.1657C>G (p.Leu553Val) c.1051C>G (p.Leu351Val) c.1621C>G (p.Leu541Val) | gnomAD v4 |
18 | g.57674882G>T | CA402560819 | ATP8B1 | c.1771C>A (p.Leu591Ile) c.1636C>A c.1657C>A (p.Leu553Ile) c.1051C>A (p.Leu351Ile) c.1621C>A (p.Leu541Ile) | gnomAD v4 |
18 | g.57674883A>C | CA504021205 | ATP8B1 | c.1770T>G (p.Val590=) c.1635T>G c.1656T>G (p.Val552=) c.1050T>G (p.Val350=) c.1620T>G (p.Val540=) | |
18 | g.57674883A>G | CA504021206 | ATP8B1 | c.1770T>C (p.Val590=) c.1635T>C c.1656T>C (p.Val552=) c.1050T>C (p.Val350=) c.1620T>C (p.Val540=) | dbSNP |
18 | g.57674883A>T | CA504021207 | ATP8B1 | c.1770T>A (p.Val590=) c.1635T>A c.1656T>A (p.Val552=) c.1050T>A (p.Val350=) c.1620T>A (p.Val540=) | |
18 | g.57674884A>C | CA402560823 | ATP8B1 | c.1769T>G (p.Val590Gly) c.1634T>G c.1655T>G (p.Val552Gly) c.1049T>G (p.Val350Gly) c.1619T>G (p.Val540Gly) | COSMIC |
18 | g.57674884A>G | CA402560827 | ATP8B1 | c.1769T>C (p.Val590Ala) c.1634T>C c.1655T>C (p.Val552Ala) c.1049T>C (p.Val350Ala) c.1619T>C (p.Val540Ala) | |
18 | g.57674884A>T | CA402560831 | ATP8B1 | c.1769T>A (p.Val590Asp) c.1634T>A c.1655T>A (p.Val552Asp) c.1049T>A (p.Val350Asp) c.1619T>A (p.Val540Asp) | |
18 | g.57674885C>A | CA402560843 | ATP8B1 | c.1768G>T (p.Val590Phe) c.1633G>T c.1654G>T (p.Val552Phe) c.1048G>T (p.Val350Phe) c.1618G>T (p.Val540Phe) | |
18 | g.57674885C= | CA2306103157 | ATP8B1 | c.1768G= (p.Val590=) c.1633G= c.1654G= (p.Val552=) c.1048G= (p.Val350=) c.1618G= (p.Val540=) | |
18 | g.57674885C>G | CA8974483 | ATP8B1 | c.1768G>C (p.Val590Leu) c.1633G>C c.1654G>C (p.Val552Leu) c.1048G>C (p.Val350Leu) c.1618G>C (p.Val540Leu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
18 | g.57674885C>T | CA402560836 | ATP8B1 | c.1768G>A (p.Val590Ile) c.1633G>A c.1654G>A (p.Val552Ile) c.1048G>A (p.Val350Ile) c.1618G>A (p.Val540Ile) | |
18 | g.57674886A= | CA2306103158 | ATP8B1 | c.1767T= (p.Asn589=) c.1632T= c.1653T= (p.Asn551=) c.1047T= (p.Asn349=) c.1617T= (p.Asn539=) | |
18 | g.57674886A>C | CA402560848 | ATP8B1 | c.1767T>G (p.Asn589Lys) c.1632T>G c.1653T>G (p.Asn551Lys) c.1047T>G (p.Asn349Lys) c.1617T>G (p.Asn539Lys) | |
18 | g.57674886A>G | CA504021208 | ATP8B1 | c.1767T>C (p.Asn589=) c.1632T>C c.1653T>C (p.Asn551=) c.1047T>C (p.Asn349=) c.1617T>C (p.Asn539=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
18 | g.57674886A>T | CA402560847 | ATP8B1 | c.1767T>A (p.Asn589Lys) c.1632T>A c.1653T>A (p.Asn551Lys) c.1047T>A (p.Asn349Lys) c.1617T>A (p.Asn539Lys) | |
18 | g.57674887T>A | CA402560849 | ATP8B1 | c.1766A>T (p.Asn589Ile) c.1631A>T c.1652A>T (p.Asn551Ile) c.1046A>T (p.Asn349Ile) c.1616A>T (p.Asn539Ile) | |
18 | g.57674887T>C | CA402560853 | ATP8B1 | c.1766A>G (p.Asn589Ser) c.1631A>G c.1652A>G (p.Asn551Ser) c.1046A>G (p.Asn349Ser) c.1616A>G (p.Asn539Ser) | gnomAD v4 |
18 | g.57674887T>G | CA402560859 | ATP8B1 | c.1766A>C (p.Asn589Thr) c.1631A>C c.1652A>C (p.Asn551Thr) c.1046A>C (p.Asn349Thr) c.1616A>C (p.Asn539Thr) | |
18 | g.57674888T>A | CA402560863 | ATP8B1 | c.1765A>T (p.Asn589Tyr) c.1630A>T c.1651A>T (p.Asn551Tyr) c.1045A>T (p.Asn349Tyr) c.1615A>T (p.Asn539Tyr) | |
18 | g.57674888T>C | CA402560866 | ATP8B1 | c.1765A>G (p.Asn589Asp) c.1630A>G c.1651A>G (p.Asn551Asp) c.1045A>G (p.Asn349Asp) c.1615A>G (p.Asn539Asp) | gnomAD v4 |
18 | g.57674888T>G | CA402560868 | ATP8B1 | c.1765A>C (p.Asn589His) c.1630A>C c.1651A>C (p.Asn551His) c.1045A>C (p.Asn349His) c.1615A>C (p.Asn539His) | |
18 | g.57674889G>A | CA504021209 | ATP8B1 | c.1764C>T (p.Tyr588=) c.1629C>T c.1650C>T (p.Tyr550=) c.1044C>T (p.Tyr348=) c.1614C>T (p.Tyr538=) | ClinVar gnomAD v4 |
18 | g.57674889G>C | CA402560871 | ATP8B1 | c.1764C>G (p.Tyr588Ter) c.1629C>G c.1650C>G (p.Tyr550Ter) c.1044C>G (p.Tyr348Ter) c.1614C>G (p.Tyr538Ter) | gnomAD v4 |
18 | g.57674889G>T | CA402560870 | ATP8B1 | c.1764C>A (p.Tyr588Ter) c.1629C>A c.1650C>A (p.Tyr550Ter) c.1044C>A (p.Tyr348Ter) c.1614C>A (p.Tyr538Ter) | gnomAD v4 |
18 | g.57674890T>A | CA402560872 | ATP8B1 | c.1763A>T (p.Tyr588Phe) c.1628A>T c.1649A>T (p.Tyr550Phe) c.1043A>T (p.Tyr348Phe) c.1613A>T (p.Tyr538Phe) | |
18 | g.57674890T>C | CA402560874 | ATP8B1 | c.1763A>G (p.Tyr588Cys) c.1628A>G c.1649A>G (p.Tyr550Cys) c.1043A>G (p.Tyr348Cys) c.1613A>G (p.Tyr538Cys) | |
18 | g.57674890T>G | CA402560877 | ATP8B1 | c.1763A>C (p.Tyr588Ser) c.1628A>C c.1649A>C (p.Tyr550Ser) c.1043A>C (p.Tyr348Ser) c.1613A>C (p.Tyr538Ser) | |
18 | g.57674891A>C | CA402560881 | ATP8B1 | c.1762T>G (p.Tyr588Asp) c.1627T>G c.1648T>G (p.Tyr550Asp) c.1042T>G (p.Tyr348Asp) c.1612T>G (p.Tyr538Asp) | |
18 | g.57674891A>G | CA402560885 | ATP8B1 | c.1762T>C (p.Tyr588His) c.1627T>C c.1648T>C (p.Tyr550His) c.1042T>C (p.Tyr348His) c.1612T>C (p.Tyr538His) | |
18 | g.57674891A>T | CA402560887 | ATP8B1 | c.1762T>A (p.Tyr588Asn) c.1627T>A c.1648T>A (p.Tyr550Asn) c.1042T>A (p.Tyr348Asn) c.1612T>A (p.Tyr538Asn) | |
18 | g.57674892A>C | CA504021210 | ATP8B1 | c.1761T>G (p.Thr587=) c.1626T>G c.1647T>G (p.Thr549=) c.1041T>G (p.Thr347=) c.1611T>G (p.Thr537=) | |
18 | g.57674892A>G | CA504021212 | ATP8B1 | c.1761T>C (p.Thr587=) c.1626T>C c.1647T>C (p.Thr549=) c.1041T>C (p.Thr347=) c.1611T>C (p.Thr537=) | |
18 | g.57674892A>T | CA504021211 | ATP8B1 | c.1761T>A (p.Thr587=) c.1626T>A c.1647T>A (p.Thr549=) c.1041T>A (p.Thr347=) c.1611T>A (p.Thr537=) | |
18 | g.57674893G>A | CA402560890 | ATP8B1 | c.1760C>T (p.Thr587Ile) c.1625C>T c.1646C>T (p.Thr549Ile) c.1040C>T (p.Thr347Ile) c.1610C>T (p.Thr537Ile) | |
18 | g.57674893G>C | CA402560894 | ATP8B1 | c.1760C>G (p.Thr587Ser) c.1625C>G c.1646C>G (p.Thr549Ser) c.1040C>G (p.Thr347Ser) c.1610C>G (p.Thr537Ser) | |
18 | g.57674893G>T | CA402560892 | ATP8B1 | c.1760C>A (p.Thr587Asn) c.1625C>A c.1646C>A (p.Thr549Asn) c.1040C>A (p.Thr347Asn) c.1610C>A (p.Thr537Asn) | |
18 | g.57674894T>A | CA402560898 | ATP8B1 | c.1759A>T (p.Thr587Ser) c.1624A>T c.1645A>T (p.Thr549Ser) c.1039A>T (p.Thr347Ser) c.1609A>T (p.Thr537Ser) | |
18 | g.57674894T>C | CA402560902 | ATP8B1 | c.1759A>G (p.Thr587Ala) c.1624A>G c.1645A>G (p.Thr549Ala) c.1039A>G (p.Thr347Ala) c.1609A>G (p.Thr537Ala) | gnomAD v4 |
18 | g.57674894T>G | CA402560903 | ATP8B1 | c.1759A>C (p.Thr587Pro) c.1624A>C c.1645A>C (p.Thr549Pro) c.1039A>C (p.Thr347Pro) c.1609A>C (p.Thr537Pro) | |
18 | g.57674895C>A | CA402560909 | ATP8B1 | c.1758G>T (p.Arg586Ser) c.1623G>T c.1644G>T (p.Arg548Ser) c.1038G>T (p.Arg346Ser) c.1608G>T (p.Arg536Ser) | |
18 | g.57674895C>G | CA402560910 | ATP8B1 | c.1758G>C (p.Arg586Ser) c.1623G>C c.1644G>C (p.Arg548Ser) c.1038G>C (p.Arg346Ser) c.1608G>C (p.Arg536Ser) | |
18 | g.57674895C>T | CA504021213 | ATP8B1 | c.1758G>A (p.Arg586=) c.1623G>A c.1644G>A (p.Arg548=) c.1038G>A (p.Arg346=) c.1608G>A (p.Arg536=) | |
18 | g.57674896C>A | CA8974484 | ATP8B1 | c.1757G>T (p.Arg586Met) c.1622G>T c.1643G>T (p.Arg548Met) c.1037G>T (p.Arg346Met) c.1607G>T (p.Arg536Met) | dbSNP ExAC gnomAD v2 |
18 | g.57674896C= | CA2306103159 | ATP8B1 | c.1757G= (p.Arg586=) c.1622G= c.1643G= (p.Arg548=) c.1037G= (p.Arg346=) c.1607G= (p.Arg536=) | |
18 | g.57674896C>G | CA402560919 | ATP8B1 | c.1757G>C (p.Arg586Thr) c.1622G>C c.1643G>C (p.Arg548Thr) c.1037G>C (p.Arg346Thr) c.1607G>C (p.Arg536Thr) | |
18 | g.57674896C>T | CA300889105 | ATP8B1 | c.1757G>A (p.Arg586Lys) c.1622G>A c.1643G>A (p.Arg548Lys) c.1037G>A (p.Arg346Lys) c.1607G>A (p.Arg536Lys) | dbSNP gnomAD v4 |
18 | g.57674897T>A | CA402560930 | ATP8B1 | c.1756A>T (p.Arg586Trp) c.1621A>T c.1642A>T (p.Arg548Trp) c.1036A>T (p.Arg346Trp) c.1606A>T (p.Arg536Trp) | |
18 | g.57674897T>C | CA402560931 | ATP8B1 | c.1756A>G (p.Arg586Gly) c.1621A>G c.1642A>G (p.Arg548Gly) c.1036A>G (p.Arg346Gly) c.1606A>G (p.Arg536Gly) | |
18 | g.57674897T>G | CA504021214 | ATP8B1 | c.1756A>C (p.Arg586=) c.1621A>C c.1642A>C (p.Arg548=) c.1036A>C (p.Arg346=) c.1606A>C (p.Arg536=) | |
18 | g.57674898T>A | CA402560933 | ATP8B1 | c.1755A>T (p.Glu585Asp) c.1620A>T c.1641A>T (p.Glu547Asp) c.1035A>T (p.Glu345Asp) c.1605A>T (p.Glu535Asp) | |
18 | g.57674898T>C | CA504021215 | ATP8B1 | c.1755A>G (p.Glu585=) c.1620A>G c.1641A>G (p.Glu547=) c.1035A>G (p.Glu345=) c.1605A>G (p.Glu535=) | |
18 | g.57674898T>G | CA402560939 | ATP8B1 | c.1755A>C (p.Glu585Asp) c.1620A>C c.1641A>C (p.Glu547Asp) c.1035A>C (p.Glu345Asp) c.1605A>C (p.Glu535Asp) | |
18 | g.57674899T>A | CA402560942 | ATP8B1 | c.1754A>T (p.Glu585Val) c.1619A>T c.1640A>T (p.Glu547Val) c.1034A>T (p.Glu345Val) c.1604A>T (p.Glu535Val) | |
18 | g.57674899T>C | CA8974485 | ATP8B1 | c.1754A>G (p.Glu585Gly) c.1619A>G c.1640A>G (p.Glu547Gly) c.1034A>G (p.Glu345Gly) c.1604A>G (p.Glu535Gly) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
18 | g.57674899T>G | CA402560944 | ATP8B1 | c.1754A>C (p.Glu585Ala) c.1619A>C c.1640A>C (p.Glu547Ala) c.1034A>C (p.Glu345Ala) c.1604A>C (p.Glu535Ala) | |
18 | g.57674899T= | CA2306103160 | ATP8B1 | c.1754A= (p.Glu585=) c.1619A= c.1640A= (p.Glu547=) c.1034A= (p.Glu345=) c.1604A= (p.Glu535=) | |
18 | g.57674900C>A | CA402560950 | ATP8B1 | c.1753G>T (p.Glu585Ter) c.1618G>T c.1639G>T (p.Glu547Ter) c.1033G>T (p.Glu345Ter) c.1603G>T (p.Glu535Ter) | dbSNP |
18 | g.57674900C= | CA2306103161 | ATP8B1 | c.1753G= (p.Glu585=) c.1618G= c.1639G= (p.Glu547=) c.1033G= (p.Glu345=) c.1603G= (p.Glu535=) | |
18 | g.57674900C>G | CA402560952 | ATP8B1 | c.1753G>C (p.Glu585Gln) c.1618G>C c.1639G>C (p.Glu547Gln) c.1033G>C (p.Glu345Gln) c.1603G>C (p.Glu535Gln) | |
18 | g.57674900C>T | CA402560960 | ATP8B1 | c.1753G>A (p.Glu585Lys) c.1618G>A c.1639G>A (p.Glu547Lys) c.1033G>A (p.Glu345Lys) c.1603G>A (p.Glu535Lys) | |
18 | g.57674901A= | CA2306103162 | ATP8B1 | c.1752T= (p.Thr584=) c.1617T= c.1638T= (p.Thr546=) c.1032T= (p.Thr344=) c.1602T= (p.Thr534=) | |
18 | g.57674901A>C | CA504021217 | ATP8B1 | c.1752T>G (p.Thr584=) c.1617T>G c.1638T>G (p.Thr546=) c.1032T>G (p.Thr344=) c.1602T>G (p.Thr534=) | |
18 | g.57674901A>G | CA8974486 | ATP8B1 | c.1752T>C (p.Thr584=) c.1617T>C c.1638T>C (p.Thr546=) c.1032T>C (p.Thr344=) c.1602T>C (p.Thr534=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
18 | g.57674901A>T | CA504021218 | ATP8B1 | c.1752T>A (p.Thr584=) c.1617T>A c.1638T>A (p.Thr546=) c.1032T>A (p.Thr344=) c.1602T>A (p.Thr534=) | |
18 | g.57674902G>A | CA8974487 | ATP8B1 | c.1751C>T (p.Thr584Ile) c.1616C>T c.1637C>T (p.Thr546Ile) c.1031C>T (p.Thr344Ile) c.1601C>T (p.Thr534Ile) | dbSNP ExAC gnomAD v2 gnomAD v4 |
18 | g.57674902G>C | CA402560967 | ATP8B1 | c.1751C>G (p.Thr584Ser) c.1616C>G c.1637C>G (p.Thr546Ser) c.1031C>G (p.Thr344Ser) c.1601C>G (p.Thr534Ser) | |
18 | g.57674902G= | CA2306103163 | ATP8B1 | c.1751C= (p.Thr584=) c.1616C= c.1637C= (p.Thr546=) c.1031C= (p.Thr344=) c.1601C= (p.Thr534=) | |
18 | g.57674902G>T | CA402560970 | ATP8B1 | c.1751C>A (p.Thr584Asn) c.1616C>A c.1637C>A (p.Thr546Asn) c.1031C>A (p.Thr344Asn) c.1601C>A (p.Thr534Asn) | |
18 | g.57674903T>A | CA8974488 | ATP8B1 | c.1750A>T (p.Thr584Ser) c.1615A>T c.1636A>T (p.Thr546Ser) c.1030A>T (p.Thr344Ser) c.1600A>T (p.Thr534Ser) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
18 | g.57674903T>C | CA402560978 | ATP8B1 | c.1750A>G (p.Thr584Ala) c.1615A>G c.1636A>G (p.Thr546Ala) c.1030A>G (p.Thr344Ala) c.1600A>G (p.Thr534Ala) | |
18 | g.57674903T>G | CA402560982 | ATP8B1 | c.1750A>C (p.Thr584Pro) c.1615A>C c.1636A>C (p.Thr546Pro) c.1030A>C (p.Thr344Pro) c.1600A>C (p.Thr534Pro) | |
18 | g.57674903T= | CA2306103164 | ATP8B1 | c.1750A= (p.Thr584=) c.1615A= c.1636A= (p.Thr546=) c.1030A= (p.Thr344=) c.1600A= (p.Thr534=) | |
18 | g.57674904G>A | CA504021219 | ATP8B1 | c.1749C>T (p.Gly583=) c.1614C>T c.1635C>T (p.Gly545=) c.1029C>T (p.Gly343=) c.1599C>T (p.Gly533=) | gnomAD v4 |
18 | g.57674904G>C | CA504021220 | ATP8B1 | c.1749C>G (p.Gly583=) c.1614C>G c.1635C>G (p.Gly545=) c.1029C>G (p.Gly343=) c.1599C>G (p.Gly533=) | |
18 | g.57674904G>T | CA504021221 | ATP8B1 | c.1749C>A (p.Gly583=) c.1614C>A c.1635C>A (p.Gly545=) c.1029C>A (p.Gly343=) c.1599C>A (p.Gly533=) | |
18 | g.57674905C>A | CA402560986 | ATP8B1 | c.1748G>T (p.Gly583Val) c.1613G>T c.1634G>T (p.Gly545Val) c.1028G>T (p.Gly343Val) c.1598G>T (p.Gly533Val) | |
18 | g.57674905C>G | CA402560988 | ATP8B1 | c.1748G>C (p.Gly583Ala) c.1613G>C c.1634G>C (p.Gly545Ala) c.1028G>C (p.Gly343Ala) c.1598G>C (p.Gly533Ala) | |
18 | g.57674905C>T | CA402560990 | ATP8B1 | c.1748G>A (p.Gly583Asp) c.1613G>A c.1634G>A (p.Gly545Asp) c.1028G>A (p.Gly343Asp) c.1598G>A (p.Gly533Asp) | |
18 | g.57674906C>A | CA402560996 | ATP8B1 | c.1747G>T (p.Gly583Cys) c.1612G>T c.1633G>T (p.Gly545Cys) c.1027G>T (p.Gly343Cys) c.1597G>T (p.Gly533Cys) | |
18 | g.57674906C>G | CA402561003 | ATP8B1 | c.1747G>C (p.Gly583Arg) c.1612G>C c.1633G>C (p.Gly545Arg) c.1027G>C (p.Gly343Arg) c.1597G>C (p.Gly533Arg) | |
18 | g.57674906C>T | CA402561000 | ATP8B1 | c.1747G>A (p.Gly583Ser) c.1612G>A c.1633G>A (p.Gly545Ser) c.1027G>A (p.Gly343Ser) c.1597G>A (p.Gly533Ser) | |
18 | g.57674907C>A | CA504021222 | ATP8B1 | c.1746G>T (p.Leu582=) c.1611G>T c.1632G>T (p.Leu544=) c.1026G>T (p.Leu342=) c.1596G>T (p.Leu532=) | |
18 | g.57674907C>G | CA504021224 | ATP8B1 | c.1746G>C (p.Leu582=) c.1611G>C c.1632G>C (p.Leu544=) c.1026G>C (p.Leu342=) c.1596G>C (p.Leu532=) | |
18 | g.57674907C>T | CA504021223 | ATP8B1 | c.1746G>A (p.Leu582=) c.1611G>A c.1632G>A (p.Leu544=) c.1026G>A (p.Leu342=) c.1596G>A (p.Leu532=) | |
18 | g.57674908del | CA2641954486 | ATP8B1 | c.1745del (p.Leu582ArgfsTer26) c.1610del c.1631del (p.Leu544ArgfsTer26) c.1025del (p.Leu342ArgfsTer26) c.1595del (p.Leu532ArgfsTer26) | gnomAD v4 |
18 | g.57674908A>C | CA402561009 | ATP8B1 | c.1745T>G (p.Leu582Arg) c.1610T>G c.1631T>G (p.Leu544Arg) c.1025T>G (p.Leu342Arg) c.1595T>G (p.Leu532Arg) | |
18 | g.57674908A>G | CA402561011 | ATP8B1 | c.1745T>C (p.Leu582Pro) c.1610T>C c.1631T>C (p.Leu544Pro) c.1025T>C (p.Leu342Pro) c.1595T>C (p.Leu532Pro) | |
18 | g.57674908A>T | CA402561012 | ATP8B1 | c.1745T>A (p.Leu582Gln) c.1610T>A c.1631T>A (p.Leu544Gln) c.1025T>A (p.Leu342Gln) c.1595T>A (p.Leu532Gln) | |
18 | g.57674909G>A | CA504021225 | ATP8B1 | c.1744C>T (p.Leu582=) c.1609C>T c.1630C>T (p.Leu544=) c.1024C>T (p.Leu342=) c.1594C>T (p.Leu532=) | |
18 | g.57674909G>C | CA402561015 | ATP8B1 | c.1744C>G (p.Leu582Val) c.1609C>G c.1630C>G (p.Leu544Val) c.1024C>G (p.Leu342Val) c.1594C>G (p.Leu532Val) | |
18 | g.57674909G>T | CA402561016 | ATP8B1 | c.1744C>A (p.Leu582Met) c.1609C>A c.1630C>A (p.Leu544Met) c.1024C>A (p.Leu342Met) c.1594C>A (p.Leu532Met) | gnomAD v4 |
18 | g.57674910T>A | CA402561017 | ATP8B1 | c.1743A>T (p.Glu581Asp) c.1608A>T c.1629A>T (p.Glu543Asp) c.1023A>T (p.Glu341Asp) c.1593A>T (p.Glu531Asp) | |
18 | g.57674910T>C | CA8974489 | ATP8B1 | c.1743A>G (p.Glu581=) c.1608A>G c.1629A>G (p.Glu543=) c.1023A>G (p.Glu341=) c.1593A>G (p.Glu531=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
18 | g.57674910T>G | CA402561019 | ATP8B1 | c.1743A>C (p.Glu581Asp) c.1608A>C c.1629A>C (p.Glu543Asp) c.1023A>C (p.Glu341Asp) c.1593A>C (p.Glu531Asp) | gnomAD v4 |
18 | g.57674910T= | CA2306103165 | ATP8B1 | c.1743A= (p.Glu581=) c.1608A= c.1629A= (p.Glu543=) c.1023A= (p.Glu341=) c.1593A= (p.Glu531=) | |
18 | g.57674911T>A | CA402561021 | ATP8B1 | c.1742A>T (p.Glu581Val) c.1607A>T c.1628A>T (p.Glu543Val) c.1022A>T (p.Glu341Val) c.1592A>T (p.Glu531Val) | |
18 | g.57674911T>C | CA402561049 | ATP8B1 | c.1742A>G (p.Glu581Gly) c.1607A>G c.1628A>G (p.Glu543Gly) c.1022A>G (p.Glu341Gly) c.1592A>G (p.Glu531Gly) | |
18 | g.57674911T>G | CA402561052 | ATP8B1 | c.1742A>C (p.Glu581Ala) c.1607A>C c.1628A>C (p.Glu543Ala) c.1022A>C (p.Glu341Ala) c.1592A>C (p.Glu531Ala) | |
18 | g.57674912C>A | CA402561061 | ATP8B1 | c.1741G>T (p.Glu581Ter) c.1606G>T c.1627G>T (p.Glu543Ter) c.1021G>T (p.Glu341Ter) c.1591G>T (p.Glu531Ter) | |
18 | g.57674912C>G | CA402561071 | ATP8B1 | c.1741G>C (p.Glu581Gln) c.1606G>C c.1627G>C (p.Glu543Gln) c.1021G>C (p.Glu341Gln) c.1591G>C (p.Glu531Gln) | |
18 | g.57674912C>T | CA402561059 | ATP8B1 | c.1741G>A (p.Glu581Lys) c.1606G>A c.1627G>A (p.Glu543Lys) c.1021G>A (p.Glu341Lys) c.1591G>A (p.Glu531Lys) | |
18 | g.57674913A>C | CA402561075 | ATP8B1 | c.1740T>G (p.Ser580Arg) c.1605T>G c.1626T>G (p.Ser542Arg) c.1020T>G (p.Ser340Arg) c.1590T>G (p.Ser530Arg) | |
18 | g.57674913A>G | CA504021226 | ATP8B1 | c.1740T>C (p.Ser580=) c.1605T>C c.1626T>C (p.Ser542=) c.1020T>C (p.Ser340=) c.1590T>C (p.Ser530=) | |
18 | g.57674913A>T | CA402561078 | ATP8B1 | c.1740T>A (p.Ser580Arg) c.1605T>A c.1626T>A (p.Ser542Arg) c.1020T>A (p.Ser340Arg) c.1590T>A (p.Ser530Arg) | |
18 | g.57674914C>A | CA402561082 | ATP8B1 | c.1739G>T (p.Ser580Ile) c.1604G>T c.1625G>T (p.Ser542Ile) c.1019G>T (p.Ser340Ile) c.1589G>T (p.Ser530Ile) | |
18 | g.57674914C= | CA2306103166 | ATP8B1 | c.1739G= (p.Ser580=) c.1604G= c.1625G= (p.Ser542=) c.1019G= (p.Ser340=) c.1589G= (p.Ser530=) | |
18 | g.57674914C>G | CA402561084 | ATP8B1 | c.1739G>C (p.Ser580Thr) c.1604G>C c.1625G>C (p.Ser542Thr) c.1019G>C (p.Ser340Thr) c.1589G>C (p.Ser530Thr) | gnomAD v4 |
18 | g.57674914C>T | CA8974490 | ATP8B1 | c.1739G>A (p.Ser580Asn) c.1604G>A c.1625G>A (p.Ser542Asn) c.1019G>A (p.Ser340Asn) c.1589G>A (p.Ser530Asn) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
18 | g.57674915T>A | CA402561086 | ATP8B1 | c.1738A>T (p.Ser580Cys) c.1603A>T c.1624A>T (p.Ser542Cys) c.1018A>T (p.Ser340Cys) c.1588A>T (p.Ser530Cys) | |
18 | g.57674915T>C | CA402561088 | ATP8B1 | c.1738A>G (p.Ser580Gly) c.1603A>G c.1624A>G (p.Ser542Gly) c.1018A>G (p.Ser340Gly) c.1588A>G (p.Ser530Gly) | |
18 | g.57674915T>G | CA402561091 | ATP8B1 | c.1738A>C (p.Ser580Arg) c.1603A>C c.1624A>C (p.Ser542Arg) c.1018A>C (p.Ser340Arg) c.1588A>C (p.Ser530Arg) | |
18 | g.57674916G>A | CA504021228 | ATP8B1 | c.1737C>T (p.Ile579=) c.1602C>T c.1623C>T (p.Ile541=) c.1017C>T (p.Ile339=) c.1587C>T (p.Ile529=) | |
18 | g.57674916G>C | CA402561094 | ATP8B1 | c.1737C>G (p.Ile579Met) c.1602C>G c.1623C>G (p.Ile541Met) c.1017C>G (p.Ile339Met) c.1587C>G (p.Ile529Met) | |
18 | g.57674916G>T | CA504021229 | ATP8B1 | c.1737C>A (p.Ile579=) c.1602C>A c.1623C>A (p.Ile541=) c.1017C>A (p.Ile339=) c.1587C>A (p.Ile529=) | |
18 | g.57674917A>C | CA402561101 | ATP8B1 | c.1736T>G (p.Ile579Ser) c.1601T>G c.1622T>G (p.Ile541Ser) c.1016T>G (p.Ile339Ser) c.1586T>G (p.Ile529Ser) | |
18 | g.57674917A>G | CA402561103 | ATP8B1 | c.1736T>C (p.Ile579Thr) c.1601T>C c.1622T>C (p.Ile541Thr) c.1016T>C (p.Ile339Thr) c.1586T>C (p.Ile529Thr) | |
18 | g.57674917A>T | CA402561112 | ATP8B1 | c.1736T>A (p.Ile579Asn) c.1601T>A c.1622T>A (p.Ile541Asn) c.1016T>A (p.Ile339Asn) c.1586T>A (p.Ile529Asn) | |
18 | g.57674918T>A | CA402561120 | ATP8B1 | c.1735A>T (p.Ile579Phe) c.1600A>T c.1621A>T (p.Ile541Phe) c.1015A>T (p.Ile339Phe) c.1585A>T (p.Ile529Phe) | |
18 | g.57674918T>C | CA402561121 | ATP8B1 | c.1735A>G (p.Ile579Val) c.1600A>G c.1621A>G (p.Ile541Val) c.1015A>G (p.Ile339Val) c.1585A>G (p.Ile529Val) | dbSNP gnomAD v3 gnomAD v4 |
18 | g.57674918T>G | CA402561126 | ATP8B1 | c.1735A>C (p.Ile579Leu) c.1600A>C c.1621A>C (p.Ile541Leu) c.1015A>C (p.Ile339Leu) c.1585A>C (p.Ile529Leu) | |
18 | g.57674918T= | CA2306103167 | ATP8B1 | c.1735A= (p.Ile579=) c.1600A= c.1621A= (p.Ile541=) c.1015A= (p.Ile339=) c.1585A= (p.Ile529=) | |
18 | g.57674919G>A | CA504021231 | ATP8B1 | c.1734C>T (p.Thr578=) c.1599C>T c.1620C>T (p.Thr540=) c.1014C>T (p.Thr338=) c.1584C>T (p.Thr528=) | ClinVar dbSNP |
18 | g.57674919G>C | CA504021233 | ATP8B1 | c.1734C>G (p.Thr578=) c.1599C>G c.1620C>G (p.Thr540=) c.1014C>G (p.Thr338=) c.1584C>G (p.Thr528=) | |
18 | g.57674919G= | CA2306103168 | ATP8B1 | c.1734C= (p.Thr578=) c.1599C= c.1620C= (p.Thr540=) c.1014C= (p.Thr338=) c.1584C= (p.Thr528=) | |
18 | g.57674919G>T | CA504021234 | ATP8B1 | c.1734C>A (p.Thr578=) c.1599C>A c.1620C>A (p.Thr540=) c.1014C>A (p.Thr338=) c.1584C>A (p.Thr528=) | |
18 | g.57674920G>A | CA402561139 | ATP8B1 | c.1733C>T (p.Thr578Ile) c.1598C>T c.1619C>T (p.Thr540Ile) c.1013C>T (p.Thr338Ile) c.1583C>T (p.Thr528Ile) | |
18 | g.57674920G>C | CA402561136 | ATP8B1 | c.1733C>G (p.Thr578Ser) c.1598C>G c.1619C>G (p.Thr540Ser) c.1013C>G (p.Thr338Ser) c.1583C>G (p.Thr528Ser) | |
18 | g.57674920G>T | CA402561133 | ATP8B1 | c.1733C>A (p.Thr578Asn) c.1598C>A c.1619C>A (p.Thr540Asn) c.1013C>A (p.Thr338Asn) c.1583C>A (p.Thr528Asn) | |
18 | g.57674921T>A | CA402561140 | ATP8B1 | c.1732A>T (p.Thr578Ser) c.1597A>T c.1618A>T (p.Thr540Ser) c.1012A>T (p.Thr338Ser) c.1582A>T (p.Thr528Ser) | |
18 | g.57674921T>C | CA402561141 | ATP8B1 | c.1732A>G (p.Thr578Ala) c.1597A>G c.1618A>G (p.Thr540Ala) c.1012A>G (p.Thr338Ala) c.1582A>G (p.Thr528Ala) | |
18 | g.57674921T>G | CA402561142 | ATP8B1 | c.1732A>C (p.Thr578Pro) c.1597A>C c.1618A>C (p.Thr540Pro) c.1012A>C (p.Thr338Pro) c.1582A>C (p.Thr528Pro) | |
18 | g.57674922G>A | CA504021236 | ATP8B1 | c.1731C>T (p.Ile577=) c.1596C>T c.1617C>T (p.Ile539=) c.1011C>T (p.Ile337=) c.1581C>T (p.Ile527=) | |
18 | g.57674922G>C | CA402561145 | ATP8B1 | c.1731C>G (p.Ile577Met) c.1596C>G c.1617C>G (p.Ile539Met) c.1011C>G (p.Ile337Met) c.1581C>G (p.Ile527Met) | |
18 | g.57674922G>T | CA504021235 | ATP8B1 | c.1731C>A (p.Ile577=) c.1596C>A c.1617C>A (p.Ile539=) c.1011C>A (p.Ile337=) c.1581C>A (p.Ile527=) | |
18 | g.57674923A>C | CA402561148 | ATP8B1 | c.1730T>G (p.Ile577Ser) c.1595T>G c.1616T>G (p.Ile539Ser) c.1010T>G (p.Ile337Ser) c.1580T>G (p.Ile527Ser) | |
18 | g.57674923A>G | CA402561151 | ATP8B1 | c.1730T>C (p.Ile577Thr) c.1595T>C c.1616T>C (p.Ile539Thr) c.1010T>C (p.Ile337Thr) c.1580T>C (p.Ile527Thr) | |
18 | g.57674923A>T | CA402561153 | ATP8B1 | c.1730T>A (p.Ile577Asn) c.1595T>A c.1616T>A (p.Ile539Asn) c.1010T>A (p.Ile337Asn) c.1580T>A (p.Ile527Asn) | |
18 | g.57674924T>A | CA402561157 | ATP8B1 | c.1729A>T (p.Ile577Phe) c.1594A>T c.1615A>T (p.Ile539Phe) c.1009A>T (p.Ile337Phe) c.1579A>T (p.Ile527Phe) | |
18 | g.57674924T>C | CA8974491 | ATP8B1 | c.1729A>G (p.Ile577Val) c.1594A>G c.1615A>G (p.Ile539Val) c.1009A>G (p.Ile337Val) c.1579A>G (p.Ile527Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
18 | g.57674924T>G | CA402561162 | ATP8B1 | c.1729A>C (p.Ile577Leu) c.1594A>C c.1615A>C (p.Ile539Leu) c.1009A>C (p.Ile337Leu) c.1579A>C (p.Ile527Leu) | |
18 | g.57674924T= | CA2306103169 | ATP8B1 | c.1729A= (p.Ile577=) c.1594A= c.1615A= (p.Ile539=) c.1009A= (p.Ile337=) c.1579A= (p.Ile527=) | |
18 | g.57674925G>A | CA504021237 | ATP8B1 | c.1728C>T (p.Thr576=) c.1593C>T c.1614C>T (p.Thr538=) c.1008C>T (p.Thr336=) c.1578C>T (p.Thr526=) | |
18 | g.57674925G>C | CA504021238 | ATP8B1 | c.1728C>G (p.Thr576=) c.1593C>G c.1614C>G (p.Thr538=) c.1008C>G (p.Thr336=) c.1578C>G (p.Thr526=) | |
18 | g.57674925G>T | CA504021239 | ATP8B1 | c.1728C>A (p.Thr576=) c.1593C>A c.1614C>A (p.Thr538=) c.1008C>A (p.Thr336=) c.1578C>A (p.Thr526=) | |
18 | g.57674926G>A | CA402561168 | ATP8B1 | c.1727C>T (p.Thr576Ile) c.1592C>T c.1613C>T (p.Thr538Ile) c.1007C>T (p.Thr336Ile) c.1577C>T (p.Thr526Ile) | |
18 | g.57674926G>C | CA402561173 | ATP8B1 | c.1727C>G (p.Thr576Ser) c.1592C>G c.1613C>G (p.Thr538Ser) c.1007C>G (p.Thr336Ser) c.1577C>G (p.Thr526Ser) | |
18 | g.57674926G>T | CA402561177 | ATP8B1 | c.1727C>A (p.Thr576Asn) c.1592C>A c.1613C>A (p.Thr538Asn) c.1007C>A (p.Thr336Asn) c.1577C>A (p.Thr526Asn) | |
18 | g.57674927T>A | CA402561183 | ATP8B1 | c.1726A>T (p.Thr576Ser) c.1591A>T c.1612A>T (p.Thr538Ser) c.1006A>T (p.Thr336Ser) c.1576A>T (p.Thr526Ser) | |
18 | g.57674927T>C | CA402561187 | ATP8B1 | c.1726A>G (p.Thr576Ala) c.1591A>G c.1612A>G (p.Thr538Ala) c.1006A>G (p.Thr336Ala) c.1576A>G (p.Thr526Ala) | |
18 | g.57674927T>G | CA402561180 | ATP8B1 | c.1726A>C (p.Thr576Pro) c.1591A>C c.1612A>C (p.Thr538Pro) c.1006A>C (p.Thr336Pro) c.1576A>C (p.Thr526Pro) | |
18 | g.57674928G>A | CA504021241 | ATP8B1 | c.1725C>T (p.Asn575=) c.1590C>T c.1611C>T (p.Asn537=) c.1005C>T (p.Asn335=) c.1575C>T (p.Asn525=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
18 | g.57674928G>C | CA402561191 | ATP8B1 | c.1725C>G (p.Asn575Lys) c.1590C>G c.1611C>G (p.Asn537Lys) c.1005C>G (p.Asn335Lys) c.1575C>G (p.Asn525Lys) | |
18 | g.57674928G= | CA2306103170 | ATP8B1 | c.1725C= (p.Asn575=) c.1590C= c.1611C= (p.Asn537=) c.1005C= (p.Asn335=) c.1575C= (p.Asn525=) | |
18 | g.57674928G>T | CA402561200 | ATP8B1 | c.1725C>A (p.Asn575Lys) c.1590C>A c.1611C>A (p.Asn537Lys) c.1005C>A (p.Asn335Lys) c.1575C>A (p.Asn525Lys) | |
18 | g.57674929T>A | CA402561206 | ATP8B1 | c.1724A>T (p.Asn575Ile) c.1589A>T c.1610A>T (p.Asn537Ile) c.1004A>T (p.Asn335Ile) c.1574A>T (p.Asn525Ile) | |
18 | g.57674929T>C | CA402561208 | ATP8B1 | c.1724A>G (p.Asn575Ser) c.1589A>G c.1610A>G (p.Asn537Ser) c.1004A>G (p.Asn335Ser) c.1574A>G (p.Asn525Ser) | |
18 | g.57674929T>G | CA402561212 | ATP8B1 | c.1724A>C (p.Asn575Thr) c.1589A>C c.1610A>C (p.Asn537Thr) c.1004A>C (p.Asn335Thr) c.1574A>C (p.Asn525Thr) | gnomAD v4 |
18 | g.57674930T>A | CA402561215 | ATP8B1 | c.1723A>T (p.Asn575Tyr) c.1588A>T c.1609A>T (p.Asn537Tyr) c.1003A>T (p.Asn335Tyr) c.1573A>T (p.Asn525Tyr) | |
18 | g.57674930T>C | CA402561219 | ATP8B1 | c.1723A>G (p.Asn575Asp) c.1588A>G c.1609A>G (p.Asn537Asp) c.1003A>G (p.Asn335Asp) c.1573A>G (p.Asn525Asp) | |
18 | g.57674930T>G | CA402561222 | ATP8B1 | c.1723A>C (p.Asn575His) c.1588A>C c.1609A>C (p.Asn537His) c.1003A>C (p.Asn335His) c.1573A>C (p.Asn525His) | |
18 | g.57674931C>A | CA402561225 | ATP8B1 | c.1722G>T (p.Gln574His) c.1587G>T c.1608G>T (p.Gln536His) c.1002G>T (p.Gln334His) c.1572G>T (p.Gln524His) | |
18 | g.57674931C>G | CA402561228 | ATP8B1 | c.1722G>C (p.Gln574His) c.1587G>C c.1608G>C (p.Gln536His) c.1002G>C (p.Gln334His) c.1572G>C (p.Gln524His) | |
18 | g.57674931C>T | CA504021244 | ATP8B1 | c.1722G>A (p.Gln574=) c.1587G>A c.1608G>A (p.Gln536=) c.1002G>A (p.Gln334=) c.1572G>A (p.Gln524=) | |
18 | g.57674932T>A | CA402561234 | ATP8B1 | c.1721A>T (p.Gln574Leu) c.1586A>T c.1607A>T (p.Gln536Leu) c.1001A>T (p.Gln334Leu) c.1571A>T (p.Gln524Leu) | |
18 | g.57674932T>C | CA402561236 | ATP8B1 | c.1721A>G (p.Gln574Arg) c.1586A>G c.1607A>G (p.Gln536Arg) c.1001A>G (p.Gln334Arg) c.1571A>G (p.Gln524Arg) | gnomAD v4 |
18 | g.57674932T>G | CA402561239 | ATP8B1 | c.1721A>C (p.Gln574Pro) c.1586A>C c.1607A>C (p.Gln536Pro) c.1001A>C (p.Gln334Pro) c.1571A>C (p.Gln524Pro) | |
18 | g.57674933G>A | CA402561244 | ATP8B1 | c.1720C>T (p.Gln574Ter) c.1585C>T c.1606C>T (p.Gln536Ter) c.1000C>T (p.Gln334Ter) c.1570C>T (p.Gln524Ter) | |
18 | g.57674933G>C | CA402561252 | ATP8B1 | c.1720C>G (p.Gln574Glu) c.1585C>G c.1606C>G (p.Gln536Glu) c.1000C>G (p.Gln334Glu) c.1570C>G (p.Gln524Glu) | |
18 | g.57674933G>T | CA402561248 | ATP8B1 | c.1720C>A (p.Gln574Lys) c.1585C>A c.1606C>A (p.Gln536Lys) c.1000C>A (p.Gln334Lys) c.1570C>A (p.Gln524Lys) | |
18 | g.57674934G>A | CA504021245 | ATP8B1 | c.1719C>T (p.Thr573=) c.1584C>T c.1605C>T (p.Thr535=) c.999C>T (p.Thr333=) c.1569C>T (p.Thr523=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
18 | g.57674934G>C | CA504021246 | ATP8B1 | c.1719C>G (p.Thr573=) c.1584C>G c.1605C>G (p.Thr535=) c.999C>G (p.Thr333=) c.1569C>G (p.Thr523=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
18 | g.57674934G= | CA2306103171 | ATP8B1 | c.1719C= (p.Thr573=) c.1584C= c.1605C= (p.Thr535=) c.999C= (p.Thr333=) c.1569C= (p.Thr523=) | |
18 | g.57674934G>T | CA504021247 | ATP8B1 | c.1719C>A (p.Thr573=) c.1584C>A c.1605C>A (p.Thr535=) c.999C>A (p.Thr333=) c.1569C>A (p.Thr523=) | gnomAD v4 |
18 | g.57674935G>A | CA402561255 | ATP8B1 | c.1718C>T (p.Thr573Ile) c.1583C>T c.1604C>T (p.Thr535Ile) c.998C>T (p.Thr333Ile) c.1568C>T (p.Thr523Ile) | gnomAD v4 |
18 | g.57674935G>C | CA402561259 | ATP8B1 | c.1718C>G (p.Thr573Ser) c.1583C>G c.1604C>G (p.Thr535Ser) c.998C>G (p.Thr333Ser) c.1568C>G (p.Thr523Ser) | |
18 | g.57674935G>T | CA402561263 | ATP8B1 | c.1718C>A (p.Thr573Asn) c.1583C>A c.1604C>A (p.Thr535Asn) c.998C>A (p.Thr333Asn) c.1568C>A (p.Thr523Asn) | COSMIC |
18 | g.57674936T>A | CA402561269 | ATP8B1 | c.1717A>T (p.Thr573Ser) c.1582A>T c.1603A>T (p.Thr535Ser) c.997A>T (p.Thr333Ser) c.1567A>T (p.Thr523Ser) | |
18 | g.57674936T>C | CA402561273 | ATP8B1 | c.1717A>G (p.Thr573Ala) c.1582A>G c.1603A>G (p.Thr535Ala) c.997A>G (p.Thr333Ala) c.1567A>G (p.Thr523Ala) | |
18 | g.57674936T>G | CA402561276 | ATP8B1 | c.1717A>C (p.Thr573Pro) c.1582A>C c.1603A>C (p.Thr535Pro) c.997A>C (p.Thr333Pro) c.1567A>C (p.Thr523Pro) | |
18 | g.57674937C>A | CA402561278 | ATP8B1 | c.1716G>T (p.Arg572Ser) c.1581G>T c.1602G>T (p.Arg534Ser) c.996G>T (p.Arg332Ser) c.1566G>T (p.Arg522Ser) | |
18 | g.57674937C>G | CA402561281 | ATP8B1 | c.1716G>C (p.Arg572Ser) c.1581G>C c.1602G>C (p.Arg534Ser) c.996G>C (p.Arg332Ser) c.1566G>C (p.Arg522Ser) | |
18 | g.57674937C>T | CA504021249 | ATP8B1 | c.1716G>A (p.Arg572=) c.1581G>A c.1602G>A (p.Arg534=) c.996G>A (p.Arg332=) c.1566G>A (p.Arg522=) | |
18 | g.57674938C>A | CA402561283 | ATP8B1 | c.1715G>T (p.Arg572Met) c.1580G>T c.1601G>T (p.Arg534Met) c.995G>T (p.Arg332Met) c.1565G>T (p.Arg522Met) | |
18 | g.57674938C>G | CA402561285 | ATP8B1 | c.1715G>C (p.Arg572Thr) c.1580G>C c.1601G>C (p.Arg534Thr) c.995G>C (p.Arg332Thr) c.1565G>C (p.Arg522Thr) | |
18 | g.57674938C>T | CA402561286 | ATP8B1 | c.1715G>A (p.Arg572Lys) c.1580G>A c.1601G>A (p.Arg534Lys) c.995G>A (p.Arg332Lys) c.1565G>A (p.Arg522Lys) | |
18 | g.57674939T>A | CA402561289 | ATP8B1 | c.1714A>T (p.Arg572Trp) c.1579A>T c.1600A>T (p.Arg534Trp) c.994A>T (p.Arg332Trp) c.1564A>T (p.Arg522Trp) | |
18 | g.57674939T>C | CA402561292 | ATP8B1 | c.1714A>G (p.Arg572Gly) c.1579A>G c.1600A>G (p.Arg534Gly) c.994A>G (p.Arg332Gly) c.1564A>G (p.Arg522Gly) | |
18 | g.57674939T>G | CA504021252 | ATP8B1 | c.1714A>C (p.Arg572=) c.1579A>C c.1600A>C (p.Arg534=) c.994A>C (p.Arg332=) c.1564A>C (p.Arg522=) | |
18 | g.57674940G>A | CA504021254 | ATP8B1 | c.1713C>T (p.Ala571=) c.1578C>T c.1599C>T (p.Ala533=) c.993C>T (p.Ala331=) c.1563C>T (p.Ala521=) | |
18 | g.57674940G>C | CA504021255 | ATP8B1 | c.1713C>G (p.Ala571=) c.1578C>G c.1599C>G (p.Ala533=) c.993C>G (p.Ala331=) c.1563C>G (p.Ala521=) | |
18 | g.57674940G>T | CA504021256 | ATP8B1 | c.1713C>A (p.Ala571=) c.1578C>A c.1599C>A (p.Ala533=) c.993C>A (p.Ala331=) c.1563C>A (p.Ala521=) | |
18 | g.57674941G>A | CA8974492 | ATP8B1 | c.1712C>T (p.Ala571Val) c.1577C>T c.1598C>T (p.Ala533Val) c.992C>T (p.Ala331Val) c.1562C>T (p.Ala521Val) | dbSNP ExAC gnomAD v2 gnomAD v4 |
18 | g.57674941G>C | CA402561299 | ATP8B1 | c.1712C>G (p.Ala571Gly) c.1577C>G c.1598C>G (p.Ala533Gly) c.992C>G (p.Ala331Gly) c.1562C>G (p.Ala521Gly) | dbSNP gnomAD v2 gnomAD v4 |
18 | g.57674941G= | CA2306103172 | ATP8B1 | c.1712C= (p.Ala571=) c.1577C= c.1598C= (p.Ala533=) c.992C= (p.Ala331=) c.1562C= (p.Ala521=) | |
18 | g.57674941G>T | CA402561301 | ATP8B1 | c.1712C>A (p.Ala571Asp) c.1577C>A c.1598C>A (p.Ala533Asp) c.992C>A (p.Ala331Asp) c.1562C>A (p.Ala521Asp) | |
18 | g.57674942C>A | CA402561308 | ATP8B1 | c.1711G>T (p.Ala571Ser) c.1576G>T c.1597G>T (p.Ala533Ser) c.991G>T (p.Ala331Ser) c.1561G>T (p.Ala521Ser) | gnomAD v4 |
18 | g.57674942C= | CA2306103173 | ATP8B1 | c.1711G= (p.Ala571=) c.1576G= c.1597G= (p.Ala533=) c.991G= (p.Ala331=) c.1561G= (p.Ala521=) | |
18 | g.57674942C>G | CA402561311 | ATP8B1 | c.1711G>C (p.Ala571Pro) c.1576G>C c.1597G>C (p.Ala533Pro) c.991G>C (p.Ala331Pro) c.1561G>C (p.Ala521Pro) | |
18 | g.57674942C>T | CA8974493 | ATP8B1 | c.1711G>A (p.Ala571Thr) c.1576G>A c.1597G>A (p.Ala533Thr) c.991G>A (p.Ala331Thr) c.1561G>A (p.Ala521Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
18 | g.57674943G>A | CA8974494 | ATP8B1 | c.1710C>T (p.Leu570=) c.1575C>T c.1596C>T (p.Leu532=) c.990C>T (p.Leu330=) c.1560C>T (p.Leu520=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
18 | g.57674943G>C | CA504021259 | ATP8B1 | c.1710C>G (p.Leu570=) c.1575C>G c.1596C>G (p.Leu532=) c.990C>G (p.Leu330=) c.1560C>G (p.Leu520=) | gnomAD v4 |
18 | g.57674943G= | CA2306103174 | ATP8B1 | c.1710C= (p.Leu570=) c.1575C= c.1596C= (p.Leu532=) c.990C= (p.Leu330=) c.1560C= (p.Leu520=) | |
18 | g.57674943G>T | CA504021260 | ATP8B1 | c.1710C>A (p.Leu570=) c.1575C>A c.1596C>A (p.Leu532=) c.990C>A (p.Leu330=) c.1560C>A (p.Leu520=) | |
18 | g.57674944A>C | CA402561330 | ATP8B1 | c.1709T>G (p.Leu570Arg) c.1574T>G c.1595T>G (p.Leu532Arg) c.989T>G (p.Leu330Arg) c.1559T>G (p.Leu520Arg) | |
18 | g.57674944A>G | CA402561324 | ATP8B1 | c.1709T>C (p.Leu570Pro) c.1574T>C c.1595T>C (p.Leu532Pro) c.989T>C (p.Leu330Pro) c.1559T>C (p.Leu520Pro) | |
18 | g.57674944A>T | CA402561328 | ATP8B1 | c.1709T>A (p.Leu570His) c.1574T>A c.1595T>A (p.Leu532His) c.989T>A (p.Leu330His) c.1559T>A (p.Leu520His) | |
18 | g.57674945G>A | CA402561338 | ATP8B1 | c.1708C>T (p.Leu570Phe) c.1573C>T c.1594C>T (p.Leu532Phe) c.988C>T (p.Leu330Phe) c.1558C>T (p.Leu520Phe) | dbSNP gnomAD v3 gnomAD v4 |
18 | g.57674945G>C | CA402561340 | ATP8B1 | c.1708C>G (p.Leu570Val) c.1573C>G c.1594C>G (p.Leu532Val) c.988C>G (p.Leu330Val) c.1558C>G (p.Leu520Val) | |
18 | g.57674945G= | CA2306103175 | ATP8B1 | c.1708C= (p.Leu570=) c.1573C= c.1594C= (p.Leu532=) c.988C= (p.Leu330=) c.1558C= (p.Leu520=) | |
18 | g.57674945G>T | CA402561345 | ATP8B1 | c.1708C>A (p.Leu570Ile) c.1573C>A c.1594C>A (p.Leu532Ile) c.988C>A (p.Leu330Ile) c.1558C>A (p.Leu520Ile) | |
18 | g.57674946G>A | CA504021263 | ATP8B1 | c.1707C>T (p.Phe569=) c.1572C>T c.1593C>T (p.Phe531=) c.987C>T (p.Phe329=) c.1557C>T (p.Phe519=) | |
18 | g.57674946G>C | CA402561349 | ATP8B1 | c.1707C>G (p.Phe569Leu) c.1572C>G c.1593C>G (p.Phe531Leu) c.987C>G (p.Phe329Leu) c.1557C>G (p.Phe519Leu) | |
18 | g.57674946G>T | CA402561352 | ATP8B1 | c.1707C>A (p.Phe569Leu) c.1572C>A c.1593C>A (p.Phe531Leu) c.987C>A (p.Phe329Leu) c.1557C>A (p.Phe519Leu) | |
18 | g.57674947A= | CA2306103176 | ATP8B1 | c.1706T= (p.Phe569=) c.1571T= c.1592T= (p.Phe531=) c.986T= (p.Phe329=) c.1556T= (p.Phe519=) | |
18 | g.57674947A>C | CA402561356 | ATP8B1 | c.1706T>G (p.Phe569Cys) c.1571T>G c.1592T>G (p.Phe531Cys) c.986T>G (p.Phe329Cys) c.1556T>G (p.Phe519Cys) | dbSNP gnomAD v2 gnomAD v4 |
18 | g.57674947A>G | CA402561368 | ATP8B1 | c.1706T>C (p.Phe569Ser) c.1571T>C c.1592T>C (p.Phe531Ser) c.986T>C (p.Phe329Ser) c.1556T>C (p.Phe519Ser) | |
18 | g.57674947A>T | CA402561360 | ATP8B1 | c.1706T>A (p.Phe569Tyr) c.1571T>A c.1592T>A (p.Phe531Tyr) c.986T>A (p.Phe329Tyr) c.1556T>A (p.Phe519Tyr) | dbSNP |
18 | g.57674948A>C | CA402561375 | ATP8B1 | c.1705T>G (p.Phe569Val) c.1570T>G c.1591T>G (p.Phe531Val) c.985T>G (p.Phe329Val) c.1555T>G (p.Phe519Val) | |
18 | g.57674948A>G | CA402561379 | ATP8B1 | c.1705T>C (p.Phe569Leu) c.1570T>C c.1591T>C (p.Phe531Leu) c.985T>C (p.Phe329Leu) c.1555T>C (p.Phe519Leu) | |
18 | g.57674948A>T | CA402561383 | ATP8B1 | c.1705T>A (p.Phe569Ile) c.1570T>A c.1591T>A (p.Phe531Ile) c.985T>A (p.Phe329Ile) c.1555T>A (p.Phe519Ile) | |
18 | g.57674949G>A | CA504021265 | ATP8B1 | c.1704C>T (p.Ala568=) c.1569C>T c.1590C>T (p.Ala530=) c.984C>T (p.Ala328=) c.1554C>T (p.Ala518=) | |
18 | g.57674949G>C | CA504021266 | ATP8B1 | c.1704C>G (p.Ala568=) c.1569C>G c.1590C>G (p.Ala530=) c.984C>G (p.Ala328=) c.1554C>G (p.Ala518=) | |
18 | g.57674949G>T | CA504021267 | ATP8B1 | c.1704C>A (p.Ala568=) c.1569C>A c.1590C>A (p.Ala530=) c.984C>A (p.Ala328=) c.1554C>A (p.Ala518=) | |
18 | g.57674950G>A | CA8974495 | ATP8B1 | c.1703C>T (p.Ala568Val) c.1568C>T c.1589C>T (p.Ala530Val) c.983C>T (p.Ala328Val) c.1553C>T (p.Ala518Val) | dbSNP ExAC gnomAD v2 gnomAD v4 |
18 | g.57674950G>C | CA402561386 | ATP8B1 | c.1703C>G (p.Ala568Gly) c.1568C>G c.1589C>G (p.Ala530Gly) c.983C>G (p.Ala328Gly) c.1553C>G (p.Ala518Gly) | |
18 | g.57674950G= | CA2306103177 | ATP8B1 | c.1703C= (p.Ala568=) c.1568C= c.1589C= (p.Ala530=) c.983C= (p.Ala328=) c.1553C= (p.Ala518=) | |
18 | g.57674950G>T | CA402561392 | ATP8B1 | c.1703C>A (p.Ala568Asp) c.1568C>A c.1589C>A (p.Ala530Asp) c.983C>A (p.Ala328Asp) c.1553C>A (p.Ala518Asp) | |
18 | g.57674951C>A | CA402561398 | ATP8B1 | c.1702G>T (p.Ala568Ser) c.1567G>T c.1588G>T (p.Ala530Ser) c.982G>T (p.Ala328Ser) c.1552G>T (p.Ala518Ser) | |
18 | g.57674951C>G | CA402561405 | ATP8B1 | c.1702G>C (p.Ala568Pro) c.1567G>C c.1588G>C (p.Ala530Pro) c.982G>C (p.Ala328Pro) c.1552G>C (p.Ala518Pro) | |
18 | g.57674951C>T | CA402561411 | ATP8B1 | c.1702G>A (p.Ala568Thr) c.1567G>A c.1588G>A (p.Ala530Thr) c.982G>A (p.Ala328Thr) c.1552G>A (p.Ala518Thr) | |
18 | g.57674952A= | CA2306103178 | ATP8B1 | c.1701T= (p.Phe567=) c.1566T= c.1587T= (p.Phe529=) c.981T= (p.Phe327=) c.1551T= (p.Phe517=) | |
18 | g.57674952A>C | CA402561414 | ATP8B1 | c.1701T>G (p.Phe567Leu) c.1566T>G c.1587T>G (p.Phe529Leu) c.981T>G (p.Phe327Leu) c.1551T>G (p.Phe517Leu) | |
18 | g.57674952A>G | CA504021268 | ATP8B1 | c.1701T>C (p.Phe567=) c.1566T>C c.1587T>C (p.Phe529=) c.981T>C (p.Phe327=) c.1551T>C (p.Phe517=) | dbSNP |
18 | g.57674952A>T | CA402561418 | ATP8B1 | c.1701T>A (p.Phe567Leu) c.1566T>A c.1587T>A (p.Phe529Leu) c.981T>A (p.Phe327Leu) c.1551T>A (p.Phe517Leu) | |
18 | g.57674953A= | CA2306103179 | ATP8B1 | c.1700T= (p.Phe567=) c.1565T= c.1586T= (p.Phe529=) c.980T= (p.Phe327=) c.1550T= (p.Phe517=) | |
18 | g.57674953A>C | CA402561425 | ATP8B1 | c.1700T>G (p.Phe567Cys) c.1565T>G c.1586T>G (p.Phe529Cys) c.980T>G (p.Phe327Cys) c.1550T>G (p.Phe517Cys) | COSMIC |
18 | g.57674953A>G | CA402561428 | ATP8B1 | c.1700T>C (p.Phe567Ser) c.1565T>C c.1586T>C (p.Phe529Ser) c.980T>C (p.Phe327Ser) c.1550T>C (p.Phe517Ser) | dbSNP gnomAD v3 gnomAD v4 |
18 | g.57674953A>T | CA402561427 | ATP8B1 | c.1700T>A (p.Phe567Tyr) c.1565T>A c.1586T>A (p.Phe529Tyr) c.980T>A (p.Phe327Tyr) c.1550T>A (p.Phe517Tyr) | |
18 | g.57674954A>C | CA402561432 | ATP8B1 | c.1699T>G (p.Phe567Val) c.1564T>G c.1585T>G (p.Phe529Val) c.979T>G (p.Phe327Val) c.1549T>G (p.Phe517Val) | gnomAD v4 |
18 | g.57674954A>G | CA402561433 | ATP8B1 | c.1699T>C (p.Phe567Leu) c.1564T>C c.1585T>C (p.Phe529Leu) c.979T>C (p.Phe327Leu) c.1549T>C (p.Phe517Leu) | |
18 | g.57674954A>T | CA402561434 | ATP8B1 | c.1699T>A (p.Phe567Ile) c.1564T>A c.1585T>A (p.Phe529Ile) c.979T>A (p.Phe327Ile) c.1549T>A (p.Phe517Ile) | |
18 | g.57674955G>A | CA504021272 | ATP8B1 | c.1698C>T (p.Gly566=) c.1563C>T c.1584C>T (p.Gly528=) c.978C>T (p.Gly326=) c.1548C>T (p.Gly516=) | dbSNP |
18 | g.57674955G>C | CA504021273 | ATP8B1 | c.1698C>G (p.Gly566=) c.1563C>G c.1584C>G (p.Gly528=) c.978C>G (p.Gly326=) c.1548C>G (p.Gly516=) | |
18 | g.57674955G= | CA2306103180 | ATP8B1 | c.1698C= (p.Gly566=) c.1563C= c.1584C= (p.Gly528=) c.978C= (p.Gly326=) c.1548C= (p.Gly516=) | |
18 | g.57674955G>T | CA504021274 | ATP8B1 | c.1698C>A (p.Gly566=) c.1563C>A c.1584C>A (p.Gly528=) c.978C>A (p.Gly326=) c.1548C>A (p.Gly516=) | |
18 | g.57674956C>A | CA402561437 | ATP8B1 | c.1697G>T (p.Gly566Val) c.1562G>T c.1583G>T (p.Gly528Val) c.977G>T (p.Gly326Val) c.1547G>T (p.Gly516Val) | |
18 | g.57674956C= | CA2306103181 | ATP8B1 | c.1697G= (p.Gly566=) c.1562G= c.1583G= (p.Gly528=) c.977G= (p.Gly326=) c.1547G= (p.Gly516=) | |
18 | g.57674956C>G | CA402561439 | ATP8B1 | c.1697G>C (p.Gly566Ala) c.1562G>C c.1583G>C (p.Gly528Ala) c.977G>C (p.Gly326Ala) c.1547G>C (p.Gly516Ala) | |
18 | g.57674956C>T | CA300889144 | ATP8B1 | c.1697G>A (p.Gly566Asp) c.1562G>A c.1583G>A (p.Gly528Asp) c.977G>A (p.Gly326Asp) c.1547G>A (p.Gly516Asp) | dbSNP gnomAD v3 gnomAD v4 |
18 | g.57674957C>A | CA402561444 | ATP8B1 | c.1696G>T (p.Gly566Cys) c.1561G>T c.1582G>T (p.Gly528Cys) c.976G>T (p.Gly326Cys) c.1546G>T (p.Gly516Cys) | |
18 | g.57674957C= | CA2306103182 | ATP8B1 | c.1696G= (p.Gly566=) c.1561G= c.1582G= (p.Gly528=) c.976G= (p.Gly326=) c.1546G= (p.Gly516=) | |
18 | g.57674957C>G | CA402561449 | ATP8B1 | c.1696G>C (p.Gly566Arg) c.1561G>C c.1582G>C (p.Gly528Arg) c.976G>C (p.Gly326Arg) c.1546G>C (p.Gly516Arg) | |
18 | g.57674957C>T | CA402561452 | ATP8B1 | c.1696G>A (p.Gly566Ser) c.1561G>A c.1582G>A (p.Gly528Ser) c.976G>A (p.Gly326Ser) c.1546G>A (p.Gly516Ser) | |
18 | g.57674958A>C | CA402561460 | ATP8B1 | c.1695T>G (p.Phe565Leu) c.1560T>G c.1581T>G (p.Phe527Leu) c.975T>G (p.Phe325Leu) c.1545T>G (p.Phe515Leu) | |
18 | g.57674958A>G | CA504021277 | ATP8B1 | c.1695T>C (p.Phe565=) c.1560T>C c.1581T>C (p.Phe527=) c.975T>C (p.Phe325=) c.1545T>C (p.Phe515=) | |
18 | g.57674958A>T | CA402561462 | ATP8B1 | c.1695T>A (p.Phe565Leu) c.1560T>A c.1581T>A (p.Phe527Leu) c.975T>A (p.Phe325Leu) c.1545T>A (p.Phe515Leu) | |
18 | g.57674960dup | CA402561457 | ATP8B1 | c.1695dup (p.Gly566TrpfsTer16) c.1560dup c.1581dup (p.Gly528TrpfsTer16) c.975dup (p.Gly326TrpfsTer16) c.1545dup (p.Gly516TrpfsTer16) | dbSNP |
18 | g.57674959A= | CA2306103183 | ATP8B1 | c.1694T= (p.Phe565=) c.1559T= c.1580T= (p.Phe527=) c.974T= (p.Phe325=) c.1544T= (p.Phe515=) | |
18 | g.57674959A>C | CA402561472 | ATP8B1 | c.1694T>G (p.Phe565Cys) c.1559T>G c.1580T>G (p.Phe527Cys) c.974T>G (p.Phe325Cys) c.1544T>G (p.Phe515Cys) | |
18 | g.57674959A>G | CA402561466 | ATP8B1 | c.1694T>C (p.Phe565Ser) c.1559T>C c.1580T>C (p.Phe527Ser) c.974T>C (p.Phe325Ser) c.1544T>C (p.Phe515Ser) | dbSNP |
18 | g.57674959A>T | CA402561468 | ATP8B1 | c.1694T>A (p.Phe565Tyr) c.1559T>A c.1580T>A (p.Phe527Tyr) c.974T>A (p.Phe325Tyr) c.1544T>A (p.Phe515Tyr) | |
18 | g.57674960A>C | CA402561476 | ATP8B1 | c.1693T>G (p.Phe565Val) c.1558T>G c.1579T>G (p.Phe527Val) c.973T>G (p.Phe325Val) c.1543T>G (p.Phe515Val) | |
18 | g.57674960A>G | CA402561478 | ATP8B1 | c.1693T>C (p.Phe565Leu) c.1558T>C c.1579T>C (p.Phe527Leu) c.973T>C (p.Phe325Leu) c.1543T>C (p.Phe515Leu) | |
18 | g.57674960A>T | CA402561481 | ATP8B1 | c.1693T>A (p.Phe565Ile) c.1558T>A c.1579T>A (p.Phe527Ile) c.973T>A (p.Phe325Ile) c.1543T>A (p.Phe515Ile) | |
18 | g.57674961G>A | CA8974496 | ATP8B1 | c.1692C>T (p.Asn564=) c.1557C>T c.1578C>T (p.Asn526=) c.972C>T (p.Asn324=) c.1542C>T (p.Asn514=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
18 | g.57674961G>C | CA402561487 | ATP8B1 | c.1692C>G (p.Asn564Lys) c.1557C>G c.1578C>G (p.Asn526Lys) c.972C>G (p.Asn324Lys) c.1542C>G (p.Asn514Lys) | |
18 | g.57674961G= | CA2306103184 | ATP8B1 | c.1692C= (p.Asn564=) c.1557C= c.1578C= (p.Asn526=) c.972C= (p.Asn324=) c.1542C= (p.Asn514=) | |
18 | g.57674961G>T | CA402561490 | ATP8B1 | c.1692C>A (p.Asn564Lys) c.1557C>A c.1578C>A (p.Asn526Lys) c.972C>A (p.Asn324Lys) c.1542C>A (p.Asn514Lys) | |
18 | g.57674962T>A | CA402561495 | ATP8B1 | c.1691A>T (p.Asn564Ile) c.1556A>T c.1577A>T (p.Asn526Ile) c.971A>T (p.Asn324Ile) c.1541A>T (p.Asn514Ile) | |
18 | g.57674962T>C | CA402561499 | ATP8B1 | c.1691A>G (p.Asn564Ser) c.1556A>G c.1577A>G (p.Asn526Ser) c.971A>G (p.Asn324Ser) c.1541A>G (p.Asn514Ser) | |
18 | g.57674962T>G | CA402561501 | ATP8B1 | c.1691A>C (p.Asn564Thr) c.1556A>C c.1577A>C (p.Asn526Thr) c.971A>C (p.Asn324Thr) c.1541A>C (p.Asn514Thr) | |
18 | g.57674963T>A | CA402561503 | ATP8B1 | c.1690A>T (p.Asn564Tyr) c.1555A>T c.1576A>T (p.Asn526Tyr) c.970A>T (p.Asn324Tyr) c.1540A>T (p.Asn514Tyr) | |
18 | g.57674963T>C | CA402561509 | ATP8B1 | c.1690A>G (p.Asn564Asp) c.1555A>G c.1576A>G (p.Asn526Asp) c.970A>G (p.Asn324Asp) c.1540A>G (p.Asn514Asp) | |
18 | g.57674963T>G | CA402561516 | ATP8B1 | c.1690A>C (p.Asn564His) c.1555A>C c.1576A>C (p.Asn526His) c.970A>C (p.Asn324His) c.1540A>C (p.Asn514His) | |
18 | g.57674964C>A | CA402561542 | ATP8B1 | c.1689G>T (p.Arg563Ser) c.1554G>T c.1575G>T (p.Arg525Ser) c.969G>T (p.Arg323Ser) c.1539G>T (p.Arg513Ser) | |
18 | g.57674964C>G | CA402561535 | ATP8B1 | c.1689G>C (p.Arg563Ser) c.1554G>C c.1575G>C (p.Arg525Ser) c.969G>C (p.Arg323Ser) c.1539G>C (p.Arg513Ser) | |
18 | g.57674964C>T | CA504021284 | ATP8B1 | c.1689G>A (p.Arg563=) c.1554G>A c.1575G>A (p.Arg525=) c.969G>A (p.Arg323=) c.1539G>A (p.Arg513=) | |
18 | g.57674965_57674979del | CA2695227681 | ATP8B1 | c.1675_1689del (p.Val559_Arg563del) c.1540_1554del c.1561_1575del (p.Val521_Arg525del) c.955_969del (p.Val319_Arg323del) c.1525_1539del (p.Val509_Arg513del) | |
18 | g.57674965C>A | CA402561543 | ATP8B1 | c.1688G>T (p.Arg563Met) c.1553G>T c.1574G>T (p.Arg525Met) c.968G>T (p.Arg323Met) c.1538G>T (p.Arg513Met) | |
18 | g.57674965C>G | CA402561545 | ATP8B1 | c.1688G>C (p.Arg563Thr) c.1553G>C c.1574G>C (p.Arg525Thr) c.968G>C (p.Arg323Thr) c.1538G>C (p.Arg513Thr) | |
18 | g.57674965C>T | CA402561544 | ATP8B1 | c.1688G>A (p.Arg563Lys) c.1553G>A c.1574G>A (p.Arg525Lys) c.968G>A (p.Arg323Lys) c.1538G>A (p.Arg513Lys) | gnomAD v4 |
18 | g.57674966T>A | CA402561549 | ATP8B1 | c.1687A>T (p.Arg563Trp) c.1552A>T c.1573A>T (p.Arg525Trp) c.967A>T (p.Arg323Trp) c.1537A>T (p.Arg513Trp) | |
18 | g.57674966T>C | CA402561553 | ATP8B1 | c.1687A>G (p.Arg563Gly) c.1552A>G c.1573A>G (p.Arg525Gly) c.967A>G (p.Arg323Gly) c.1537A>G (p.Arg513Gly) | |
18 | g.57674966T>G | CA504021286 | ATP8B1 | c.1687A>C (p.Arg563=) c.1552A>C c.1573A>C (p.Arg525=) c.967A>C (p.Arg323=) c.1537A>C (p.Arg513=) | |
18 | g.57674967G>A | CA504021287 | ATP8B1 | c.1686C>T (p.Ala562=) c.1551C>T c.1572C>T (p.Ala524=) c.966C>T (p.Ala322=) c.1536C>T (p.Ala512=) | |
18 | g.57674967G>C | CA504021288 | ATP8B1 | c.1686C>G (p.Ala562=) c.1551C>G c.1572C>G (p.Ala524=) c.966C>G (p.Ala322=) c.1536C>G (p.Ala512=) | |
18 | g.57674967G>T | CA504021290 | ATP8B1 | c.1686C>A (p.Ala562=) c.1551C>A c.1572C>A (p.Ala524=) c.966C>A (p.Ala322=) c.1536C>A (p.Ala512=) | |
18 | g.57674968G>A | CA402561554 | ATP8B1 | c.1685C>T (p.Ala562Val) c.1550C>T c.1571C>T (p.Ala524Val) c.965C>T (p.Ala322Val) c.1535C>T (p.Ala512Val) | gnomAD v4 |
18 | g.57674968G>C | CA402561555 | ATP8B1 | c.1685C>G (p.Ala562Gly) c.1550C>G c.1571C>G (p.Ala524Gly) c.965C>G (p.Ala322Gly) c.1535C>G (p.Ala512Gly) | |
18 | g.57674968G>T | CA402561558 | ATP8B1 | c.1685C>A (p.Ala562Asp) c.1550C>A c.1571C>A (p.Ala524Asp) c.965C>A (p.Ala322Asp) c.1535C>A (p.Ala512Asp) | |
18 | g.57674969C>A | CA402561562 | ATP8B1 | c.1684G>T (p.Ala562Ser) c.1549G>T c.1570G>T (p.Ala524Ser) c.964G>T (p.Ala322Ser) c.1534G>T (p.Ala512Ser) | |
18 | g.57674969C>G | CA402561568 | ATP8B1 | c.1684G>C (p.Ala562Pro) c.1549G>C c.1570G>C (p.Ala524Pro) c.964G>C (p.Ala322Pro) c.1534G>C (p.Ala512Pro) | |
18 | g.57674969C>T | CA402561573 | ATP8B1 | c.1684G>A (p.Ala562Thr) c.1549G>A c.1570G>A (p.Ala524Thr) c.964G>A (p.Ala322Thr) c.1534G>A (p.Ala512Thr) | |
18 | g.57674970A= | CA2306103185 | ATP8B1 | c.1683T= (p.Ala561=) c.1548T= c.1569T= (p.Ala523=) c.963T= (p.Ala321=) c.1533T= (p.Ala511=) | |
18 | g.57674970A>C | CA8974497 | ATP8B1 | c.1683T>G (p.Ala561=) c.1548T>G c.1569T>G (p.Ala523=) c.963T>G (p.Ala321=) c.1533T>G (p.Ala511=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
18 | g.57674970A>G | CA504021296 | ATP8B1 | c.1683T>C (p.Ala561=) c.1548T>C c.1569T>C (p.Ala523=) c.963T>C (p.Ala321=) c.1533T>C (p.Ala511=) | |
18 | g.57674970A>T | CA504021294 | ATP8B1 | c.1683T>A (p.Ala561=) c.1548T>A c.1569T>A (p.Ala523=) c.963T>A (p.Ala321=) c.1533T>A (p.Ala511=) | |
18 | g.57674971G>A | CA402561580 | ATP8B1 | c.1682C>T (p.Ala561Val) c.1547C>T c.1568C>T (p.Ala523Val) c.962C>T (p.Ala321Val) c.1532C>T (p.Ala511Val) | |
18 | g.57674971G>C | CA402561586 | ATP8B1 | c.1682C>G (p.Ala561Gly) c.1547C>G c.1568C>G (p.Ala523Gly) c.962C>G (p.Ala321Gly) c.1532C>G (p.Ala511Gly) | |
18 | g.57674971G>T | CA402561593 | ATP8B1 | c.1682C>A (p.Ala561Asp) c.1547C>A c.1568C>A (p.Ala523Asp) c.962C>A (p.Ala321Asp) c.1532C>A (p.Ala511Asp) | |
18 | g.57674972C>A | CA402561598 | ATP8B1 | c.1681G>T (p.Ala561Ser) c.1546G>T c.1567G>T (p.Ala523Ser) c.961G>T (p.Ala321Ser) c.1531G>T (p.Ala511Ser) | |
18 | g.57674972C= | CA2306103186 | ATP8B1 | c.1681G= (p.Ala561=) c.1546G= c.1567G= (p.Ala523=) c.961G= (p.Ala321=) c.1531G= (p.Ala511=) | |
18 | g.57674972C>G | CA402561600 | ATP8B1 | c.1681G>C (p.Ala561Pro) c.1546G>C c.1567G>C (p.Ala523Pro) c.961G>C (p.Ala321Pro) c.1531G>C (p.Ala511Pro) | |
18 | g.57674972C>T | CA8974498 | ATP8B1 | c.1681G>A (p.Ala561Thr) c.1546G>A c.1567G>A (p.Ala523Thr) c.961G>A (p.Ala321Thr) c.1531G>A (p.Ala511Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
18 | g.57674973G>A | CA8974499 | ATP8B1 | c.1680C>T (p.Asn560=) c.1545C>T c.1566C>T (p.Asn522=) c.960C>T (p.Asn320=) c.1530C>T (p.Asn510=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
18 | g.57674973G>C | CA402561608 | ATP8B1 | c.1680C>G (p.Asn560Lys) c.1545C>G c.1566C>G (p.Asn522Lys) c.960C>G (p.Asn320Lys) c.1530C>G (p.Asn510Lys) | |
18 | g.57674973G= | CA2306103187 | ATP8B1 | c.1680C= (p.Asn560=) c.1545C= c.1566C= (p.Asn522=) c.960C= (p.Asn320=) c.1530C= (p.Asn510=) | |
18 | g.57674973G>T | CA402561610 | ATP8B1 | c.1680C>A (p.Asn560Lys) c.1545C>A c.1566C>A (p.Asn522Lys) c.960C>A (p.Asn320Lys) c.1530C>A (p.Asn510Lys) | |
18 | g.57674973dup | CA2831039023 | ATP8B1 | c.1680dup (p.Ala561ArgfsTer21) c.1545dup c.1566dup (p.Ala523ArgfsTer21) c.960dup (p.Ala321ArgfsTer21) c.1530dup (p.Ala511ArgfsTer21) | |
18 | g.57674974T>A | CA402561616 | ATP8B1 | c.1679A>T (p.Asn560Ile) c.1544A>T c.1565A>T (p.Asn522Ile) c.959A>T (p.Asn320Ile) c.1529A>T (p.Asn510Ile) | |
18 | g.57674974T>C | CA402561620 | ATP8B1 | c.1679A>G (p.Asn560Ser) c.1544A>G c.1565A>G (p.Asn522Ser) c.959A>G (p.Asn320Ser) c.1529A>G (p.Asn510Ser) | |
18 | g.57674974T>G | CA402561625 | ATP8B1 | c.1679A>C (p.Asn560Thr) c.1544A>C c.1565A>C (p.Asn522Thr) c.959A>C (p.Asn320Thr) c.1529A>C (p.Asn510Thr) | |
18 | g.57674975T>A | CA402561630 | ATP8B1 | c.1678A>T (p.Asn560Tyr) c.1543A>T c.1564A>T (p.Asn522Tyr) c.958A>T (p.Asn320Tyr) c.1528A>T (p.Asn510Tyr) | |
18 | g.57674975T>C | CA402561632 | ATP8B1 | c.1678A>G (p.Asn560Asp) c.1543A>G c.1564A>G (p.Asn522Asp) c.958A>G (p.Asn320Asp) c.1528A>G (p.Asn510Asp) | gnomAD v4 |
18 | g.57674975T>G | CA402561642 | ATP8B1 | c.1678A>C (p.Asn560His) c.1543A>C c.1564A>C (p.Asn522His) c.958A>C (p.Asn320His) c.1528A>C (p.Asn510His) | |
18 | g.57674976T>A | CA504021304 | ATP8B1 | c.1677A>T (p.Val559=) c.1542A>T c.1563A>T (p.Val521=) c.957A>T (p.Val319=) c.1527A>T (p.Val509=) | |
18 | g.57674976T>C | CA504021306 | ATP8B1 | c.1677A>G (p.Val559=) c.1542A>G c.1563A>G (p.Val521=) c.957A>G (p.Val319=) c.1527A>G (p.Val509=) | |
18 | g.57674976T>G | CA504021307 | ATP8B1 | c.1677A>C (p.Val559=) c.1542A>C c.1563A>C (p.Val521=) c.957A>C (p.Val319=) c.1527A>C (p.Val509=) | |
18 | g.57674976_57674977insGGCTTCCGCCGCCCCAGCATCGCCCTTGCGTAGTGGGCCAGCCAGCATCCCCGCCAGTTTCCACACCAGCGCTTCGGTGAAGGTCGCCGGGTACAGCGCCGGGTCGTCGGCGGTGGCGATGTAGCGC | CA2515259107 | ATP8B1 | c.1676_1677insGCGCTACATCGCCACCGCCGACGACCCGGCGCTGTACCCGGCGACCTTCACCGAAGCGCTGGTGTGGAAACTGGCGGGGATGCTGGCTGGCCCACTACGCAAGGGCGATGCTGGGGCGGCGGAAGCC (p.Asn560ArgfsTer64) c.1541_1542insGCGCTACATCGCCACCGCCGACGACCCGGCGCTGTACCCGGCGACCTTCACCGAAGCGCTGGTGTGGAAACTGGCGGGGATGCTGGCTGGCCCACTACGCAAGGGCGATGCTGGGGCGGCGGAAGCC c.1562_1563insGCGCTACATCGCCACCGCCGACGACCCGGCGCTGTACCCGGCGACCTTCACCGAAGCGCTGGTGTGGAAACTGGCGGGGATGCTGGCTGGCCCACTACGCAAGGGCGATGCTGGGGCGGCGGAAGCC (p.Asn522ArgfsTer64) c.956_957insGCGCTACATCGCCACCGCCGACGACCCGGCGCTGTACCCGGCGACCTTCACCGAAGCGCTGGTGTGGAAACTGGCGGGGATGCTGGCTGGCCCACTACGCAAGGGCGATGCTGGGGCGGCGGAAGCC (p.Asn320ArgfsTer64) c.1526_1527insGCGCTACATCGCCACCGCCGACGACCCGGCGCTGTACCCGGCGACCTTCACCGAAGCGCTGGTGTGGAAACTGGCGGGGATGCTGGCTGGCCCACTACGCAAGGGCGATGCTGGGGCGGCGGAAGCC (p.Asn510ArgfsTer64) | |
18 | g.57674977A>C | CA402561658 | ATP8B1 | c.1676T>G (p.Val559Gly) c.1541T>G c.1562T>G (p.Val521Gly) c.956T>G (p.Val319Gly) c.1526T>G (p.Val509Gly) | |
18 | g.57674977A>G | CA402561664 | ATP8B1 | c.1676T>C (p.Val559Ala) c.1541T>C c.1562T>C (p.Val521Ala) c.956T>C (p.Val319Ala) c.1526T>C (p.Val509Ala) | |
18 | g.57674977A>T | CA402561671 | ATP8B1 | c.1676T>A (p.Val559Glu) c.1541T>A c.1562T>A (p.Val521Glu) c.956T>A (p.Val319Glu) c.1526T>A (p.Val509Glu) | |
18 | g.57674978C>A | CA402561676 | ATP8B1 | c.1675G>T (p.Val559Leu) c.1540G>T c.1561G>T (p.Val521Leu) c.955G>T (p.Val319Leu) c.1525G>T (p.Val509Leu) | |
18 | g.57674978C= | CA2306103188 | ATP8B1 | c.1675G= (p.Val559=) c.1540G= c.1561G= (p.Val521=) c.955G= (p.Val319=) c.1525G= (p.Val509=) | |
18 | g.57674978C>G | CA402561681 | ATP8B1 | c.1675G>C (p.Val559Leu) c.1540G>C c.1561G>C (p.Val521Leu) c.955G>C (p.Val319Leu) c.1525G>C (p.Val509Leu) | |
18 | g.57674978C>T | CA402561682 | ATP8B1 | c.1675G>A (p.Val559Ile) c.1540G>A c.1561G>A (p.Val521Ile) c.955G>A (p.Val319Ile) c.1525G>A (p.Val509Ile) | dbSNP gnomAD v2 |