Chr Mutation (hg38) CAid Gene Transcript Linkouts
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=)
3g.119413982A=CA1396548500ARHGAP31c.2053A= (p.Ile685=)
c.1960A= (p.Ile654=)
c.1993A= (p.Ile665=)
c.1561A= (p.Ile521=)
3g.119413982A>CCA354048658ARHGAP31c.2053A>C (p.Ile685Leu)
c.1960A>C (p.Ile654Leu)
c.1993A>C (p.Ile665Leu)
c.1561A>C (p.Ile521Leu)
3g.119413982A>GCA354048661ARHGAP31c.2053A>G (p.Ile685Val)
c.1960A>G (p.Ile654Val)
c.1993A>G (p.Ile665Val)
c.1561A>G (p.Ile521Val)
 dbSNP gnomAD v4
3g.119413982A>TCA354048664ARHGAP31c.2053A>T (p.Ile685Phe)
c.1960A>T (p.Ile654Phe)
c.1993A>T (p.Ile665Phe)
c.1561A>T (p.Ile521Phe)
3g.119413983T>ACA354048667ARHGAP31c.2054T>A (p.Ile685Asn)
c.1961T>A (p.Ile654Asn)
c.1994T>A (p.Ile665Asn)
c.1562T>A (p.Ile521Asn)
3g.119413983T>CCA354048672ARHGAP31c.2054T>C (p.Ile685Thr)
c.1961T>C (p.Ile654Thr)
c.1994T>C (p.Ile665Thr)
c.1562T>C (p.Ile521Thr)
3g.119413983T>GCA354048680ARHGAP31c.2054T>G (p.Ile685Ser)
c.1961T>G (p.Ile654Ser)
c.1994T>G (p.Ile665Ser)
c.1562T>G (p.Ile521Ser)
3g.119413984T>ACA435411491ARHGAP31c.2055T>A (p.Ile685=)
c.1962T>A (p.Ile654=)
c.1995T>A (p.Ile665=)
c.1563T>A (p.Ile521=)
3g.119413984T>CCA435411492ARHGAP31c.2055T>C (p.Ile685=)
c.1962T>C (p.Ile654=)
c.1995T>C (p.Ile665=)
c.1563T>C (p.Ile521=)
3g.119413984T>GCA354048692ARHGAP31c.2055T>G (p.Ile685Met)
c.1962T>G (p.Ile654Met)
c.1995T>G (p.Ile665Met)
c.1563T>G (p.Ile521Met)
3g.119413985C>ACA354048700ARHGAP31c.2056C>A (p.Leu686Ile)
c.1963C>A (p.Leu655Ile)
c.1996C>A (p.Leu666Ile)
c.1564C>A (p.Leu522Ile)
 gnomAD v4 COSMIC
3g.119413985C>GCA354048704ARHGAP31c.2056C>G (p.Leu686Val)
c.1963C>G (p.Leu655Val)
c.1996C>G (p.Leu666Val)
c.1564C>G (p.Leu522Val)
3g.119413985C>TCA354048698ARHGAP31c.2056C>T (p.Leu686Phe)
c.1963C>T (p.Leu655Phe)
c.1996C>T (p.Leu666Phe)
c.1564C>T (p.Leu522Phe)
3g.119413986T>ACA354048707ARHGAP31c.2057T>A (p.Leu686His)
c.1964T>A (p.Leu655His)
c.1997T>A (p.Leu666His)
c.1565T>A (p.Leu522His)
3g.119413986T>CCA354048708ARHGAP31c.2057T>C (p.Leu686Pro)
c.1964T>C (p.Leu655Pro)
c.1997T>C (p.Leu666Pro)
c.1565T>C (p.Leu522Pro)
3g.119413986T>GCA354048709ARHGAP31c.2057T>G (p.Leu686Arg)
c.1964T>G (p.Leu655Arg)
c.1997T>G (p.Leu666Arg)
c.1565T>G (p.Leu522Arg)
3g.119413993_119413997delCA2577942208ARHGAP31c.2064_2068del (p.Ser689GlyfsTer?)
c.1971_1975del (p.Ser658GlyfsTer?)
c.2004_2008del (p.Ser669GlyfsTer?)
c.1572_1576del (p.Ser525GlyfsTer?)
3g.119413987C>ACA435411493ARHGAP31c.2058C>A (p.Leu686=)
c.1965C>A (p.Leu655=)
c.1998C>A (p.Leu666=)
c.1566C>A (p.Leu522=)
3g.119413987C=CA1396548501ARHGAP31c.2058C= (p.Leu686=)
c.1965C= (p.Leu655=)
c.1998C= (p.Leu666=)
c.1566C= (p.Leu522=)
3g.119413987C>GCA2553958ARHGAP31c.2058C>G (p.Leu686=)
c.1965C>G (p.Leu655=)
c.1998C>G (p.Leu666=)
c.1566C>G (p.Leu522=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.119413987C>TCA81697356ARHGAP31c.2058C>T (p.Leu686=)
c.1965C>T (p.Leu655=)
c.1998C>T (p.Leu666=)
c.1566C>T (p.Leu522=)
 dbSNP gnomAD v3 gnomAD v4
3g.119413988G>ACA2553959ARHGAP31c.2059G>A (p.Glu687Lys)
c.1966G>A (p.Glu656Lys)
c.1999G>A (p.Glu667Lys)
c.1567G>A (p.Glu523Lys)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.119413988G>CCA354048724ARHGAP31c.2059G>C (p.Glu687Gln)
c.1966G>C (p.Glu656Gln)
c.1999G>C (p.Glu667Gln)
c.1567G>C (p.Glu523Gln)
 dbSNP gnomAD v4
3g.119413988G=CA1396548502ARHGAP31c.2059G= (p.Glu687=)
c.1966G= (p.Glu656=)
c.1999G= (p.Glu667=)
c.1567G= (p.Glu523=)
3g.119413988G>TCA354048730ARHGAP31c.2059G>T (p.Glu687Ter)
c.1966G>T (p.Glu656Ter)
c.1999G>T (p.Glu667Ter)
c.1567G>T (p.Glu523Ter)
3g.119413989A>CCA354048737ARHGAP31c.2060A>C (p.Glu687Ala)
c.1967A>C (p.Glu656Ala)
c.2000A>C (p.Glu667Ala)
c.1568A>C (p.Glu523Ala)
3g.119413989A>GCA354048739ARHGAP31c.2060A>G (p.Glu687Gly)
c.1967A>G (p.Glu656Gly)
c.2000A>G (p.Glu667Gly)
c.1568A>G (p.Glu523Gly)
3g.119413989A>TCA354048742ARHGAP31c.2060A>T (p.Glu687Val)
c.1967A>T (p.Glu656Val)
c.2000A>T (p.Glu667Val)
c.1568A>T (p.Glu523Val)
3g.119413990G>ACA435411497ARHGAP31c.2061G>A (p.Glu687=)
c.1968G>A (p.Glu656=)
c.2001G>A (p.Glu667=)
c.1569G>A (p.Glu523=)
3g.119413990G>CCA354048748ARHGAP31c.2061G>C (p.Glu687Asp)
c.1968G>C (p.Glu656Asp)
c.2001G>C (p.Glu667Asp)
c.1569G>C (p.Glu523Asp)
3g.119413990G>TCA354048755ARHGAP31c.2061G>T (p.Glu687Asp)
c.1968G>T (p.Glu656Asp)
c.2001G>T (p.Glu667Asp)
c.1569G>T (p.Glu523Asp)
 COSMIC
3g.119413991T>ACA354048767ARHGAP31c.2062T>A (p.Ser688Thr)
c.1969T>A (p.Ser657Thr)
c.2002T>A (p.Ser668Thr)
c.1570T>A (p.Ser524Thr)
3g.119413991T>CCA354048761ARHGAP31c.2062T>C (p.Ser688Pro)
c.1969T>C (p.Ser657Pro)
c.2002T>C (p.Ser668Pro)
c.1570T>C (p.Ser524Pro)
3g.119413991T>GCA354048764ARHGAP31c.2062T>G (p.Ser688Ala)
c.1969T>G (p.Ser657Ala)
c.2002T>G (p.Ser668Ala)
c.1570T>G (p.Ser524Ala)
 gnomAD v4
3g.119413992C>ACA354048771ARHGAP31c.2063C>A (p.Ser688Ter)
c.1970C>A (p.Ser657Ter)
c.2003C>A (p.Ser668Ter)
c.1571C>A (p.Ser524Ter)
 gnomAD v4
3g.119413992C=CA1396548503ARHGAP31c.2063C= (p.Ser688=)
c.1970C= (p.Ser657=)
c.2003C= (p.Ser668=)
c.1571C= (p.Ser524=)
3g.119413992C>GCA2553960ARHGAP31c.2063C>G (p.Ser688Trp)
c.1970C>G (p.Ser657Trp)
c.2003C>G (p.Ser668Trp)
c.1571C>G (p.Ser524Trp)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.119413992C>TCA354048776ARHGAP31c.2063C>T (p.Ser688Leu)
c.1970C>T (p.Ser657Leu)
c.2003C>T (p.Ser668Leu)
c.1571C>T (p.Ser524Leu)
 dbSNP gnomAD v3 gnomAD v4 COSMIC
3g.119413992_119413993insTTCA2586965849ARHGAP31c.2063_2064insTT (p.Ser689Ter)
c.1970_1971insTT (p.Ser658Ter)
c.2003_2004insTT (p.Ser669Ter)
c.1571_1572insTT (p.Ser525Ter)
3g.119413993G>ACA2553961ARHGAP31c.2064G>A (p.Ser688=)
c.1971G>A (p.Ser657=)
c.2004G>A (p.Ser668=)
c.1572G>A (p.Ser524=)
 dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
3g.119413993G>CCA435411498ARHGAP31c.2064G>C (p.Ser688=)
c.1971G>C (p.Ser657=)
c.2004G>C (p.Ser668=)
c.1572G>C (p.Ser524=)
 gnomAD v4
3g.119413993G=CA1396548504ARHGAP31c.2064G= (p.Ser688=)
c.1971G= (p.Ser657=)
c.2004G= (p.Ser668=)
c.1572G= (p.Ser524=)
3g.119413993G>TCA435411499ARHGAP31c.2064G>T (p.Ser688=)
c.1971G>T (p.Ser657=)
c.2004G>T (p.Ser668=)
c.1572G>T (p.Ser524=)
3g.119413994A>CCA354048785ARHGAP31c.2065A>C (p.Ser689Arg)
c.1972A>C (p.Ser658Arg)
c.2005A>C (p.Ser669Arg)
c.1573A>C (p.Ser525Arg)
3g.119413994A>GCA354048791ARHGAP31c.2065A>G (p.Ser689Gly)
c.1972A>G (p.Ser658Gly)
c.2005A>G (p.Ser669Gly)
c.1573A>G (p.Ser525Gly)
3g.119413994A>TCA354048813ARHGAP31c.2065A>T (p.Ser689Cys)
c.1972A>T (p.Ser658Cys)
c.2005A>T (p.Ser669Cys)
c.1573A>T (p.Ser525Cys)
3g.119413995G>ACA354048818ARHGAP31c.2066G>A (p.Ser689Asn)
c.1973G>A (p.Ser658Asn)
c.2006G>A (p.Ser669Asn)
c.1574G>A (p.Ser525Asn)
3g.119413995G>CCA354048819ARHGAP31c.2066G>C (p.Ser689Thr)
c.1973G>C (p.Ser658Thr)
c.2006G>C (p.Ser669Thr)
c.1574G>C (p.Ser525Thr)
 dbSNP gnomAD v4
3g.119413995G=CA1396548505ARHGAP31c.2066G= (p.Ser689=)
c.1973G= (p.Ser658=)
c.2006G= (p.Ser669=)
c.1574G= (p.Ser525=)
3g.119413995G>TCA354048820ARHGAP31c.2066G>T (p.Ser689Ile)
c.1973G>T (p.Ser658Ile)
c.2006G>T (p.Ser669Ile)
c.1574G>T (p.Ser525Ile)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.119413996T>ACA354048821ARHGAP31c.2067T>A (p.Ser689Arg)
c.1974T>A (p.Ser658Arg)
c.2007T>A (p.Ser669Arg)
c.1575T>A (p.Ser525Arg)
 dbSNP gnomAD v3 gnomAD v4
3g.119413996T>CCA435411500ARHGAP31c.2067T>C (p.Ser689=)
c.1974T>C (p.Ser658=)
c.2007T>C (p.Ser669=)
c.1575T>C (p.Ser525=)
 dbSNP
3g.119413996T>GCA354048825ARHGAP31c.2067T>G (p.Ser689Arg)
c.1974T>G (p.Ser658Arg)
c.2007T>G (p.Ser669Arg)
c.1575T>G (p.Ser525Arg)
3g.119413996T=CA1396548506ARHGAP31c.2067T= (p.Ser689=)
c.1974T= (p.Ser658=)
c.2007T= (p.Ser669=)
c.1575T= (p.Ser525=)
3g.119413996_119413997insGCA81697371ARHGAP31c.2067_2068insG (p.Leu690AlafsTer?)
c.1974_1975insG (p.Leu659AlafsTer?)
c.2007_2008insG (p.Leu670AlafsTer?)
c.1575_1576insG (p.Leu526AlafsTer?)
 dbSNP
3g.119413997C>ACA354048849ARHGAP31c.2068C>A (p.Leu690Met)
c.1975C>A (p.Leu659Met)
c.2008C>A (p.Leu670Met)
c.1576C>A (p.Leu526Met)
3g.119413997C>GCA354048847ARHGAP31c.2068C>G (p.Leu690Val)
c.1975C>G (p.Leu659Val)
c.2008C>G (p.Leu670Val)
c.1576C>G (p.Leu526Val)
3g.119413997C>TCA435411503ARHGAP31c.2068C>T (p.Leu690=)
c.1975C>T (p.Leu659=)
c.2008C>T (p.Leu670=)
c.1576C>T (p.Leu526=)
 gnomAD v4
3g.119413998T>ACA354048862ARHGAP31c.2069T>A (p.Leu690Gln)
c.1976T>A (p.Leu659Gln)
c.2009T>A (p.Leu670Gln)
c.1577T>A (p.Leu526Gln)
3g.119413998T>CCA354048870ARHGAP31c.2069T>C (p.Leu690Pro)
c.1976T>C (p.Leu659Pro)
c.2009T>C (p.Leu670Pro)
c.1577T>C (p.Leu526Pro)
 dbSNP gnomAD v4
3g.119413998T>GCA354048866ARHGAP31c.2069T>G (p.Leu690Arg)
c.1976T>G (p.Leu659Arg)
c.2009T>G (p.Leu670Arg)
c.1577T>G (p.Leu526Arg)
3g.119413998T=CA1396548507ARHGAP31c.2069T= (p.Leu690=)
c.1976T= (p.Leu659=)
c.2009T= (p.Leu670=)
c.1577T= (p.Leu526=)
3g.119413999G>ACA435411504ARHGAP31c.2070G>A (p.Leu690=)
c.1977G>A (p.Leu659=)
c.2010G>A (p.Leu670=)
c.1578G>A (p.Leu526=)
3g.119413999G>CCA2553962ARHGAP31c.2070G>C (p.Leu690=)
c.1977G>C (p.Leu659=)
c.2010G>C (p.Leu670=)
c.1578G>C (p.Leu526=)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.119413999G=CA1396548508ARHGAP31c.2070G= (p.Leu690=)
c.1977G= (p.Leu659=)
c.2010G= (p.Leu670=)
c.1578G= (p.Leu526=)
3g.119413999G>TCA435411506ARHGAP31c.2070G>T (p.Leu690=)
c.1977G>T (p.Leu659=)
c.2010G>T (p.Leu670=)
c.1578G>T (p.Leu526=)
3g.119414000G>ACA2553963ARHGAP31c.2071G>A (p.Gly691Arg)
c.1978G>A (p.Gly660Arg)
c.2011G>A (p.Gly671Arg)
c.1579G>A (p.Gly527Arg)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.119414000G>CCA354048881ARHGAP31c.2071G>C (p.Gly691Arg)
c.1978G>C (p.Gly660Arg)
c.2011G>C (p.Gly671Arg)
c.1579G>C (p.Gly527Arg)
3g.119414000G=CA1396548509ARHGAP31c.2071G= (p.Gly691=)
c.1978G= (p.Gly660=)
c.2011G= (p.Gly671=)
c.1579G= (p.Gly527=)
3g.119414000G>TCA354048884ARHGAP31c.2071G>T (p.Gly691Trp)
c.1978G>T (p.Gly660Trp)
c.2011G>T (p.Gly671Trp)
c.1579G>T (p.Gly527Trp)
3g.119414001G>ACA354048901ARHGAP31c.2072G>A (p.Gly691Glu)
c.1979G>A (p.Gly660Glu)
c.2012G>A (p.Gly671Glu)
c.1580G>A (p.Gly527Glu)
 gnomAD v4
3g.119414001G>CCA2553964ARHGAP31c.2072G>C (p.Gly691Ala)
c.1979G>C (p.Gly660Ala)
c.2012G>C (p.Gly671Ala)
c.1580G>C (p.Gly527Ala)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.119414001G=CA1396548510ARHGAP31c.2072G= (p.Gly691=)
c.1979G= (p.Gly660=)
c.2012G= (p.Gly671=)
c.1580G= (p.Gly527=)
3g.119414001G>TCA354048905ARHGAP31c.2072G>T (p.Gly691Val)
c.1979G>T (p.Gly660Val)
c.2012G>T (p.Gly671Val)
c.1580G>T (p.Gly527Val)
3g.119414002G>ACA435411510ARHGAP31c.2073G>A (p.Gly691=)
c.1980G>A (p.Gly660=)
c.2013G>A (p.Gly671=)
c.1581G>A (p.Gly527=)
3g.119414002G>CCA435411511ARHGAP31c.2073G>C (p.Gly691=)
c.1980G>C (p.Gly660=)
c.2013G>C (p.Gly671=)
c.1581G>C (p.Gly527=)
3g.119414002G>TCA435411512ARHGAP31c.2073G>T (p.Gly691=)
c.1980G>T (p.Gly660=)
c.2013G>T (p.Gly671=)
c.1581G>T (p.Gly527=)
3g.119414003C>ACA2553965ARHGAP31c.2074C>A (p.Pro692Thr)
c.1981C>A (p.Pro661Thr)
c.2014C>A (p.Pro672Thr)
c.1582C>A (p.Pro528Thr)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.119414003C=CA1396548511ARHGAP31c.2074C= (p.Pro692=)
c.1981C= (p.Pro661=)
c.2014C= (p.Pro672=)
c.1582C= (p.Pro528=)
3g.119414003C>GCA354048934ARHGAP31c.2074C>G (p.Pro692Ala)
c.1981C>G (p.Pro661Ala)
c.2014C>G (p.Pro672Ala)
c.1582C>G (p.Pro528Ala)
3g.119414003C>TCA354048938ARHGAP31c.2074C>T (p.Pro692Ser)
c.1981C>T (p.Pro661Ser)
c.2014C>T (p.Pro672Ser)
c.1582C>T (p.Pro528Ser)
 gnomAD v4
3g.119414004C>ACA354048945ARHGAP31c.2075C>A (p.Pro692His)
c.1982C>A (p.Pro661His)
c.2015C>A (p.Pro672His)
c.1583C>A (p.Pro528His)
3g.119414004C=CA1396548512ARHGAP31c.2075C= (p.Pro692=)
c.1982C= (p.Pro661=)
c.2015C= (p.Pro672=)
c.1583C= (p.Pro528=)
3g.119414004C>GCA354048948ARHGAP31c.2075C>G (p.Pro692Arg)
c.1982C>G (p.Pro661Arg)
c.2015C>G (p.Pro672Arg)
c.1583C>G (p.Pro528Arg)
3g.119414004C>TCA354048952ARHGAP31c.2075C>T (p.Pro692Leu)
c.1982C>T (p.Pro661Leu)
c.2015C>T (p.Pro672Leu)
c.1583C>T (p.Pro528Leu)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.119414005C>ACA2553966ARHGAP31c.2076C>A (p.Pro692=)
c.1983C>A (p.Pro661=)
c.2016C>A (p.Pro672=)
c.1584C>A (p.Pro528=)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.119414005C=CA1396548513ARHGAP31c.2076C= (p.Pro692=)
c.1983C= (p.Pro661=)
c.2016C= (p.Pro672=)
c.1584C= (p.Pro528=)
3g.119414005C>GCA435411513ARHGAP31c.2076C>G (p.Pro692=)
c.1983C>G (p.Pro661=)
c.2016C>G (p.Pro672=)
c.1584C>G (p.Pro528=)
3g.119414005C>TCA435411514ARHGAP31c.2076C>T (p.Pro692=)
c.1983C>T (p.Pro661=)
c.2016C>T (p.Pro672=)
c.1584C>T (p.Pro528=)
3g.119414006T>ACA354048960ARHGAP31c.2077T>A (p.Phe693Ile)
c.1984T>A (p.Phe662Ile)
c.2017T>A (p.Phe673Ile)
c.1585T>A (p.Phe529Ile)
3g.119414006T>CCA354048964ARHGAP31c.2077T>C (p.Phe693Leu)
c.1984T>C (p.Phe662Leu)
c.2017T>C (p.Phe673Leu)
c.1585T>C (p.Phe529Leu)
3g.119414006T>GCA354048966ARHGAP31c.2077T>G (p.Phe693Val)
c.1984T>G (p.Phe662Val)
c.2017T>G (p.Phe673Val)
c.1585T>G (p.Phe529Val)
3g.119414007T>ACA354048967ARHGAP31c.2078T>A (p.Phe693Tyr)
c.1985T>A (p.Phe662Tyr)
c.2018T>A (p.Phe673Tyr)
c.1586T>A (p.Phe529Tyr)
3g.119414007T>CCA354048968ARHGAP31c.2078T>C (p.Phe693Ser)
c.1985T>C (p.Phe662Ser)
c.2018T>C (p.Phe673Ser)
c.1586T>C (p.Phe529Ser)
 gnomAD v4
3g.119414007T>GCA354048969ARHGAP31c.2078T>G (p.Phe693Cys)
c.1985T>G (p.Phe662Cys)
c.2018T>G (p.Phe673Cys)
c.1586T>G (p.Phe529Cys)
3g.119414008T>ACA354048973ARHGAP31c.2079T>A (p.Phe693Leu)
c.1986T>A (p.Phe662Leu)
c.2019T>A (p.Phe673Leu)
c.1587T>A (p.Phe529Leu)
3g.119414008T>CCA2553967ARHGAP31c.2079T>C (p.Phe693=)
c.1986T>C (p.Phe662=)
c.2019T>C (p.Phe673=)
c.1587T>C (p.Phe529=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.119414008T>GCA354048977ARHGAP31c.2079T>G (p.Phe693Leu)
c.1986T>G (p.Phe662Leu)
c.2019T>G (p.Phe673Leu)
c.1587T>G (p.Phe529Leu)
3g.119414008T=CA1396548514ARHGAP31c.2079T= (p.Phe693=)
c.1986T= (p.Phe662=)
c.2019T= (p.Phe673=)
c.1587T= (p.Phe529=)
3g.119414009A>CCA354048981ARHGAP31c.2080A>C (p.Ile694Leu)
c.1987A>C (p.Ile663Leu)
c.2020A>C (p.Ile674Leu)
c.1588A>C (p.Ile530Leu)
3g.119414009A>GCA354048984ARHGAP31c.2080A>G (p.Ile694Val)
c.1987A>G (p.Ile663Val)
c.2020A>G (p.Ile674Val)
c.1588A>G (p.Ile530Val)
3g.119414009A>TCA354048989ARHGAP31c.2080A>T (p.Ile694Phe)
c.1987A>T (p.Ile663Phe)
c.2020A>T (p.Ile674Phe)
c.1588A>T (p.Ile530Phe)
3g.119414010T>ACA354049001ARHGAP31c.2081T>A (p.Ile694Asn)
c.1988T>A (p.Ile663Asn)
c.2021T>A (p.Ile674Asn)
c.1589T>A (p.Ile530Asn)
3g.119414010T>CCA354049000ARHGAP31c.2081T>C (p.Ile694Thr)
c.1988T>C (p.Ile663Thr)
c.2021T>C (p.Ile674Thr)
c.1589T>C (p.Ile530Thr)
 dbSNP gnomAD v2 gnomAD v4
3g.119414010T>GCA354048993ARHGAP31c.2081T>G (p.Ile694Ser)
c.1988T>G (p.Ile663Ser)
c.2021T>G (p.Ile674Ser)
c.1589T>G (p.Ile530Ser)
 gnomAD v4
3g.119414010T=CA1396548515ARHGAP31c.2081T= (p.Ile694=)
c.1988T= (p.Ile663=)
c.2021T= (p.Ile674=)
c.1589T= (p.Ile530=)
3g.119414011T>ACA435411517ARHGAP31c.2082T>A (p.Ile694=)
c.1989T>A (p.Ile663=)
c.2022T>A (p.Ile674=)
c.1590T>A (p.Ile530=)
 dbSNP
3g.119414011T>CCA435411518ARHGAP31c.2082T>C (p.Ile694=)
c.1989T>C (p.Ile663=)
c.2022T>C (p.Ile674=)
c.1590T>C (p.Ile530=)
3g.119414011T>GCA354049006ARHGAP31c.2082T>G (p.Ile694Met)
c.1989T>G (p.Ile663Met)
c.2022T>G (p.Ile674Met)
c.1590T>G (p.Ile530Met)
 dbSNP
3g.119414011T=CA1396548516ARHGAP31c.2082T= (p.Ile694=)
c.1989T= (p.Ile663=)
c.2022T= (p.Ile674=)
c.1590T= (p.Ile530=)
3g.119414012C>ACA354049010ARHGAP31c.2083C>A (p.Pro695Thr)
c.1990C>A (p.Pro664Thr)
c.2023C>A (p.Pro675Thr)
c.1591C>A (p.Pro531Thr)
3g.119414012C>GCA354049011ARHGAP31c.2083C>G (p.Pro695Ala)
c.1990C>G (p.Pro664Ala)
c.2023C>G (p.Pro675Ala)
c.1591C>G (p.Pro531Ala)
3g.119414012C>TCA354049013ARHGAP31c.2083C>T (p.Pro695Ser)
c.1990C>T (p.Pro664Ser)
c.2023C>T (p.Pro675Ser)
c.1591C>T (p.Pro531Ser)
3g.119414013C>ACA354049016ARHGAP31c.2084C>A (p.Pro695His)
c.1991C>A (p.Pro664His)
c.2024C>A (p.Pro675His)
c.1592C>A (p.Pro531His)
3g.119414013C>GCA354049018ARHGAP31c.2084C>G (p.Pro695Arg)
c.1991C>G (p.Pro664Arg)
c.2024C>G (p.Pro675Arg)
c.1592C>G (p.Pro531Arg)
3g.119414013C>TCA354049022ARHGAP31c.2084C>T (p.Pro695Leu)
c.1991C>T (p.Pro664Leu)
c.2024C>T (p.Pro675Leu)
c.1592C>T (p.Pro531Leu)
3g.119414014C>ACA435411519ARHGAP31c.2085C>A (p.Pro695=)
c.1992C>A (p.Pro664=)
c.2025C>A (p.Pro675=)
c.1593C>A (p.Pro531=)
3g.119414014C>GCA435411521ARHGAP31c.2085C>G (p.Pro695=)
c.1992C>G (p.Pro664=)
c.2025C>G (p.Pro675=)
c.1593C>G (p.Pro531=)
3g.119414014C>TCA435411520ARHGAP31c.2085C>T (p.Pro695=)
c.1992C>T (p.Pro664=)
c.2025C>T (p.Pro675=)
c.1593C>T (p.Pro531=)
3g.119414015T>ACA354049028ARHGAP31c.2086T>A (p.Ser696Thr)
c.1993T>A (p.Ser665Thr)
c.2026T>A (p.Ser676Thr)
c.1594T>A (p.Ser532Thr)
3g.119414015T>CCA354049031ARHGAP31c.2086T>C (p.Ser696Pro)
c.1993T>C (p.Ser665Pro)
c.2026T>C (p.Ser676Pro)
c.1594T>C (p.Ser532Pro)
3g.119414015T>GCA354049029ARHGAP31c.2086T>G (p.Ser696Ala)
c.1993T>G (p.Ser665Ala)
c.2026T>G (p.Ser676Ala)
c.1594T>G (p.Ser532Ala)
3g.119414016C>ACA354049037ARHGAP31c.2087C>A (p.Ser696Ter)
c.1994C>A (p.Ser665Ter)
c.2027C>A (p.Ser676Ter)
c.1595C>A (p.Ser532Ter)
3g.119414016C>GCA354049042ARHGAP31c.2087C>G (p.Ser696Ter)
c.1994C>G (p.Ser665Ter)
c.2027C>G (p.Ser676Ter)
c.1595C>G (p.Ser532Ter)
3g.119414016C>TCA354049046ARHGAP31c.2087C>T (p.Ser696Leu)
c.1994C>T (p.Ser665Leu)
c.2027C>T (p.Ser676Leu)
c.1595C>T (p.Ser532Leu)
3g.119414017A=CA1396548517ARHGAP31c.2088A= (p.Ser696=)
c.1995A= (p.Ser665=)
c.2028A= (p.Ser676=)
c.1596A= (p.Ser532=)
3g.119414017A>CCA435411523ARHGAP31c.2088A>C (p.Ser696=)
c.1995A>C (p.Ser665=)
c.2028A>C (p.Ser676=)
c.1596A>C (p.Ser532=)
3g.119414017A>GCA2553968ARHGAP31c.2088A>G (p.Ser696=)
c.1995A>G (p.Ser665=)
c.2028A>G (p.Ser676=)
c.1596A>G (p.Ser532=)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.119414017A>TCA435411524ARHGAP31c.2088A>T (p.Ser696=)
c.1995A>T (p.Ser665=)
c.2028A>T (p.Ser676=)
c.1596A>T (p.Ser532=)
3g.119414018G>ACA354049056ARHGAP31c.2089G>A (p.Glu697Lys)
c.1996G>A (p.Glu666Lys)
c.2029G>A (p.Glu677Lys)
c.1597G>A (p.Glu533Lys)
3g.119414018G>CCA354049065ARHGAP31c.2089G>C (p.Glu697Gln)
c.1996G>C (p.Glu666Gln)
c.2029G>C (p.Glu677Gln)
c.1597G>C (p.Glu533Gln)
3g.119414018G>TCA354049059ARHGAP31c.2089G>T (p.Glu697Ter)
c.1996G>T (p.Glu666Ter)
c.2029G>T (p.Glu677Ter)
c.1597G>T (p.Glu533Ter)
3g.119414019A>CCA354049069ARHGAP31c.2090A>C (p.Glu697Ala)
c.1997A>C (p.Glu666Ala)
c.2030A>C (p.Glu677Ala)
c.1598A>C (p.Glu533Ala)
3g.119414019A>GCA354049073ARHGAP31c.2090A>G (p.Glu697Gly)
c.1997A>G (p.Glu666Gly)
c.2030A>G (p.Glu677Gly)
c.1598A>G (p.Glu533Gly)
3g.119414019A>TCA354049075ARHGAP31c.2090A>T (p.Glu697Val)
c.1997A>T (p.Glu666Val)
c.2030A>T (p.Glu677Val)
c.1598A>T (p.Glu533Val)
3g.119414020G>ACA435411526ARHGAP31c.2091G>A (p.Glu697=)
c.1998G>A (p.Glu666=)
c.2031G>A (p.Glu677=)
c.1599G>A (p.Glu533=)
3g.119414020G>CCA354049079ARHGAP31c.2091G>C (p.Glu697Asp)
c.1998G>C (p.Glu666Asp)
c.2031G>C (p.Glu677Asp)
c.1599G>C (p.Glu533Asp)
3g.119414020G>TCA354049082ARHGAP31c.2091G>T (p.Glu697Asp)
c.1998G>T (p.Glu666Asp)
c.2031G>T (p.Glu677Asp)
c.1599G>T (p.Glu533Asp)
3g.119414021C>ACA354049087ARHGAP31c.2092C>A (p.Pro698Thr)
c.1999C>A (p.Pro667Thr)
c.2032C>A (p.Pro678Thr)
c.1600C>A (p.Pro534Thr)
3g.119414021C>GCA354049088ARHGAP31c.2092C>G (p.Pro698Ala)
c.1999C>G (p.Pro667Ala)
c.2032C>G (p.Pro678Ala)
c.1600C>G (p.Pro534Ala)
3g.119414021C>TCA354049089ARHGAP31c.2092C>T (p.Pro698Ser)
c.1999C>T (p.Pro667Ser)
c.2032C>T (p.Pro678Ser)
c.1600C>T (p.Pro534Ser)
 gnomAD v4
3g.119414022C>ACA354049090ARHGAP31c.2093C>A (p.Pro698His)
c.2000C>A (p.Pro667His)
c.2033C>A (p.Pro678His)
c.1601C>A (p.Pro534His)
3g.119414022C=CA1396548518ARHGAP31c.2093C= (p.Pro698=)
c.2000C= (p.Pro667=)
c.2033C= (p.Pro678=)
c.1601C= (p.Pro534=)
3g.119414022C>GCA2553969ARHGAP31c.2093C>G (p.Pro698Arg)
c.2000C>G (p.Pro667Arg)
c.2033C>G (p.Pro678Arg)
c.1601C>G (p.Pro534Arg)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.119414022C>TCA354049094ARHGAP31c.2093C>T (p.Pro698Leu)
c.2000C>T (p.Pro667Leu)
c.2033C>T (p.Pro678Leu)
c.1601C>T (p.Pro534Leu)
3g.119414023T>ACA435411530ARHGAP31c.2094T>A (p.Pro698=)
c.2001T>A (p.Pro667=)
c.2034T>A (p.Pro678=)
c.1602T>A (p.Pro534=)
3g.119414023T>CCA435411531ARHGAP31c.2094T>C (p.Pro698=)
c.2001T>C (p.Pro667=)
c.2034T>C (p.Pro678=)
c.1602T>C (p.Pro534=)
3g.119414023T>GCA435411532ARHGAP31c.2094T>G (p.Pro698=)
c.2001T>G (p.Pro667=)
c.2034T>G (p.Pro678=)
c.1602T>G (p.Pro534=)
3g.119414024C>ACA354049097ARHGAP31c.2095C>A (p.Pro699Thr)
c.2002C>A (p.Pro668Thr)
c.2035C>A (p.Pro679Thr)
c.1603C>A (p.Pro535Thr)
3g.119414024C>GCA354049102ARHGAP31c.2095C>G (p.Pro699Ala)
c.2002C>G (p.Pro668Ala)
c.2035C>G (p.Pro679Ala)
c.1603C>G (p.Pro535Ala)
 gnomAD v4
3g.119414024C>TCA354049100ARHGAP31c.2095C>T (p.Pro699Ser)
c.2002C>T (p.Pro668Ser)
c.2035C>T (p.Pro679Ser)
c.1603C>T (p.Pro535Ser)
3g.119414025C>ACA354049106ARHGAP31c.2096C>A (p.Pro699His)
c.2003C>A (p.Pro668His)
c.2036C>A (p.Pro679His)
c.1604C>A (p.Pro535His)
3g.119414025C>GCA354049123ARHGAP31c.2096C>G (p.Pro699Arg)
c.2003C>G (p.Pro668Arg)
c.2036C>G (p.Pro679Arg)
c.1604C>G (p.Pro535Arg)
3g.119414025C>TCA354049119ARHGAP31c.2096C>T (p.Pro699Leu)
c.2003C>T (p.Pro668Leu)
c.2036C>T (p.Pro679Leu)
c.1604C>T (p.Pro535Leu)
 gnomAD v4
3g.119414026T>ACA435411534ARHGAP31c.2097T>A (p.Pro699=)
c.2004T>A (p.Pro668=)
c.2037T>A (p.Pro679=)
c.1605T>A (p.Pro535=)
3g.119414026T>CCA435411536ARHGAP31c.2097T>C (p.Pro699=)
c.2004T>C (p.Pro668=)
c.2037T>C (p.Pro679=)
c.1605T>C (p.Pro535=)
3g.119414026T>GCA435411535ARHGAP31c.2097T>G (p.Pro699=)
c.2004T>G (p.Pro668=)
c.2037T>G (p.Pro679=)
c.1605T>G (p.Pro535=)
 gnomAD v4
3g.119414027G>ACA354049125ARHGAP31c.2098G>A (p.Gly700Arg)
c.2005G>A (p.Gly669Arg)
c.2038G>A (p.Gly680Arg)
c.1606G>A (p.Gly536Arg)
3g.119414027G>CCA354049126ARHGAP31c.2098G>C (p.Gly700Arg)
c.2005G>C (p.Gly669Arg)
c.2038G>C (p.Gly680Arg)
c.1606G>C (p.Gly536Arg)
3g.119414027G>TCA354049127ARHGAP31c.2098G>T (p.Gly700Trp)
c.2005G>T (p.Gly669Trp)
c.2038G>T (p.Gly680Trp)
c.1606G>T (p.Gly536Trp)
 COSMIC
3g.119414028G>ACA2553970ARHGAP31c.2099G>A (p.Gly700Glu)
c.2006G>A (p.Gly669Glu)
c.2039G>A (p.Gly680Glu)
c.1607G>A (p.Gly536Glu)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.119414028G>CCA354049129ARHGAP31c.2099G>C (p.Gly700Ala)
c.2006G>C (p.Gly669Ala)
c.2039G>C (p.Gly680Ala)
c.1607G>C (p.Gly536Ala)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.119414028G=CA1396548519ARHGAP31c.2099G= (p.Gly700=)
c.2006G= (p.Gly669=)
c.2039G= (p.Gly680=)
c.1607G= (p.Gly536=)
3g.119414028G>TCA354049131ARHGAP31c.2099G>T (p.Gly700Val)
c.2006G>T (p.Gly669Val)
c.2039G>T (p.Gly680Val)
c.1607G>T (p.Gly536Val)
3g.119414029G>ACA435411537ARHGAP31c.2100G>A (p.Gly700=)
c.2007G>A (p.Gly669=)
c.2040G>A (p.Gly680=)
c.1608G>A (p.Gly536=)
3g.119414029G>CCA435411538ARHGAP31c.2100G>C (p.Gly700=)
c.2007G>C (p.Gly669=)
c.2040G>C (p.Gly680=)
c.1608G>C (p.Gly536=)
3g.119414029G>TCA435411540ARHGAP31c.2100G>T (p.Gly700=)
c.2007G>T (p.Gly669=)
c.2040G>T (p.Gly680=)
c.1608G>T (p.Gly536=)
3g.119414030A>CCA354049134ARHGAP31c.2101A>C (p.Ser701Arg)
c.2008A>C (p.Ser670Arg)
c.2041A>C (p.Ser681Arg)
c.1609A>C (p.Ser537Arg)
3g.119414030A>GCA354049137ARHGAP31c.2101A>G (p.Ser701Gly)
c.2008A>G (p.Ser670Gly)
c.2041A>G (p.Ser681Gly)
c.1609A>G (p.Ser537Gly)
3g.119414030A>TCA354049140ARHGAP31c.2101A>T (p.Ser701Cys)
c.2008A>T (p.Ser670Cys)
c.2041A>T (p.Ser681Cys)
c.1609A>T (p.Ser537Cys)
3g.119414031G>ACA354049142ARHGAP31c.2102G>A (p.Ser701Asn)
c.2009G>A (p.Ser670Asn)
c.2042G>A (p.Ser681Asn)
c.1610G>A (p.Ser537Asn)
3g.119414031G>CCA354049144ARHGAP31c.2102G>C (p.Ser701Thr)
c.2009G>C (p.Ser670Thr)
c.2042G>C (p.Ser681Thr)
c.1610G>C (p.Ser537Thr)
3g.119414031G>TCA354049146ARHGAP31c.2102G>T (p.Ser701Ile)
c.2009G>T (p.Ser670Ile)
c.2042G>T (p.Ser681Ile)
c.1610G>T (p.Ser537Ile)
3g.119414032C>ACA354049152ARHGAP31c.2103C>A (p.Ser701Arg)
c.2010C>A (p.Ser670Arg)
c.2043C>A (p.Ser681Arg)
c.1611C>A (p.Ser537Arg)
3g.119414032C>GCA354049150ARHGAP31c.2103C>G (p.Ser701Arg)
c.2010C>G (p.Ser670Arg)
c.2043C>G (p.Ser681Arg)
c.1611C>G (p.Ser537Arg)
3g.119414032C>TCA435411544ARHGAP31c.2103C>T (p.Ser701=)
c.2010C>T (p.Ser670=)
c.2043C>T (p.Ser681=)
c.1611C>T (p.Ser537=)
3g.119414033T>ACA354049154ARHGAP31c.2104T>A (p.Leu702Met)
c.2011T>A (p.Leu671Met)
c.2044T>A (p.Leu682Met)
c.1612T>A (p.Leu538Met)
3g.119414033T>CCA435411545ARHGAP31c.2104T>C (p.Leu702=)
c.2011T>C (p.Leu671=)
c.2044T>C (p.Leu682=)
c.1612T>C (p.Leu538=)
3g.119414033T>GCA354049157ARHGAP31c.2104T>G (p.Leu702Val)
c.2011T>G (p.Leu671Val)
c.2044T>G (p.Leu682Val)
c.1612T>G (p.Leu538Val)
3g.119414034T>ACA354049161ARHGAP31c.2105T>A (p.Leu702Ter)
c.2012T>A (p.Leu671Ter)
c.2045T>A (p.Leu682Ter)
c.1613T>A (p.Leu538Ter)
3g.119414034T>CCA354049163ARHGAP31c.2105T>C (p.Leu702Ser)
c.2012T>C (p.Leu671Ser)
c.2045T>C (p.Leu682Ser)
c.1613T>C (p.Leu538Ser)
3g.119414034T>GCA354049165ARHGAP31c.2105T>G (p.Leu702Trp)
c.2012T>G (p.Leu671Trp)
c.2045T>G (p.Leu682Trp)
c.1613T>G (p.Leu538Trp)
3g.119414035G>ACA81697392ARHGAP31c.2106G>A (p.Leu702=)
c.2013G>A (p.Leu671=)
c.2046G>A (p.Leu682=)
c.1614G>A (p.Leu538=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.119414035G>CCA354049172ARHGAP31c.2106G>C (p.Leu702Phe)
c.2013G>C (p.Leu671Phe)
c.2046G>C (p.Leu682Phe)
c.1614G>C (p.Leu538Phe)
3g.119414035G=CA1396548520ARHGAP31c.2106G= (p.Leu702=)
c.2013G= (p.Leu671=)
c.2046G= (p.Leu682=)
c.1614G= (p.Leu538=)
3g.119414035G>TCA354049169ARHGAP31c.2106G>T (p.Leu702Phe)
c.2013G>T (p.Leu671Phe)
c.2046G>T (p.Leu682Phe)
c.1614G>T (p.Leu538Phe)
3g.119414036C>ACA354049176ARHGAP31c.2107C>A (p.Pro703Thr)
c.2014C>A (p.Pro672Thr)
c.2047C>A (p.Pro683Thr)
c.1615C>A (p.Pro539Thr)
3g.119414036C>GCA354049179ARHGAP31c.2107C>G (p.Pro703Ala)
c.2014C>G (p.Pro672Ala)
c.2047C>G (p.Pro683Ala)
c.1615C>G (p.Pro539Ala)
3g.119414036C>TCA354049182ARHGAP31c.2107C>T (p.Pro703Ser)
c.2014C>T (p.Pro672Ser)
c.2047C>T (p.Pro683Ser)
c.1615C>T (p.Pro539Ser)
3g.119414037C>ACA354049187ARHGAP31c.2108C>A (p.Pro703His)
c.2015C>A (p.Pro672His)
c.2048C>A (p.Pro683His)
c.1616C>A (p.Pro539His)
3g.119414037C>GCA354049188ARHGAP31c.2108C>G (p.Pro703Arg)
c.2015C>G (p.Pro672Arg)
c.2048C>G (p.Pro683Arg)
c.1616C>G (p.Pro539Arg)
3g.119414037C>TCA354049190ARHGAP31c.2108C>T (p.Pro703Leu)
c.2015C>T (p.Pro672Leu)
c.2048C>T (p.Pro683Leu)
c.1616C>T (p.Pro539Leu)
3g.119414038T>ACA435411547ARHGAP31c.2109T>A (p.Pro703=)
c.2016T>A (p.Pro672=)
c.2049T>A (p.Pro683=)
c.1617T>A (p.Pro539=)
3g.119414038T>CCA435411548ARHGAP31c.2109T>C (p.Pro703=)
c.2016T>C (p.Pro672=)
c.2049T>C (p.Pro683=)
c.1617T>C (p.Pro539=)
 dbSNP gnomAD v2 gnomAD v4
3g.119414038T>GCA435411549ARHGAP31c.2109T>G (p.Pro703=)
c.2016T>G (p.Pro672=)
c.2049T>G (p.Pro683=)
c.1617T>G (p.Pro539=)
3g.119414038T=CA1396548521ARHGAP31c.2109T= (p.Pro703=)
c.2016T= (p.Pro672=)
c.2049T= (p.Pro683=)
c.1617T= (p.Pro539=)
3g.119414039T>ACA354049200ARHGAP31c.2110T>A (p.Cys704Ser)
c.2017T>A (p.Cys673Ser)
c.2050T>A (p.Cys684Ser)
c.1618T>A (p.Cys540Ser)
3g.119414039T>CCA354049205ARHGAP31c.2110T>C (p.Cys704Arg)
c.2017T>C (p.Cys673Arg)
c.2050T>C (p.Cys684Arg)
c.1618T>C (p.Cys540Arg)
3g.119414039T>GCA354049203ARHGAP31c.2110T>G (p.Cys704Gly)
c.2017T>G (p.Cys673Gly)
c.2050T>G (p.Cys684Gly)
c.1618T>G (p.Cys540Gly)
3g.119414040G>ACA354049209ARHGAP31c.2111G>A (p.Cys704Tyr)
c.2018G>A (p.Cys673Tyr)
c.2051G>A (p.Cys684Tyr)
c.1619G>A (p.Cys540Tyr)
 gnomAD v4
3g.119414040G>CCA354049212ARHGAP31c.2111G>C (p.Cys704Ser)
c.2018G>C (p.Cys673Ser)
c.2051G>C (p.Cys684Ser)
c.1619G>C (p.Cys540Ser)
 dbSNP gnomAD v4
3g.119414040G=CA1396548522ARHGAP31c.2111G= (p.Cys704=)
c.2018G= (p.Cys673=)
c.2051G= (p.Cys684=)
c.1619G= (p.Cys540=)
3g.119414040G>TCA354049213ARHGAP31c.2111G>T (p.Cys704Phe)
c.2018G>T (p.Cys673Phe)
c.2051G>T (p.Cys684Phe)
c.1619G>T (p.Cys540Phe)
3g.119414041T>ACA354049215ARHGAP31c.2112T>A (p.Cys704Ter)
c.2019T>A (p.Cys673Ter)
c.2052T>A (p.Cys684Ter)
c.1620T>A (p.Cys540Ter)
3g.119414041T>CCA435411552ARHGAP31c.2112T>C (p.Cys704=)
c.2019T>C (p.Cys673=)
c.2052T>C (p.Cys684=)
c.1620T>C (p.Cys540=)
3g.119414041T>GCA354049217ARHGAP31c.2112T>G (p.Cys704Trp)
c.2019T>G (p.Cys673Trp)
c.2052T>G (p.Cys684Trp)
c.1620T>G (p.Cys540Trp)
3g.119414042G>ACA354049223ARHGAP31c.2113G>A (p.Gly705Ser)
c.2020G>A (p.Gly674Ser)
c.2053G>A (p.Gly685Ser)
c.1621G>A (p.Gly541Ser)
3g.119414042G>CCA354049222ARHGAP31c.2113G>C (p.Gly705Arg)
c.2020G>C (p.Gly674Arg)
c.2053G>C (p.Gly685Arg)
c.1621G>C (p.Gly541Arg)
3g.119414042G>TCA354049219ARHGAP31c.2113G>T (p.Gly705Cys)
c.2020G>T (p.Gly674Cys)
c.2053G>T (p.Gly685Cys)
c.1621G>T (p.Gly541Cys)
3g.119414043G>ACA354049226ARHGAP31c.2114G>A (p.Gly705Asp)
c.2021G>A (p.Gly674Asp)
c.2054G>A (p.Gly685Asp)
c.1622G>A (p.Gly541Asp)
 gnomAD v4
3g.119414043G>CCA354049228ARHGAP31c.2114G>C (p.Gly705Ala)
c.2021G>C (p.Gly674Ala)
c.2054G>C (p.Gly685Ala)
c.1622G>C (p.Gly541Ala)
3g.119414043G>TCA354049232ARHGAP31c.2114G>T (p.Gly705Val)
c.2021G>T (p.Gly674Val)
c.2054G>T (p.Gly685Val)
c.1622G>T (p.Gly541Val)
3g.119414044C>ACA435411553ARHGAP31c.2115C>A (p.Gly705=)
c.2022C>A (p.Gly674=)
c.2055C>A (p.Gly685=)
c.1623C>A (p.Gly541=)
3g.119414044C>GCA435411554ARHGAP31c.2115C>G (p.Gly705=)
c.2022C>G (p.Gly674=)
c.2055C>G (p.Gly685=)
c.1623C>G (p.Gly541=)
3g.119414044C>TCA435411555ARHGAP31c.2115C>T (p.Gly705=)
c.2022C>T (p.Gly674=)
c.2055C>T (p.Gly685=)
c.1623C>T (p.Gly541=)
3g.119414045T>ACA354049236ARHGAP31c.2116T>A (p.Ser706Thr)
c.2023T>A (p.Ser675Thr)
c.2056T>A (p.Ser686Thr)
c.1624T>A (p.Ser542Thr)
3g.119414045T>CCA354049238ARHGAP31c.2116T>C (p.Ser706Pro)
c.2023T>C (p.Ser675Pro)
c.2056T>C (p.Ser686Pro)
c.1624T>C (p.Ser542Pro)
3g.119414045T>GCA354049239ARHGAP31c.2116T>G (p.Ser706Ala)
c.2023T>G (p.Ser675Ala)
c.2056T>G (p.Ser686Ala)
c.1624T>G (p.Ser542Ala)
 gnomAD v4 COSMIC
3g.119414046C>ACA354049244ARHGAP31c.2117C>A (p.Ser706Tyr)
c.2024C>A (p.Ser675Tyr)
c.2057C>A (p.Ser686Tyr)
c.1625C>A (p.Ser542Tyr)
3g.119414046C=CA1396548523ARHGAP31c.2117C= (p.Ser706=)
c.2024C= (p.Ser675=)
c.2057C= (p.Ser686=)
c.1625C= (p.Ser542=)
3g.119414046C>GCA354049248ARHGAP31c.2117C>G (p.Ser706Cys)
c.2024C>G (p.Ser675Cys)
c.2057C>G (p.Ser686Cys)
c.1625C>G (p.Ser542Cys)
3g.119414046C>TCA354049245ARHGAP31c.2117C>T (p.Ser706Phe)
c.2024C>T (p.Ser675Phe)
c.2057C>T (p.Ser686Phe)
c.1625C>T (p.Ser542Phe)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.119414047C>ACA435411557ARHGAP31c.2118C>A (p.Ser706=)
c.2025C>A (p.Ser675=)
c.2058C>A (p.Ser686=)
c.1626C>A (p.Ser542=)
3g.119414047C>GCA435411559ARHGAP31c.2118C>G (p.Ser706=)
c.2025C>G (p.Ser675=)
c.2058C>G (p.Ser686=)
c.1626C>G (p.Ser542=)
3g.119414047C>TCA435411558ARHGAP31c.2118C>T (p.Ser706=)
c.2025C>T (p.Ser675=)
c.2058C>T (p.Ser686=)
c.1626C>T (p.Ser542=)
3g.119414048T>ACA354049250ARHGAP31c.2119T>A (p.Phe707Ile)
c.2026T>A (p.Phe676Ile)
c.2059T>A (p.Phe687Ile)
c.1627T>A (p.Phe543Ile)
3g.119414048T>CCA2553971ARHGAP31c.2119T>C (p.Phe707Leu)
c.2026T>C (p.Phe676Leu)
c.2059T>C (p.Phe687Leu)
c.1627T>C (p.Phe543Leu)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.119414048T>GCA354049253ARHGAP31c.2119T>G (p.Phe707Val)
c.2026T>G (p.Phe676Val)
c.2059T>G (p.Phe687Val)
c.1627T>G (p.Phe543Val)
3g.119414048T=CA1396548524ARHGAP31c.2119T= (p.Phe707=)
c.2026T= (p.Phe676=)
c.2059T= (p.Phe687=)
c.1627T= (p.Phe543=)
3g.119414049T>ACA354049255ARHGAP31c.2120T>A (p.Phe707Tyr)
c.2027T>A (p.Phe676Tyr)
c.2060T>A (p.Phe687Tyr)
c.1628T>A (p.Phe543Tyr)
3g.119414049T>CCA354049257ARHGAP31c.2120T>C (p.Phe707Ser)
c.2027T>C (p.Phe676Ser)
c.2060T>C (p.Phe687Ser)
c.1628T>C (p.Phe543Ser)
3g.119414049T>GCA354049259ARHGAP31c.2120T>G (p.Phe707Cys)
c.2027T>G (p.Phe676Cys)
c.2060T>G (p.Phe687Cys)
c.1628T>G (p.Phe543Cys)
3g.119414050C>ACA354049266ARHGAP31c.2121C>A (p.Phe707Leu)
c.2028C>A (p.Phe676Leu)
c.2061C>A (p.Phe687Leu)
c.1629C>A (p.Phe543Leu)
3g.119414050C>GCA354049268ARHGAP31c.2121C>G (p.Phe707Leu)
c.2028C>G (p.Phe676Leu)
c.2061C>G (p.Phe687Leu)
c.1629C>G (p.Phe543Leu)
3g.119414050C>TCA435411563ARHGAP31c.2121C>T (p.Phe707=)
c.2028C>T (p.Phe676=)
c.2061C>T (p.Phe687=)
c.1629C>T (p.Phe543=)
3g.119414051C>ACA354049274ARHGAP31c.2122C>A (p.Pro708Thr)
c.2029C>A (p.Pro677Thr)
c.2062C>A (p.Pro688Thr)
c.1630C>A (p.Pro544Thr)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.119414051C=CA1396548525ARHGAP31c.2122C= (p.Pro708=)
c.2029C= (p.Pro677=)
c.2062C= (p.Pro688=)
c.1630C= (p.Pro544=)
3g.119414051C>GCA354049276ARHGAP31c.2122C>G (p.Pro708Ala)
c.2029C>G (p.Pro677Ala)
c.2062C>G (p.Pro688Ala)
c.1630C>G (p.Pro544Ala)
3g.119414051C>TCA354049279ARHGAP31c.2122C>T (p.Pro708Ser)
c.2029C>T (p.Pro677Ser)
c.2062C>T (p.Pro688Ser)
c.1630C>T (p.Pro544Ser)
3g.119414052C>ACA354049282ARHGAP31c.2123C>A (p.Pro708His)
c.2030C>A (p.Pro677His)
c.2063C>A (p.Pro688His)
c.1631C>A (p.Pro544His)
3g.119414052C>GCA354049288ARHGAP31c.2123C>G (p.Pro708Arg)
c.2030C>G (p.Pro677Arg)
c.2063C>G (p.Pro688Arg)
c.1631C>G (p.Pro544Arg)
3g.119414052C>TCA354049284ARHGAP31c.2123C>T (p.Pro708Leu)
c.2030C>T (p.Pro677Leu)
c.2063C>T (p.Pro688Leu)
c.1631C>T (p.Pro544Leu)
3g.119414053T>ACA435411564ARHGAP31c.2124T>A (p.Pro708=)
c.2031T>A (p.Pro677=)
c.2064T>A (p.Pro688=)
c.1632T>A (p.Pro544=)
3g.119414053T>CCA435411565ARHGAP31c.2124T>C (p.Pro708=)
c.2031T>C (p.Pro677=)
c.2064T>C (p.Pro688=)
c.1632T>C (p.Pro544=)
 gnomAD v4
3g.119414053T>GCA435411566ARHGAP31c.2124T>G (p.Pro708=)
c.2031T>G (p.Pro677=)
c.2064T>G (p.Pro688=)
c.1632T>G (p.Pro544=)
3g.119414054G>ACA2553972ARHGAP31c.2125G>A (p.Ala709Thr)
c.2032G>A (p.Ala678Thr)
c.2065G>A (p.Ala689Thr)
c.1633G>A (p.Ala545Thr)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.119414054G>CCA354049293ARHGAP31c.2125G>C (p.Ala709Pro)
c.2032G>C (p.Ala678Pro)
c.2065G>C (p.Ala689Pro)
c.1633G>C (p.Ala545Pro)
3g.119414054G=CA1396548526ARHGAP31c.2125G= (p.Ala709=)
c.2032G= (p.Ala678=)
c.2065G= (p.Ala689=)
c.1633G= (p.Ala545=)
3g.119414054G>TCA354049296ARHGAP31c.2125G>T (p.Ala709Ser)
c.2032G>T (p.Ala678Ser)
c.2065G>T (p.Ala689Ser)
c.1633G>T (p.Ala545Ser)
3g.119414055C>ACA354049301ARHGAP31c.2126C>A (p.Ala709Asp)
c.2033C>A (p.Ala678Asp)
c.2066C>A (p.Ala689Asp)
c.1634C>A (p.Ala545Asp)
3g.119414055C>GCA354049304ARHGAP31c.2126C>G (p.Ala709Gly)
c.2033C>G (p.Ala678Gly)
c.2066C>G (p.Ala689Gly)
c.1634C>G (p.Ala545Gly)
3g.119414055C>TCA354049305ARHGAP31c.2126C>T (p.Ala709Val)
c.2033C>T (p.Ala678Val)
c.2066C>T (p.Ala689Val)
c.1634C>T (p.Ala545Val)
3g.119414056T>ACA435411569ARHGAP31c.2127T>A (p.Ala709=)
c.2034T>A (p.Ala678=)
c.2067T>A (p.Ala689=)
c.1635T>A (p.Ala545=)
3g.119414056T>CCA435411570ARHGAP31c.2127T>C (p.Ala709=)
c.2034T>C (p.Ala678=)
c.2067T>C (p.Ala689=)
c.1635T>C (p.Ala545=)
 gnomAD v4
3g.119414056T>GCA435411568ARHGAP31c.2127T>G (p.Ala709=)
c.2034T>G (p.Ala678=)
c.2067T>G (p.Ala689=)
c.1635T>G (p.Ala545=)
3g.119414057C>ACA354049313ARHGAP31c.2128C>A (p.Pro710Thr)
c.2035C>A (p.Pro679Thr)
c.2068C>A (p.Pro690Thr)
c.1636C>A (p.Pro546Thr)
3g.119414057C>GCA354049312ARHGAP31c.2128C>G (p.Pro710Ala)
c.2035C>G (p.Pro679Ala)
c.2068C>G (p.Pro690Ala)
c.1636C>G (p.Pro546Ala)
3g.119414057C>TCA354049309ARHGAP31c.2128C>T (p.Pro710Ser)
c.2035C>T (p.Pro679Ser)
c.2068C>T (p.Pro690Ser)
c.1636C>T (p.Pro546Ser)
 COSMIC
3g.119414058C>ACA354049314ARHGAP31c.2129C>A (p.Pro710Gln)
c.2036C>A (p.Pro679Gln)
c.2069C>A (p.Pro690Gln)
c.1637C>A (p.Pro546Gln)
3g.119414058C>GCA354049315ARHGAP31c.2129C>G (p.Pro710Arg)
c.2036C>G (p.Pro679Arg)
c.2069C>G (p.Pro690Arg)
c.1637C>G (p.Pro546Arg)
3g.119414058C>TCA354049317ARHGAP31c.2129C>T (p.Pro710Leu)
c.2036C>T (p.Pro679Leu)
c.2069C>T (p.Pro690Leu)
c.1637C>T (p.Pro546Leu)
3g.119414059A=CA1396548527ARHGAP31c.2130A= (p.Pro710=)
c.2037A= (p.Pro679=)
c.2070A= (p.Pro690=)
c.1638A= (p.Pro546=)
3g.119414059A>CCA435411571ARHGAP31c.2130A>C (p.Pro710=)
c.2037A>C (p.Pro679=)
c.2070A>C (p.Pro690=)
c.1638A>C (p.Pro546=)
 dbSNP
3g.119414059A>GCA435411573ARHGAP31c.2130A>G (p.Pro710=)
c.2037A>G (p.Pro679=)
c.2070A>G (p.Pro690=)
c.1638A>G (p.Pro546=)
 dbSNP gnomAD v3 gnomAD v4
3g.119414059A>TCA435411575ARHGAP31c.2130A>T (p.Pro710=)
c.2037A>T (p.Pro679=)
c.2070A>T (p.Pro690=)
c.1638A>T (p.Pro546=)
3g.119414060G>ACA354049319ARHGAP31c.2131G>A (p.Val711Ile)
c.2038G>A (p.Val680Ile)
c.2071G>A (p.Val691Ile)
c.1639G>A (p.Val547Ile)
3g.119414060G>CCA354049321ARHGAP31c.2131G>C (p.Val711Leu)
c.2038G>C (p.Val680Leu)
c.2071G>C (p.Val691Leu)
c.1639G>C (p.Val547Leu)
3g.119414060G>TCA354049325ARHGAP31c.2131G>T (p.Val711Phe)
c.2038G>T (p.Val680Phe)
c.2071G>T (p.Val691Phe)
c.1639G>T (p.Val547Phe)
3g.119414061T>ACA354049327ARHGAP31c.2132T>A (p.Val711Asp)
c.2039T>A (p.Val680Asp)
c.2072T>A (p.Val691Asp)
c.1640T>A (p.Val547Asp)
3g.119414061T>CCA354049332ARHGAP31c.2132T>C (p.Val711Ala)
c.2039T>C (p.Val680Ala)
c.2072T>C (p.Val691Ala)
c.1640T>C (p.Val547Ala)
3g.119414061T>GCA354049329ARHGAP31c.2132T>G (p.Val711Gly)
c.2039T>G (p.Val680Gly)
c.2072T>G (p.Val691Gly)
c.1640T>G (p.Val547Gly)
3g.119414061_119414067delinsTCTCCACCA1396548528ARHGAP31c.2132_2138delinsTCTCCAC (p.Val711=)
c.2039_2045delinsTCTCCAC (p.Val680=)
c.2072_2078delinsTCTCCAC (p.Val691=)
c.1640_1646delinsTCTCCAC (p.Val547=)
3g.119414062C>ACA435411577ARHGAP31c.2133C>A (p.Val711=)
c.2040C>A (p.Val680=)
c.2073C>A (p.Val691=)
c.1641C>A (p.Val547=)
3g.119414062C>GCA435411578ARHGAP31c.2133C>G (p.Val711=)
c.2040C>G (p.Val680=)
c.2073C>G (p.Val691=)
c.1641C>G (p.Val547=)
3g.119414062C>TCA435411579ARHGAP31c.2133C>T (p.Val711=)
c.2040C>T (p.Val680=)
c.2073C>T (p.Val691=)
c.1641C>T (p.Val547=)
3g.119414063_119414068delCA2553973ARHGAP31c.2134_2139del (p.Ser712_Thr713del)
c.2041_2046del (p.Ser681_Thr682del)
c.2074_2079del (p.Ser692_Thr693del)
c.1642_1647del (p.Ser548_Thr549del)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.119414063T>ACA354049344ARHGAP31c.2134T>A (p.Ser712Thr)
c.2041T>A (p.Ser681Thr)
c.2074T>A (p.Ser692Thr)
c.1642T>A (p.Ser548Thr)
3g.119414063T>CCA354049346ARHGAP31c.2134T>C (p.Ser712Pro)
c.2041T>C (p.Ser681Pro)
c.2074T>C (p.Ser692Pro)
c.1642T>C (p.Ser548Pro)
 dbSNP gnomAD v2 gnomAD v4
3g.119414063T>GCA354049348ARHGAP31c.2134T>G (p.Ser712Ala)
c.2041T>G (p.Ser681Ala)
c.2074T>G (p.Ser692Ala)
c.1642T>G (p.Ser548Ala)
3g.119414063T=CA1396548529ARHGAP31c.2134T= (p.Ser712=)
c.2041T= (p.Ser681=)
c.2074T= (p.Ser692=)
c.1642T= (p.Ser548=)
3g.119414064C>ACA354049352ARHGAP31c.2135C>A (p.Ser712Tyr)
c.2042C>A (p.Ser681Tyr)
c.2075C>A (p.Ser692Tyr)
c.1643C>A (p.Ser548Tyr)
3g.119414064C=CA1396548530ARHGAP31c.2135C= (p.Ser712=)
c.2042C= (p.Ser681=)
c.2075C= (p.Ser692=)
c.1643C= (p.Ser548=)
3g.119414064C>GCA354049355ARHGAP31c.2135C>G (p.Ser712Cys)
c.2042C>G (p.Ser681Cys)
c.2075C>G (p.Ser692Cys)
c.1643C>G (p.Ser548Cys)
 gnomAD v4
3g.119414064C>TCA81697411ARHGAP31c.2135C>T (p.Ser712Phe)
c.2042C>T (p.Ser681Phe)
c.2075C>T (p.Ser692Phe)
c.1643C>T (p.Ser548Phe)
 dbSNP gnomAD v2 gnomAD v4
3g.119414065C>ACA435411583ARHGAP31c.2136C>A (p.Ser712=)
c.2043C>A (p.Ser681=)
c.2076C>A (p.Ser692=)
c.1644C>A (p.Ser548=)
3g.119414065C>GCA435411584ARHGAP31c.2136C>G (p.Ser712=)
c.2043C>G (p.Ser681=)
c.2076C>G (p.Ser692=)
c.1644C>G (p.Ser548=)
3g.119414065C>TCA435411585ARHGAP31c.2136C>T (p.Ser712=)
c.2043C>T (p.Ser681=)
c.2076C>T (p.Ser692=)
c.1644C>T (p.Ser548=)
3g.119414066A=CA1396548531ARHGAP31c.2137A= (p.Thr713=)
c.2044A= (p.Thr682=)
c.2077A= (p.Thr693=)
c.1645A= (p.Thr549=)
3g.119414066A>CCA354049359ARHGAP31c.2137A>C (p.Thr713Pro)
c.2044A>C (p.Thr682Pro)
c.2077A>C (p.Thr693Pro)
c.1645A>C (p.Thr549Pro)
 dbSNP
3g.119414066A>GCA354049361ARHGAP31c.2137A>G (p.Thr713Ala)
c.2044A>G (p.Thr682Ala)
c.2077A>G (p.Thr693Ala)
c.1645A>G (p.Thr549Ala)
 dbSNP
3g.119414066A>TCA354049368ARHGAP31c.2137A>T (p.Thr713Ser)
c.2044A>T (p.Thr682Ser)
c.2077A>T (p.Thr693Ser)
c.1645A>T (p.Thr549Ser)
3g.119414067C>ACA354049373ARHGAP31c.2138C>A (p.Thr713Asn)
c.2045C>A (p.Thr682Asn)
c.2078C>A (p.Thr693Asn)
c.1646C>A (p.Thr549Asn)
 dbSNP gnomAD v3 gnomAD v4
3g.119414067C=CA1396548532ARHGAP31c.2138C= (p.Thr713=)
c.2045C= (p.Thr682=)
c.2078C= (p.Thr693=)
c.1646C= (p.Thr549=)
3g.119414067C>GCA354049379ARHGAP31c.2138C>G (p.Thr713Ser)
c.2045C>G (p.Thr682Ser)
c.2078C>G (p.Thr693Ser)
c.1646C>G (p.Thr549Ser)
3g.119414067C>TCA354049376ARHGAP31c.2138C>T (p.Thr713Ile)
c.2045C>T (p.Thr682Ile)
c.2078C>T (p.Thr693Ile)
c.1646C>T (p.Thr549Ile)
3g.119414068C>ACA435411587ARHGAP31c.2139C>A (p.Thr713=)
c.2046C>A (p.Thr682=)
c.2079C>A (p.Thr693=)
c.1647C>A (p.Thr549=)
3g.119414068C=CA1396548533ARHGAP31c.2139C= (p.Thr713=)
c.2046C= (p.Thr682=)
c.2079C= (p.Thr693=)
c.1647C= (p.Thr549=)
3g.119414068C>GCA435411589ARHGAP31c.2139C>G (p.Thr713=)
c.2046C>G (p.Thr682=)
c.2079C>G (p.Thr693=)
c.1647C>G (p.Thr549=)
 gnomAD v4
3g.119414068C>TCA435411588ARHGAP31c.2139C>T (p.Thr713=)
c.2046C>T (p.Thr682=)
c.2079C>T (p.Thr693=)
c.1647C>T (p.Thr549=)
 dbSNP gnomAD v3 gnomAD v4
3g.119414069C>ACA354049382ARHGAP31c.2140C>A (p.Pro714Thr)
c.2047C>A (p.Pro683Thr)
c.2080C>A (p.Pro694Thr)
c.1648C>A (p.Pro550Thr)
3g.119414069C=CA1396548534ARHGAP31c.2140C= (p.Pro714=)
c.2047C= (p.Pro683=)
c.2080C= (p.Pro694=)
c.1648C= (p.Pro550=)
3g.119414069C>GCA354049383ARHGAP31c.2140C>G (p.Pro714Ala)
c.2047C>G (p.Pro683Ala)
c.2080C>G (p.Pro694Ala)
c.1648C>G (p.Pro550Ala)
3g.119414069C>TCA2553974ARHGAP31c.2140C>T (p.Pro714Ser)
c.2047C>T (p.Pro683Ser)
c.2080C>T (p.Pro694Ser)
c.1648C>T (p.Pro550Ser)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.119414070C>ACA81697424ARHGAP31c.2141C>A (p.Pro714His)
c.2048C>A (p.Pro683His)
c.2081C>A (p.Pro694His)
c.1649C>A (p.Pro550His)
 dbSNP gnomAD v4
3g.119414070C=CA1396548535ARHGAP31c.2141C= (p.Pro714=)
c.2048C= (p.Pro683=)
c.2081C= (p.Pro694=)
c.1649C= (p.Pro550=)
3g.119414070C>GCA354049391ARHGAP31c.2141C>G (p.Pro714Arg)
c.2048C>G (p.Pro683Arg)
c.2081C>G (p.Pro694Arg)
c.1649C>G (p.Pro550Arg)
3g.119414070C>TCA354049394ARHGAP31c.2141C>T (p.Pro714Leu)
c.2048C>T (p.Pro683Leu)
c.2081C>T (p.Pro694Leu)
c.1649C>T (p.Pro550Leu)
3g.119414071T>ACA435411590ARHGAP31c.2142T>A (p.Pro714=)
c.2049T>A (p.Pro683=)
c.2082T>A (p.Pro694=)
c.1650T>A (p.Pro550=)
3g.119414071T>CCA2553975ARHGAP31c.2142T>C (p.Pro714=)
c.2049T>C (p.Pro683=)
c.2082T>C (p.Pro694=)
c.1650T>C (p.Pro550=)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.119414071T>GCA435411591ARHGAP31c.2142T>G (p.Pro714=)
c.2049T>G (p.Pro683=)
c.2082T>G (p.Pro694=)
c.1650T>G (p.Pro550=)
3g.119414071T=CA1396548536ARHGAP31c.2142T= (p.Pro714=)
c.2049T= (p.Pro683=)
c.2082T= (p.Pro694=)
c.1650T= (p.Pro550=)
3g.119414072C>ACA354049398ARHGAP31c.2143C>A (p.Leu715Met)
c.2050C>A (p.Leu684Met)
c.2083C>A (p.Leu695Met)
c.1651C>A (p.Leu551Met)
3g.119414072C=CA1396548537ARHGAP31c.2143C= (p.Leu715=)
c.2050C= (p.Leu684=)
c.2083C= (p.Leu695=)
c.1651C= (p.Leu551=)
3g.119414072C>GCA2553976ARHGAP31c.2143C>G (p.Leu715Val)
c.2050C>G (p.Leu684Val)
c.2083C>G (p.Leu695Val)
c.1651C>G (p.Leu551Val)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.119414072C>TCA435411593ARHGAP31c.2143C>T (p.Leu715=)
c.2050C>T (p.Leu684=)
c.2083C>T (p.Leu695=)
c.1651C>T (p.Leu551=)
3g.119414073T>ACA354049404ARHGAP31c.2144T>A (p.Leu715Gln)
c.2051T>A (p.Leu684Gln)
c.2084T>A (p.Leu695Gln)
c.1652T>A (p.Leu551Gln)
3g.119414073T>CCA354049407ARHGAP31c.2144T>C (p.Leu715Pro)
c.2051T>C (p.Leu684Pro)
c.2084T>C (p.Leu695Pro)
c.1652T>C (p.Leu551Pro)
3g.119414073T>GCA354049410ARHGAP31c.2144T>G (p.Leu715Arg)
c.2051T>G (p.Leu684Arg)
c.2084T>G (p.Leu695Arg)
c.1652T>G (p.Leu551Arg)
3g.119414074G>ACA435411594ARHGAP31c.2145G>A (p.Leu715=)
c.2052G>A (p.Leu684=)
c.2085G>A (p.Leu695=)
c.1653G>A (p.Leu551=)
 dbSNP gnomAD v3 gnomAD v4
3g.119414074G>CCA435411595ARHGAP31c.2145G>C (p.Leu715=)
c.2052G>C (p.Leu684=)
c.2085G>C (p.Leu695=)
c.1653G>C (p.Leu551=)
3g.119414074G>TCA435411596ARHGAP31c.2145G>T (p.Leu715=)
c.2052G>T (p.Leu684=)
c.2085G>T (p.Leu695=)
c.1653G>T (p.Leu551=)
3g.119414075G>ACA354049419ARHGAP31c.2146G>A (p.Glu716Lys)
c.2053G>A (p.Glu685Lys)
c.2086G>A (p.Glu696Lys)
c.1654G>A (p.Glu552Lys)
 dbSNP
3g.119414075G>CCA354049413ARHGAP31c.2146G>C (p.Glu716Gln)
c.2053G>C (p.Glu685Gln)
c.2086G>C (p.Glu696Gln)
c.1654G>C (p.Glu552Gln)
3g.119414075G=CA1396548538ARHGAP31c.2146G= (p.Glu716=)
c.2053G= (p.Glu685=)
c.2086G= (p.Glu696=)
c.1654G= (p.Glu552=)
3g.119414075G>TCA354049416ARHGAP31c.2146G>T (p.Glu716Ter)
c.2053G>T (p.Glu685Ter)
c.2086G>T (p.Glu696Ter)
c.1654G>T (p.Glu552Ter)
3g.119414076A>CCA354049423ARHGAP31c.2147A>C (p.Glu716Ala)
c.2054A>C (p.Glu685Ala)
c.2087A>C (p.Glu696Ala)
c.1655A>C (p.Glu552Ala)
3g.119414076A>GCA354049426ARHGAP31c.2147A>G (p.Glu716Gly)
c.2054A>G (p.Glu685Gly)
c.2087A>G (p.Glu696Gly)
c.1655A>G (p.Glu552Gly)
3g.119414076A>TCA354049428ARHGAP31c.2147A>T (p.Glu716Val)
c.2054A>T (p.Glu685Val)
c.2087A>T (p.Glu696Val)
c.1655A>T (p.Glu552Val)

Number of alleles fetched