Chr Mutation (hg38) CAid Gene Transcript Linkouts
16g.28900692G>ACA395411137ATP2A1c.1876G>A (p.Gly626Arg)
c.1501G>A (p.Gly501Arg)
16g.28900692G>CCA395411138ATP2A1c.1876G>C (p.Gly626Arg)
c.1501G>C (p.Gly501Arg)
16g.28900692G>TCA395411139ATP2A1c.1876G>T (p.Gly626Trp)
c.1501G>T (p.Gly501Trp)
16g.28900693G>ACA395411140ATP2A1c.1877G>A (p.Gly626Glu)
c.1502G>A (p.Gly501Glu)
 gnomAD v4
16g.28900693G>CCA395411141ATP2A1c.1877G>C (p.Gly626Ala)
c.1502G>C (p.Gly501Ala)
16g.28900693G>TCA395411142ATP2A1c.1877G>T (p.Gly626Val)
c.1502G>T (p.Gly501Val)
16g.28900694G>ACA494874352ATP2A1c.1878G>A (p.Gly626=)
c.1503G>A (p.Gly501=)
16g.28900694G>CCA494874350ATP2A1c.1878G>C (p.Gly626=)
c.1503G>C (p.Gly501=)
 gnomAD v4
16g.28900694G>TCA494874351ATP2A1c.1878G>T (p.Gly626=)
c.1503G>T (p.Gly501=)
16g.28900695G>ACA395411145ATP2A1c.1879G>A (p.Asp627Asn)
c.1504G>A (p.Asp502Asn)
 dbSNP gnomAD v2 gnomAD v4
16g.28900695G>CCA395411143ATP2A1c.1879G>C (p.Asp627His)
c.1504G>C (p.Asp502His)
16g.28900695G=CA2215884692ATP2A1c.1879G= (p.Asp627=)
c.1504G= (p.Asp502=)
16g.28900695G>TCA395411144ATP2A1c.1879G>T (p.Asp627Tyr)
c.1504G>T (p.Asp502Tyr)
16g.28900696A>CCA395411146ATP2A1c.1880A>C (p.Asp627Ala)
c.1505A>C (p.Asp502Ala)
16g.28900696A>GCA395411147ATP2A1c.1880A>G (p.Asp627Gly)
c.1505A>G (p.Asp502Gly)
16g.28900696A>TCA395411148ATP2A1c.1880A>T (p.Asp627Val)
c.1505A>T (p.Asp502Val)
16g.28900700_28900702delCA2575960521ATP2A1c.1884_1886del (p.Asn628del)
c.1509_1511del (p.Asn503del)
 gnomAD v4
16g.28900697C>ACA395411149ATP2A1c.1881C>A (p.Asp627Glu)
c.1506C>A (p.Asp502Glu)
16g.28900697C>GCA395411150ATP2A1c.1881C>G (p.Asp627Glu)
c.1506C>G (p.Asp502Glu)
 gnomAD v4
16g.28900697C>TCA494874353ATP2A1c.1881C>T (p.Asp627=)
c.1506C>T (p.Asp502=)
16g.28900698A=CA2215884695ATP2A1c.1882A= (p.Asn628=)
c.1507A= (p.Asn503=)
16g.28900698A>CCA395411151ATP2A1c.1882A>C (p.Asn628His)
c.1507A>C (p.Asn503His)
16g.28900698A>GCA395411153ATP2A1c.1882A>G (p.Asn628Asp)
c.1507A>G (p.Asn503Asp)
 dbSNP gnomAD v3 gnomAD v4
16g.28900698A>TCA395411152ATP2A1c.1882A>T (p.Asn628Tyr)
c.1507A>T (p.Asn503Tyr)
16g.28900699A=CA2215884702ATP2A1c.1883A= (p.Asn628=)
c.1508A= (p.Asn503=)
16g.28900699A>CCA395411154ATP2A1c.1883A>C (p.Asn628Thr)
c.1508A>C (p.Asn503Thr)
16g.28900699A>GCA7987107ATP2A1c.1883A>G (p.Asn628Ser)
c.1508A>G (p.Asn503Ser)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.28900699A>TCA395411155ATP2A1c.1883A>T (p.Asn628Ile)
c.1508A>T (p.Asn503Ile)
16g.28900700C>ACA395411156ATP2A1c.1884C>A (p.Asn628Lys)
c.1509C>A (p.Asn503Lys)
16g.28900700C>GCA395411157ATP2A1c.1884C>G (p.Asn628Lys)
c.1509C>G (p.Asn503Lys)
16g.28900700C>TCA494874354ATP2A1c.1884C>T (p.Asn628=)
c.1509C>T (p.Asn503=)
16g.28900700_28900701delinsCACA2215884706ATP2A1c.1884_1885delinsCA (p.Asn628=)
c.1509_1510delinsCA (p.Asn503=)
16g.28900701A>CCA395411158ATP2A1c.1885A>C (p.Lys629Gln)
c.1510A>C (p.Lys504Gln)
16g.28900701A>GCA395411159ATP2A1c.1885A>G (p.Lys629Glu)
c.1510A>G (p.Lys504Glu)
 gnomAD v4
16g.28900701A>TCA395411160ATP2A1c.1885A>T (p.Lys629Ter)
c.1510A>T (p.Lys504Ter)
16g.28900702dupCA2632539944ATP2A1c.1886dup (p.Thr631HisfsTer?)
c.1511dup (p.Thr506HisfsTer?)
 gnomAD v4
16g.28900702delCA2215884709ATP2A1c.1886del (p.Lys629ArgfsTer?)
c.1511del (p.Lys504ArgfsTer?)
 dbSNP
16g.28900702A=CA2215884716ATP2A1c.1886A= (p.Lys629=)
c.1511A= (p.Lys504=)
16g.28900702A>CCA7987108ATP2A1c.1886A>C (p.Lys629Thr)
c.1511A>C (p.Lys504Thr)
 dbSNP ExAC gnomAD v2 gnomAD v4
16g.28900702A>GCA395411161ATP2A1c.1886A>G (p.Lys629Arg)
c.1511A>G (p.Lys504Arg)
 gnomAD v4
16g.28900702A>TCA395411162ATP2A1c.1886A>T (p.Lys629Met)
c.1511A>T (p.Lys504Met)
16g.28900703G>ACA494874355ATP2A1c.1887G>A (p.Lys629=)
c.1512G>A (p.Lys504=)
16g.28900703G>CCA395411163ATP2A1c.1887G>C (p.Lys629Asn)
c.1512G>C (p.Lys504Asn)
 gnomAD v4
16g.28900703G>TCA395411164ATP2A1c.1887G>T (p.Lys629Asn)
c.1512G>T (p.Lys504Asn)
16g.28900704G>ACA279240229ATP2A1c.1888G>A (p.Gly630Ser)
c.1513G>A (p.Gly505Ser)
 dbSNP gnomAD v3 gnomAD v4
16g.28900704G>CCA395411166ATP2A1c.1888G>C (p.Gly630Arg)
c.1513G>C (p.Gly505Arg)
16g.28900704G=CA2215884723ATP2A1c.1888G= (p.Gly630=)
c.1513G= (p.Gly505=)
16g.28900704G>TCA395411165ATP2A1c.1888G>T (p.Gly630Cys)
c.1513G>T (p.Gly505Cys)
16g.28900705G>ACA395411167ATP2A1c.1889G>A (p.Gly630Asp)
c.1514G>A (p.Gly505Asp)
16g.28900705G>CCA395411168ATP2A1c.1889G>C (p.Gly630Ala)
c.1514G>C (p.Gly505Ala)
16g.28900705G>TCA395411169ATP2A1c.1889G>T (p.Gly630Val)
c.1514G>T (p.Gly505Val)
16g.28900706C>ACA494874356ATP2A1c.1890C>A (p.Gly630=)
c.1515C>A (p.Gly505=)
16g.28900706C>GCA494874357ATP2A1c.1890C>G (p.Gly630=)
c.1515C>G (p.Gly505=)
16g.28900706C>TCA494874358ATP2A1c.1890C>T (p.Gly630=)
c.1515C>T (p.Gly505=)
16g.28900707A>CCA395411170ATP2A1c.1891A>C (p.Thr631Pro)
c.1516A>C (p.Thr506Pro)
16g.28900707A>GCA395411171ATP2A1c.1891A>G (p.Thr631Ala)
c.1516A>G (p.Thr506Ala)
16g.28900707A>TCA395411172ATP2A1c.1891A>T (p.Thr631Ser)
c.1516A>T (p.Thr506Ser)
16g.28900708C>ACA395411173ATP2A1c.1892C>A (p.Thr631Lys)
c.1517C>A (p.Thr506Lys)
16g.28900708C=CA2215884727ATP2A1c.1892C= (p.Thr631=)
c.1517C= (p.Thr506=)
16g.28900708C>GCA7987109ATP2A1c.1892C>G (p.Thr631Arg)
c.1517C>G (p.Thr506Arg)
 dbSNP ExAC gnomAD v2 gnomAD v4
16g.28900708C>TCA395411174ATP2A1c.1892C>T (p.Thr631Ile)
c.1517C>T (p.Thr506Ile)
 gnomAD v4
16g.28900709A=CA2215884733ATP2A1c.1893A= (p.Thr631=)
c.1518A= (p.Thr506=)
16g.28900709A>CCA494874359ATP2A1c.1893A>C (p.Thr631=)
c.1518A>C (p.Thr506=)
16g.28900709A>GCA494874360ATP2A1c.1893A>G (p.Thr631=)
c.1518A>G (p.Thr506=)
 dbSNP
16g.28900709A>TCA494874361ATP2A1c.1893A>T (p.Thr631=)
c.1518A>T (p.Thr506=)
16g.28900710G>ACA395411175ATP2A1c.1894G>A (p.Ala632Thr)
c.1519G>A (p.Ala507Thr)
16g.28900710G>CCA395411176ATP2A1c.1894G>C (p.Ala632Pro)
c.1519G>C (p.Ala507Pro)
 gnomAD v4
16g.28900710G>TCA395411177ATP2A1c.1894G>T (p.Ala632Ser)
c.1519G>T (p.Ala507Ser)
16g.28900711C>ACA395411180ATP2A1c.1895C>A (p.Ala632Asp)
c.1520C>A (p.Ala507Asp)
16g.28900711C>GCA395411178ATP2A1c.1895C>G (p.Ala632Gly)
c.1520C>G (p.Ala507Gly)
16g.28900711C>TCA395411179ATP2A1c.1895C>T (p.Ala632Val)
c.1520C>T (p.Ala507Val)
16g.28900712C>ACA494874362ATP2A1c.1896C>A (p.Ala632=)
c.1521C>A (p.Ala507=)
16g.28900712C=CA2215884736ATP2A1c.1896C= (p.Ala632=)
c.1521C= (p.Ala507=)
16g.28900712C>GCA494874363ATP2A1c.1896C>G (p.Ala632=)
c.1521C>G (p.Ala507=)
16g.28900712C>TCA494874364ATP2A1c.1896C>T (p.Ala632=)
c.1521C>T (p.Ala507=)
 dbSNP gnomAD v2
16g.28900713A>CCA395411181ATP2A1c.1897A>C (p.Ile633Leu)
c.1522A>C (p.Ile508Leu)
16g.28900713A>GCA395411182ATP2A1c.1897A>G (p.Ile633Val)
c.1522A>G (p.Ile508Val)
16g.28900713A>TCA395411183ATP2A1c.1897A>T (p.Ile633Phe)
c.1522A>T (p.Ile508Phe)
16g.28900714T>ACA395411184ATP2A1c.1898T>A (p.Ile633Asn)
c.1523T>A (p.Ile508Asn)
16g.28900714T>CCA395411185ATP2A1c.1898T>C (p.Ile633Thr)
c.1523T>C (p.Ile508Thr)
16g.28900714T>GCA395411186ATP2A1c.1898T>G (p.Ile633Ser)
c.1523T>G (p.Ile508Ser)
16g.28900715T>ACA494874365ATP2A1c.1899T>A (p.Ile633=)
c.1524T>A (p.Ile508=)
16g.28900715T>CCA279240233ATP2A1c.1899T>C (p.Ile633=)
c.1524T>C (p.Ile508=)
 ClinVar dbSNP
16g.28900715T>GCA395411187ATP2A1c.1899T>G (p.Ile633Met)
c.1524T>G (p.Ile508Met)
16g.28900715T=CA2215884746ATP2A1c.1899T= (p.Ile633=)
c.1524T= (p.Ile508=)
16g.28900716G>ACA395411188ATP2A1c.1900G>A (p.Ala634Thr)
c.1525G>A (p.Ala509Thr)
16g.28900716G>CCA395411189ATP2A1c.1900G>C (p.Ala634Pro)
c.1525G>C (p.Ala509Pro)
16g.28900716G>TCA395411190ATP2A1c.1900G>T (p.Ala634Ser)
c.1525G>T (p.Ala509Ser)
16g.28900717C>ACA395411193ATP2A1c.1901C>A (p.Ala634Asp)
c.1526C>A (p.Ala509Asp)
16g.28900717C>GCA395411192ATP2A1c.1901C>G (p.Ala634Gly)
c.1526C>G (p.Ala509Gly)
16g.28900717C>TCA395411191ATP2A1c.1901C>T (p.Ala634Val)
c.1526C>T (p.Ala509Val)
 gnomAD v4
16g.28900718C>ACA494874366ATP2A1c.1902C>A (p.Ala634=)
c.1527C>A (p.Ala509=)
16g.28900718C>GCA494874367ATP2A1c.1902C>G (p.Ala634=)
c.1527C>G (p.Ala509=)
16g.28900718C>TCA494874368ATP2A1c.1902C>T (p.Ala634=)
c.1527C>T (p.Ala509=)
16g.28900719A>CCA395411196ATP2A1c.1903A>C (p.Ile635Leu)
c.1528A>C (p.Ile510Leu)
16g.28900719A>GCA395411194ATP2A1c.1903A>G (p.Ile635Val)
c.1528A>G (p.Ile510Val)
16g.28900719A>TCA395411195ATP2A1c.1903A>T (p.Ile635Phe)
c.1528A>T (p.Ile510Phe)
16g.28900720T>ACA395411197ATP2A1c.1904T>A (p.Ile635Asn)
c.1529T>A (p.Ile510Asn)
16g.28900720T>CCA395411198ATP2A1c.1904T>C (p.Ile635Thr)
c.1529T>C (p.Ile510Thr)
16g.28900720T>GCA395411199ATP2A1c.1904T>G (p.Ile635Ser)
c.1529T>G (p.Ile510Ser)
16g.28900721C>ACA494874369ATP2A1c.1905C>A (p.Ile635=)
c.1530C>A (p.Ile510=)
16g.28900721C=CA2215884750ATP2A1c.1905C= (p.Ile635=)
c.1530C= (p.Ile510=)
16g.28900721C>GCA395411200ATP2A1c.1905C>G (p.Ile635Met)
c.1530C>G (p.Ile510Met)
16g.28900721C>TCA7987110ATP2A1c.1905C>T (p.Ile635=)
c.1530C>T (p.Ile510=)
 dbSNP ExAC gnomAD v2
16g.28900722T>ACA395411201ATP2A1c.1906T>A (p.Cys636Ser)
c.1531T>A (p.Cys511Ser)
16g.28900722T>CCA395411202ATP2A1c.1906T>C (p.Cys636Arg)
c.1531T>C (p.Cys511Arg)
16g.28900722T>GCA395411203ATP2A1c.1906T>G (p.Cys636Gly)
c.1531T>G (p.Cys511Gly)
16g.28900723G>ACA395411204ATP2A1c.1907G>A (p.Cys636Tyr)
c.1532G>A (p.Cys511Tyr)
16g.28900723G>CCA395411205ATP2A1c.1907G>C (p.Cys636Ser)
c.1532G>C (p.Cys511Ser)
16g.28900723G>TCA395411206ATP2A1c.1907G>T (p.Cys636Phe)
c.1532G>T (p.Cys511Phe)
16g.28900724C>ACA395411208ATP2A1c.1908C>A (p.Cys636Ter)
c.1533C>A (p.Cys511Ter)
16g.28900724C=CA2215884754ATP2A1c.1908C= (p.Cys636=)
c.1533C= (p.Cys511=)
16g.28900724C>GCA395411207ATP2A1c.1908C>G (p.Cys636Trp)
c.1533C>G (p.Cys511Trp)
16g.28900724C>TCA494874370ATP2A1c.1908C>T (p.Cys636=)
c.1533C>T (p.Cys511=)
 dbSNP gnomAD v2 gnomAD v4
16g.28900725C>ACA494874371ATP2A1c.1909C>A (p.Arg637=)
c.1534C>A (p.Arg512=)
16g.28900725C=CA2215884766ATP2A1c.1909C= (p.Arg637=)
c.1534C= (p.Arg512=)
16g.28900725C>GCA395411209ATP2A1c.1909C>G (p.Arg637Gly)
c.1534C>G (p.Arg512Gly)
16g.28900725C>TCA7987111ATP2A1c.1909C>T (p.Arg637Trp)
c.1534C>T (p.Arg512Trp)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.28900726G>ACA7987112ATP2A1c.1910G>A (p.Arg637Gln)
c.1535G>A (p.Arg512Gln)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.28900726G>CCA395411210ATP2A1c.1910G>C (p.Arg637Pro)
c.1535G>C (p.Arg512Pro)
16g.28900726G=CA2215884780ATP2A1c.1910G= (p.Arg637=)
c.1535G= (p.Arg512=)
16g.28900726G>TCA395411211ATP2A1c.1910G>T (p.Arg637Leu)
c.1535G>T (p.Arg512Leu)
16g.28900727G>ACA7987113ATP2A1c.1911G>A (p.Arg637=)
c.1536G>A (p.Arg512=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.28900727G>CCA494874373ATP2A1c.1911G>C (p.Arg637=)
c.1536G>C (p.Arg512=)
16g.28900727G=CA2215884788ATP2A1c.1911G= (p.Arg637=)
c.1536G= (p.Arg512=)
16g.28900727G>TCA494874372ATP2A1c.1911G>T (p.Arg637=)
c.1536G>T (p.Arg512=)
16g.28900728C>ACA494874374ATP2A1c.1912C>A (p.Arg638=)
c.1537C>A (p.Arg513=)
16g.28900728C=CA2215884796ATP2A1c.1912C= (p.Arg638=)
c.1537C= (p.Arg513=)
16g.28900728C>GCA395411212ATP2A1c.1912C>G (p.Arg638Gly)
c.1537C>G (p.Arg513Gly)
16g.28900728C>TCA7987114ATP2A1c.1912C>T (p.Arg638Ter)
c.1537C>T (p.Arg513Ter)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
16g.28900729G>ACA7987115ATP2A1c.1913G>A (p.Arg638Gln)
c.1538G>A (p.Arg513Gln)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
16g.28900729G>CCA395411213ATP2A1c.1913G>C (p.Arg638Pro)
c.1538G>C (p.Arg513Pro)
16g.28900729G=CA2215884801ATP2A1c.1913G= (p.Arg638=)
c.1538G= (p.Arg513=)
16g.28900729G>TCA395411214ATP2A1c.1913G>T (p.Arg638Leu)
c.1538G>T (p.Arg513Leu)
16g.28900730A=CA2215884808ATP2A1c.1914A= (p.Arg638=)
c.1539A= (p.Arg513=)
16g.28900730A>CCA494874375ATP2A1c.1914A>C (p.Arg638=)
c.1539A>C (p.Arg513=)
 dbSNP
16g.28900730A>GCA494874376ATP2A1c.1914A>G (p.Arg638=)
c.1539A>G (p.Arg513=)
 ClinVar gnomAD v4
16g.28900730A>TCA494874377ATP2A1c.1914A>T (p.Arg638=)
c.1539A>T (p.Arg513=)
16g.28900731A>CCA395411215ATP2A1c.1915A>C (p.Ile639Leu)
c.1540A>C (p.Ile514Leu)
16g.28900731A>GCA395411216ATP2A1c.1915A>G (p.Ile639Val)
c.1540A>G (p.Ile514Val)
16g.28900731A>TCA395411217ATP2A1c.1915A>T (p.Ile639Phe)
c.1540A>T (p.Ile514Phe)
16g.28900732T>ACA7987117ATP2A1c.1916T>A (p.Ile639Asn)
c.1541T>A (p.Ile514Asn)
 dbSNP ExAC gnomAD v2
16g.28900732T>CCA7987116ATP2A1c.1916T>C (p.Ile639Thr)
c.1541T>C (p.Ile514Thr)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.28900732T>GCA395411218ATP2A1c.1916T>G (p.Ile639Ser)
c.1541T>G (p.Ile514Ser)
16g.28900732T=CA2215884815ATP2A1c.1916T= (p.Ile639=)
c.1541T= (p.Ile514=)
16g.28900733T>ACA494874378ATP2A1c.1917T>A (p.Ile639=)
c.1542T>A (p.Ile514=)
16g.28900733T>CCA494874379ATP2A1c.1917T>C (p.Ile639=)
c.1542T>C (p.Ile514=)
 dbSNP
16g.28900733T>GCA7987118ATP2A1c.1917T>G (p.Ile639Met)
c.1542T>G (p.Ile514Met)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.28900733T=CA2215884821ATP2A1c.1917T= (p.Ile639=)
c.1542T= (p.Ile514=)
16g.28900734G>ACA395411219ATP2A1c.1918G>A (p.Gly640Ser)
c.1543G>A (p.Gly515Ser)
 gnomAD v4
16g.28900734G>CCA395411220ATP2A1c.1918G>C (p.Gly640Arg)
c.1543G>C (p.Gly515Arg)
16g.28900734G>TCA395411221ATP2A1c.1918G>T (p.Gly640Cys)
c.1543G>T (p.Gly515Cys)
16g.28900735G>ACA395411222ATP2A1c.1919G>A (p.Gly640Asp)
c.1544G>A (p.Gly515Asp)
 gnomAD v4
16g.28900735G>CCA395411223ATP2A1c.1919G>C (p.Gly640Ala)
c.1544G>C (p.Gly515Ala)
16g.28900735G>TCA395411224ATP2A1c.1919G>T (p.Gly640Val)
c.1544G>T (p.Gly515Val)
16g.28900736C>ACA494874380ATP2A1c.1920C>A (p.Gly640=)
c.1545C>A (p.Gly515=)
16g.28900736C>GCA494874381ATP2A1c.1920C>G (p.Gly640=)
c.1545C>G (p.Gly515=)
16g.28900736C>TCA494874382ATP2A1c.1920C>T (p.Gly640=)
c.1545C>T (p.Gly515=)
16g.28900737A=CA2215884835ATP2A1c.1921A= (p.Ile641=)
c.1546A= (p.Ile516=)
16g.28900737A>CCA395411227ATP2A1c.1921A>C (p.Ile641Leu)
c.1546A>C (p.Ile516Leu)
16g.28900737A>GCA395411225ATP2A1c.1921A>G (p.Ile641Val)
c.1546A>G (p.Ile516Val)
 dbSNP
16g.28900737A>TCA395411226ATP2A1c.1921A>T (p.Ile641Phe)
c.1546A>T (p.Ile516Phe)
16g.28900738T>ACA395411228ATP2A1c.1922T>A (p.Ile641Asn)
c.1547T>A (p.Ile516Asn)
16g.28900738T>CCA395411229ATP2A1c.1922T>C (p.Ile641Thr)
c.1547T>C (p.Ile516Thr)
16g.28900738T>GCA395411230ATP2A1c.1922T>G (p.Ile641Ser)
c.1547T>G (p.Ile516Ser)
16g.28900739C>ACA494874383ATP2A1c.1923C>A (p.Ile641=)
c.1548C>A (p.Ile516=)
 dbSNP gnomAD v2 gnomAD v4
16g.28900739C=CA2215884842ATP2A1c.1923C= (p.Ile641=)
c.1548C= (p.Ile516=)
16g.28900739C>GCA395411231ATP2A1c.1923C>G (p.Ile641Met)
c.1548C>G (p.Ile516Met)
16g.28900739C>TCA7987119ATP2A1c.1923C>T (p.Ile641=)
c.1548C>T (p.Ile516=)
 dbSNP ExAC gnomAD v2 gnomAD v4
16g.28900740T>ACA395411232ATP2A1c.1924T>A (p.Phe642Ile)
c.1549T>A (p.Phe517Ile)
16g.28900740T>CCA395411234ATP2A1c.1924T>C (p.Phe642Leu)
c.1549T>C (p.Phe517Leu)
16g.28900740T>GCA395411233ATP2A1c.1924T>G (p.Phe642Val)
c.1549T>G (p.Phe517Val)
16g.28900741T>ACA395411235ATP2A1c.1925T>A (p.Phe642Tyr)
c.1550T>A (p.Phe517Tyr)
16g.28900741T>CCA395411236ATP2A1c.1925T>C (p.Phe642Ser)
c.1550T>C (p.Phe517Ser)
 dbSNP
16g.28900741T>GCA395411237ATP2A1c.1925T>G (p.Phe642Cys)
c.1550T>G (p.Phe517Cys)
16g.28900741T=CA2215884848ATP2A1c.1925T= (p.Phe642=)
c.1550T= (p.Phe517=)
16g.28900742T>ACA395411238ATP2A1c.1926T>A (p.Phe642Leu)
c.1551T>A (p.Phe517Leu)
16g.28900742T>CCA494874384ATP2A1c.1926T>C (p.Phe642=)
c.1551T>C (p.Phe517=)
 dbSNP
16g.28900742T>GCA395411239ATP2A1c.1926T>G (p.Phe642Leu)
c.1551T>G (p.Phe517Leu)
16g.28900742T=CA2215884855ATP2A1c.1926T= (p.Phe642=)
c.1551T= (p.Phe517=)
16g.28900743G>ACA395411240ATP2A1c.1927G>A (p.Gly643Arg)
c.1552G>A (p.Gly518Arg)
16g.28900743G>CCA395411241ATP2A1c.1927G>C (p.Gly643Arg)
c.1552G>C (p.Gly518Arg)
16g.28900743G>TCA395411242ATP2A1c.1927G>T (p.Gly643Trp)
c.1552G>T (p.Gly518Trp)
16g.28900746delCA2632539945ATP2A1c.1930del (p.Glu644ArgfsTer?)
c.1555del (p.Glu519ArgfsTer?)
 gnomAD v4
16g.28900744G>ACA395411243ATP2A1c.1928G>A (p.Gly643Glu)
c.1553G>A (p.Gly518Glu)
 gnomAD v4
16g.28900744G>CCA279240302ATP2A1c.1928G>C (p.Gly643Ala)
c.1553G>C (p.Gly518Ala)
 dbSNP
16g.28900744G=CA2215884858ATP2A1c.1928G= (p.Gly643=)
c.1553G= (p.Gly518=)
16g.28900744G>TCA395411244ATP2A1c.1928G>T (p.Gly643Val)
c.1553G>T (p.Gly518Val)
16g.28900745G>ACA279240303ATP2A1c.1929G>A (p.Gly643=)
c.1554G>A (p.Gly518=)
 dbSNP gnomAD v3 gnomAD v4
16g.28900745G>CCA494874385ATP2A1c.1929G>C (p.Gly643=)
c.1554G>C (p.Gly518=)
16g.28900745G=CA2215884865ATP2A1c.1929G= (p.Gly643=)
c.1554G= (p.Gly518=)
16g.28900745G>TCA494874386ATP2A1c.1929G>T (p.Gly643=)
c.1554G>T (p.Gly518=)
 gnomAD v4
16g.28900746G>ACA395411247ATP2A1c.1930G>A (p.Glu644Lys)
c.1555G>A (p.Glu519Lys)
16g.28900746G>CCA395411245ATP2A1c.1930G>C (p.Glu644Gln)
c.1555G>C (p.Glu519Gln)
16g.28900746G>TCA395411246ATP2A1c.1930G>T (p.Glu644Ter)
c.1555G>T (p.Glu519Ter)
16g.28900747A>CCA395411248ATP2A1c.1931A>C (p.Glu644Ala)
c.1556A>C (p.Glu519Ala)
16g.28900747A>GCA395411249ATP2A1c.1931A>G (p.Glu644Gly)
c.1556A>G (p.Glu519Gly)
 gnomAD v4
16g.28900747A>TCA395411250ATP2A1c.1931A>T (p.Glu644Val)
c.1556A>T (p.Glu519Val)
16g.28900748G>ACA279240308ATP2A1c.1932G>A (p.Glu644=)
c.1557G>A (p.Glu519=)
 dbSNP gnomAD v3 gnomAD v4
16g.28900748G>CCA395411251ATP2A1c.1932G>C (p.Glu644Asp)
c.1557G>C (p.Glu519Asp)
16g.28900748G=CA2215884877ATP2A1c.1932G= (p.Glu644=)
c.1557G= (p.Glu519=)
16g.28900748G>TCA395411252ATP2A1c.1932G>T (p.Glu644Asp)
c.1557G>T (p.Glu519Asp)
16g.28900749A>CCA395411255ATP2A1c.1933A>C (p.Asn645His)
c.1558A>C (p.Asn520His)
16g.28900749A>GCA395411254ATP2A1c.1933A>G (p.Asn645Asp)
c.1558A>G (p.Asn520Asp)
16g.28900749A>TCA395411253ATP2A1c.1933A>T (p.Asn645Tyr)
c.1558A>T (p.Asn520Tyr)
16g.28900750A>CCA395411256ATP2A1c.1934A>C (p.Asn645Thr)
c.1559A>C (p.Asn520Thr)
16g.28900750A>GCA395411257ATP2A1c.1934A>G (p.Asn645Ser)
c.1559A>G (p.Asn520Ser)
16g.28900750A>TCA395411258ATP2A1c.1934A>T (p.Asn645Ile)
c.1559A>T (p.Asn520Ile)
16g.28900751C>ACA395411259ATP2A1c.1935C>A (p.Asn645Lys)
c.1560C>A (p.Asn520Lys)
16g.28900751C=CA2215884885ATP2A1c.1935C= (p.Asn645=)
c.1560C= (p.Asn520=)
16g.28900751C>GCA395411260ATP2A1c.1935C>G (p.Asn645Lys)
c.1560C>G (p.Asn520Lys)
16g.28900751C>TCA7987120ATP2A1c.1935C>T (p.Asn645=)
c.1560C>T (p.Asn520=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
16g.28900752G>ACA7987121ATP2A1c.1936G>A (p.Glu646Lys)
c.1561G>A (p.Glu521Lys)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.28900752G>CCA7987122ATP2A1c.1936G>C (p.Glu646Gln)
c.1561G>C (p.Glu521Gln)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.28900752G=CA2215884907ATP2A1c.1936G= (p.Glu646=)
c.1561G= (p.Glu521=)
16g.28900752G>TCA395411261ATP2A1c.1936G>T (p.Glu646Ter)
c.1561G>T (p.Glu521Ter)
16g.28900756_28900758delCA645573195ATP2A1c.1940_1942del (p.Glu647del)
c.1565_1567del (p.Glu522del)
 COSMIC COSMIC
16g.28900753A>CCA395411262ATP2A1c.1937A>C (p.Glu646Ala)
c.1562A>C (p.Glu521Ala)
16g.28900753A>GCA395411263ATP2A1c.1937A>G (p.Glu646Gly)
c.1562A>G (p.Glu521Gly)
16g.28900753A>TCA395411264ATP2A1c.1937A>T (p.Glu646Val)
c.1562A>T (p.Glu521Val)
16g.28900754G>ACA494874387ATP2A1c.1938G>A (p.Glu646=)
c.1563G>A (p.Glu521=)
 dbSNP
16g.28900754G>CCA395411265ATP2A1c.1938G>C (p.Glu646Asp)
c.1563G>C (p.Glu521Asp)
 ClinVar
16g.28900754G=CA2215884917ATP2A1c.1938G= (p.Glu646=)
c.1563G= (p.Glu521=)
16g.28900754G>TCA395411266ATP2A1c.1938G>T (p.Glu646Asp)
c.1563G>T (p.Glu521Asp)
16g.28900755G>ACA395411267ATP2A1c.1939G>A (p.Glu647Lys)
c.1564G>A (p.Glu522Lys)
 gnomAD v4
16g.28900755G>CCA395411268ATP2A1c.1939G>C (p.Glu647Gln)
c.1564G>C (p.Glu522Gln)
16g.28900755G>TCA395411269ATP2A1c.1939G>T (p.Glu647Ter)
c.1564G>T (p.Glu522Ter)
16g.28900756A>CCA395411270ATP2A1c.1940A>C (p.Glu647Ala)
c.1565A>C (p.Glu522Ala)
16g.28900756A>GCA395411271ATP2A1c.1940A>G (p.Glu647Gly)
c.1565A>G (p.Glu522Gly)
16g.28900756A>TCA395411272ATP2A1c.1940A>T (p.Glu647Val)
c.1565A>T (p.Glu522Val)
 gnomAD v4
16g.28900757G>ACA10643415ATP2A1c.1941G>A (p.Glu647=)
c.1566G>A (p.Glu522=)
 ClinVar dbSNP gnomAD v4
16g.28900757G>CCA395411274ATP2A1c.1941G>C (p.Glu647Asp)
c.1566G>C (p.Glu522Asp)
16g.28900757G=CA2215884921ATP2A1c.1941G= (p.Glu647=)
c.1566G= (p.Glu522=)
16g.28900757G>TCA395411273ATP2A1c.1941G>T (p.Glu647Asp)
c.1566G>T (p.Glu522Asp)
16g.28900758G>ACA395411275ATP2A1c.1942G>A (p.Val648Met)
c.1567G>A (p.Val523Met)
 dbSNP gnomAD v3 gnomAD v4
16g.28900758G>CCA395411277ATP2A1c.1942G>C (p.Val648Leu)
c.1567G>C (p.Val523Leu)
16g.28900758G=CA2215884925ATP2A1c.1942G= (p.Val648=)
c.1567G= (p.Val523=)
16g.28900758G>TCA395411276ATP2A1c.1942G>T (p.Val648Leu)
c.1567G>T (p.Val523Leu)
16g.28900759T>ACA395411278ATP2A1c.1943T>A (p.Val648Glu)
c.1568T>A (p.Val523Glu)
16g.28900759T>CCA395411280ATP2A1c.1943T>C (p.Val648Ala)
c.1568T>C (p.Val523Ala)
16g.28900759T>GCA395411279ATP2A1c.1943T>G (p.Val648Gly)
c.1568T>G (p.Val523Gly)
16g.28900760G>ACA494874388ATP2A1c.1944G>A (p.Val648=)
c.1569G>A (p.Val523=)
16g.28900760G>CCA494874389ATP2A1c.1944G>C (p.Val648=)
c.1569G>C (p.Val523=)
16g.28900760G>TCA494874390ATP2A1c.1944G>T (p.Val648=)
c.1569G>T (p.Val523=)
16g.28900761G>ACA395411281ATP2A1c.1945G>A (p.Ala649Thr)
c.1570G>A (p.Ala524Thr)
 dbSNP
16g.28900761G>CCA395411282ATP2A1c.1945G>C (p.Ala649Pro)
c.1570G>C (p.Ala524Pro)
16g.28900761G=CA2215884932ATP2A1c.1945G= (p.Ala649=)
c.1570G= (p.Ala524=)
16g.28900761G>TCA395411283ATP2A1c.1945G>T (p.Ala649Ser)
c.1570G>T (p.Ala524Ser)
16g.28900762C>ACA395411284ATP2A1c.1946C>A (p.Ala649Asp)
c.1571C>A (p.Ala524Asp)
16g.28900762C=CA2215884936ATP2A1c.1946C= (p.Ala649=)
c.1571C= (p.Ala524=)
16g.28900762C>GCA395411285ATP2A1c.1946C>G (p.Ala649Gly)
c.1571C>G (p.Ala524Gly)
16g.28900762C>TCA395411286ATP2A1c.1946C>T (p.Ala649Val)
c.1571C>T (p.Ala524Val)
 dbSNP gnomAD v2 gnomAD v4
16g.28900763C>ACA494874392ATP2A1c.1947C>A (p.Ala649=)
c.1572C>A (p.Ala524=)
16g.28900763C=CA2215884942ATP2A1c.1947C= (p.Ala649=)
c.1572C= (p.Ala524=)
16g.28900763C>GCA494874393ATP2A1c.1947C>G (p.Ala649=)
c.1572C>G (p.Ala524=)
 dbSNP
16g.28900763C>TCA494874391ATP2A1c.1947C>T (p.Ala649=)
c.1572C>T (p.Ala524=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.28900764G>ACA7987123ATP2A1c.1948G>A (p.Asp650Asn)
c.1573G>A (p.Asp525Asn)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.28900764G>CCA395411287ATP2A1c.1948G>C (p.Asp650His)
c.1573G>C (p.Asp525His)
16g.28900764G=CA2215884950ATP2A1c.1948G= (p.Asp650=)
c.1573G= (p.Asp525=)
16g.28900764G>TCA7987124ATP2A1c.1948G>T (p.Asp650Tyr)
c.1573G>T (p.Asp525Tyr)
 dbSNP ExAC gnomAD v2
16g.28900765A=CA2215884952ATP2A1c.1949A= (p.Asp650=)
c.1574A= (p.Asp525=)
16g.28900765A>CCA395411288ATP2A1c.1949A>C (p.Asp650Ala)
c.1574A>C (p.Asp525Ala)
 dbSNP gnomAD v3 gnomAD v4
16g.28900765A>GCA395411289ATP2A1c.1949A>G (p.Asp650Gly)
c.1574A>G (p.Asp525Gly)
16g.28900765A>TCA395411290ATP2A1c.1949A>T (p.Asp650Val)
c.1574A>T (p.Asp525Val)
 dbSNP gnomAD v3 gnomAD v4
16g.28900766T>ACA395411291ATP2A1c.1950T>A (p.Asp650Glu)
c.1575T>A (p.Asp525Glu)
16g.28900766T>CCA494874394ATP2A1c.1950T>C (p.Asp650=)
c.1575T>C (p.Asp525=)
 dbSNP
16g.28900766T>GCA395411292ATP2A1c.1950T>G (p.Asp650Glu)
c.1575T>G (p.Asp525Glu)
16g.28900766T=CA2215884957ATP2A1c.1950T= (p.Asp650=)
c.1575T= (p.Asp525=)
16g.28900767C>ACA395411293ATP2A1c.1951C>A (p.Arg651Ser)
c.1576C>A (p.Arg526Ser)
 COSMIC COSMIC
16g.28900767C=CA2215884966ATP2A1c.1951C= (p.Arg651=)
c.1576C= (p.Arg526=)
16g.28900767C>GCA395411294ATP2A1c.1951C>G (p.Arg651Gly)
c.1576C>G (p.Arg526Gly)
 dbSNP gnomAD v4
16g.28900767C>TCA279240353ATP2A1c.1951C>T (p.Arg651Cys)
c.1576C>T (p.Arg526Cys)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
16g.28900768G>ACA7987125ATP2A1c.1952G>A (p.Arg651His)
c.1577G>A (p.Arg526His)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
16g.28900768G>CCA395411295ATP2A1c.1952G>C (p.Arg651Pro)
c.1577G>C (p.Arg526Pro)
16g.28900768G=CA2215884971ATP2A1c.1952G= (p.Arg651=)
c.1577G= (p.Arg526=)
16g.28900768G>TCA395411296ATP2A1c.1952G>T (p.Arg651Leu)
c.1577G>T (p.Arg526Leu)
16g.28900769C>ACA494874395ATP2A1c.1953C>A (p.Arg651=)
c.1578C>A (p.Arg526=)
 dbSNP
16g.28900769C=CA2215884978ATP2A1c.1953C= (p.Arg651=)
c.1578C= (p.Arg526=)
16g.28900769C>GCA494874396ATP2A1c.1953C>G (p.Arg651=)
c.1578C>G (p.Arg526=)
16g.28900769C>TCA7987126ATP2A1c.1953C>T (p.Arg651=)
c.1578C>T (p.Arg526=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.28900770G>ACA7987127ATP2A1c.1954G>A (p.Ala652Thr)
c.1579G>A (p.Ala527Thr)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
16g.28900770G>CCA395411297ATP2A1c.1954G>C (p.Ala652Pro)
c.1579G>C (p.Ala527Pro)
16g.28900770G=CA2215884985ATP2A1c.1954G= (p.Ala652=)
c.1579G= (p.Ala527=)
16g.28900770G>TCA395411298ATP2A1c.1954G>T (p.Ala652Ser)
c.1579G>T (p.Ala527Ser)
16g.28900771C>ACA395411300ATP2A1c.1955C>A (p.Ala652Asp)
c.1580C>A (p.Ala527Asp)
16g.28900771C>GCA395411301ATP2A1c.1955C>G (p.Ala652Gly)
c.1580C>G (p.Ala527Gly)
16g.28900771C>TCA395411299ATP2A1c.1955C>T (p.Ala652Val)
c.1580C>T (p.Ala527Val)
 gnomAD v4
16g.28900772C>ACA494874397ATP2A1c.1956C>A (p.Ala652=)
c.1581C>A (p.Ala527=)
16g.28900772C=CA2215884994ATP2A1c.1956C= (p.Ala652=)
c.1581C= (p.Ala527=)
16g.28900772C>GCA494874398ATP2A1c.1956C>G (p.Ala652=)
c.1581C>G (p.Ala527=)
16g.28900772C>TCA7987128ATP2A1c.1956C>T (p.Ala652=)
c.1581C>T (p.Ala527=)
 dbSNP ExAC gnomAD v2
16g.28900773T>ACA395411302ATP2A1c.1957T>A (p.Tyr653Asn)
c.1582T>A (p.Tyr528Asn)
16g.28900773T>CCA395411303ATP2A1c.1957T>C (p.Tyr653His)
c.1582T>C (p.Tyr528His)
 ClinVar
16g.28900773T>GCA395411304ATP2A1c.1957T>G (p.Tyr653Asp)
c.1582T>G (p.Tyr528Asp)
16g.28900774A=CA2215885000ATP2A1c.1958A= (p.Tyr653=)
c.1583A= (p.Tyr528=)
16g.28900774A>CCA395411305ATP2A1c.1958A>C (p.Tyr653Ser)
c.1583A>C (p.Tyr528Ser)
16g.28900774A>GCA7987129ATP2A1c.1958A>G (p.Tyr653Cys)
c.1583A>G (p.Tyr528Cys)
 dbSNP ExAC gnomAD v3 gnomAD v4
16g.28900774A>TCA395411306ATP2A1c.1958A>T (p.Tyr653Phe)
c.1583A>T (p.Tyr528Phe)
16g.28900775C>ACA395411307ATP2A1c.1959C>A (p.Tyr653Ter)
c.1584C>A (p.Tyr528Ter)
16g.28900775C>GCA395411308ATP2A1c.1959C>G (p.Tyr653Ter)
c.1584C>G (p.Tyr528Ter)
16g.28900775C>TCA494874399ATP2A1c.1959C>T (p.Tyr653=)
c.1584C>T (p.Tyr528=)
16g.28900776A>CCA395411309ATP2A1c.1960A>C (p.Thr654Pro)
c.1585A>C (p.Thr529Pro)
16g.28900776A>GCA395411310ATP2A1c.1960A>G (p.Thr654Ala)
c.1585A>G (p.Thr529Ala)
 gnomAD v4
16g.28900776A>TCA395411311ATP2A1c.1960A>T (p.Thr654Ser)
c.1585A>T (p.Thr529Ser)
16g.28900777C>ACA395411312ATP2A1c.1961C>A (p.Thr654Lys)
c.1586C>A (p.Thr529Lys)
 ClinVar dbSNP gnomAD v2 gnomAD v4
16g.28900777C=CA2215885019ATP2A1c.1961C= (p.Thr654=)
c.1586C= (p.Thr529=)
16g.28900777C>GCA395411313ATP2A1c.1961C>G (p.Thr654Arg)
c.1586C>G (p.Thr529Arg)
16g.28900777C>TCA7987130ATP2A1c.1961C>T (p.Thr654Met)
c.1586C>T (p.Thr529Met)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
16g.28900778G>ACA7987131ATP2A1c.1962G>A (p.Thr654=)
c.1587G>A (p.Thr529=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.28900778G>CCA494874400ATP2A1c.1962G>C (p.Thr654=)
c.1587G>C (p.Thr529=)
 dbSNP
16g.28900778G=CA2215885025ATP2A1c.1962G= (p.Thr654=)
c.1587G= (p.Thr529=)
16g.28900778G>TCA494874401ATP2A1c.1962G>T (p.Thr654=)
c.1587G>T (p.Thr529=)
16g.28900779G>ACA395411314ATP2A1c.1963G>A (p.Gly655Ser)
c.1588G>A (p.Gly530Ser)
16g.28900779G>CCA395411315ATP2A1c.1963G>C (p.Gly655Arg)
c.1588G>C (p.Gly530Arg)
16g.28900779G>TCA395411316ATP2A1c.1963G>T (p.Gly655Cys)
c.1588G>T (p.Gly530Cys)
16g.28900780G>ACA395411319ATP2A1c.1964G>A (p.Gly655Asp)
c.1589G>A (p.Gly530Asp)
16g.28900780G>CCA395411318ATP2A1c.1964G>C (p.Gly655Ala)
c.1589G>C (p.Gly530Ala)
16g.28900780G>TCA395411317ATP2A1c.1964G>T (p.Gly655Val)
c.1589G>T (p.Gly530Val)
16g.28900781C>ACA494874402ATP2A1c.1965C>A (p.Gly655=)
c.1590C>A (p.Gly530=)
16g.28900781C=CA2215885030ATP2A1c.1965C= (p.Gly655=)
c.1590C= (p.Gly530=)
16g.28900781C>GCA494874403ATP2A1c.1965C>G (p.Gly655=)
c.1590C>G (p.Gly530=)
16g.28900781C>TCA494874404ATP2A1c.1965C>T (p.Gly655=)
c.1590C>T (p.Gly530=)
 dbSNP
16g.28900782C>ACA7987133ATP2A1c.1966C>A (p.Arg656=)
c.1591C>A (p.Arg531=)
 dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC COSMIC
16g.28900782C=CA2215885034ATP2A1c.1966C= (p.Arg656=)
c.1591C= (p.Arg531=)
16g.28900782C>GCA395411320ATP2A1c.1966C>G (p.Arg656Gly)
c.1591C>G (p.Arg531Gly)
16g.28900782C>TCA7987132ATP2A1c.1966C>T (p.Arg656Ter)
c.1591C>T (p.Arg531Ter)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.28900783G>ACA7987134ATP2A1c.1967G>A (p.Arg656Gln)
c.1592G>A (p.Arg531Gln)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
16g.28900783G>CCA395411321ATP2A1c.1967G>C (p.Arg656Pro)
c.1592G>C (p.Arg531Pro)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.28900783G=CA2215885039ATP2A1c.1967G= (p.Arg656=)
c.1592G= (p.Arg531=)
16g.28900783G>TCA7987135ATP2A1c.1967G>T (p.Arg656Leu)
c.1592G>T (p.Arg531Leu)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.28900786_28900787delCA2632539976ATP2A1c.1970_1971del (p.Glu657ValfsTer8)
c.1595_1596del (p.Glu532ValfsTer8)
 gnomAD v4
16g.28900784A=CA2215885043ATP2A1c.1968A= (p.Arg656=)
c.1593A= (p.Arg531=)
16g.28900784A>CCA494874405ATP2A1c.1968A>C (p.Arg656=)
c.1593A>C (p.Arg531=)
16g.28900784A>GCA494874407ATP2A1c.1968A>G (p.Arg656=)
c.1593A>G (p.Arg531=)
 dbSNP
16g.28900784A>TCA494874406ATP2A1c.1968A>T (p.Arg656=)
c.1593A>T (p.Arg531=)
16g.28900784dupCA622162501ATP2A1c.1968dup (p.Glu657ArgfsTer9)
c.1593dup (p.Glu532ArgfsTer9)
 dbSNP gnomAD v2 gnomAD v4
16g.28900785G>ACA395411324ATP2A1c.1969G>A (p.Glu657Lys)
c.1594G>A (p.Glu532Lys)
 COSMIC
16g.28900785G>CCA395411323ATP2A1c.1969G>C (p.Glu657Gln)
c.1594G>C (p.Glu532Gln)
 dbSNP
16g.28900785G=CA2215885049ATP2A1c.1969G= (p.Glu657=)
c.1594G= (p.Glu532=)
16g.28900785G>TCA395411322ATP2A1c.1969G>T (p.Glu657Ter)
c.1594G>T (p.Glu532Ter)
16g.28900786A>CCA395411325ATP2A1c.1970A>C (p.Glu657Ala)
c.1595A>C (p.Glu532Ala)
16g.28900786A>GCA395411327ATP2A1c.1970A>G (p.Glu657Gly)
c.1595A>G (p.Glu532Gly)
16g.28900786A>TCA395411326ATP2A1c.1970A>T (p.Glu657Val)
c.1595A>T (p.Glu532Val)
16g.28900787G>ACA494874408ATP2A1c.1971G>A (p.Glu657=)
c.1596G>A (p.Glu532=)
16g.28900787G>CCA395411328ATP2A1c.1971G>C (p.Glu657Asp)
c.1596G>C (p.Glu532Asp)
 dbSNP
16g.28900787G>TCA395411329ATP2A1c.1971G>T (p.Glu657Asp)
c.1596G>T (p.Glu532Asp)
16g.28900788T>ACA395411330ATP2A1c.1972T>A (p.Phe658Ile)
c.1597T>A (p.Phe533Ile)
16g.28900788T>CCA395411331ATP2A1c.1972T>C (p.Phe658Leu)
c.1597T>C (p.Phe533Leu)
16g.28900788T>GCA395411332ATP2A1c.1972T>G (p.Phe658Val)
c.1597T>G (p.Phe533Val)
16g.28900789T>ACA395411333ATP2A1c.1973T>A (p.Phe658Tyr)
c.1598T>A (p.Phe533Tyr)
16g.28900789T>CCA395411334ATP2A1c.1973T>C (p.Phe658Ser)
c.1598T>C (p.Phe533Ser)
16g.28900789T>GCA395411335ATP2A1c.1973T>G (p.Phe658Cys)
c.1598T>G (p.Phe533Cys)
16g.28900790C>ACA395411336ATP2A1c.1974C>A (p.Phe658Leu)
c.1599C>A (p.Phe533Leu)
 ClinVar dbSNP gnomAD v2
16g.28900790C=CA2215885060ATP2A1c.1974C= (p.Phe658=)
c.1599C= (p.Phe533=)
16g.28900790C>GCA395411337ATP2A1c.1974C>G (p.Phe658Leu)
c.1599C>G (p.Phe533Leu)
 gnomAD v4
16g.28900790C>TCA7987136ATP2A1c.1974C>T (p.Phe658=)
c.1599C>T (p.Phe533=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.28900791G>ACA7987137ATP2A1c.1975G>A (p.Asp659Asn)
c.1600G>A (p.Asp534Asn)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.28900791G>CCA395411339ATP2A1c.1975G>C (p.Asp659His)
c.1600G>C (p.Asp534His)
16g.28900791G=CA2215885080ATP2A1c.1975G= (p.Asp659=)
c.1600G= (p.Asp534=)
16g.28900791G>TCA395411338ATP2A1c.1975G>T (p.Asp659Tyr)
c.1600G>T (p.Asp534Tyr)
16g.28900792A=CA2215885087ATP2A1c.1976A= (p.Asp659=)
c.1601A= (p.Asp534=)
16g.28900792A>CCA395411340ATP2A1c.1976A>C (p.Asp659Ala)
c.1601A>C (p.Asp534Ala)
16g.28900792A>GCA395411341ATP2A1c.1976A>G (p.Asp659Gly)
c.1601A>G (p.Asp534Gly)
 ClinVar dbSNP
16g.28900792A>TCA395411342ATP2A1c.1976A>T (p.Asp659Val)
c.1601A>T (p.Asp534Val)

Number of alleles fetched