Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.119413875_119413891dupCA545960933ARHGAP31c.1946_1962dup (p.Glu655MetfsTer3)
c.1853_1869dup (p.Glu624MetfsTer3)
c.1886_1902dup (p.Glu635MetfsTer3)
c.1454_1470dup (p.Glu491MetfsTer3)
 dbSNP gnomAD v2 gnomAD v4
3g.119413881T>ACA354047872ARHGAP31c.1952T>A (p.Leu651Gln)
c.1859T>A (p.Leu620Gln)
c.1892T>A (p.Leu631Gln)
c.1460T>A (p.Leu487Gln)
 ClinVar dbSNP gnomAD v3 gnomAD v4
3g.119413881T>CCA354047873ARHGAP31c.1952T>C (p.Leu651Pro)
c.1859T>C (p.Leu620Pro)
c.1892T>C (p.Leu631Pro)
c.1460T>C (p.Leu487Pro)
 gnomAD v4
3g.119413881T>GCA354047874ARHGAP31c.1952T>G (p.Leu651Arg)
c.1859T>G (p.Leu620Arg)
c.1892T>G (p.Leu631Arg)
c.1460T>G (p.Leu487Arg)
3g.119413881T=CA1396548469ARHGAP31c.1952T= (p.Leu651=)
c.1859T= (p.Leu620=)
c.1892T= (p.Leu631=)
c.1460T= (p.Leu487=)
3g.119413882G>ACA435411419ARHGAP31c.1953G>A (p.Leu651=)
c.1860G>A (p.Leu620=)
c.1893G>A (p.Leu631=)
c.1461G>A (p.Leu487=)
3g.119413882G>CCA435411420ARHGAP31c.1953G>C (p.Leu651=)
c.1860G>C (p.Leu620=)
c.1893G>C (p.Leu631=)
c.1461G>C (p.Leu487=)
3g.119413882G>TCA435411421ARHGAP31c.1953G>T (p.Leu651=)
c.1860G>T (p.Leu620=)
c.1893G>T (p.Leu631=)
c.1461G>T (p.Leu487=)
 gnomAD v4
3g.119413883A>CCA354047879ARHGAP31c.1954A>C (p.Ile652Leu)
c.1861A>C (p.Ile621Leu)
c.1894A>C (p.Ile632Leu)
c.1462A>C (p.Ile488Leu)
3g.119413883A>GCA354047877ARHGAP31c.1954A>G (p.Ile652Val)
c.1861A>G (p.Ile621Val)
c.1894A>G (p.Ile632Val)
c.1462A>G (p.Ile488Val)
3g.119413883A>TCA354047878ARHGAP31c.1954A>T (p.Ile652Phe)
c.1861A>T (p.Ile621Phe)
c.1894A>T (p.Ile632Phe)
c.1462A>T (p.Ile488Phe)
3g.119413884T>ACA354047880ARHGAP31c.1955T>A (p.Ile652Asn)
c.1862T>A (p.Ile621Asn)
c.1895T>A (p.Ile632Asn)
c.1463T>A (p.Ile488Asn)
3g.119413884T>CCA354047882ARHGAP31c.1955T>C (p.Ile652Thr)
c.1862T>C (p.Ile621Thr)
c.1895T>C (p.Ile632Thr)
c.1463T>C (p.Ile488Thr)
3g.119413884T>GCA354047893ARHGAP31c.1955T>G (p.Ile652Ser)
c.1862T>G (p.Ile621Ser)
c.1895T>G (p.Ile632Ser)
c.1463T>G (p.Ile488Ser)
3g.119413885C>ACA435411425ARHGAP31c.1956C>A (p.Ile652=)
c.1863C>A (p.Ile621=)
c.1896C>A (p.Ile632=)
c.1464C>A (p.Ile488=)
3g.119413885C=CA1396548470ARHGAP31c.1956C= (p.Ile652=)
c.1863C= (p.Ile621=)
c.1896C= (p.Ile632=)
c.1464C= (p.Ile488=)
3g.119413885C>GCA354047895ARHGAP31c.1956C>G (p.Ile652Met)
c.1863C>G (p.Ile621Met)
c.1896C>G (p.Ile632Met)
c.1464C>G (p.Ile488Met)
 gnomAD v4
3g.119413885C>TCA2553945ARHGAP31c.1956C>T (p.Ile652=)
c.1863C>T (p.Ile621=)
c.1896C>T (p.Ile632=)
c.1464C>T (p.Ile488=)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.119413886T>ACA354047903ARHGAP31c.1957T>A (p.Trp653Arg)
c.1864T>A (p.Trp622Arg)
c.1897T>A (p.Trp633Arg)
c.1465T>A (p.Trp489Arg)
3g.119413886T>CCA354047896ARHGAP31c.1957T>C (p.Trp653Arg)
c.1864T>C (p.Trp622Arg)
c.1897T>C (p.Trp633Arg)
c.1465T>C (p.Trp489Arg)
3g.119413886T>GCA354047898ARHGAP31c.1957T>G (p.Trp653Gly)
c.1864T>G (p.Trp622Gly)
c.1897T>G (p.Trp633Gly)
c.1465T>G (p.Trp489Gly)
3g.119413887G>ACA354047911ARHGAP31c.1958G>A (p.Trp653Ter)
c.1865G>A (p.Trp622Ter)
c.1898G>A (p.Trp633Ter)
c.1466G>A (p.Trp489Ter)
3g.119413887G>CCA354047920ARHGAP31c.1958G>C (p.Trp653Ser)
c.1865G>C (p.Trp622Ser)
c.1898G>C (p.Trp633Ser)
c.1466G>C (p.Trp489Ser)
3g.119413887G>TCA354047926ARHGAP31c.1958G>T (p.Trp653Leu)
c.1865G>T (p.Trp622Leu)
c.1898G>T (p.Trp633Leu)
c.1466G>T (p.Trp489Leu)
3g.119413888G>ACA354047930ARHGAP31c.1959G>A (p.Trp653Ter)
c.1866G>A (p.Trp622Ter)
c.1899G>A (p.Trp633Ter)
c.1467G>A (p.Trp489Ter)
3g.119413888G>CCA354047936ARHGAP31c.1959G>C (p.Trp653Cys)
c.1866G>C (p.Trp622Cys)
c.1899G>C (p.Trp633Cys)
c.1467G>C (p.Trp489Cys)
3g.119413888G>TCA354047938ARHGAP31c.1959G>T (p.Trp653Cys)
c.1866G>T (p.Trp622Cys)
c.1899G>T (p.Trp633Cys)
c.1467G>T (p.Trp489Cys)
3g.119413889C>ACA354047942ARHGAP31c.1960C>A (p.Pro654Thr)
c.1867C>A (p.Pro623Thr)
c.1900C>A (p.Pro634Thr)
c.1468C>A (p.Pro490Thr)
3g.119413889C>GCA354047944ARHGAP31c.1960C>G (p.Pro654Ala)
c.1867C>G (p.Pro623Ala)
c.1900C>G (p.Pro634Ala)
c.1468C>G (p.Pro490Ala)
3g.119413889C>TCA354047954ARHGAP31c.1960C>T (p.Pro654Ser)
c.1867C>T (p.Pro623Ser)
c.1900C>T (p.Pro634Ser)
c.1468C>T (p.Pro490Ser)
3g.119413890C>ACA354047965ARHGAP31c.1961C>A (p.Pro654His)
c.1868C>A (p.Pro623His)
c.1901C>A (p.Pro634His)
c.1469C>A (p.Pro490His)
3g.119413890C>GCA354047968ARHGAP31c.1961C>G (p.Pro654Arg)
c.1868C>G (p.Pro623Arg)
c.1901C>G (p.Pro634Arg)
c.1469C>G (p.Pro490Arg)
3g.119413890C>TCA354047974ARHGAP31c.1961C>T (p.Pro654Leu)
c.1868C>T (p.Pro623Leu)
c.1901C>T (p.Pro634Leu)
c.1469C>T (p.Pro490Leu)
3g.119413891T>ACA435411437ARHGAP31c.1962T>A (p.Pro654=)
c.1869T>A (p.Pro623=)
c.1902T>A (p.Pro634=)
c.1470T>A (p.Pro490=)
3g.119413891T>CCA435411438ARHGAP31c.1962T>C (p.Pro654=)
c.1869T>C (p.Pro623=)
c.1902T>C (p.Pro634=)
c.1470T>C (p.Pro490=)
3g.119413891T>GCA435411439ARHGAP31c.1962T>G (p.Pro654=)
c.1869T>G (p.Pro623=)
c.1902T>G (p.Pro634=)
c.1470T>G (p.Pro490=)
3g.119413892G>ACA354047976ARHGAP31c.1963G>A (p.Glu655Lys)
c.1870G>A (p.Glu624Lys)
c.1903G>A (p.Glu635Lys)
c.1471G>A (p.Glu491Lys)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.119413892G>CCA354047984ARHGAP31c.1963G>C (p.Glu655Gln)
c.1870G>C (p.Glu624Gln)
c.1903G>C (p.Glu635Gln)
c.1471G>C (p.Glu491Gln)
3g.119413892G=CA1396548471ARHGAP31c.1963G= (p.Glu655=)
c.1870G= (p.Glu624=)
c.1903G= (p.Glu635=)
c.1471G= (p.Glu491=)
3g.119413892G>TCA354047979ARHGAP31c.1963G>T (p.Glu655Ter)
c.1870G>T (p.Glu624Ter)
c.1903G>T (p.Glu635Ter)
c.1471G>T (p.Glu491Ter)
3g.119413893A>CCA354047992ARHGAP31c.1964A>C (p.Glu655Ala)
c.1871A>C (p.Glu624Ala)
c.1904A>C (p.Glu635Ala)
c.1472A>C (p.Glu491Ala)
 gnomAD v4
3g.119413893A>GCA354048003ARHGAP31c.1964A>G (p.Glu655Gly)
c.1871A>G (p.Glu624Gly)
c.1904A>G (p.Glu635Gly)
c.1472A>G (p.Glu491Gly)
3g.119413893A>TCA354047996ARHGAP31c.1964A>T (p.Glu655Val)
c.1871A>T (p.Glu624Val)
c.1904A>T (p.Glu635Val)
c.1472A>T (p.Glu491Val)
3g.119413894G>ACA435411337ARHGAP31c.1965G>A (p.Glu655=)
c.1872G>A (p.Glu624=)
c.1905G>A (p.Glu635=)
c.1473G>A (p.Glu491=)
3g.119413894G>CCA354048005ARHGAP31c.1965G>C (p.Glu655Asp)
c.1872G>C (p.Glu624Asp)
c.1905G>C (p.Glu635Asp)
c.1473G>C (p.Glu491Asp)
3g.119413894G>TCA354048007ARHGAP31c.1965G>T (p.Glu655Asp)
c.1872G>T (p.Glu624Asp)
c.1905G>T (p.Glu635Asp)
c.1473G>T (p.Glu491Asp)
3g.119413895A>CCA354048009ARHGAP31c.1966A>C (p.Ile656Leu)
c.1873A>C (p.Ile625Leu)
c.1906A>C (p.Ile636Leu)
c.1474A>C (p.Ile492Leu)
3g.119413895A>GCA354048015ARHGAP31c.1966A>G (p.Ile656Val)
c.1873A>G (p.Ile625Val)
c.1906A>G (p.Ile636Val)
c.1474A>G (p.Ile492Val)
3g.119413895A>TCA354048017ARHGAP31c.1966A>T (p.Ile656Phe)
c.1873A>T (p.Ile625Phe)
c.1906A>T (p.Ile636Phe)
c.1474A>T (p.Ile492Phe)
3g.119413896T>ACA354048019ARHGAP31c.1967T>A (p.Ile656Asn)
c.1874T>A (p.Ile625Asn)
c.1907T>A (p.Ile636Asn)
c.1475T>A (p.Ile492Asn)
3g.119413896T>CCA354048020ARHGAP31c.1967T>C (p.Ile656Thr)
c.1874T>C (p.Ile625Thr)
c.1907T>C (p.Ile636Thr)
c.1475T>C (p.Ile492Thr)
3g.119413896T>GCA354048021ARHGAP31c.1967T>G (p.Ile656Ser)
c.1874T>G (p.Ile625Ser)
c.1907T>G (p.Ile636Ser)
c.1475T>G (p.Ile492Ser)
3g.119413897T>ACA435411340ARHGAP31c.1968T>A (p.Ile656=)
c.1875T>A (p.Ile625=)
c.1908T>A (p.Ile636=)
c.1476T>A (p.Ile492=)
3g.119413897T>CCA435411341ARHGAP31c.1968T>C (p.Ile656=)
c.1875T>C (p.Ile625=)
c.1908T>C (p.Ile636=)
c.1476T>C (p.Ile492=)
3g.119413897T>GCA354048022ARHGAP31c.1968T>G (p.Ile656Met)
c.1875T>G (p.Ile625Met)
c.1908T>G (p.Ile636Met)
c.1476T>G (p.Ile492Met)
3g.119413898C>ACA354048024ARHGAP31c.1969C>A (p.Gln657Lys)
c.1876C>A (p.Gln626Lys)
c.1909C>A (p.Gln637Lys)
c.1477C>A (p.Gln493Lys)
3g.119413898C>GCA354048026ARHGAP31c.1969C>G (p.Gln657Glu)
c.1876C>G (p.Gln626Glu)
c.1909C>G (p.Gln637Glu)
c.1477C>G (p.Gln493Glu)
3g.119413898C>TCA354048028ARHGAP31c.1969C>T (p.Gln657Ter)
c.1876C>T (p.Gln626Ter)
c.1909C>T (p.Gln637Ter)
c.1477C>T (p.Gln493Ter)
3g.119413899A>CCA354048035ARHGAP31c.1970A>C (p.Gln657Pro)
c.1877A>C (p.Gln626Pro)
c.1910A>C (p.Gln637Pro)
c.1478A>C (p.Gln493Pro)
3g.119413899A>GCA354048037ARHGAP31c.1970A>G (p.Gln657Arg)
c.1877A>G (p.Gln626Arg)
c.1910A>G (p.Gln637Arg)
c.1478A>G (p.Gln493Arg)
3g.119413899A>TCA354048036ARHGAP31c.1970A>T (p.Gln657Leu)
c.1877A>T (p.Gln626Leu)
c.1910A>T (p.Gln637Leu)
c.1478A>T (p.Gln493Leu)
3g.119413900A>CCA354048038ARHGAP31c.1971A>C (p.Gln657His)
c.1878A>C (p.Gln626His)
c.1911A>C (p.Gln637His)
c.1479A>C (p.Gln493His)
 gnomAD v4
3g.119413900A>GCA435411347ARHGAP31c.1971A>G (p.Gln657=)
c.1878A>G (p.Gln626=)
c.1911A>G (p.Gln637=)
c.1479A>G (p.Gln493=)
 gnomAD v4
3g.119413900A>TCA354048039ARHGAP31c.1971A>T (p.Gln657His)
c.1878A>T (p.Gln626His)
c.1911A>T (p.Gln637His)
c.1479A>T (p.Gln493His)
3g.119413901C>ACA354048041ARHGAP31c.1972C>A (p.Gln658Lys)
c.1879C>A (p.Gln627Lys)
c.1912C>A (p.Gln638Lys)
c.1480C>A (p.Gln494Lys)
 COSMIC
3g.119413901C>GCA354048046ARHGAP31c.1972C>G (p.Gln658Glu)
c.1879C>G (p.Gln627Glu)
c.1912C>G (p.Gln638Glu)
c.1480C>G (p.Gln494Glu)
3g.119413901C>TCA354048047ARHGAP31c.1972C>T (p.Gln658Ter)
c.1879C>T (p.Gln627Ter)
c.1912C>T (p.Gln638Ter)
c.1480C>T (p.Gln494Ter)
3g.119413902A>CCA354048052ARHGAP31c.1973A>C (p.Gln658Pro)
c.1880A>C (p.Gln627Pro)
c.1913A>C (p.Gln638Pro)
c.1481A>C (p.Gln494Pro)
3g.119413902A>GCA354048053ARHGAP31c.1973A>G (p.Gln658Arg)
c.1880A>G (p.Gln627Arg)
c.1913A>G (p.Gln638Arg)
c.1481A>G (p.Gln494Arg)
3g.119413902A>TCA354048054ARHGAP31c.1973A>T (p.Gln658Leu)
c.1880A>T (p.Gln627Leu)
c.1913A>T (p.Gln638Leu)
c.1481A>T (p.Gln494Leu)
3g.119413903G>ACA435411350ARHGAP31c.1974G>A (p.Gln658=)
c.1881G>A (p.Gln627=)
c.1914G>A (p.Gln638=)
c.1482G>A (p.Gln494=)
3g.119413903G>CCA354048055ARHGAP31c.1974G>C (p.Gln658His)
c.1881G>C (p.Gln627His)
c.1914G>C (p.Gln638His)
c.1482G>C (p.Gln494His)
3g.119413903G>TCA354048056ARHGAP31c.1974G>T (p.Gln658His)
c.1881G>T (p.Gln627His)
c.1914G>T (p.Gln638His)
c.1482G>T (p.Gln494His)
3g.119413904G>ACA354048063ARHGAP31c.1975G>A (p.Glu659Lys)
c.1882G>A (p.Glu628Lys)
c.1915G>A (p.Glu639Lys)
c.1483G>A (p.Glu495Lys)
3g.119413904G>CCA354048067ARHGAP31c.1975G>C (p.Glu659Gln)
c.1882G>C (p.Glu628Gln)
c.1915G>C (p.Glu639Gln)
c.1483G>C (p.Glu495Gln)
3g.119413904G>TCA354048058ARHGAP31c.1975G>T (p.Glu659Ter)
c.1882G>T (p.Glu628Ter)
c.1915G>T (p.Glu639Ter)
c.1483G>T (p.Glu495Ter)
3g.119413905A>CCA354048072ARHGAP31c.1976A>C (p.Glu659Ala)
c.1883A>C (p.Glu628Ala)
c.1916A>C (p.Glu639Ala)
c.1484A>C (p.Glu495Ala)
3g.119413905A>GCA354048074ARHGAP31c.1976A>G (p.Glu659Gly)
c.1883A>G (p.Glu628Gly)
c.1916A>G (p.Glu639Gly)
c.1484A>G (p.Glu495Gly)
3g.119413905A>TCA354048075ARHGAP31c.1976A>T (p.Glu659Val)
c.1883A>T (p.Glu628Val)
c.1916A>T (p.Glu639Val)
c.1484A>T (p.Glu495Val)
3g.119413906G>ACA435411354ARHGAP31c.1977G>A (p.Glu659=)
c.1884G>A (p.Glu628=)
c.1917G>A (p.Glu639=)
c.1485G>A (p.Glu495=)
3g.119413906G>CCA354048076ARHGAP31c.1977G>C (p.Glu659Asp)
c.1884G>C (p.Glu628Asp)
c.1917G>C (p.Glu639Asp)
c.1485G>C (p.Glu495Asp)
3g.119413906G>TCA354048077ARHGAP31c.1977G>T (p.Glu659Asp)
c.1884G>T (p.Glu628Asp)
c.1917G>T (p.Glu639Asp)
c.1485G>T (p.Glu495Asp)
3g.119413907C>ACA81697274ARHGAP31c.1978C>A (p.Leu660Met)
c.1885C>A (p.Leu629Met)
c.1918C>A (p.Leu640Met)
c.1486C>A (p.Leu496Met)
 dbSNP gnomAD v4
3g.119413907C=CA1396548472ARHGAP31c.1978C= (p.Leu660=)
c.1885C= (p.Leu629=)
c.1918C= (p.Leu640=)
c.1486C= (p.Leu496=)
3g.119413907C>GCA354048078ARHGAP31c.1978C>G (p.Leu660Val)
c.1885C>G (p.Leu629Val)
c.1918C>G (p.Leu640Val)
c.1486C>G (p.Leu496Val)
3g.119413907C>TCA435411358ARHGAP31c.1978C>T (p.Leu660=)
c.1885C>T (p.Leu629=)
c.1918C>T (p.Leu640=)
c.1486C>T (p.Leu496=)
3g.119413908T>ACA354048081ARHGAP31c.1979T>A (p.Leu660Gln)
c.1886T>A (p.Leu629Gln)
c.1919T>A (p.Leu640Gln)
c.1487T>A (p.Leu496Gln)
3g.119413908T>CCA354048083ARHGAP31c.1979T>C (p.Leu660Pro)
c.1886T>C (p.Leu629Pro)
c.1919T>C (p.Leu640Pro)
c.1487T>C (p.Leu496Pro)
3g.119413908T>GCA354048085ARHGAP31c.1979T>G (p.Leu660Arg)
c.1886T>G (p.Leu629Arg)
c.1919T>G (p.Leu640Arg)
c.1487T>G (p.Leu496Arg)
3g.119413909G>ACA435411359ARHGAP31c.1980G>A (p.Leu660=)
c.1887G>A (p.Leu629=)
c.1920G>A (p.Leu640=)
c.1488G>A (p.Leu496=)
3g.119413909G>CCA435411360ARHGAP31c.1980G>C (p.Leu660=)
c.1887G>C (p.Leu629=)
c.1920G>C (p.Leu640=)
c.1488G>C (p.Leu496=)
3g.119413909G>TCA435411361ARHGAP31c.1980G>T (p.Leu660=)
c.1887G>T (p.Leu629=)
c.1920G>T (p.Leu640=)
c.1488G>T (p.Leu496=)
3g.119413910A=CA1396548473ARHGAP31c.1981A= (p.Lys661=)
c.1888A= (p.Lys630=)
c.1921A= (p.Lys641=)
c.1489A= (p.Lys497=)
3g.119413910A>CCA354048088ARHGAP31c.1981A>C (p.Lys661Gln)
c.1888A>C (p.Lys630Gln)
c.1921A>C (p.Lys641Gln)
c.1489A>C (p.Lys497Gln)
 dbSNP gnomAD v2 gnomAD v4
3g.119413910A>GCA354048090ARHGAP31c.1981A>G (p.Lys661Glu)
c.1888A>G (p.Lys630Glu)
c.1921A>G (p.Lys641Glu)
c.1489A>G (p.Lys497Glu)
 COSMIC
3g.119413910A>TCA354048093ARHGAP31c.1981A>T (p.Lys661Ter)
c.1888A>T (p.Lys630Ter)
c.1921A>T (p.Lys641Ter)
c.1489A>T (p.Lys497Ter)
3g.119413911A>CCA354048104ARHGAP31c.1982A>C (p.Lys661Thr)
c.1889A>C (p.Lys630Thr)
c.1922A>C (p.Lys641Thr)
c.1490A>C (p.Lys497Thr)
3g.119413911A>GCA354048102ARHGAP31c.1982A>G (p.Lys661Arg)
c.1889A>G (p.Lys630Arg)
c.1922A>G (p.Lys641Arg)
c.1490A>G (p.Lys497Arg)
3g.119413911A>TCA354048096ARHGAP31c.1982A>T (p.Lys661Ile)
c.1889A>T (p.Lys630Ile)
c.1922A>T (p.Lys641Ile)
c.1490A>T (p.Lys497Ile)
3g.119413912A=CA1396548474ARHGAP31c.1983A= (p.Lys661=)
c.1890A= (p.Lys630=)
c.1923A= (p.Lys641=)
c.1491A= (p.Lys497=)
3g.119413912A>CCA2553946ARHGAP31c.1983A>C (p.Lys661Asn)
c.1890A>C (p.Lys630Asn)
c.1923A>C (p.Lys641Asn)
c.1491A>C (p.Lys497Asn)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.119413912A>GCA435411365ARHGAP31c.1983A>G (p.Lys661=)
c.1890A>G (p.Lys630=)
c.1923A>G (p.Lys641=)
c.1491A>G (p.Lys497=)
3g.119413912A>TCA354048111ARHGAP31c.1983A>T (p.Lys661Asn)
c.1890A>T (p.Lys630Asn)
c.1923A>T (p.Lys641Asn)
c.1491A>T (p.Lys497Asn)
3g.119413913A=CA1396548475ARHGAP31c.1984A= (p.Ile662=)
c.1891A= (p.Ile631=)
c.1924A= (p.Ile642=)
c.1492A= (p.Ile498=)
3g.119413913A>CCA354048114ARHGAP31c.1984A>C (p.Ile662Leu)
c.1891A>C (p.Ile631Leu)
c.1924A>C (p.Ile642Leu)
c.1492A>C (p.Ile498Leu)
 dbSNP gnomAD v2 gnomAD v4
3g.119413913A>GCA354048115ARHGAP31c.1984A>G (p.Ile662Val)
c.1891A>G (p.Ile631Val)
c.1924A>G (p.Ile642Val)
c.1492A>G (p.Ile498Val)
3g.119413913A>TCA354048117ARHGAP31c.1984A>T (p.Ile662Phe)
c.1891A>T (p.Ile631Phe)
c.1924A>T (p.Ile642Phe)
c.1492A>T (p.Ile498Phe)
3g.119413914T>ACA354048119ARHGAP31c.1985T>A (p.Ile662Asn)
c.1892T>A (p.Ile631Asn)
c.1925T>A (p.Ile642Asn)
c.1493T>A (p.Ile498Asn)
 gnomAD v4
3g.119413914T>CCA354048121ARHGAP31c.1985T>C (p.Ile662Thr)
c.1892T>C (p.Ile631Thr)
c.1925T>C (p.Ile642Thr)
c.1493T>C (p.Ile498Thr)
3g.119413914T>GCA354048123ARHGAP31c.1985T>G (p.Ile662Ser)
c.1892T>G (p.Ile631Ser)
c.1925T>G (p.Ile642Ser)
c.1493T>G (p.Ile498Ser)
3g.119413915C>ACA435411366ARHGAP31c.1986C>A (p.Ile662=)
c.1893C>A (p.Ile631=)
c.1926C>A (p.Ile642=)
c.1494C>A (p.Ile498=)
3g.119413915C>GCA354048126ARHGAP31c.1986C>G (p.Ile662Met)
c.1893C>G (p.Ile631Met)
c.1926C>G (p.Ile642Met)
c.1494C>G (p.Ile498Met)
3g.119413915C>TCA435411369ARHGAP31c.1986C>T (p.Ile662=)
c.1893C>T (p.Ile631=)
c.1926C>T (p.Ile642=)
c.1494C>T (p.Ile498=)
 gnomAD v4
3g.119413916A>CCA354048127ARHGAP31c.1987A>C (p.Ile663Leu)
c.1894A>C (p.Ile632Leu)
c.1927A>C (p.Ile643Leu)
c.1495A>C (p.Ile499Leu)
3g.119413916A>GCA354048128ARHGAP31c.1987A>G (p.Ile663Val)
c.1894A>G (p.Ile632Val)
c.1927A>G (p.Ile643Val)
c.1495A>G (p.Ile499Val)
3g.119413916A>TCA354048129ARHGAP31c.1987A>T (p.Ile663Phe)
c.1894A>T (p.Ile632Phe)
c.1927A>T (p.Ile643Phe)
c.1495A>T (p.Ile499Phe)
 gnomAD v4
3g.119413917T>ACA354048132ARHGAP31c.1988T>A (p.Ile663Asn)
c.1895T>A (p.Ile632Asn)
c.1928T>A (p.Ile643Asn)
c.1496T>A (p.Ile499Asn)
 gnomAD v4
3g.119413917T>CCA81697278ARHGAP31c.1988T>C (p.Ile663Thr)
c.1895T>C (p.Ile632Thr)
c.1928T>C (p.Ile643Thr)
c.1496T>C (p.Ile499Thr)
 dbSNP gnomAD v2 gnomAD v4
3g.119413917T>GCA354048135ARHGAP31c.1988T>G (p.Ile663Ser)
c.1895T>G (p.Ile632Ser)
c.1928T>G (p.Ile643Ser)
c.1496T>G (p.Ile499Ser)
3g.119413917T=CA1396548476ARHGAP31c.1988T= (p.Ile663=)
c.1895T= (p.Ile632=)
c.1928T= (p.Ile643=)
c.1496T= (p.Ile499=)
3g.119413918T>ACA435411372ARHGAP31c.1989T>A (p.Ile663=)
c.1896T>A (p.Ile632=)
c.1929T>A (p.Ile643=)
c.1497T>A (p.Ile499=)
3g.119413918T>CCA435411374ARHGAP31c.1989T>C (p.Ile663=)
c.1896T>C (p.Ile632=)
c.1929T>C (p.Ile643=)
c.1497T>C (p.Ile499=)
3g.119413918T>GCA354048139ARHGAP31c.1989T>G (p.Ile663Met)
c.1896T>G (p.Ile632Met)
c.1929T>G (p.Ile643Met)
c.1497T>G (p.Ile499Met)
3g.119413919delCA2667110268ARHGAP31c.1990del (p.Glu664AsnfsTer14)
c.1897del (p.Glu633AsnfsTer14)
c.1930del (p.Glu644AsnfsTer14)
c.1498del (p.Glu500AsnfsTer14)
 gnomAD v4
3g.119413919G>ACA354048147ARHGAP31c.1990G>A (p.Glu664Lys)
c.1897G>A (p.Glu633Lys)
c.1930G>A (p.Glu644Lys)
c.1498G>A (p.Glu500Lys)
3g.119413919G>CCA354048144ARHGAP31c.1990G>C (p.Glu664Gln)
c.1897G>C (p.Glu633Gln)
c.1930G>C (p.Glu644Gln)
c.1498G>C (p.Glu500Gln)
3g.119413919G>TCA354048146ARHGAP31c.1990G>T (p.Glu664Ter)
c.1897G>T (p.Glu633Ter)
c.1930G>T (p.Glu644Ter)
c.1498G>T (p.Glu500Ter)
3g.119413920A>CCA354048148ARHGAP31c.1991A>C (p.Glu664Ala)
c.1898A>C (p.Glu633Ala)
c.1931A>C (p.Glu644Ala)
c.1499A>C (p.Glu500Ala)
3g.119413920A>GCA354048149ARHGAP31c.1991A>G (p.Glu664Gly)
c.1898A>G (p.Glu633Gly)
c.1931A>G (p.Glu644Gly)
c.1499A>G (p.Glu500Gly)
3g.119413920A>TCA354048150ARHGAP31c.1991A>T (p.Glu664Val)
c.1898A>T (p.Glu633Val)
c.1931A>T (p.Glu644Val)
c.1499A>T (p.Glu500Val)
3g.119413921A>CCA354048152ARHGAP31c.1992A>C (p.Glu664Asp)
c.1899A>C (p.Glu633Asp)
c.1932A>C (p.Glu644Asp)
c.1500A>C (p.Glu500Asp)
3g.119413921A>GCA435411379ARHGAP31c.1992A>G (p.Glu664=)
c.1899A>G (p.Glu633=)
c.1932A>G (p.Glu644=)
c.1500A>G (p.Glu500=)
3g.119413921A>TCA354048161ARHGAP31c.1992A>T (p.Glu664Asp)
c.1899A>T (p.Glu633Asp)
c.1932A>T (p.Glu644Asp)
c.1500A>T (p.Glu500Asp)
3g.119413922T>ACA354048166ARHGAP31c.1993T>A (p.Ser665Thr)
c.1900T>A (p.Ser634Thr)
c.1933T>A (p.Ser645Thr)
c.1501T>A (p.Ser501Thr)
3g.119413922T>CCA354048169ARHGAP31c.1993T>C (p.Ser665Pro)
c.1900T>C (p.Ser634Pro)
c.1933T>C (p.Ser645Pro)
c.1501T>C (p.Ser501Pro)
3g.119413922T>GCA354048170ARHGAP31c.1993T>G (p.Ser665Ala)
c.1900T>G (p.Ser634Ala)
c.1933T>G (p.Ser645Ala)
c.1501T>G (p.Ser501Ala)
3g.119413923C>ACA354048171ARHGAP31c.1994C>A (p.Ser665Tyr)
c.1901C>A (p.Ser634Tyr)
c.1934C>A (p.Ser645Tyr)
c.1502C>A (p.Ser501Tyr)
 COSMIC
3g.119413923C>GCA354048172ARHGAP31c.1994C>G (p.Ser665Cys)
c.1901C>G (p.Ser634Cys)
c.1934C>G (p.Ser645Cys)
c.1502C>G (p.Ser501Cys)
3g.119413923C>TCA354048173ARHGAP31c.1994C>T (p.Ser665Phe)
c.1901C>T (p.Ser634Phe)
c.1934C>T (p.Ser645Phe)
c.1502C>T (p.Ser501Phe)
3g.119413924T>ACA435411384ARHGAP31c.1995T>A (p.Ser665=)
c.1902T>A (p.Ser634=)
c.1935T>A (p.Ser645=)
c.1503T>A (p.Ser501=)
3g.119413924T>CCA435411386ARHGAP31c.1995T>C (p.Ser665=)
c.1902T>C (p.Ser634=)
c.1935T>C (p.Ser645=)
c.1503T>C (p.Ser501=)
3g.119413924T>GCA435411387ARHGAP31c.1995T>G (p.Ser665=)
c.1902T>G (p.Ser634=)
c.1935T>G (p.Ser645=)
c.1503T>G (p.Ser501=)
3g.119413925G>ACA354048175ARHGAP31c.1996G>A (p.Glu666Lys)
c.1903G>A (p.Glu635Lys)
c.1936G>A (p.Glu646Lys)
c.1504G>A (p.Glu502Lys)
3g.119413925G>CCA354048177ARHGAP31c.1996G>C (p.Glu666Gln)
c.1903G>C (p.Glu635Gln)
c.1936G>C (p.Glu646Gln)
c.1504G>C (p.Glu502Gln)
3g.119413925G>TCA354048176ARHGAP31c.1996G>T (p.Glu666Ter)
c.1903G>T (p.Glu635Ter)
c.1936G>T (p.Glu646Ter)
c.1504G>T (p.Glu502Ter)
3g.119413926A>CCA354048178ARHGAP31c.1997A>C (p.Glu666Ala)
c.1904A>C (p.Glu635Ala)
c.1937A>C (p.Glu646Ala)
c.1505A>C (p.Glu502Ala)
3g.119413926A>GCA354048180ARHGAP31c.1997A>G (p.Glu666Gly)
c.1904A>G (p.Glu635Gly)
c.1937A>G (p.Glu646Gly)
c.1505A>G (p.Glu502Gly)
3g.119413926A>TCA354048182ARHGAP31c.1997A>T (p.Glu666Val)
c.1904A>T (p.Glu635Val)
c.1937A>T (p.Glu646Val)
c.1505A>T (p.Glu502Val)
3g.119413927G>ACA435411393ARHGAP31c.1998G>A (p.Glu666=)
c.1905G>A (p.Glu635=)
c.1938G>A (p.Glu646=)
c.1506G>A (p.Glu502=)
3g.119413927G>CCA354048185ARHGAP31c.1998G>C (p.Glu666Asp)
c.1905G>C (p.Glu635Asp)
c.1938G>C (p.Glu646Asp)
c.1506G>C (p.Glu502Asp)
3g.119413927G>TCA354048186ARHGAP31c.1998G>T (p.Glu666Asp)
c.1905G>T (p.Glu635Asp)
c.1938G>T (p.Glu646Asp)
c.1506G>T (p.Glu502Asp)
3g.119413928G>ACA354048190ARHGAP31c.1999G>A (p.Glu667Lys)
c.1906G>A (p.Glu636Lys)
c.1939G>A (p.Glu647Lys)
c.1507G>A (p.Glu503Lys)
3g.119413928G>CCA354048193ARHGAP31c.1999G>C (p.Glu667Gln)
c.1906G>C (p.Glu636Gln)
c.1939G>C (p.Glu647Gln)
c.1507G>C (p.Glu503Gln)
3g.119413928G>TCA354048194ARHGAP31c.1999G>T (p.Glu667Ter)
c.1906G>T (p.Glu636Ter)
c.1939G>T (p.Glu647Ter)
c.1507G>T (p.Glu503Ter)
3g.119413929A>CCA354048195ARHGAP31c.2000A>C (p.Glu667Ala)
c.1907A>C (p.Glu636Ala)
c.1940A>C (p.Glu647Ala)
c.1508A>C (p.Glu503Ala)
3g.119413929A>GCA354048196ARHGAP31c.2000A>G (p.Glu667Gly)
c.1907A>G (p.Glu636Gly)
c.1940A>G (p.Glu647Gly)
c.1508A>G (p.Glu503Gly)
3g.119413929A>TCA354048197ARHGAP31c.2000A>T (p.Glu667Val)
c.1907A>T (p.Glu636Val)
c.1940A>T (p.Glu647Val)
c.1508A>T (p.Glu503Val)
3g.119413930G>ACA435411401ARHGAP31c.2001G>A (p.Glu667=)
c.1908G>A (p.Glu636=)
c.1941G>A (p.Glu647=)
c.1509G>A (p.Glu503=)
3g.119413930G>CCA354048201ARHGAP31c.2001G>C (p.Glu667Asp)
c.1908G>C (p.Glu636Asp)
c.1941G>C (p.Glu647Asp)
c.1509G>C (p.Glu503Asp)
3g.119413930G>TCA354048199ARHGAP31c.2001G>T (p.Glu667Asp)
c.1908G>T (p.Glu636Asp)
c.1941G>T (p.Glu647Asp)
c.1509G>T (p.Glu503Asp)
3g.119413931G>ACA354048204ARHGAP31c.2002G>A (p.Glu668Lys)
c.1909G>A (p.Glu637Lys)
c.1942G>A (p.Glu648Lys)
c.1510G>A (p.Glu504Lys)
3g.119413931G>CCA354048208ARHGAP31c.2002G>C (p.Glu668Gln)
c.1909G>C (p.Glu637Gln)
c.1942G>C (p.Glu648Gln)
c.1510G>C (p.Glu504Gln)
3g.119413931G>TCA354048211ARHGAP31c.2002G>T (p.Glu668Ter)
c.1909G>T (p.Glu637Ter)
c.1942G>T (p.Glu648Ter)
c.1510G>T (p.Glu504Ter)
3g.119413932A=CA1396548477ARHGAP31c.2003A= (p.Glu668=)
c.1910A= (p.Glu637=)
c.1943A= (p.Glu648=)
c.1511A= (p.Glu504=)
3g.119413932A>CCA354048214ARHGAP31c.2003A>C (p.Glu668Ala)
c.1910A>C (p.Glu637Ala)
c.1943A>C (p.Glu648Ala)
c.1511A>C (p.Glu504Ala)
 dbSNP
3g.119413932A>GCA354048216ARHGAP31c.2003A>G (p.Glu668Gly)
c.1910A>G (p.Glu637Gly)
c.1943A>G (p.Glu648Gly)
c.1511A>G (p.Glu504Gly)
3g.119413932A>TCA354048220ARHGAP31c.2003A>T (p.Glu668Val)
c.1910A>T (p.Glu637Val)
c.1943A>T (p.Glu648Val)
c.1511A>T (p.Glu504Val)
3g.119413933G>ACA435411405ARHGAP31c.2004G>A (p.Glu668=)
c.1911G>A (p.Glu637=)
c.1944G>A (p.Glu648=)
c.1512G>A (p.Glu504=)
3g.119413933G>CCA354048232ARHGAP31c.2004G>C (p.Glu668Asp)
c.1911G>C (p.Glu637Asp)
c.1944G>C (p.Glu648Asp)
c.1512G>C (p.Glu504Asp)
3g.119413933G>TCA354048227ARHGAP31c.2004G>T (p.Glu668Asp)
c.1911G>T (p.Glu637Asp)
c.1944G>T (p.Glu648Asp)
c.1512G>T (p.Glu504Asp)
3g.119413934C>ACA354048236ARHGAP31c.2005C>A (p.Leu669Ile)
c.1912C>A (p.Leu638Ile)
c.1945C>A (p.Leu649Ile)
c.1513C>A (p.Leu505Ile)
3g.119413934C=CA1396548478ARHGAP31c.2005C= (p.Leu669=)
c.1912C= (p.Leu638=)
c.1945C= (p.Leu649=)
c.1513C= (p.Leu505=)
3g.119413934C>GCA81697286ARHGAP31c.2005C>G (p.Leu669Val)
c.1912C>G (p.Leu638Val)
c.1945C>G (p.Leu649Val)
c.1513C>G (p.Leu505Val)
 dbSNP
3g.119413934C>TCA354048242ARHGAP31c.2005C>T (p.Leu669Phe)
c.1912C>T (p.Leu638Phe)
c.1945C>T (p.Leu649Phe)
c.1513C>T (p.Leu505Phe)
 gnomAD v4
3g.119413935T>ACA354048246ARHGAP31c.2006T>A (p.Leu669His)
c.1913T>A (p.Leu638His)
c.1946T>A (p.Leu649His)
c.1514T>A (p.Leu505His)
3g.119413935T>CCA354048249ARHGAP31c.2006T>C (p.Leu669Pro)
c.1913T>C (p.Leu638Pro)
c.1946T>C (p.Leu649Pro)
c.1514T>C (p.Leu505Pro)
3g.119413935T>GCA354048252ARHGAP31c.2006T>G (p.Leu669Arg)
c.1913T>G (p.Leu638Arg)
c.1946T>G (p.Leu649Arg)
c.1514T>G (p.Leu505Arg)
3g.119413936C>ACA435411409ARHGAP31c.2007C>A (p.Leu669=)
c.1914C>A (p.Leu638=)
c.1947C>A (p.Leu649=)
c.1515C>A (p.Leu505=)
3g.119413936C=CA1396548479ARHGAP31c.2007C= (p.Leu669=)
c.1914C= (p.Leu638=)
c.1947C= (p.Leu649=)
c.1515C= (p.Leu505=)
3g.119413936C>GCA81697288ARHGAP31c.2007C>G (p.Leu669=)
c.1914C>G (p.Leu638=)
c.1947C>G (p.Leu649=)
c.1515C>G (p.Leu505=)
 dbSNP gnomAD v4
3g.119413936C>TCA435411411ARHGAP31c.2007C>T (p.Leu669=)
c.1914C>T (p.Leu638=)
c.1947C>T (p.Leu649=)
c.1515C>T (p.Leu505=)
 dbSNP gnomAD v3 gnomAD v4
3g.119413937T>ACA354048263ARHGAP31c.2008T>A (p.Ser670Thr)
c.1915T>A (p.Ser639Thr)
c.1948T>A (p.Ser650Thr)
c.1516T>A (p.Ser506Thr)
3g.119413937T>CCA354048257ARHGAP31c.2008T>C (p.Ser670Pro)
c.1915T>C (p.Ser639Pro)
c.1948T>C (p.Ser650Pro)
c.1516T>C (p.Ser506Pro)
3g.119413937T>GCA354048260ARHGAP31c.2008T>G (p.Ser670Ala)
c.1915T>G (p.Ser639Ala)
c.1948T>G (p.Ser650Ala)
c.1516T>G (p.Ser506Ala)
3g.119413938C>ACA354048266ARHGAP31c.2009C>A (p.Ser670Ter)
c.1916C>A (p.Ser639Ter)
c.1949C>A (p.Ser650Ter)
c.1517C>A (p.Ser506Ter)
3g.119413938C>GCA354048269ARHGAP31c.2009C>G (p.Ser670Ter)
c.1916C>G (p.Ser639Ter)
c.1949C>G (p.Ser650Ter)
c.1517C>G (p.Ser506Ter)
3g.119413938C>TCA354048271ARHGAP31c.2009C>T (p.Ser670Leu)
c.1916C>T (p.Ser639Leu)
c.1949C>T (p.Ser650Leu)
c.1517C>T (p.Ser506Leu)
3g.119413939A=CA1396548480ARHGAP31c.2010A= (p.Ser670=)
c.1917A= (p.Ser639=)
c.1950A= (p.Ser650=)
c.1518A= (p.Ser506=)
3g.119413939A>CCA435411423ARHGAP31c.2010A>C (p.Ser670=)
c.1917A>C (p.Ser639=)
c.1950A>C (p.Ser650=)
c.1518A>C (p.Ser506=)
 gnomAD v4
3g.119413939A>GCA435411422ARHGAP31c.2010A>G (p.Ser670=)
c.1917A>G (p.Ser639=)
c.1950A>G (p.Ser650=)
c.1518A>G (p.Ser506=)
3g.119413939A>TCA81697298ARHGAP31c.2010A>T (p.Ser670=)
c.1917A>T (p.Ser639=)
c.1950A>T (p.Ser650=)
c.1518A>T (p.Ser506=)
 dbSNP
3g.119413940T>ACA354048274ARHGAP31c.2011T>A (p.Ser671Thr)
c.1918T>A (p.Ser640Thr)
c.1951T>A (p.Ser651Thr)
c.1519T>A (p.Ser507Thr)
3g.119413940T>CCA354048275ARHGAP31c.2011T>C (p.Ser671Pro)
c.1918T>C (p.Ser640Pro)
c.1951T>C (p.Ser651Pro)
c.1519T>C (p.Ser507Pro)
3g.119413940T>GCA354048276ARHGAP31c.2011T>G (p.Ser671Ala)
c.1918T>G (p.Ser640Ala)
c.1951T>G (p.Ser651Ala)
c.1519T>G (p.Ser507Ala)
3g.119413941C>ACA354048278ARHGAP31c.2012C>A (p.Ser671Ter)
c.1919C>A (p.Ser640Ter)
c.1952C>A (p.Ser651Ter)
c.1520C>A (p.Ser507Ter)
3g.119413941C=CA1396548481ARHGAP31c.2012C= (p.Ser671=)
c.1919C= (p.Ser640=)
c.1952C= (p.Ser651=)
c.1520C= (p.Ser507=)
3g.119413941C>GCA354048280ARHGAP31c.2012C>G (p.Ser671Trp)
c.1919C>G (p.Ser640Trp)
c.1952C>G (p.Ser651Trp)
c.1520C>G (p.Ser507Trp)
3g.119413941C>TCA354048283ARHGAP31c.2012C>T (p.Ser671Leu)
c.1919C>T (p.Ser640Leu)
c.1952C>T (p.Ser651Leu)
c.1520C>T (p.Ser507Leu)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.119413942G>ACA435411432ARHGAP31c.2013G>A (p.Ser671=)
c.1920G>A (p.Ser640=)
c.1953G>A (p.Ser651=)
c.1521G>A (p.Ser507=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
3g.119413942G>CCA435411433ARHGAP31c.2013G>C (p.Ser671=)
c.1920G>C (p.Ser640=)
c.1953G>C (p.Ser651=)
c.1521G>C (p.Ser507=)
3g.119413942G=CA1396548482ARHGAP31c.2013G= (p.Ser671=)
c.1920G= (p.Ser640=)
c.1953G= (p.Ser651=)
c.1521G= (p.Ser507=)
3g.119413942G>TCA2553947ARHGAP31c.2013G>T (p.Ser671=)
c.1920G>T (p.Ser640=)
c.1953G>T (p.Ser651=)
c.1521G>T (p.Ser507=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.119413943T>ACA354048288ARHGAP31c.2014T>A (p.Leu672Met)
c.1921T>A (p.Leu641Met)
c.1954T>A (p.Leu652Met)
c.1522T>A (p.Leu508Met)
3g.119413943T>CCA435411434ARHGAP31c.2014T>C (p.Leu672=)
c.1921T>C (p.Leu641=)
c.1954T>C (p.Leu652=)
c.1522T>C (p.Leu508=)
3g.119413943T>GCA354048290ARHGAP31c.2014T>G (p.Leu672Val)
c.1921T>G (p.Leu641Val)
c.1954T>G (p.Leu652Val)
c.1522T>G (p.Leu508Val)
3g.119413944T>ACA354048294ARHGAP31c.2015T>A (p.Leu672Ter)
c.1922T>A (p.Leu641Ter)
c.1955T>A (p.Leu652Ter)
c.1523T>A (p.Leu508Ter)
3g.119413944T>CCA354048299ARHGAP31c.2015T>C (p.Leu672Ser)
c.1922T>C (p.Leu641Ser)
c.1955T>C (p.Leu652Ser)
c.1523T>C (p.Leu508Ser)
3g.119413944T>GCA354048295ARHGAP31c.2015T>G (p.Leu672Trp)
c.1922T>G (p.Leu641Trp)
c.1955T>G (p.Leu652Trp)
c.1523T>G (p.Leu508Trp)
3g.119413945G>ACA2553948ARHGAP31c.2016G>A (p.Leu672=)
c.1923G>A (p.Leu641=)
c.1956G>A (p.Leu652=)
c.1524G>A (p.Leu508=)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.119413945G>CCA354048312ARHGAP31c.2016G>C (p.Leu672Phe)
c.1923G>C (p.Leu641Phe)
c.1956G>C (p.Leu652Phe)
c.1524G>C (p.Leu508Phe)
3g.119413945G=CA1396548483ARHGAP31c.2016G= (p.Leu672=)
c.1923G= (p.Leu641=)
c.1956G= (p.Leu652=)
c.1524G= (p.Leu508=)
3g.119413945G>TCA354048311ARHGAP31c.2016G>T (p.Leu672Phe)
c.1923G>T (p.Leu641Phe)
c.1956G>T (p.Leu652Phe)
c.1524G>T (p.Leu508Phe)
3g.119413946C>ACA354048313ARHGAP31c.2017C>A (p.Pro673Thr)
c.1924C>A (p.Pro642Thr)
c.1957C>A (p.Pro653Thr)
c.1525C>A (p.Pro509Thr)
3g.119413946C>GCA354048318ARHGAP31c.2017C>G (p.Pro673Ala)
c.1924C>G (p.Pro642Ala)
c.1957C>G (p.Pro653Ala)
c.1525C>G (p.Pro509Ala)
3g.119413946C>TCA354048319ARHGAP31c.2017C>T (p.Pro673Ser)
c.1924C>T (p.Pro642Ser)
c.1957C>T (p.Pro653Ser)
c.1525C>T (p.Pro509Ser)
 COSMIC
3g.119413947C>ACA354048325ARHGAP31c.2018C>A (p.Pro673Gln)
c.1925C>A (p.Pro642Gln)
c.1958C>A (p.Pro653Gln)
c.1526C>A (p.Pro509Gln)
3g.119413947C>GCA354048328ARHGAP31c.2018C>G (p.Pro673Arg)
c.1925C>G (p.Pro642Arg)
c.1958C>G (p.Pro653Arg)
c.1526C>G (p.Pro509Arg)
3g.119413947C>TCA354048330ARHGAP31c.2018C>T (p.Pro673Leu)
c.1925C>T (p.Pro642Leu)
c.1958C>T (p.Pro653Leu)
c.1526C>T (p.Pro509Leu)
3g.119413948A=CA1396548484ARHGAP31c.2019A= (p.Pro673=)
c.1926A= (p.Pro642=)
c.1959A= (p.Pro653=)
c.1527A= (p.Pro509=)
3g.119413948A>CCA435411443ARHGAP31c.2019A>C (p.Pro673=)
c.1926A>C (p.Pro642=)
c.1959A>C (p.Pro653=)
c.1527A>C (p.Pro509=)
3g.119413948A>GCA2553949ARHGAP31c.2019A>G (p.Pro673=)
c.1926A>G (p.Pro642=)
c.1959A>G (p.Pro653=)
c.1527A>G (p.Pro509=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.119413948A>TCA435411444ARHGAP31c.2019A>T (p.Pro673=)
c.1926A>T (p.Pro642=)
c.1959A>T (p.Pro653=)
c.1527A>T (p.Pro509=)
3g.119413949C>ACA354048336ARHGAP31c.2020C>A (p.Pro674Thr)
c.1927C>A (p.Pro643Thr)
c.1960C>A (p.Pro654Thr)
c.1528C>A (p.Pro510Thr)
 gnomAD v4 COSMIC
3g.119413949C=CA1396548485ARHGAP31c.2020C= (p.Pro674=)
c.1927C= (p.Pro643=)
c.1960C= (p.Pro654=)
c.1528C= (p.Pro510=)
3g.119413949C>GCA354048339ARHGAP31c.2020C>G (p.Pro674Ala)
c.1927C>G (p.Pro643Ala)
c.1960C>G (p.Pro654Ala)
c.1528C>G (p.Pro510Ala)
3g.119413949C>TCA81697308ARHGAP31c.2020C>T (p.Pro674Ser)
c.1927C>T (p.Pro643Ser)
c.1960C>T (p.Pro654Ser)
c.1528C>T (p.Pro510Ser)
 dbSNP
3g.119413950C>ACA354048344ARHGAP31c.2021C>A (p.Pro674His)
c.1928C>A (p.Pro643His)
c.1961C>A (p.Pro654His)
c.1529C>A (p.Pro510His)
3g.119413950C>GCA354048351ARHGAP31c.2021C>G (p.Pro674Arg)
c.1928C>G (p.Pro643Arg)
c.1961C>G (p.Pro654Arg)
c.1529C>G (p.Pro510Arg)
3g.119413950C>TCA354048353ARHGAP31c.2021C>T (p.Pro674Leu)
c.1928C>T (p.Pro643Leu)
c.1961C>T (p.Pro654Leu)
c.1529C>T (p.Pro510Leu)
 ClinVar
3g.119413951T>ACA435411450ARHGAP31c.2022T>A (p.Pro674=)
c.1929T>A (p.Pro643=)
c.1962T>A (p.Pro654=)
c.1530T>A (p.Pro510=)
3g.119413951T>CCA435411448ARHGAP31c.2022T>C (p.Pro674=)
c.1929T>C (p.Pro643=)
c.1962T>C (p.Pro654=)
c.1530T>C (p.Pro510=)
3g.119413951T>GCA435411449ARHGAP31c.2022T>G (p.Pro674=)
c.1929T>G (p.Pro643=)
c.1962T>G (p.Pro654=)
c.1530T>G (p.Pro510=)
3g.119413952C>ACA354048363ARHGAP31c.2023C>A (p.Pro675Thr)
c.1930C>A (p.Pro644Thr)
c.1963C>A (p.Pro655Thr)
c.1531C>A (p.Pro511Thr)
3g.119413952C>GCA354048373ARHGAP31c.2023C>G (p.Pro675Ala)
c.1930C>G (p.Pro644Ala)
c.1963C>G (p.Pro655Ala)
c.1531C>G (p.Pro511Ala)
3g.119413952C>TCA354048370ARHGAP31c.2023C>T (p.Pro675Ser)
c.1930C>T (p.Pro644Ser)
c.1963C>T (p.Pro655Ser)
c.1531C>T (p.Pro511Ser)
3g.119413953C>ACA354048383ARHGAP31c.2024C>A (p.Pro675His)
c.1931C>A (p.Pro644His)
c.1964C>A (p.Pro655His)
c.1532C>A (p.Pro511His)
3g.119413953C>GCA354048387ARHGAP31c.2024C>G (p.Pro675Arg)
c.1931C>G (p.Pro644Arg)
c.1964C>G (p.Pro655Arg)
c.1532C>G (p.Pro511Arg)
3g.119413953C>TCA354048390ARHGAP31c.2024C>T (p.Pro675Leu)
c.1931C>T (p.Pro644Leu)
c.1964C>T (p.Pro655Leu)
c.1532C>T (p.Pro511Leu)
3g.119413954T>ACA435411455ARHGAP31c.2025T>A (p.Pro675=)
c.1932T>A (p.Pro644=)
c.1965T>A (p.Pro655=)
c.1533T>A (p.Pro511=)
3g.119413954T>CCA435411456ARHGAP31c.2025T>C (p.Pro675=)
c.1932T>C (p.Pro644=)
c.1965T>C (p.Pro655=)
c.1533T>C (p.Pro511=)
3g.119413954T>GCA435411457ARHGAP31c.2025T>G (p.Pro675=)
c.1932T>G (p.Pro644=)
c.1965T>G (p.Pro655=)
c.1533T>G (p.Pro511=)
3g.119413955G>ACA2553950ARHGAP31c.2026G>A (p.Ala676Thr)
c.1933G>A (p.Ala645Thr)
c.1966G>A (p.Ala656Thr)
c.1534G>A (p.Ala512Thr)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.119413955G>CCA354048394ARHGAP31c.2026G>C (p.Ala676Pro)
c.1933G>C (p.Ala645Pro)
c.1966G>C (p.Ala656Pro)
c.1534G>C (p.Ala512Pro)
3g.119413955G=CA1396548486ARHGAP31c.2026G= (p.Ala676=)
c.1933G= (p.Ala645=)
c.1966G= (p.Ala656=)
c.1534G= (p.Ala512=)
3g.119413955G>TCA354048398ARHGAP31c.2026G>T (p.Ala676Ser)
c.1933G>T (p.Ala645Ser)
c.1966G>T (p.Ala656Ser)
c.1534G>T (p.Ala512Ser)
3g.119413956C>ACA354048404ARHGAP31c.2027C>A (p.Ala676Asp)
c.1934C>A (p.Ala645Asp)
c.1967C>A (p.Ala656Asp)
c.1535C>A (p.Ala512Asp)
 dbSNP
3g.119413956C>GCA354048406ARHGAP31c.2027C>G (p.Ala676Gly)
c.1934C>G (p.Ala645Gly)
c.1967C>G (p.Ala656Gly)
c.1535C>G (p.Ala512Gly)
3g.119413956C>TCA354048416ARHGAP31c.2027C>T (p.Ala676Val)
c.1934C>T (p.Ala645Val)
c.1967C>T (p.Ala656Val)
c.1535C>T (p.Ala512Val)
3g.119413957T>ACA2553951ARHGAP31c.2028T>A (p.Ala676=)
c.1935T>A (p.Ala645=)
c.1968T>A (p.Ala656=)
c.1536T>A (p.Ala512=)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.119413957T>CCA435411463ARHGAP31c.2028T>C (p.Ala676=)
c.1935T>C (p.Ala645=)
c.1968T>C (p.Ala656=)
c.1536T>C (p.Ala512=)
 gnomAD v4
3g.119413957T>GCA435411465ARHGAP31c.2028T>G (p.Ala676=)
c.1935T>G (p.Ala645=)
c.1968T>G (p.Ala656=)
c.1536T>G (p.Ala512=)
3g.119413957T=CA1396548487ARHGAP31c.2028T= (p.Ala676=)
c.1935T= (p.Ala645=)
c.1968T= (p.Ala656=)
c.1536T= (p.Ala512=)
3g.119413958C>ACA354048422ARHGAP31c.2029C>A (p.Leu677Met)
c.1936C>A (p.Leu646Met)
c.1969C>A (p.Leu657Met)
c.1537C>A (p.Leu513Met)
3g.119413958C>GCA354048423ARHGAP31c.2029C>G (p.Leu677Val)
c.1936C>G (p.Leu646Val)
c.1969C>G (p.Leu657Val)
c.1537C>G (p.Leu513Val)
3g.119413958C>TCA435411466ARHGAP31c.2029C>T (p.Leu677=)
c.1936C>T (p.Leu646=)
c.1969C>T (p.Leu657=)
c.1537C>T (p.Leu513=)
 COSMIC
3g.119413959T>ACA354048424ARHGAP31c.2030T>A (p.Leu677Gln)
c.1937T>A (p.Leu646Gln)
c.1970T>A (p.Leu657Gln)
c.1538T>A (p.Leu513Gln)
3g.119413959T>CCA354048425ARHGAP31c.2030T>C (p.Leu677Pro)
c.1937T>C (p.Leu646Pro)
c.1970T>C (p.Leu657Pro)
c.1538T>C (p.Leu513Pro)
3g.119413959T>GCA354048428ARHGAP31c.2030T>G (p.Leu677Arg)
c.1937T>G (p.Leu646Arg)
c.1970T>G (p.Leu657Arg)
c.1538T>G (p.Leu513Arg)
 gnomAD v4
3g.119413960G>ACA435411467ARHGAP31c.2031G>A (p.Leu677=)
c.1938G>A (p.Leu646=)
c.1971G>A (p.Leu657=)
c.1539G>A (p.Leu513=)
3g.119413960G>CCA435411468ARHGAP31c.2031G>C (p.Leu677=)
c.1938G>C (p.Leu646=)
c.1971G>C (p.Leu657=)
c.1539G>C (p.Leu513=)
3g.119413960G>TCA435411470ARHGAP31c.2031G>T (p.Leu677=)
c.1938G>T (p.Leu646=)
c.1971G>T (p.Leu657=)
c.1539G>T (p.Leu513=)
3g.119413961A>CCA354048436ARHGAP31c.2032A>C (p.Lys678Gln)
c.1939A>C (p.Lys647Gln)
c.1972A>C (p.Lys658Gln)
c.1540A>C (p.Lys514Gln)
3g.119413961A>GCA354048439ARHGAP31c.2032A>G (p.Lys678Glu)
c.1939A>G (p.Lys647Glu)
c.1972A>G (p.Lys658Glu)
c.1540A>G (p.Lys514Glu)
3g.119413961A>TCA354048443ARHGAP31c.2032A>T (p.Lys678Ter)
c.1939A>T (p.Lys647Ter)
c.1972A>T (p.Lys658Ter)
c.1540A>T (p.Lys514Ter)
3g.119413962A>CCA354048444ARHGAP31c.2033A>C (p.Lys678Thr)
c.1940A>C (p.Lys647Thr)
c.1973A>C (p.Lys658Thr)
c.1541A>C (p.Lys514Thr)
3g.119413962A>GCA354048445ARHGAP31c.2033A>G (p.Lys678Arg)
c.1940A>G (p.Lys647Arg)
c.1973A>G (p.Lys658Arg)
c.1541A>G (p.Lys514Arg)
3g.119413962A>TCA354048446ARHGAP31c.2033A>T (p.Lys678Met)
c.1940A>T (p.Lys647Met)
c.1973A>T (p.Lys658Met)
c.1541A>T (p.Lys514Met)
3g.119413963G>ACA435411472ARHGAP31c.2034G>A (p.Lys678=)
c.1941G>A (p.Lys647=)
c.1974G>A (p.Lys658=)
c.1542G>A (p.Lys514=)
3g.119413963G>CCA354048449ARHGAP31c.2034G>C (p.Lys678Asn)
c.1941G>C (p.Lys647Asn)
c.1974G>C (p.Lys658Asn)
c.1542G>C (p.Lys514Asn)
 dbSNP gnomAD v3 gnomAD v4
3g.119413963G=CA1396548488ARHGAP31c.2034G= (p.Lys678=)
c.1941G= (p.Lys647=)
c.1974G= (p.Lys658=)
c.1542G= (p.Lys514=)
3g.119413963G>TCA354048452ARHGAP31c.2034G>T (p.Lys678Asn)
c.1941G>T (p.Lys647Asn)
c.1974G>T (p.Lys658Asn)
c.1542G>T (p.Lys514Asn)
3g.119413964A>CCA354048463ARHGAP31c.2035A>C (p.Thr679Pro)
c.1942A>C (p.Thr648Pro)
c.1975A>C (p.Thr659Pro)
c.1543A>C (p.Thr515Pro)
3g.119413964A>GCA354048461ARHGAP31c.2035A>G (p.Thr679Ala)
c.1942A>G (p.Thr648Ala)
c.1975A>G (p.Thr659Ala)
c.1543A>G (p.Thr515Ala)
 gnomAD v4
3g.119413964A>TCA354048458ARHGAP31c.2035A>T (p.Thr679Ser)
c.1942A>T (p.Thr648Ser)
c.1975A>T (p.Thr659Ser)
c.1543A>T (p.Thr515Ser)
3g.119413964_119413965delinsACCA1396548489ARHGAP31c.2035_2036delinsAC (p.Thr679=)
c.1942_1943delinsAC (p.Thr648=)
c.1975_1976delinsAC (p.Thr659=)
c.1543_1544delinsAC (p.Thr515=)
3g.119413965C>ACA354048467ARHGAP31c.2036C>A (p.Thr679Asn)
c.1943C>A (p.Thr648Asn)
c.1976C>A (p.Thr659Asn)
c.1544C>A (p.Thr515Asn)
3g.119413965C=CA1396548490ARHGAP31c.2036C= (p.Thr679=)
c.1943C= (p.Thr648=)
c.1976C= (p.Thr659=)
c.1544C= (p.Thr515=)
3g.119413965C>GCA354048471ARHGAP31c.2036C>G (p.Thr679Ser)
c.1943C>G (p.Thr648Ser)
c.1976C>G (p.Thr659Ser)
c.1544C>G (p.Thr515Ser)
 gnomAD v4
3g.119413965C>TCA2553952ARHGAP31c.2036C>T (p.Thr679Ile)
c.1943C>T (p.Thr648Ile)
c.1976C>T (p.Thr659Ile)
c.1544C>T (p.Thr515Ile)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.119413966delCA81697309ARHGAP31c.2037del (p.Ser680AlafsTer?)
c.1944del (p.Ser649AlafsTer?)
c.1977del (p.Ser660AlafsTer?)
c.1545del (p.Ser516AlafsTer?)
 dbSNP
3g.119413966C>ACA435411476ARHGAP31c.2037C>A (p.Thr679=)
c.1944C>A (p.Thr648=)
c.1977C>A (p.Thr659=)
c.1545C>A (p.Thr515=)
3g.119413966C=CA1396548491ARHGAP31c.2037C= (p.Thr679=)
c.1944C= (p.Thr648=)
c.1977C= (p.Thr659=)
c.1545C= (p.Thr515=)
3g.119413966C>GCA2553953ARHGAP31c.2037C>G (p.Thr679=)
c.1944C>G (p.Thr648=)
c.1977C>G (p.Thr659=)
c.1545C>G (p.Thr515=)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.119413966C>TCA2553954ARHGAP31c.2037C>T (p.Thr679=)
c.1944C>T (p.Thr648=)
c.1977C>T (p.Thr659=)
c.1545C>T (p.Thr515=)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.119413967A>CCA354048501ARHGAP31c.2038A>C (p.Ser680Arg)
c.1945A>C (p.Ser649Arg)
c.1978A>C (p.Ser660Arg)
c.1546A>C (p.Ser516Arg)
3g.119413967A>GCA354048505ARHGAP31c.2038A>G (p.Ser680Gly)
c.1945A>G (p.Ser649Gly)
c.1978A>G (p.Ser660Gly)
c.1546A>G (p.Ser516Gly)
3g.119413967A>TCA354048512ARHGAP31c.2038A>T (p.Ser680Cys)
c.1945A>T (p.Ser649Cys)
c.1978A>T (p.Ser660Cys)
c.1546A>T (p.Ser516Cys)
3g.119413968G>ACA2553955ARHGAP31c.2039G>A (p.Ser680Asn)
c.1946G>A (p.Ser649Asn)
c.1979G>A (p.Ser660Asn)
c.1547G>A (p.Ser516Asn)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.119413968G>CCA354048518ARHGAP31c.2039G>C (p.Ser680Thr)
c.1946G>C (p.Ser649Thr)
c.1979G>C (p.Ser660Thr)
c.1547G>C (p.Ser516Thr)
3g.119413968G=CA1396548492ARHGAP31c.2039G= (p.Ser680=)
c.1946G= (p.Ser649=)
c.1979G= (p.Ser660=)
c.1547G= (p.Ser516=)
3g.119413968G>TCA354048521ARHGAP31c.2039G>T (p.Ser680Ile)
c.1946G>T (p.Ser649Ile)
c.1979G>T (p.Ser660Ile)
c.1547G>T (p.Ser516Ile)
3g.119413969C>ACA354048531ARHGAP31c.2040C>A (p.Ser680Arg)
c.1947C>A (p.Ser649Arg)
c.1980C>A (p.Ser660Arg)
c.1548C>A (p.Ser516Arg)
 gnomAD v4
3g.119413969C>GCA354048532ARHGAP31c.2040C>G (p.Ser680Arg)
c.1947C>G (p.Ser649Arg)
c.1980C>G (p.Ser660Arg)
c.1548C>G (p.Ser516Arg)
3g.119413969C>TCA435411479ARHGAP31c.2040C>T (p.Ser680=)
c.1947C>T (p.Ser649=)
c.1980C>T (p.Ser660=)
c.1548C>T (p.Ser516=)
3g.119413970C>ACA354048537ARHGAP31c.2041C>A (p.Pro681Thr)
c.1948C>A (p.Pro650Thr)
c.1981C>A (p.Pro661Thr)
c.1549C>A (p.Pro517Thr)
3g.119413970C=CA1396548493ARHGAP31c.2041C= (p.Pro681=)
c.1948C= (p.Pro650=)
c.1981C= (p.Pro661=)
c.1549C= (p.Pro517=)
3g.119413970C>GCA354048555ARHGAP31c.2041C>G (p.Pro681Ala)
c.1948C>G (p.Pro650Ala)
c.1981C>G (p.Pro661Ala)
c.1549C>G (p.Pro517Ala)
3g.119413970C>TCA81697334ARHGAP31c.2041C>T (p.Pro681Ser)
c.1948C>T (p.Pro650Ser)
c.1981C>T (p.Pro661Ser)
c.1549C>T (p.Pro517Ser)
 dbSNP gnomAD v3 gnomAD v4
3g.119413971C>ACA354048560ARHGAP31c.2042C>A (p.Pro681Gln)
c.1949C>A (p.Pro650Gln)
c.1982C>A (p.Pro661Gln)
c.1550C>A (p.Pro517Gln)
3g.119413971C=CA1396548494ARHGAP31c.2042C= (p.Pro681=)
c.1949C= (p.Pro650=)
c.1982C= (p.Pro661=)
c.1550C= (p.Pro517=)
3g.119413971C>GCA2553956ARHGAP31c.2042C>G (p.Pro681Arg)
c.1949C>G (p.Pro650Arg)
c.1982C>G (p.Pro661Arg)
c.1550C>G (p.Pro517Arg)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.119413971C>TCA2553957ARHGAP31c.2042C>T (p.Pro681Leu)
c.1949C>T (p.Pro650Leu)
c.1982C>T (p.Pro661Leu)
c.1550C>T (p.Pro517Leu)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.119413972A>CCA435411481ARHGAP31c.2043A>C (p.Pro681=)
c.1950A>C (p.Pro650=)
c.1983A>C (p.Pro661=)
c.1551A>C (p.Pro517=)
3g.119413972A>GCA435411483ARHGAP31c.2043A>G (p.Pro681=)
c.1950A>G (p.Pro650=)
c.1983A>G (p.Pro661=)
c.1551A>G (p.Pro517=)
3g.119413972A>TCA435411482ARHGAP31c.2043A>T (p.Pro681=)
c.1950A>T (p.Pro650=)
c.1983A>T (p.Pro661=)
c.1551A>T (p.Pro517=)
3g.119413973A>CCA354048572ARHGAP31c.2044A>C (p.Ile682Leu)
c.1951A>C (p.Ile651Leu)
c.1984A>C (p.Ile662Leu)
c.1552A>C (p.Ile518Leu)
3g.119413973A>GCA354048585ARHGAP31c.2044A>G (p.Ile682Val)
c.1951A>G (p.Ile651Val)
c.1984A>G (p.Ile662Val)
c.1552A>G (p.Ile518Val)
 gnomAD v4
3g.119413973A>TCA354048587ARHGAP31c.2044A>T (p.Ile682Phe)
c.1951A>T (p.Ile651Phe)
c.1984A>T (p.Ile662Phe)
c.1552A>T (p.Ile518Phe)
3g.119413974T>ACA354048589ARHGAP31c.2045T>A (p.Ile682Asn)
c.1952T>A (p.Ile651Asn)
c.1985T>A (p.Ile662Asn)
c.1553T>A (p.Ile518Asn)
3g.119413974T>CCA354048591ARHGAP31c.2045T>C (p.Ile682Thr)
c.1952T>C (p.Ile651Thr)
c.1985T>C (p.Ile662Thr)
c.1553T>C (p.Ile518Thr)
 gnomAD v4
3g.119413974T>GCA354048600ARHGAP31c.2045T>G (p.Ile682Ser)
c.1952T>G (p.Ile651Ser)
c.1985T>G (p.Ile662Ser)
c.1553T>G (p.Ile518Ser)
3g.119413975T>ACA435411485ARHGAP31c.2046T>A (p.Ile682=)
c.1953T>A (p.Ile651=)
c.1986T>A (p.Ile662=)
c.1554T>A (p.Ile518=)
3g.119413975T>CCA435411486ARHGAP31c.2046T>C (p.Ile682=)
c.1953T>C (p.Ile651=)
c.1986T>C (p.Ile662=)
c.1554T>C (p.Ile518=)
3g.119413975T>GCA354048603ARHGAP31c.2046T>G (p.Ile682Met)
c.1953T>G (p.Ile651Met)
c.1986T>G (p.Ile662Met)
c.1554T>G (p.Ile518Met)
3g.119413976C>ACA354048606ARHGAP31c.2047C>A (p.Gln683Lys)
c.1954C>A (p.Gln652Lys)
c.1987C>A (p.Gln663Lys)
c.1555C>A (p.Gln519Lys)
3g.119413976C=CA1396548495ARHGAP31c.2047C= (p.Gln683=)
c.1954C= (p.Gln652=)
c.1987C= (p.Gln663=)
c.1555C= (p.Gln519=)
3g.119413976C>GCA354048608ARHGAP31c.2047C>G (p.Gln683Glu)
c.1954C>G (p.Gln652Glu)
c.1987C>G (p.Gln663Glu)
c.1555C>G (p.Gln519Glu)
3g.119413976C>TCA129505ARHGAP31c.2047C>T (p.Gln683Ter)
c.1954C>T (p.Gln652Ter)
c.1987C>T (p.Gln663Ter)
c.1555C>T (p.Gln519Ter)
 ClinVar dbSNP gnomAD v4
3g.119413977A=CA1396548496ARHGAP31c.2048A= (p.Gln683=)
c.1955A= (p.Gln652=)
c.1988A= (p.Gln663=)
c.1556A= (p.Gln519=)
3g.119413977A>CCA354048617ARHGAP31c.2048A>C (p.Gln683Pro)
c.1955A>C (p.Gln652Pro)
c.1988A>C (p.Gln663Pro)
c.1556A>C (p.Gln519Pro)
3g.119413977A>GCA81697349ARHGAP31c.2048A>G (p.Gln683Arg)
c.1955A>G (p.Gln652Arg)
c.1988A>G (p.Gln663Arg)
c.1556A>G (p.Gln519Arg)
 ClinVar dbSNP gnomAD v4
3g.119413977A>TCA354048612ARHGAP31c.2048A>T (p.Gln683Leu)
c.1955A>T (p.Gln652Leu)
c.1988A>T (p.Gln663Leu)
c.1556A>T (p.Gln519Leu)
3g.119413978G>ACA435411487ARHGAP31c.2049G>A (p.Gln683=)
c.1956G>A (p.Gln652=)
c.1989G>A (p.Gln663=)
c.1557G>A (p.Gln519=)
 dbSNP gnomAD v4
3g.119413978G>CCA354048624ARHGAP31c.2049G>C (p.Gln683His)
c.1956G>C (p.Gln652His)
c.1989G>C (p.Gln663His)
c.1557G>C (p.Gln519His)
3g.119413978G=CA1396548497ARHGAP31c.2049G= (p.Gln683=)
c.1956G= (p.Gln652=)
c.1989G= (p.Gln663=)
c.1557G= (p.Gln519=)
3g.119413978G>TCA354048639ARHGAP31c.2049G>T (p.Gln683His)
c.1956G>T (p.Gln652His)
c.1989G>T (p.Gln663His)
c.1557G>T (p.Gln519His)
3g.119413979C>ACA354048644ARHGAP31c.2050C>A (p.Pro684Thr)
c.1957C>A (p.Pro653Thr)
c.1990C>A (p.Pro664Thr)
c.1558C>A (p.Pro520Thr)
3g.119413979C=CA1396548498ARHGAP31c.2050C= (p.Pro684=)
c.1957C= (p.Pro653=)
c.1990C= (p.Pro664=)
c.1558C= (p.Pro520=)
3g.119413979C>GCA354048648ARHGAP31c.2050C>G (p.Pro684Ala)
c.1957C>G (p.Pro653Ala)
c.1990C>G (p.Pro664Ala)
c.1558C>G (p.Pro520Ala)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.119413979C>TCA354048650ARHGAP31c.2050C>T (p.Pro684Ser)
c.1957C>T (p.Pro653Ser)
c.1990C>T (p.Pro664Ser)
c.1558C>T (p.Pro520Ser)
3g.119413980C>ACA354048652ARHGAP31c.2051C>A (p.Pro684His)
c.1958C>A (p.Pro653His)
c.1991C>A (p.Pro664His)
c.1559C>A (p.Pro520His)
3g.119413980C>GCA354048653ARHGAP31c.2051C>G (p.Pro684Arg)
c.1958C>G (p.Pro653Arg)
c.1991C>G (p.Pro664Arg)
c.1559C>G (p.Pro520Arg)
 gnomAD v4
3g.119413980C>TCA354048655ARHGAP31c.2051C>T (p.Pro684Leu)
c.1958C>T (p.Pro653Leu)
c.1991C>T (p.Pro664Leu)
c.1559C>T (p.Pro520Leu)
 COSMIC
3g.119413981T>ACA435411488ARHGAP31c.2052T>A (p.Pro684=)
c.1959T>A (p.Pro653=)
c.1992T>A (p.Pro664=)
c.1560T>A (p.Pro520=)
3g.119413981T>CCA435411489ARHGAP31c.2052T>C (p.Pro684=)
c.1959T>C (p.Pro653=)
c.1992T>C (p.Pro664=)
c.1560T>C (p.Pro520=)
3g.119413981T>GCA81697353ARHGAP31c.2052T>G (p.Pro684=)
c.1959T>G (p.Pro653=)
c.1992T>G (p.Pro664=)
c.1560T>G (p.Pro520=)
 dbSNP gnomAD v3 gnomAD v4
3g.119413981T=CA1396548499ARHGAP31c.2052T= (p.Pro684=)
c.1959T= (p.Pro653=)
c.1992T= (p.Pro664=)
c.1560T= (p.Pro520=)

Number of alleles fetched