Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.119414097C>ACA354049559ARHGAP31c.2168C>A (p.Ala723Asp)
c.2075C>A (p.Ala692Asp)
c.2108C>A (p.Ala703Asp)
c.1676C>A (p.Ala559Asp)
3g.119414097C>GCA354049562ARHGAP31c.2168C>G (p.Ala723Gly)
c.2075C>G (p.Ala692Gly)
c.2108C>G (p.Ala703Gly)
c.1676C>G (p.Ala559Gly)
3g.119414097C>TCA354049563ARHGAP31c.2168C>T (p.Ala723Val)
c.2075C>T (p.Ala692Val)
c.2108C>T (p.Ala703Val)
c.1676C>T (p.Ala559Val)
3g.119414098C>ACA435411608ARHGAP31c.2169C>A (p.Ala723=)
c.2076C>A (p.Ala692=)
c.2109C>A (p.Ala703=)
c.1677C>A (p.Ala559=)
3g.119414098C>GCA435411610ARHGAP31c.2169C>G (p.Ala723=)
c.2076C>G (p.Ala692=)
c.2109C>G (p.Ala703=)
c.1677C>G (p.Ala559=)
3g.119414098C>TCA435411609ARHGAP31c.2169C>T (p.Ala723=)
c.2076C>T (p.Ala692=)
c.2109C>T (p.Ala703=)
c.1677C>T (p.Ala559=)
3g.119414099A>CCA354049567ARHGAP31c.2170A>C (p.Asn724His)
c.2077A>C (p.Asn693His)
c.2110A>C (p.Asn704His)
c.1678A>C (p.Asn560His)
3g.119414099A>GCA354049569ARHGAP31c.2170A>G (p.Asn724Asp)
c.2077A>G (p.Asn693Asp)
c.2110A>G (p.Asn704Asp)
c.1678A>G (p.Asn560Asp)
3g.119414099A>TCA354049571ARHGAP31c.2170A>T (p.Asn724Tyr)
c.2077A>T (p.Asn693Tyr)
c.2110A>T (p.Asn704Tyr)
c.1678A>T (p.Asn560Tyr)
3g.119414100A=CA1396548547ARHGAP31c.2171A= (p.Asn724=)
c.2078A= (p.Asn693=)
c.2111A= (p.Asn704=)
c.1679A= (p.Asn560=)
3g.119414100A>CCA354049580ARHGAP31c.2171A>C (p.Asn724Thr)
c.2078A>C (p.Asn693Thr)
c.2111A>C (p.Asn704Thr)
c.1679A>C (p.Asn560Thr)
3g.119414100A>GCA354049574ARHGAP31c.2171A>G (p.Asn724Ser)
c.2078A>G (p.Asn693Ser)
c.2111A>G (p.Asn704Ser)
c.1679A>G (p.Asn560Ser)
 dbSNP gnomAD v4
3g.119414100A>TCA354049576ARHGAP31c.2171A>T (p.Asn724Ile)
c.2078A>T (p.Asn693Ile)
c.2111A>T (p.Asn704Ile)
c.1679A>T (p.Asn560Ile)
3g.119414101T>ACA354049583ARHGAP31c.2172T>A (p.Asn724Lys)
c.2079T>A (p.Asn693Lys)
c.2112T>A (p.Asn704Lys)
c.1680T>A (p.Asn560Lys)
3g.119414101T>CCA435411611ARHGAP31c.2172T>C (p.Asn724=)
c.2079T>C (p.Asn693=)
c.2112T>C (p.Asn704=)
c.1680T>C (p.Asn560=)
3g.119414101T>GCA354049586ARHGAP31c.2172T>G (p.Asn724Lys)
c.2079T>G (p.Asn693Lys)
c.2112T>G (p.Asn704Lys)
c.1680T>G (p.Asn560Lys)
3g.119414102C>ACA354049589ARHGAP31c.2173C>A (p.Gln725Lys)
c.2080C>A (p.Gln694Lys)
c.2113C>A (p.Gln705Lys)
c.1681C>A (p.Gln561Lys)
3g.119414102C>GCA354049592ARHGAP31c.2173C>G (p.Gln725Glu)
c.2080C>G (p.Gln694Glu)
c.2113C>G (p.Gln705Glu)
c.1681C>G (p.Gln561Glu)
 gnomAD v4
3g.119414102C>TCA354049595ARHGAP31c.2173C>T (p.Gln725Ter)
c.2080C>T (p.Gln694Ter)
c.2113C>T (p.Gln705Ter)
c.1681C>T (p.Gln561Ter)
3g.119414103A>CCA354049598ARHGAP31c.2174A>C (p.Gln725Pro)
c.2081A>C (p.Gln694Pro)
c.2114A>C (p.Gln705Pro)
c.1682A>C (p.Gln561Pro)
3g.119414103A>GCA354049602ARHGAP31c.2174A>G (p.Gln725Arg)
c.2081A>G (p.Gln694Arg)
c.2114A>G (p.Gln705Arg)
c.1682A>G (p.Gln561Arg)
3g.119414103A>TCA354049601ARHGAP31c.2174A>T (p.Gln725Leu)
c.2081A>T (p.Gln694Leu)
c.2114A>T (p.Gln705Leu)
c.1682A>T (p.Gln561Leu)
3g.119414104G>ACA435411612ARHGAP31c.2175G>A (p.Gln725=)
c.2082G>A (p.Gln694=)
c.2115G>A (p.Gln705=)
c.1683G>A (p.Gln561=)
3g.119414104G>CCA354049604ARHGAP31c.2175G>C (p.Gln725His)
c.2082G>C (p.Gln694His)
c.2115G>C (p.Gln705His)
c.1683G>C (p.Gln561His)
 dbSNP
3g.119414104G=CA1396548548ARHGAP31c.2175G= (p.Gln725=)
c.2082G= (p.Gln694=)
c.2115G= (p.Gln705=)
c.1683G= (p.Gln561=)
3g.119414104G>TCA354049607ARHGAP31c.2175G>T (p.Gln725His)
c.2082G>T (p.Gln694His)
c.2115G>T (p.Gln705His)
c.1683G>T (p.Gln561His)
3g.119414105A>CCA354049611ARHGAP31c.2176A>C (p.Ser726Arg)
c.2083A>C (p.Ser695Arg)
c.2116A>C (p.Ser706Arg)
c.1684A>C (p.Ser562Arg)
3g.119414105A>GCA354049613ARHGAP31c.2176A>G (p.Ser726Gly)
c.2083A>G (p.Ser695Gly)
c.2116A>G (p.Ser706Gly)
c.1684A>G (p.Ser562Gly)
3g.119414105A>TCA354049615ARHGAP31c.2176A>T (p.Ser726Cys)
c.2083A>T (p.Ser695Cys)
c.2116A>T (p.Ser706Cys)
c.1684A>T (p.Ser562Cys)
3g.119414106G>ACA354049619ARHGAP31c.2177G>A (p.Ser726Asn)
c.2084G>A (p.Ser695Asn)
c.2117G>A (p.Ser706Asn)
c.1685G>A (p.Ser562Asn)
 gnomAD v4
3g.119414106G>CCA354049622ARHGAP31c.2177G>C (p.Ser726Thr)
c.2084G>C (p.Ser695Thr)
c.2117G>C (p.Ser706Thr)
c.1685G>C (p.Ser562Thr)
3g.119414106G>TCA354049625ARHGAP31c.2177G>T (p.Ser726Ile)
c.2084G>T (p.Ser695Ile)
c.2117G>T (p.Ser706Ile)
c.1685G>T (p.Ser562Ile)
3g.119414107C>ACA354049628ARHGAP31c.2178C>A (p.Ser726Arg)
c.2085C>A (p.Ser695Arg)
c.2118C>A (p.Ser706Arg)
c.1686C>A (p.Ser562Arg)
3g.119414107C>GCA354049630ARHGAP31c.2178C>G (p.Ser726Arg)
c.2085C>G (p.Ser695Arg)
c.2118C>G (p.Ser706Arg)
c.1686C>G (p.Ser562Arg)
3g.119414107C>TCA435411613ARHGAP31c.2178C>T (p.Ser726=)
c.2085C>T (p.Ser695=)
c.2118C>T (p.Ser706=)
c.1686C>T (p.Ser562=)
3g.119414108A>CCA354049638ARHGAP31c.2179A>C (p.Thr727Pro)
c.2086A>C (p.Thr696Pro)
c.2119A>C (p.Thr707Pro)
c.1687A>C (p.Thr563Pro)
3g.119414108A>GCA354049636ARHGAP31c.2179A>G (p.Thr727Ala)
c.2086A>G (p.Thr696Ala)
c.2119A>G (p.Thr707Ala)
c.1687A>G (p.Thr563Ala)
3g.119414108A>TCA354049634ARHGAP31c.2179A>T (p.Thr727Ser)
c.2086A>T (p.Thr696Ser)
c.2119A>T (p.Thr707Ser)
c.1687A>T (p.Thr563Ser)
3g.119414109C>ACA354049640ARHGAP31c.2180C>A (p.Thr727Lys)
c.2087C>A (p.Thr696Lys)
c.2120C>A (p.Thr707Lys)
c.1688C>A (p.Thr563Lys)
3g.119414109C=CA1396548549ARHGAP31c.2180C= (p.Thr727=)
c.2087C= (p.Thr696=)
c.2120C= (p.Thr707=)
c.1688C= (p.Thr563=)
3g.119414109C>GCA354049642ARHGAP31c.2180C>G (p.Thr727Arg)
c.2087C>G (p.Thr696Arg)
c.2120C>G (p.Thr707Arg)
c.1688C>G (p.Thr563Arg)
3g.119414109C>TCA2553982ARHGAP31c.2180C>T (p.Thr727Ile)
c.2087C>T (p.Thr696Ile)
c.2120C>T (p.Thr707Ile)
c.1688C>T (p.Thr563Ile)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.119414110A>CCA435411614ARHGAP31c.2181A>C (p.Thr727=)
c.2088A>C (p.Thr696=)
c.2121A>C (p.Thr707=)
c.1689A>C (p.Thr563=)
3g.119414110A>GCA435411615ARHGAP31c.2181A>G (p.Thr727=)
c.2088A>G (p.Thr696=)
c.2121A>G (p.Thr707=)
c.1689A>G (p.Thr563=)
3g.119414110A>TCA435411616ARHGAP31c.2181A>T (p.Thr727=)
c.2088A>T (p.Thr696=)
c.2121A>T (p.Thr707=)
c.1689A>T (p.Thr563=)
 gnomAD v4
3g.119414111C>ACA354049644ARHGAP31c.2182C>A (p.Gln728Lys)
c.2089C>A (p.Gln697Lys)
c.2122C>A (p.Gln708Lys)
c.1690C>A (p.Gln564Lys)
 gnomAD v4
3g.119414111C=CA1396548550ARHGAP31c.2182C= (p.Gln728=)
c.2089C= (p.Gln697=)
c.2122C= (p.Gln708=)
c.1690C= (p.Gln564=)
3g.119414111C>GCA354049646ARHGAP31c.2182C>G (p.Gln728Glu)
c.2089C>G (p.Gln697Glu)
c.2122C>G (p.Gln708Glu)
c.1690C>G (p.Gln564Glu)
3g.119414111C>TCA354049648ARHGAP31c.2182C>T (p.Gln728Ter)
c.2089C>T (p.Gln697Ter)
c.2122C>T (p.Gln708Ter)
c.1690C>T (p.Gln564Ter)
 ClinVar dbSNP
3g.119414112A=CA1396548551ARHGAP31c.2183A= (p.Gln728=)
c.2090A= (p.Gln697=)
c.2123A= (p.Gln708=)
c.1691A= (p.Gln564=)
3g.119414112A>CCA354049653ARHGAP31c.2183A>C (p.Gln728Pro)
c.2090A>C (p.Gln697Pro)
c.2123A>C (p.Gln708Pro)
c.1691A>C (p.Gln564Pro)
3g.119414112A>GCA354049650ARHGAP31c.2183A>G (p.Gln728Arg)
c.2090A>G (p.Gln697Arg)
c.2123A>G (p.Gln708Arg)
c.1691A>G (p.Gln564Arg)
 gnomAD v4
3g.119414112A>TCA354049651ARHGAP31c.2183A>T (p.Gln728Leu)
c.2090A>T (p.Gln697Leu)
c.2123A>T (p.Gln708Leu)
c.1691A>T (p.Gln564Leu)
 dbSNP gnomAD v3 gnomAD v4
3g.119414112_119414113delCA2740452930ARHGAP31c.2183_2184del (p.Gln728ArgfsTer14)
c.2090_2091del (p.Gln697ArgfsTer14)
c.2123_2124del (p.Gln708ArgfsTer14)
c.1691_1692del (p.Gln564ArgfsTer14)
3g.119414113G>ACA435411617ARHGAP31c.2184G>A (p.Gln728=)
c.2091G>A (p.Gln697=)
c.2124G>A (p.Gln708=)
c.1692G>A (p.Gln564=)
 gnomAD v4
3g.119414113G>CCA354049655ARHGAP31c.2184G>C (p.Gln728His)
c.2091G>C (p.Gln697His)
c.2124G>C (p.Gln708His)
c.1692G>C (p.Gln564His)
3g.119414113G>TCA354049657ARHGAP31c.2184G>T (p.Gln728His)
c.2091G>T (p.Gln697His)
c.2124G>T (p.Gln708His)
c.1692G>T (p.Gln564His)
3g.119414114G>ACA2553983ARHGAP31c.2185G>A (p.Gly729Arg)
c.2092G>A (p.Gly698Arg)
c.2125G>A (p.Gly709Arg)
c.1693G>A (p.Gly565Arg)
 dbSNP ExAC gnomAD v2
3g.119414114G>CCA354049660ARHGAP31c.2185G>C (p.Gly729Arg)
c.2092G>C (p.Gly698Arg)
c.2125G>C (p.Gly709Arg)
c.1693G>C (p.Gly565Arg)
 dbSNP
3g.119414114G=CA1396548552ARHGAP31c.2185G= (p.Gly729=)
c.2092G= (p.Gly698=)
c.2125G= (p.Gly709=)
c.1693G= (p.Gly565=)
3g.119414114G>TCA354049662ARHGAP31c.2185G>T (p.Gly729Trp)
c.2092G>T (p.Gly698Trp)
c.2125G>T (p.Gly709Trp)
c.1693G>T (p.Gly565Trp)
3g.119414115G>ACA354049668ARHGAP31c.2186G>A (p.Gly729Glu)
c.2093G>A (p.Gly698Glu)
c.2126G>A (p.Gly709Glu)
c.1694G>A (p.Gly565Glu)
 dbSNP gnomAD v4 COSMIC
3g.119414115G>CCA354049664ARHGAP31c.2186G>C (p.Gly729Ala)
c.2093G>C (p.Gly698Ala)
c.2126G>C (p.Gly709Ala)
c.1694G>C (p.Gly565Ala)
3g.119414115G=CA1396548553ARHGAP31c.2186G= (p.Gly729=)
c.2093G= (p.Gly698=)
c.2126G= (p.Gly709=)
c.1694G= (p.Gly565=)
3g.119414115G>TCA354049666ARHGAP31c.2186G>T (p.Gly729Val)
c.2093G>T (p.Gly698Val)
c.2126G>T (p.Gly709Val)
c.1694G>T (p.Gly565Val)
3g.119414116G>ACA435411618ARHGAP31c.2187G>A (p.Gly729=)
c.2094G>A (p.Gly698=)
c.2127G>A (p.Gly709=)
c.1695G>A (p.Gly565=)
 dbSNP
3g.119414116G>CCA435411619ARHGAP31c.2187G>C (p.Gly729=)
c.2094G>C (p.Gly698=)
c.2127G>C (p.Gly709=)
c.1695G>C (p.Gly565=)
3g.119414116G>TCA435411620ARHGAP31c.2187G>T (p.Gly729=)
c.2094G>T (p.Gly698=)
c.2127G>T (p.Gly709=)
c.1695G>T (p.Gly565=)
3g.119414117G>ACA354049670ARHGAP31c.2188G>A (p.Ala730Thr)
c.2095G>A (p.Ala699Thr)
c.2128G>A (p.Ala710Thr)
c.1696G>A (p.Ala566Thr)
3g.119414117G>CCA354049672ARHGAP31c.2188G>C (p.Ala730Pro)
c.2095G>C (p.Ala699Pro)
c.2128G>C (p.Ala710Pro)
c.1696G>C (p.Ala566Pro)
3g.119414117G>TCA354049674ARHGAP31c.2188G>T (p.Ala730Ser)
c.2095G>T (p.Ala699Ser)
c.2128G>T (p.Ala710Ser)
c.1696G>T (p.Ala566Ser)
 gnomAD v4
3g.119414118C>ACA354049676ARHGAP31c.2189C>A (p.Ala730Asp)
c.2096C>A (p.Ala699Asp)
c.2129C>A (p.Ala710Asp)
c.1697C>A (p.Ala566Asp)
3g.119414118C=CA1396548554ARHGAP31c.2189C= (p.Ala730=)
c.2096C= (p.Ala699=)
c.2129C= (p.Ala710=)
c.1697C= (p.Ala566=)
3g.119414118C>GCA81697459ARHGAP31c.2189C>G (p.Ala730Gly)
c.2096C>G (p.Ala699Gly)
c.2129C>G (p.Ala710Gly)
c.1697C>G (p.Ala566Gly)
 dbSNP
3g.119414118C>TCA354049678ARHGAP31c.2189C>T (p.Ala730Val)
c.2096C>T (p.Ala699Val)
c.2129C>T (p.Ala710Val)
c.1697C>T (p.Ala566Val)
3g.119414119T>ACA81697462ARHGAP31c.2190T>A (p.Ala730=)
c.2097T>A (p.Ala699=)
c.2130T>A (p.Ala710=)
c.1698T>A (p.Ala566=)
 dbSNP gnomAD v3 gnomAD v4
3g.119414119T>CCA435411622ARHGAP31c.2190T>C (p.Ala730=)
c.2097T>C (p.Ala699=)
c.2130T>C (p.Ala710=)
c.1698T>C (p.Ala566=)
3g.119414119T>GCA435411621ARHGAP31c.2190T>G (p.Ala730=)
c.2097T>G (p.Ala699=)
c.2130T>G (p.Ala710=)
c.1698T>G (p.Ala566=)
3g.119414119T=CA1396548555ARHGAP31c.2190T= (p.Ala730=)
c.2097T= (p.Ala699=)
c.2130T= (p.Ala710=)
c.1698T= (p.Ala566=)
3g.119414120T>ACA354049682ARHGAP31c.2191T>A (p.Ser731Thr)
c.2098T>A (p.Ser700Thr)
c.2131T>A (p.Ser711Thr)
c.1699T>A (p.Ser567Thr)
 COSMIC
3g.119414120T>CCA354049683ARHGAP31c.2191T>C (p.Ser731Pro)
c.2098T>C (p.Ser700Pro)
c.2131T>C (p.Ser711Pro)
c.1699T>C (p.Ser567Pro)
3g.119414120T>GCA354049685ARHGAP31c.2191T>G (p.Ser731Ala)
c.2098T>G (p.Ser700Ala)
c.2131T>G (p.Ser711Ala)
c.1699T>G (p.Ser567Ala)
3g.119414121C>ACA354049688ARHGAP31c.2192C>A (p.Ser731Tyr)
c.2099C>A (p.Ser700Tyr)
c.2132C>A (p.Ser711Tyr)
c.1700C>A (p.Ser567Tyr)
3g.119414121C=CA1396548556ARHGAP31c.2192C= (p.Ser731=)
c.2099C= (p.Ser700=)
c.2132C= (p.Ser711=)
c.1700C= (p.Ser567=)
3g.119414121C>GCA354049689ARHGAP31c.2192C>G (p.Ser731Cys)
c.2099C>G (p.Ser700Cys)
c.2132C>G (p.Ser711Cys)
c.1700C>G (p.Ser567Cys)
 dbSNP gnomAD v2 gnomAD v4
3g.119414121C>TCA354049692ARHGAP31c.2192C>T (p.Ser731Phe)
c.2099C>T (p.Ser700Phe)
c.2132C>T (p.Ser711Phe)
c.1700C>T (p.Ser567Phe)
3g.119414122C>ACA435411625ARHGAP31c.2193C>A (p.Ser731=)
c.2100C>A (p.Ser700=)
c.2133C>A (p.Ser711=)
c.1701C>A (p.Ser567=)
3g.119414122C>GCA435411624ARHGAP31c.2193C>G (p.Ser731=)
c.2100C>G (p.Ser700=)
c.2133C>G (p.Ser711=)
c.1701C>G (p.Ser567=)
3g.119414122C>TCA435411623ARHGAP31c.2193C>T (p.Ser731=)
c.2100C>T (p.Ser700=)
c.2133C>T (p.Ser711=)
c.1701C>T (p.Ser567=)
3g.119414123A=CA1396548557ARHGAP31c.2194A= (p.Thr732=)
c.2101A= (p.Thr701=)
c.2134A= (p.Thr712=)
c.1702A= (p.Thr568=)
3g.119414123A>CCA354049695ARHGAP31c.2194A>C (p.Thr732Pro)
c.2101A>C (p.Thr701Pro)
c.2134A>C (p.Thr712Pro)
c.1702A>C (p.Thr568Pro)
3g.119414123A>GCA354049698ARHGAP31c.2194A>G (p.Thr732Ala)
c.2101A>G (p.Thr701Ala)
c.2134A>G (p.Thr712Ala)
c.1702A>G (p.Thr568Ala)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.119414123A>TCA354049697ARHGAP31c.2194A>T (p.Thr732Ser)
c.2101A>T (p.Thr701Ser)
c.2134A>T (p.Thr712Ser)
c.1702A>T (p.Thr568Ser)
3g.119414124C>ACA354049701ARHGAP31c.2195C>A (p.Thr732Lys)
c.2102C>A (p.Thr701Lys)
c.2135C>A (p.Thr712Lys)
c.1703C>A (p.Thr568Lys)
3g.119414124C=CA1396548558ARHGAP31c.2195C= (p.Thr732=)
c.2102C= (p.Thr701=)
c.2135C= (p.Thr712=)
c.1703C= (p.Thr568=)
3g.119414124C>GCA354049703ARHGAP31c.2195C>G (p.Thr732Arg)
c.2102C>G (p.Thr701Arg)
c.2135C>G (p.Thr712Arg)
c.1703C>G (p.Thr568Arg)
3g.119414124C>TCA354049704ARHGAP31c.2195C>T (p.Thr732Ile)
c.2102C>T (p.Thr701Ile)
c.2135C>T (p.Thr712Ile)
c.1703C>T (p.Thr568Ile)
 ClinVar dbSNP gnomAD v3 gnomAD v4
3g.119414125A>CCA435411626ARHGAP31c.2196A>C (p.Thr732=)
c.2103A>C (p.Thr701=)
c.2136A>C (p.Thr712=)
c.1704A>C (p.Thr568=)
3g.119414125A>GCA435411628ARHGAP31c.2196A>G (p.Thr732=)
c.2103A>G (p.Thr701=)
c.2136A>G (p.Thr712=)
c.1704A>G (p.Thr568=)
 gnomAD v4
3g.119414125A>TCA435411627ARHGAP31c.2196A>T (p.Thr732=)
c.2103A>T (p.Thr701=)
c.2136A>T (p.Thr712=)
c.1704A>T (p.Thr568=)
3g.119414126G>ACA354049706ARHGAP31c.2197G>A (p.Ala733Thr)
c.2104G>A (p.Ala702Thr)
c.2137G>A (p.Ala713Thr)
c.1705G>A (p.Ala569Thr)
3g.119414126G>CCA354049708ARHGAP31c.2197G>C (p.Ala733Pro)
c.2104G>C (p.Ala702Pro)
c.2137G>C (p.Ala713Pro)
c.1705G>C (p.Ala569Pro)
3g.119414126G>TCA354049709ARHGAP31c.2197G>T (p.Ala733Ser)
c.2104G>T (p.Ala702Ser)
c.2137G>T (p.Ala713Ser)
c.1705G>T (p.Ala569Ser)
3g.119414127C>ACA354049711ARHGAP31c.2198C>A (p.Ala733Glu)
c.2105C>A (p.Ala702Glu)
c.2138C>A (p.Ala713Glu)
c.1706C>A (p.Ala569Glu)
3g.119414127C=CA1396548559ARHGAP31c.2198C= (p.Ala733=)
c.2105C= (p.Ala702=)
c.2138C= (p.Ala713=)
c.1706C= (p.Ala569=)
3g.119414127C>GCA354049713ARHGAP31c.2198C>G (p.Ala733Gly)
c.2105C>G (p.Ala702Gly)
c.2138C>G (p.Ala713Gly)
c.1706C>G (p.Ala569Gly)
3g.119414127C>TCA354049715ARHGAP31c.2198C>T (p.Ala733Val)
c.2105C>T (p.Ala702Val)
c.2138C>T (p.Ala713Val)
c.1706C>T (p.Ala569Val)
 dbSNP gnomAD v4
3g.119414128A=CA1396548560ARHGAP31c.2199A= (p.Ala733=)
c.2106A= (p.Ala702=)
c.2139A= (p.Ala713=)
c.1707A= (p.Ala569=)
3g.119414128A>CCA435411629ARHGAP31c.2199A>C (p.Ala733=)
c.2106A>C (p.Ala702=)
c.2139A>C (p.Ala713=)
c.1707A>C (p.Ala569=)
 dbSNP gnomAD v2 gnomAD v4
3g.119414128A>GCA435411630ARHGAP31c.2199A>G (p.Ala733=)
c.2106A>G (p.Ala702=)
c.2139A>G (p.Ala713=)
c.1707A>G (p.Ala569=)
 dbSNP gnomAD v2 gnomAD v4
3g.119414128A>TCA2553984ARHGAP31c.2199A>T (p.Ala733=)
c.2106A>T (p.Ala702=)
c.2139A>T (p.Ala713=)
c.1707A>T (p.Ala569=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.119414129G>ACA354049719ARHGAP31c.2200G>A (p.Ala734Thr)
c.2107G>A (p.Ala703Thr)
c.2140G>A (p.Ala714Thr)
c.1708G>A (p.Ala570Thr)
3g.119414129G>CCA354049720ARHGAP31c.2200G>C (p.Ala734Pro)
c.2107G>C (p.Ala703Pro)
c.2140G>C (p.Ala714Pro)
c.1708G>C (p.Ala570Pro)
3g.119414129G>TCA354049723ARHGAP31c.2200G>T (p.Ala734Ser)
c.2107G>T (p.Ala703Ser)
c.2140G>T (p.Ala714Ser)
c.1708G>T (p.Ala570Ser)
3g.119414130C>ACA2553985ARHGAP31c.2201C>A (p.Ala734Asp)
c.2108C>A (p.Ala703Asp)
c.2141C>A (p.Ala714Asp)
c.1709C>A (p.Ala570Asp)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.119414130C=CA1396548561ARHGAP31c.2201C= (p.Ala734=)
c.2108C= (p.Ala703=)
c.2141C= (p.Ala714=)
c.1709C= (p.Ala570=)
3g.119414130C>GCA354049728ARHGAP31c.2201C>G (p.Ala734Gly)
c.2108C>G (p.Ala703Gly)
c.2141C>G (p.Ala714Gly)
c.1709C>G (p.Ala570Gly)
3g.119414130C>TCA354049726ARHGAP31c.2201C>T (p.Ala734Val)
c.2108C>T (p.Ala703Val)
c.2141C>T (p.Ala714Val)
c.1709C>T (p.Ala570Val)
3g.119414131C>ACA435411631ARHGAP31c.2202C>A (p.Ala734=)
c.2109C>A (p.Ala703=)
c.2142C>A (p.Ala714=)
c.1710C>A (p.Ala570=)
3g.119414131C>GCA435411632ARHGAP31c.2202C>G (p.Ala734=)
c.2109C>G (p.Ala703=)
c.2142C>G (p.Ala714=)
c.1710C>G (p.Ala570=)
3g.119414131C>TCA435411633ARHGAP31c.2202C>T (p.Ala734=)
c.2109C>T (p.Ala703=)
c.2142C>T (p.Ala714=)
c.1710C>T (p.Ala570=)
3g.119414132A=CA1396548562ARHGAP31c.2203A= (p.Ser735=)
c.2110A= (p.Ser704=)
c.2143A= (p.Ser715=)
c.1711A= (p.Ser571=)
3g.119414132A>CCA354049730ARHGAP31c.2203A>C (p.Ser735Arg)
c.2110A>C (p.Ser704Arg)
c.2143A>C (p.Ser715Arg)
c.1711A>C (p.Ser571Arg)
 gnomAD v4
3g.119414132A>GCA2553986ARHGAP31c.2203A>G (p.Ser735Gly)
c.2110A>G (p.Ser704Gly)
c.2143A>G (p.Ser715Gly)
c.1711A>G (p.Ser571Gly)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.119414132A>TCA354049732ARHGAP31c.2203A>T (p.Ser735Cys)
c.2110A>T (p.Ser704Cys)
c.2143A>T (p.Ser715Cys)
c.1711A>T (p.Ser571Cys)
3g.119414133G>ACA354049735ARHGAP31c.2204G>A (p.Ser735Asn)
c.2111G>A (p.Ser704Asn)
c.2144G>A (p.Ser715Asn)
c.1712G>A (p.Ser571Asn)
 gnomAD v4
3g.119414133G>CCA354049737ARHGAP31c.2204G>C (p.Ser735Thr)
c.2111G>C (p.Ser704Thr)
c.2144G>C (p.Ser715Thr)
c.1712G>C (p.Ser571Thr)
3g.119414133G>TCA354049738ARHGAP31c.2204G>T (p.Ser735Ile)
c.2111G>T (p.Ser704Ile)
c.2144G>T (p.Ser715Ile)
c.1712G>T (p.Ser571Ile)
3g.119414134C>ACA354049741ARHGAP31c.2205C>A (p.Ser735Arg)
c.2112C>A (p.Ser704Arg)
c.2145C>A (p.Ser715Arg)
c.1713C>A (p.Ser571Arg)
3g.119414134C>GCA354049742ARHGAP31c.2205C>G (p.Ser735Arg)
c.2112C>G (p.Ser704Arg)
c.2145C>G (p.Ser715Arg)
c.1713C>G (p.Ser571Arg)
3g.119414134C>TCA435411634ARHGAP31c.2205C>T (p.Ser735=)
c.2112C>T (p.Ser704=)
c.2145C>T (p.Ser715=)
c.1713C>T (p.Ser571=)
3g.119414135A>CCA435411635ARHGAP31c.2206A>C (p.Arg736=)
c.2113A>C (p.Arg705=)
c.2146A>C (p.Arg716=)
c.1714A>C (p.Arg572=)
3g.119414135A>GCA354049744ARHGAP31c.2206A>G (p.Arg736Gly)
c.2113A>G (p.Arg705Gly)
c.2146A>G (p.Arg716Gly)
c.1714A>G (p.Arg572Gly)
3g.119414135A>TCA354049745ARHGAP31c.2206A>T (p.Arg736Ter)
c.2113A>T (p.Arg705Ter)
c.2146A>T (p.Arg716Ter)
c.1714A>T (p.Arg572Ter)
3g.119414140_119414141delCA2667110269ARHGAP31c.2211_2212del (p.Lys738AlafsTer4)
c.2118_2119del (p.Lys707AlafsTer4)
c.2151_2152del (p.Lys718AlafsTer4)
c.1719_1720del (p.Lys574AlafsTer4)
 gnomAD v4
3g.119414136G>ACA354049751ARHGAP31c.2207G>A (p.Arg736Lys)
c.2114G>A (p.Arg705Lys)
c.2147G>A (p.Arg716Lys)
c.1715G>A (p.Arg572Lys)
 gnomAD v4
3g.119414136G>CCA354049749ARHGAP31c.2207G>C (p.Arg736Thr)
c.2114G>C (p.Arg705Thr)
c.2147G>C (p.Arg716Thr)
c.1715G>C (p.Arg572Thr)
3g.119414136G>TCA354049747ARHGAP31c.2207G>T (p.Arg736Ile)
c.2114G>T (p.Arg705Ile)
c.2147G>T (p.Arg716Ile)
c.1715G>T (p.Arg572Ile)
3g.119414137A=CA1396548563ARHGAP31c.2208A= (p.Arg736=)
c.2115A= (p.Arg705=)
c.2148A= (p.Arg716=)
c.1716A= (p.Arg572=)
3g.119414137A>CCA354049753ARHGAP31c.2208A>C (p.Arg736Ser)
c.2115A>C (p.Arg705Ser)
c.2148A>C (p.Arg716Ser)
c.1716A>C (p.Arg572Ser)
3g.119414137A>GCA81697470ARHGAP31c.2208A>G (p.Arg736=)
c.2115A>G (p.Arg705=)
c.2148A>G (p.Arg716=)
c.1716A>G (p.Arg572=)
 dbSNP
3g.119414137A>TCA354049755ARHGAP31c.2208A>T (p.Arg736Ser)
c.2115A>T (p.Arg705Ser)
c.2148A>T (p.Arg716Ser)
c.1716A>T (p.Arg572Ser)
 gnomAD v4
3g.119414138G>ACA81697471ARHGAP31c.2209G>A (p.Glu737Lys)
c.2116G>A (p.Glu706Lys)
c.2149G>A (p.Glu717Lys)
c.1717G>A (p.Glu573Lys)
 dbSNP gnomAD v3 gnomAD v4
3g.119414138G>CCA354049759ARHGAP31c.2209G>C (p.Glu737Gln)
c.2116G>C (p.Glu706Gln)
c.2149G>C (p.Glu717Gln)
c.1717G>C (p.Glu573Gln)
3g.119414138G=CA1396548564ARHGAP31c.2209G= (p.Glu737=)
c.2116G= (p.Glu706=)
c.2149G= (p.Glu717=)
c.1717G= (p.Glu573=)
3g.119414138G>TCA354049761ARHGAP31c.2209G>T (p.Glu737Ter)
c.2116G>T (p.Glu706Ter)
c.2149G>T (p.Glu717Ter)
c.1717G>T (p.Glu573Ter)
3g.119414139A=CA1396548565ARHGAP31c.2210A= (p.Glu737=)
c.2117A= (p.Glu706=)
c.2150A= (p.Glu717=)
c.1718A= (p.Glu573=)
3g.119414139A>CCA354049763ARHGAP31c.2210A>C (p.Glu737Ala)
c.2117A>C (p.Glu706Ala)
c.2150A>C (p.Glu717Ala)
c.1718A>C (p.Glu573Ala)
3g.119414139A>GCA354049766ARHGAP31c.2210A>G (p.Glu737Gly)
c.2117A>G (p.Glu706Gly)
c.2150A>G (p.Glu717Gly)
c.1718A>G (p.Glu573Gly)
 dbSNP
3g.119414139A>TCA354049769ARHGAP31c.2210A>T (p.Glu737Val)
c.2117A>T (p.Glu706Val)
c.2150A>T (p.Glu717Val)
c.1718A>T (p.Glu573Val)
3g.119414140G>ACA435411636ARHGAP31c.2211G>A (p.Glu737=)
c.2118G>A (p.Glu706=)
c.2151G>A (p.Glu717=)
c.1719G>A (p.Glu573=)
3g.119414140G>CCA354049771ARHGAP31c.2211G>C (p.Glu737Asp)
c.2118G>C (p.Glu706Asp)
c.2151G>C (p.Glu717Asp)
c.1719G>C (p.Glu573Asp)
3g.119414140G>TCA354049773ARHGAP31c.2211G>T (p.Glu737Asp)
c.2118G>T (p.Glu706Asp)
c.2151G>T (p.Glu717Asp)
c.1719G>T (p.Glu573Asp)
3g.119414141A>CCA354049778ARHGAP31c.2212A>C (p.Lys738Gln)
c.2119A>C (p.Lys707Gln)
c.2152A>C (p.Lys718Gln)
c.1720A>C (p.Lys574Gln)
3g.119414141A>GCA354049781ARHGAP31c.2212A>G (p.Lys738Glu)
c.2119A>G (p.Lys707Glu)
c.2152A>G (p.Lys718Glu)
c.1720A>G (p.Lys574Glu)
3g.119414141A>TCA354049784ARHGAP31c.2212A>T (p.Lys738Ter)
c.2119A>T (p.Lys707Ter)
c.2152A>T (p.Lys718Ter)
c.1720A>T (p.Lys574Ter)
3g.119414142A>CCA354049787ARHGAP31c.2213A>C (p.Lys738Thr)
c.2120A>C (p.Lys707Thr)
c.2153A>C (p.Lys718Thr)
c.1721A>C (p.Lys574Thr)
3g.119414142A>GCA354049790ARHGAP31c.2213A>G (p.Lys738Arg)
c.2120A>G (p.Lys707Arg)
c.2153A>G (p.Lys718Arg)
c.1721A>G (p.Lys574Arg)
3g.119414142A>TCA354049792ARHGAP31c.2213A>T (p.Lys738Met)
c.2120A>T (p.Lys707Met)
c.2153A>T (p.Lys718Met)
c.1721A>T (p.Lys574Met)
3g.119414143G>ACA435411637ARHGAP31c.2214G>A (p.Lys738=)
c.2121G>A (p.Lys707=)
c.2154G>A (p.Lys718=)
c.1722G>A (p.Lys574=)
3g.119414143G>CCA354049795ARHGAP31c.2214G>C (p.Lys738Asn)
c.2121G>C (p.Lys707Asn)
c.2154G>C (p.Lys718Asn)
c.1722G>C (p.Lys574Asn)
 ClinVar
3g.119414143G>TCA354049798ARHGAP31c.2214G>T (p.Lys738Asn)
c.2121G>T (p.Lys707Asn)
c.2154G>T (p.Lys718Asn)
c.1722G>T (p.Lys574Asn)
3g.119414144C>ACA354049801ARHGAP31c.2215C>A (p.Pro739Thr)
c.2122C>A (p.Pro708Thr)
c.2155C>A (p.Pro719Thr)
c.1723C>A (p.Pro575Thr)
 gnomAD v4
3g.119414144C>GCA354049804ARHGAP31c.2215C>G (p.Pro739Ala)
c.2122C>G (p.Pro708Ala)
c.2155C>G (p.Pro719Ala)
c.1723C>G (p.Pro575Ala)
3g.119414144C>TCA354049806ARHGAP31c.2215C>T (p.Pro739Ser)
c.2122C>T (p.Pro708Ser)
c.2155C>T (p.Pro719Ser)
c.1723C>T (p.Pro575Ser)
3g.119414145delCA2580068644ARHGAP31c.2216del (p.Pro739ArgfsTer19)
c.2123del (p.Pro708ArgfsTer19)
c.2156del (p.Pro719ArgfsTer19)
c.1724del (p.Pro575ArgfsTer19)
 ClinVar
3g.119414145C>ACA354049809ARHGAP31c.2216C>A (p.Pro739Gln)
c.2123C>A (p.Pro708Gln)
c.2156C>A (p.Pro719Gln)
c.1724C>A (p.Pro575Gln)
 gnomAD v4
3g.119414145C=CA1396548566ARHGAP31c.2216C= (p.Pro739=)
c.2123C= (p.Pro708=)
c.2156C= (p.Pro719=)
c.1724C= (p.Pro575=)
3g.119414145C>GCA354049811ARHGAP31c.2216C>G (p.Pro739Arg)
c.2123C>G (p.Pro708Arg)
c.2156C>G (p.Pro719Arg)
c.1724C>G (p.Pro575Arg)
 dbSNP gnomAD v2 gnomAD v4
3g.119414145C>TCA2553987ARHGAP31c.2216C>T (p.Pro739Leu)
c.2123C>T (p.Pro708Leu)
c.2156C>T (p.Pro719Leu)
c.1724C>T (p.Pro575Leu)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
3g.119414146G>ACA435411640ARHGAP31c.2217G>A (p.Pro739=)
c.2124G>A (p.Pro708=)
c.2157G>A (p.Pro719=)
c.1725G>A (p.Pro575=)
 dbSNP gnomAD v3 gnomAD v4 COSMIC
3g.119414146G>CCA435411639ARHGAP31c.2217G>C (p.Pro739=)
c.2124G>C (p.Pro708=)
c.2157G>C (p.Pro719=)
c.1725G>C (p.Pro575=)
 dbSNP gnomAD v4
3g.119414146G=CA1396548567ARHGAP31c.2217G= (p.Pro739=)
c.2124G= (p.Pro708=)
c.2157G= (p.Pro719=)
c.1725G= (p.Pro575=)
3g.119414146G>TCA435411638ARHGAP31c.2217G>T (p.Pro739=)
c.2124G>T (p.Pro708=)
c.2157G>T (p.Pro719=)
c.1725G>T (p.Pro575=)
 dbSNP gnomAD v2 gnomAD v4
3g.119414147G>ACA354049817ARHGAP31c.2218G>A (p.Glu740Lys)
c.2125G>A (p.Glu709Lys)
c.2158G>A (p.Glu720Lys)
c.1726G>A (p.Glu576Lys)
 gnomAD v4
3g.119414147G>CCA354049818ARHGAP31c.2218G>C (p.Glu740Gln)
c.2125G>C (p.Glu709Gln)
c.2158G>C (p.Glu720Gln)
c.1726G>C (p.Glu576Gln)
 gnomAD v4
3g.119414147G>TCA354049820ARHGAP31c.2218G>T (p.Glu740Ter)
c.2125G>T (p.Glu709Ter)
c.2158G>T (p.Glu720Ter)
c.1726G>T (p.Glu576Ter)
3g.119414148A>CCA354049824ARHGAP31c.2219A>C (p.Glu740Ala)
c.2126A>C (p.Glu709Ala)
c.2159A>C (p.Glu720Ala)
c.1727A>C (p.Glu576Ala)
3g.119414148A>GCA354049826ARHGAP31c.2219A>G (p.Glu740Gly)
c.2126A>G (p.Glu709Gly)
c.2159A>G (p.Glu720Gly)
c.1727A>G (p.Glu576Gly)
3g.119414148A>TCA354049829ARHGAP31c.2219A>T (p.Glu740Val)
c.2126A>T (p.Glu709Val)
c.2159A>T (p.Glu720Val)
c.1727A>T (p.Glu576Val)
3g.119414149A=CA1396548568ARHGAP31c.2220A= (p.Glu740=)
c.2127A= (p.Glu709=)
c.2160A= (p.Glu720=)
c.1728A= (p.Glu576=)
3g.119414149A>CCA354049834ARHGAP31c.2220A>C (p.Glu740Asp)
c.2127A>C (p.Glu709Asp)
c.2160A>C (p.Glu720Asp)
c.1728A>C (p.Glu576Asp)
 dbSNP gnomAD v3 gnomAD v4
3g.119414149A>GCA435411641ARHGAP31c.2220A>G (p.Glu740=)
c.2127A>G (p.Glu709=)
c.2160A>G (p.Glu720=)
c.1728A>G (p.Glu576=)
 dbSNP
3g.119414149A>TCA354049832ARHGAP31c.2220A>T (p.Glu740Asp)
c.2127A>T (p.Glu709Asp)
c.2160A>T (p.Glu720Asp)
c.1728A>T (p.Glu576Asp)
3g.119414150C>ACA354049839ARHGAP31c.2221C>A (p.Pro741Thr)
c.2128C>A (p.Pro710Thr)
c.2161C>A (p.Pro721Thr)
c.1729C>A (p.Pro577Thr)
 dbSNP gnomAD v4
3g.119414150C=CA1396548569ARHGAP31c.2221C= (p.Pro741=)
c.2128C= (p.Pro710=)
c.2161C= (p.Pro721=)
c.1729C= (p.Pro577=)
3g.119414150C>GCA354049841ARHGAP31c.2221C>G (p.Pro741Ala)
c.2128C>G (p.Pro710Ala)
c.2161C>G (p.Pro721Ala)
c.1729C>G (p.Pro577Ala)
 gnomAD v4
3g.119414150C>TCA354049843ARHGAP31c.2221C>T (p.Pro741Ser)
c.2128C>T (p.Pro710Ser)
c.2161C>T (p.Pro721Ser)
c.1729C>T (p.Pro577Ser)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.119414151C>ACA354049847ARHGAP31c.2222C>A (p.Pro741His)
c.2129C>A (p.Pro710His)
c.2162C>A (p.Pro721His)
c.1730C>A (p.Pro577His)
3g.119414151C=CA1396548570ARHGAP31c.2222C= (p.Pro741=)
c.2129C= (p.Pro710=)
c.2162C= (p.Pro721=)
c.1730C= (p.Pro577=)
3g.119414151C>GCA354049849ARHGAP31c.2222C>G (p.Pro741Arg)
c.2129C>G (p.Pro710Arg)
c.2162C>G (p.Pro721Arg)
c.1730C>G (p.Pro577Arg)
3g.119414151C>TCA2553988ARHGAP31c.2222C>T (p.Pro741Leu)
c.2129C>T (p.Pro710Leu)
c.2162C>T (p.Pro721Leu)
c.1730C>T (p.Pro577Leu)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.119414152T>ACA435411642ARHGAP31c.2223T>A (p.Pro741=)
c.2130T>A (p.Pro710=)
c.2163T>A (p.Pro721=)
c.1731T>A (p.Pro577=)
3g.119414152T>CCA435411644ARHGAP31c.2223T>C (p.Pro741=)
c.2130T>C (p.Pro710=)
c.2163T>C (p.Pro721=)
c.1731T>C (p.Pro577=)
 dbSNP gnomAD v2 gnomAD v4
3g.119414152T>GCA435411643ARHGAP31c.2223T>G (p.Pro741=)
c.2130T>G (p.Pro710=)
c.2163T>G (p.Pro721=)
c.1731T>G (p.Pro577=)
3g.119414152T=CA1396548571ARHGAP31c.2223T= (p.Pro741=)
c.2130T= (p.Pro710=)
c.2163T= (p.Pro721=)
c.1731T= (p.Pro577=)
3g.119414153G>ACA354049862ARHGAP31c.2224G>A (p.Glu742Lys)
c.2131G>A (p.Glu711Lys)
c.2164G>A (p.Glu722Lys)
c.1732G>A (p.Glu578Lys)
 dbSNP gnomAD v2 gnomAD v4
3g.119414153G>CCA354049859ARHGAP31c.2224G>C (p.Glu742Gln)
c.2131G>C (p.Glu711Gln)
c.2164G>C (p.Glu722Gln)
c.1732G>C (p.Glu578Gln)
 gnomAD v4 COSMIC
3g.119414153G=CA1396548572ARHGAP31c.2224G= (p.Glu742=)
c.2131G= (p.Glu711=)
c.2164G= (p.Glu722=)
c.1732G= (p.Glu578=)
3g.119414153G>TCA354049861ARHGAP31c.2224G>T (p.Glu742Ter)
c.2131G>T (p.Glu711Ter)
c.2164G>T (p.Glu722Ter)
c.1732G>T (p.Glu578Ter)
3g.119414154A=CA1396548573ARHGAP31c.2225A= (p.Glu742=)
c.2132A= (p.Glu711=)
c.2165A= (p.Glu722=)
c.1733A= (p.Glu578=)
3g.119414154A>CCA354049865ARHGAP31c.2225A>C (p.Glu742Ala)
c.2132A>C (p.Glu711Ala)
c.2165A>C (p.Glu722Ala)
c.1733A>C (p.Glu578Ala)
3g.119414154A>GCA81697476ARHGAP31c.2225A>G (p.Glu742Gly)
c.2132A>G (p.Glu711Gly)
c.2165A>G (p.Glu722Gly)
c.1733A>G (p.Glu578Gly)
 dbSNP
3g.119414154A>TCA354049870ARHGAP31c.2225A>T (p.Glu742Val)
c.2132A>T (p.Glu711Val)
c.2165A>T (p.Glu722Val)
c.1733A>T (p.Glu578Val)
3g.119414155G>ACA435411645ARHGAP31c.2226G>A (p.Glu742=)
c.2133G>A (p.Glu711=)
c.2166G>A (p.Glu722=)
c.1734G>A (p.Glu578=)
 dbSNP gnomAD v4
3g.119414155G>CCA354049873ARHGAP31c.2226G>C (p.Glu742Asp)
c.2133G>C (p.Glu711Asp)
c.2166G>C (p.Glu722Asp)
c.1734G>C (p.Glu578Asp)
3g.119414155G>TCA354049875ARHGAP31c.2226G>T (p.Glu742Asp)
c.2133G>T (p.Glu711Asp)
c.2166G>T (p.Glu722Asp)
c.1734G>T (p.Glu578Asp)
3g.119414156C>ACA354049882ARHGAP31c.2227C>A (p.Gln743Lys)
c.2134C>A (p.Gln712Lys)
c.2167C>A (p.Gln723Lys)
c.1735C>A (p.Gln579Lys)
3g.119414156C>GCA354049877ARHGAP31c.2227C>G (p.Gln743Glu)
c.2134C>G (p.Gln712Glu)
c.2167C>G (p.Gln723Glu)
c.1735C>G (p.Gln579Glu)
3g.119414156C>TCA354049880ARHGAP31c.2227C>T (p.Gln743Ter)
c.2134C>T (p.Gln712Ter)
c.2167C>T (p.Gln723Ter)
c.1735C>T (p.Gln579Ter)
3g.119414157A=CA1396548574ARHGAP31c.2228A= (p.Gln743=)
c.2135A= (p.Gln712=)
c.2168A= (p.Gln723=)
c.1736A= (p.Gln579=)
3g.119414157A>CCA354049885ARHGAP31c.2228A>C (p.Gln743Pro)
c.2135A>C (p.Gln712Pro)
c.2168A>C (p.Gln723Pro)
c.1736A>C (p.Gln579Pro)
3g.119414157A>GCA2553989ARHGAP31c.2228A>G (p.Gln743Arg)
c.2135A>G (p.Gln712Arg)
c.2168A>G (p.Gln723Arg)
c.1736A>G (p.Gln579Arg)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.119414157A>TCA354049887ARHGAP31c.2228A>T (p.Gln743Leu)
c.2135A>T (p.Gln712Leu)
c.2168A>T (p.Gln723Leu)
c.1736A>T (p.Gln579Leu)
3g.119414158G>ACA435411646ARHGAP31c.2229G>A (p.Gln743=)
c.2136G>A (p.Gln712=)
c.2169G>A (p.Gln723=)
c.1737G>A (p.Gln579=)
3g.119414158G>CCA354049890ARHGAP31c.2229G>C (p.Gln743His)
c.2136G>C (p.Gln712His)
c.2169G>C (p.Gln723His)
c.1737G>C (p.Gln579His)
3g.119414158G>TCA354049893ARHGAP31c.2229G>T (p.Gln743His)
c.2136G>T (p.Gln712His)
c.2169G>T (p.Gln723His)
c.1737G>T (p.Gln579His)
3g.119414160delCA2667110270ARHGAP31c.2231del (p.Gly744AlafsTer14)
c.2138del (p.Gly713AlafsTer14)
c.2171del (p.Gly724AlafsTer14)
c.1739del (p.Gly580AlafsTer14)
 gnomAD v4
3g.119414159G>ACA354049896ARHGAP31c.2230G>A (p.Gly744Ser)
c.2137G>A (p.Gly713Ser)
c.2170G>A (p.Gly724Ser)
c.1738G>A (p.Gly580Ser)
 dbSNP gnomAD v2 gnomAD v4
3g.119414159G>CCA354049899ARHGAP31c.2230G>C (p.Gly744Arg)
c.2137G>C (p.Gly713Arg)
c.2170G>C (p.Gly724Arg)
c.1738G>C (p.Gly580Arg)
 dbSNP
3g.119414159G=CA1396548575ARHGAP31c.2230G= (p.Gly744=)
c.2137G= (p.Gly713=)
c.2170G= (p.Gly724=)
c.1738G= (p.Gly580=)
3g.119414159G>TCA354049901ARHGAP31c.2230G>T (p.Gly744Cys)
c.2137G>T (p.Gly713Cys)
c.2170G>T (p.Gly724Cys)
c.1738G>T (p.Gly580Cys)
3g.119414160G>ACA81697477ARHGAP31c.2231G>A (p.Gly744Asp)
c.2138G>A (p.Gly713Asp)
c.2171G>A (p.Gly724Asp)
c.1739G>A (p.Gly580Asp)
 dbSNP gnomAD v2 gnomAD v4
3g.119414160G>CCA354049907ARHGAP31c.2231G>C (p.Gly744Ala)
c.2138G>C (p.Gly713Ala)
c.2171G>C (p.Gly724Ala)
c.1739G>C (p.Gly580Ala)
3g.119414160G=CA1396548576ARHGAP31c.2231G= (p.Gly744=)
c.2138G= (p.Gly713=)
c.2171G= (p.Gly724=)
c.1739G= (p.Gly580=)
3g.119414160G>TCA354049909ARHGAP31c.2231G>T (p.Gly744Val)
c.2138G>T (p.Gly713Val)
c.2171G>T (p.Gly724Val)
c.1739G>T (p.Gly580Val)
3g.119414161C>ACA435411647ARHGAP31c.2232C>A (p.Gly744=)
c.2139C>A (p.Gly713=)
c.2172C>A (p.Gly724=)
c.1740C>A (p.Gly580=)
3g.119414161C>GCA435411648ARHGAP31c.2232C>G (p.Gly744=)
c.2139C>G (p.Gly713=)
c.2172C>G (p.Gly724=)
c.1740C>G (p.Gly580=)
3g.119414161C>TCA435411649ARHGAP31c.2232C>T (p.Gly744=)
c.2139C>T (p.Gly713=)
c.2172C>T (p.Gly724=)
c.1740C>T (p.Gly580=)
3g.119414162C>ACA354049913ARHGAP31c.2233C>A (p.Leu745Met)
c.2140C>A (p.Leu714Met)
c.2173C>A (p.Leu725Met)
c.1741C>A (p.Leu581Met)
3g.119414162C>GCA354049914ARHGAP31c.2233C>G (p.Leu745Val)
c.2140C>G (p.Leu714Val)
c.2173C>G (p.Leu725Val)
c.1741C>G (p.Leu581Val)
3g.119414162C>TCA435411650ARHGAP31c.2233C>T (p.Leu745=)
c.2140C>T (p.Leu714=)
c.2173C>T (p.Leu725=)
c.1741C>T (p.Leu581=)
3g.119414163T>ACA354049915ARHGAP31c.2234T>A (p.Leu745Gln)
c.2141T>A (p.Leu714Gln)
c.2174T>A (p.Leu725Gln)
c.1742T>A (p.Leu581Gln)
3g.119414163T>CCA354049919ARHGAP31c.2234T>C (p.Leu745Pro)
c.2141T>C (p.Leu714Pro)
c.2174T>C (p.Leu725Pro)
c.1742T>C (p.Leu581Pro)
3g.119414163T>GCA354049918ARHGAP31c.2234T>G (p.Leu745Arg)
c.2141T>G (p.Leu714Arg)
c.2174T>G (p.Leu725Arg)
c.1742T>G (p.Leu581Arg)
3g.119414164G>ACA435411651ARHGAP31c.2235G>A (p.Leu745=)
c.2142G>A (p.Leu714=)
c.2175G>A (p.Leu725=)
c.1743G>A (p.Leu581=)
3g.119414164G>CCA81697478ARHGAP31c.2235G>C (p.Leu745=)
c.2142G>C (p.Leu714=)
c.2175G>C (p.Leu725=)
c.1743G>C (p.Leu581=)
 ClinVar dbSNP gnomAD v3 gnomAD v4
3g.119414164G=CA1396548577ARHGAP31c.2235G= (p.Leu745=)
c.2142G= (p.Leu714=)
c.2175G= (p.Leu725=)
c.1743G= (p.Leu581=)
3g.119414164G>TCA435411652ARHGAP31c.2235G>T (p.Leu745=)
c.2142G>T (p.Leu714=)
c.2175G>T (p.Leu725=)
c.1743G>T (p.Leu581=)
3g.119414165C>ACA354049930ARHGAP31c.2236C>A (p.His746Asn)
c.2143C>A (p.His715Asn)
c.2176C>A (p.His726Asn)
c.1744C>A (p.His582Asn)
3g.119414165C>GCA354049925ARHGAP31c.2236C>G (p.His746Asp)
c.2143C>G (p.His715Asp)
c.2176C>G (p.His726Asp)
c.1744C>G (p.His582Asp)
3g.119414165C>TCA354049928ARHGAP31c.2236C>T (p.His746Tyr)
c.2143C>T (p.His715Tyr)
c.2176C>T (p.His726Tyr)
c.1744C>T (p.His582Tyr)
3g.119414166A>CCA354049932ARHGAP31c.2237A>C (p.His746Pro)
c.2144A>C (p.His715Pro)
c.2177A>C (p.His726Pro)
c.1745A>C (p.His582Pro)
3g.119414166A>GCA354049935ARHGAP31c.2237A>G (p.His746Arg)
c.2144A>G (p.His715Arg)
c.2177A>G (p.His726Arg)
c.1745A>G (p.His582Arg)
 gnomAD v4
3g.119414166A>TCA354049937ARHGAP31c.2237A>T (p.His746Leu)
c.2144A>T (p.His715Leu)
c.2177A>T (p.His726Leu)
c.1745A>T (p.His582Leu)
3g.119414167C>ACA354049940ARHGAP31c.2238C>A (p.His746Gln)
c.2145C>A (p.His715Gln)
c.2178C>A (p.His726Gln)
c.1746C>A (p.His582Gln)
 ClinVar
3g.119414167C=CA1396548578ARHGAP31c.2238C= (p.His746=)
c.2145C= (p.His715=)
c.2178C= (p.His726=)
c.1746C= (p.His582=)
3g.119414167C>GCA354049948ARHGAP31c.2238C>G (p.His746Gln)
c.2145C>G (p.His715Gln)
c.2178C>G (p.His726Gln)
c.1746C>G (p.His582Gln)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.119414167C>TCA435411653ARHGAP31c.2238C>T (p.His746=)
c.2145C>T (p.His715=)
c.2178C>T (p.His726=)
c.1746C>T (p.His582=)
 gnomAD v4
3g.119414169delCA2524516268ARHGAP31c.2240del (p.Pro747GlnfsTer11)
c.2147del (p.Pro716GlnfsTer11)
c.2180del (p.Pro727GlnfsTer11)
c.1748del (p.Pro583GlnfsTer11)
3g.119414168C>ACA354049951ARHGAP31c.2239C>A (p.Pro747Thr)
c.2146C>A (p.Pro716Thr)
c.2179C>A (p.Pro727Thr)
c.1747C>A (p.Pro583Thr)
3g.119414168C=CA1396548579ARHGAP31c.2239C= (p.Pro747=)
c.2146C= (p.Pro716=)
c.2179C= (p.Pro727=)
c.1747C= (p.Pro583=)
3g.119414168C>GCA354049953ARHGAP31c.2239C>G (p.Pro747Ala)
c.2146C>G (p.Pro716Ala)
c.2179C>G (p.Pro727Ala)
c.1747C>G (p.Pro583Ala)
3g.119414168C>TCA354049956ARHGAP31c.2239C>T (p.Pro747Ser)
c.2146C>T (p.Pro716Ser)
c.2179C>T (p.Pro727Ser)
c.1747C>T (p.Pro583Ser)
 dbSNP
3g.119414169C>ACA354049962ARHGAP31c.2240C>A (p.Pro747Gln)
c.2147C>A (p.Pro716Gln)
c.2180C>A (p.Pro727Gln)
c.1748C>A (p.Pro583Gln)
3g.119414169C>GCA354049965ARHGAP31c.2240C>G (p.Pro747Arg)
c.2147C>G (p.Pro716Arg)
c.2180C>G (p.Pro727Arg)
c.1748C>G (p.Pro583Arg)
3g.119414169C>TCA354049970ARHGAP31c.2240C>T (p.Pro747Leu)
c.2147C>T (p.Pro716Leu)
c.2180C>T (p.Pro727Leu)
c.1748C>T (p.Pro583Leu)
3g.119414170A=CA1396548580ARHGAP31c.2241A= (p.Pro747=)
c.2148A= (p.Pro716=)
c.2181A= (p.Pro727=)
c.1749A= (p.Pro583=)
3g.119414170A>CCA2553990ARHGAP31c.2241A>C (p.Pro747=)
c.2148A>C (p.Pro716=)
c.2181A>C (p.Pro727=)
c.1749A>C (p.Pro583=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.119414170A>GCA435411654ARHGAP31c.2241A>G (p.Pro747=)
c.2148A>G (p.Pro716=)
c.2181A>G (p.Pro727=)
c.1749A>G (p.Pro583=)
3g.119414170A>TCA435411655ARHGAP31c.2241A>T (p.Pro747=)
c.2148A>T (p.Pro716=)
c.2181A>T (p.Pro727=)
c.1749A>T (p.Pro583=)
3g.119414171G>ACA354049975ARHGAP31c.2242G>A (p.Asp748Asn)
c.2149G>A (p.Asp717Asn)
c.2182G>A (p.Asp728Asn)
c.1750G>A (p.Asp584Asn)
3g.119414171G>CCA354049977ARHGAP31c.2242G>C (p.Asp748His)
c.2149G>C (p.Asp717His)
c.2182G>C (p.Asp728His)
c.1750G>C (p.Asp584His)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.119414171G=CA1396548581ARHGAP31c.2242G= (p.Asp748=)
c.2149G= (p.Asp717=)
c.2182G= (p.Asp728=)
c.1750G= (p.Asp584=)
3g.119414171G>TCA354049981ARHGAP31c.2242G>T (p.Asp748Tyr)
c.2149G>T (p.Asp717Tyr)
c.2182G>T (p.Asp728Tyr)
c.1750G>T (p.Asp584Tyr)
3g.119414172A=CA1396548582ARHGAP31c.2243A= (p.Asp748=)
c.2150A= (p.Asp717=)
c.2183A= (p.Asp728=)
c.1751A= (p.Asp584=)
3g.119414172A>CCA354049994ARHGAP31c.2243A>C (p.Asp748Ala)
c.2150A>C (p.Asp717Ala)
c.2183A>C (p.Asp728Ala)
c.1751A>C (p.Asp584Ala)
3g.119414172A>GCA354049997ARHGAP31c.2243A>G (p.Asp748Gly)
c.2150A>G (p.Asp717Gly)
c.2183A>G (p.Asp728Gly)
c.1751A>G (p.Asp584Gly)
 dbSNP gnomAD v2 gnomAD v4
3g.119414172A>TCA354049999ARHGAP31c.2243A>T (p.Asp748Val)
c.2150A>T (p.Asp717Val)
c.2183A>T (p.Asp728Val)
c.1751A>T (p.Asp584Val)
3g.119414173C>ACA354050011ARHGAP31c.2244C>A (p.Asp748Glu)
c.2151C>A (p.Asp717Glu)
c.2184C>A (p.Asp728Glu)
c.1752C>A (p.Asp584Glu)
3g.119414173C=CA1396548583ARHGAP31c.2244C= (p.Asp748=)
c.2151C= (p.Asp717=)
c.2184C= (p.Asp728=)
c.1752C= (p.Asp584=)
3g.119414173C>GCA354050018ARHGAP31c.2244C>G (p.Asp748Glu)
c.2151C>G (p.Asp717Glu)
c.2184C>G (p.Asp728Glu)
c.1752C>G (p.Asp584Glu)
 dbSNP
3g.119414173C>TCA2553991ARHGAP31c.2244C>T (p.Asp748=)
c.2151C>T (p.Asp717=)
c.2184C>T (p.Asp728=)
c.1752C>T (p.Asp584=)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.119414174C>ACA354050023ARHGAP31c.2245C>A (p.Leu749Ile)
c.2152C>A (p.Leu718Ile)
c.2185C>A (p.Leu729Ile)
c.1753C>A (p.Leu585Ile)
3g.119414174C=CA1396548584ARHGAP31c.2245C= (p.Leu749=)
c.2152C= (p.Leu718=)
c.2185C= (p.Leu729=)
c.1753C= (p.Leu585=)
3g.119414174C>GCA354050026ARHGAP31c.2245C>G (p.Leu749Val)
c.2152C>G (p.Leu718Val)
c.2185C>G (p.Leu729Val)
c.1753C>G (p.Leu585Val)
3g.119414174C>TCA2553992ARHGAP31c.2245C>T (p.Leu749Phe)
c.2152C>T (p.Leu718Phe)
c.2185C>T (p.Leu729Phe)
c.1753C>T (p.Leu585Phe)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.119414175T>ACA2553993ARHGAP31c.2246T>A (p.Leu749His)
c.2153T>A (p.Leu718His)
c.2186T>A (p.Leu729His)
c.1754T>A (p.Leu585His)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.119414175T>CCA354050040ARHGAP31c.2246T>C (p.Leu749Pro)
c.2153T>C (p.Leu718Pro)
c.2186T>C (p.Leu729Pro)
c.1754T>C (p.Leu585Pro)
3g.119414175T>GCA354050032ARHGAP31c.2246T>G (p.Leu749Arg)
c.2153T>G (p.Leu718Arg)
c.2186T>G (p.Leu729Arg)
c.1754T>G (p.Leu585Arg)
3g.119414175T=CA1396548585ARHGAP31c.2246T= (p.Leu749=)
c.2153T= (p.Leu718=)
c.2186T= (p.Leu729=)
c.1754T= (p.Leu585=)
3g.119414176C>ACA435411656ARHGAP31c.2247C>A (p.Leu749=)
c.2154C>A (p.Leu718=)
c.2187C>A (p.Leu729=)
c.1755C>A (p.Leu585=)
 dbSNP
3g.119414176C=CA1396548586ARHGAP31c.2247C= (p.Leu749=)
c.2154C= (p.Leu718=)
c.2187C= (p.Leu729=)
c.1755C= (p.Leu585=)
3g.119414176C>GCA435411657ARHGAP31c.2247C>G (p.Leu749=)
c.2154C>G (p.Leu718=)
c.2187C>G (p.Leu729=)
c.1755C>G (p.Leu585=)
 gnomAD v4
3g.119414176C>TCA435411658ARHGAP31c.2247C>T (p.Leu749=)
c.2154C>T (p.Leu718=)
c.2187C>T (p.Leu729=)
c.1755C>T (p.Leu585=)
 dbSNP gnomAD v3 gnomAD v4
3g.119414177G>ACA354050043ARHGAP31c.2248G>A (p.Ala750Thr)
c.2155G>A (p.Ala719Thr)
c.2188G>A (p.Ala730Thr)
c.1756G>A (p.Ala586Thr)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
3g.119414177G>CCA354050046ARHGAP31c.2248G>C (p.Ala750Pro)
c.2155G>C (p.Ala719Pro)
c.2188G>C (p.Ala730Pro)
c.1756G>C (p.Ala586Pro)
3g.119414177G=CA1396548587ARHGAP31c.2248G= (p.Ala750=)
c.2155G= (p.Ala719=)
c.2188G= (p.Ala730=)
c.1756G= (p.Ala586=)
3g.119414177G>TCA354050048ARHGAP31c.2248G>T (p.Ala750Ser)
c.2155G>T (p.Ala719Ser)
c.2188G>T (p.Ala730Ser)
c.1756G>T (p.Ala586Ser)
3g.119414178C>ACA354050050ARHGAP31c.2249C>A (p.Ala750Asp)
c.2156C>A (p.Ala719Asp)
c.2189C>A (p.Ala730Asp)
c.1757C>A (p.Ala586Asp)
 ClinVar dbSNP
3g.119414178C>GCA354050052ARHGAP31c.2249C>G (p.Ala750Gly)
c.2156C>G (p.Ala719Gly)
c.2189C>G (p.Ala730Gly)
c.1757C>G (p.Ala586Gly)
3g.119414178C>TCA354050055ARHGAP31c.2249C>T (p.Ala750Val)
c.2156C>T (p.Ala719Val)
c.2189C>T (p.Ala730Val)
c.1757C>T (p.Ala586Val)
3g.119414179C>ACA435411659ARHGAP31c.2250C>A (p.Ala750=)
c.2157C>A (p.Ala719=)
c.2190C>A (p.Ala730=)
c.1758C>A (p.Ala586=)
3g.119414179C>GCA435411660ARHGAP31c.2250C>G (p.Ala750=)
c.2157C>G (p.Ala719=)
c.2190C>G (p.Ala730=)
c.1758C>G (p.Ala586=)
3g.119414179C>TCA435411661ARHGAP31c.2250C>T (p.Ala750=)
c.2157C>T (p.Ala719=)
c.2190C>T (p.Ala730=)
c.1758C>T (p.Ala586=)
3g.119414180A=CA1396548588ARHGAP31c.2251A= (p.Ser751=)
c.2158A= (p.Ser720=)
c.2191A= (p.Ser731=)
c.1759A= (p.Ser587=)
3g.119414180A>CCA354050060ARHGAP31c.2251A>C (p.Ser751Arg)
c.2158A>C (p.Ser720Arg)
c.2191A>C (p.Ser731Arg)
c.1759A>C (p.Ser587Arg)
 dbSNP gnomAD v4
3g.119414180A>GCA354050061ARHGAP31c.2251A>G (p.Ser751Gly)
c.2158A>G (p.Ser720Gly)
c.2191A>G (p.Ser731Gly)
c.1759A>G (p.Ser587Gly)
3g.119414180A>TCA354050063ARHGAP31c.2251A>T (p.Ser751Cys)
c.2158A>T (p.Ser720Cys)
c.2191A>T (p.Ser731Cys)
c.1759A>T (p.Ser587Cys)
3g.119414181G>ACA354050069ARHGAP31c.2252G>A (p.Ser751Asn)
c.2159G>A (p.Ser720Asn)
c.2192G>A (p.Ser731Asn)
c.1760G>A (p.Ser587Asn)
 dbSNP gnomAD v3 gnomAD v4
3g.119414181G>CCA354050070ARHGAP31c.2252G>C (p.Ser751Thr)
c.2159G>C (p.Ser720Thr)
c.2192G>C (p.Ser731Thr)
c.1760G>C (p.Ser587Thr)
3g.119414181G=CA1396548589ARHGAP31c.2252G= (p.Ser751=)
c.2159G= (p.Ser720=)
c.2192G= (p.Ser731=)
c.1760G= (p.Ser587=)
3g.119414181G>TCA354050072ARHGAP31c.2252G>T (p.Ser751Ile)
c.2159G>T (p.Ser720Ile)
c.2192G>T (p.Ser731Ile)
c.1760G>T (p.Ser587Ile)
 dbSNP gnomAD v4
3g.119414182C>ACA354050075ARHGAP31c.2253C>A (p.Ser751Arg)
c.2160C>A (p.Ser720Arg)
c.2193C>A (p.Ser731Arg)
c.1761C>A (p.Ser587Arg)
3g.119414182C>GCA354050077ARHGAP31c.2253C>G (p.Ser751Arg)
c.2160C>G (p.Ser720Arg)
c.2193C>G (p.Ser731Arg)
c.1761C>G (p.Ser587Arg)
3g.119414182C>TCA435411662ARHGAP31c.2253C>T (p.Ser751=)
c.2160C>T (p.Ser720=)
c.2193C>T (p.Ser731=)
c.1761C>T (p.Ser587=)
3g.119414183C>ACA354050079ARHGAP31c.2254C>A (p.Leu752Met)
c.2161C>A (p.Leu721Met)
c.2194C>A (p.Leu732Met)
c.1762C>A (p.Leu588Met)
3g.119414183C=CA1396548590ARHGAP31c.2254C= (p.Leu752=)
c.2161C= (p.Leu721=)
c.2194C= (p.Leu732=)
c.1762C= (p.Leu588=)
3g.119414183C>GCA2553994ARHGAP31c.2254C>G (p.Leu752Val)
c.2161C>G (p.Leu721Val)
c.2194C>G (p.Leu732Val)
c.1762C>G (p.Leu588Val)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.119414183C>TCA435411663ARHGAP31c.2254C>T (p.Leu752=)
c.2161C>T (p.Leu721=)
c.2194C>T (p.Leu732=)
c.1762C>T (p.Leu588=)
3g.119414184T>ACA354050084ARHGAP31c.2255T>A (p.Leu752Gln)
c.2162T>A (p.Leu721Gln)
c.2195T>A (p.Leu732Gln)
c.1763T>A (p.Leu588Gln)
 gnomAD v4
3g.119414184T>CCA354050088ARHGAP31c.2255T>C (p.Leu752Pro)
c.2162T>C (p.Leu721Pro)
c.2195T>C (p.Leu732Pro)
c.1763T>C (p.Leu588Pro)
3g.119414184T>GCA354050091ARHGAP31c.2255T>G (p.Leu752Arg)
c.2162T>G (p.Leu721Arg)
c.2195T>G (p.Leu732Arg)
c.1763T>G (p.Leu588Arg)
3g.119414185G>ACA435411667ARHGAP31c.2256G>A (p.Leu752=)
c.2163G>A (p.Leu721=)
c.2196G>A (p.Leu732=)
c.1764G>A (p.Leu588=)
3g.119414185G>CCA435411668ARHGAP31c.2256G>C (p.Leu752=)
c.2163G>C (p.Leu721=)
c.2196G>C (p.Leu732=)
c.1764G>C (p.Leu588=)
3g.119414185G>TCA435411669ARHGAP31c.2256G>T (p.Leu752=)
c.2163G>T (p.Leu721=)
c.2196G>T (p.Leu732=)
c.1764G>T (p.Leu588=)
3g.119414186G>ACA354050093ARHGAP31c.2257G>A (p.Ala753Thr)
c.2164G>A (p.Ala722Thr)
c.2197G>A (p.Ala733Thr)
c.1765G>A (p.Ala589Thr)
 COSMIC
3g.119414186G>CCA81697486ARHGAP31c.2257G>C (p.Ala753Pro)
c.2164G>C (p.Ala722Pro)
c.2197G>C (p.Ala733Pro)
c.1765G>C (p.Ala589Pro)
 dbSNP gnomAD v4
3g.119414186G=CA1396548591ARHGAP31c.2257G= (p.Ala753=)
c.2164G= (p.Ala722=)
c.2197G= (p.Ala733=)
c.1765G= (p.Ala589=)
3g.119414186G>TCA354050103ARHGAP31c.2257G>T (p.Ala753Ser)
c.2164G>T (p.Ala722Ser)
c.2197G>T (p.Ala733Ser)
c.1765G>T (p.Ala589Ser)
3g.119414187C>ACA354050106ARHGAP31c.2258C>A (p.Ala753Asp)
c.2165C>A (p.Ala722Asp)
c.2198C>A (p.Ala733Asp)
c.1766C>A (p.Ala589Asp)
3g.119414187C>GCA354050111ARHGAP31c.2258C>G (p.Ala753Gly)
c.2165C>G (p.Ala722Gly)
c.2198C>G (p.Ala733Gly)
c.1766C>G (p.Ala589Gly)
3g.119414187C>TCA354050115ARHGAP31c.2258C>T (p.Ala753Val)
c.2165C>T (p.Ala722Val)
c.2198C>T (p.Ala733Val)
c.1766C>T (p.Ala589Val)
 gnomAD v4
3g.119414188T>ACA435411673ARHGAP31c.2259T>A (p.Ala753=)
c.2166T>A (p.Ala722=)
c.2199T>A (p.Ala733=)
c.1767T>A (p.Ala589=)
3g.119414188T>CCA435411671ARHGAP31c.2259T>C (p.Ala753=)
c.2166T>C (p.Ala722=)
c.2199T>C (p.Ala733=)
c.1767T>C (p.Ala589=)
 dbSNP
3g.119414188T>GCA435411672ARHGAP31c.2259T>G (p.Ala753=)
c.2166T>G (p.Ala722=)
c.2199T>G (p.Ala733=)
c.1767T>G (p.Ala589=)
 gnomAD v4
3g.119414188T=CA1396548592ARHGAP31c.2259T= (p.Ala753=)
c.2166T= (p.Ala722=)
c.2199T= (p.Ala733=)
c.1767T= (p.Ala589=)
3g.119414189C>ACA354050119ARHGAP31c.2260C>A (p.Pro754Thr)
c.2167C>A (p.Pro723Thr)
c.2200C>A (p.Pro734Thr)
c.1768C>A (p.Pro590Thr)
3g.119414189C>GCA354050120ARHGAP31c.2260C>G (p.Pro754Ala)
c.2167C>G (p.Pro723Ala)
c.2200C>G (p.Pro734Ala)
c.1768C>G (p.Pro590Ala)
3g.119414189C>TCA354050123ARHGAP31c.2260C>T (p.Pro754Ser)
c.2167C>T (p.Pro723Ser)
c.2200C>T (p.Pro734Ser)
c.1768C>T (p.Pro590Ser)
 gnomAD v4
3g.119414190C>ACA2553995ARHGAP31c.2261C>A (p.Pro754His)
c.2168C>A (p.Pro723His)
c.2201C>A (p.Pro734His)
c.1769C>A (p.Pro590His)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.119414190C=CA1396548593ARHGAP31c.2261C= (p.Pro754=)
c.2168C= (p.Pro723=)
c.2201C= (p.Pro734=)
c.1769C= (p.Pro590=)
3g.119414190C>GCA354050137ARHGAP31c.2261C>G (p.Pro754Arg)
c.2168C>G (p.Pro723Arg)
c.2201C>G (p.Pro734Arg)
c.1769C>G (p.Pro590Arg)
3g.119414190C>TCA354050131ARHGAP31c.2261C>T (p.Pro754Leu)
c.2168C>T (p.Pro723Leu)
c.2201C>T (p.Pro734Leu)
c.1769C>T (p.Pro590Leu)
 gnomAD v4
3g.119414191T>ACA435411674ARHGAP31c.2262T>A (p.Pro754=)
c.2169T>A (p.Pro723=)
c.2202T>A (p.Pro734=)
c.1770T>A (p.Pro590=)
3g.119414191T>CCA435411675ARHGAP31c.2262T>C (p.Pro754=)
c.2169T>C (p.Pro723=)
c.2202T>C (p.Pro734=)
c.1770T>C (p.Pro590=)
3g.119414191T>GCA435411676ARHGAP31c.2262T>G (p.Pro754=)
c.2169T>G (p.Pro723=)
c.2202T>G (p.Pro734=)
c.1770T>G (p.Pro590=)
3g.119414192C>ACA354050142ARHGAP31c.2263C>A (p.Leu755Met)
c.2170C>A (p.Leu724Met)
c.2203C>A (p.Leu735Met)
c.1771C>A (p.Leu591Met)
3g.119414192C>GCA354050144ARHGAP31c.2263C>G (p.Leu755Val)
c.2170C>G (p.Leu724Val)
c.2203C>G (p.Leu735Val)
c.1771C>G (p.Leu591Val)
3g.119414192C>TCA435411677ARHGAP31c.2263C>T (p.Leu755=)
c.2170C>T (p.Leu724=)
c.2203C>T (p.Leu735=)
c.1771C>T (p.Leu591=)
 COSMIC
3g.119414193T>ACA354050147ARHGAP31c.2264T>A (p.Leu755Gln)
c.2171T>A (p.Leu724Gln)
c.2204T>A (p.Leu735Gln)
c.1772T>A (p.Leu591Gln)
3g.119414193T>CCA354050152ARHGAP31c.2264T>C (p.Leu755Pro)
c.2171T>C (p.Leu724Pro)
c.2204T>C (p.Leu735Pro)
c.1772T>C (p.Leu591Pro)
3g.119414193T>GCA354050149ARHGAP31c.2264T>G (p.Leu755Arg)
c.2171T>G (p.Leu724Arg)
c.2204T>G (p.Leu735Arg)
c.1772T>G (p.Leu591Arg)
3g.119414194G>ACA435411682ARHGAP31c.2265G>A (p.Leu755=)
c.2172G>A (p.Leu724=)
c.2205G>A (p.Leu735=)
c.1773G>A (p.Leu591=)
 dbSNP gnomAD v2 gnomAD v4
3g.119414194G>CCA435411681ARHGAP31c.2265G>C (p.Leu755=)
c.2172G>C (p.Leu724=)
c.2205G>C (p.Leu735=)
c.1773G>C (p.Leu591=)
3g.119414194G=CA1396548594ARHGAP31c.2265G= (p.Leu755=)
c.2172G= (p.Leu724=)
c.2205G= (p.Leu735=)
c.1773G= (p.Leu591=)
3g.119414194G>TCA435411683ARHGAP31c.2265G>T (p.Leu755=)
c.2172G>T (p.Leu724=)
c.2205G>T (p.Leu735=)
c.1773G>T (p.Leu591=)
3g.119414195G>ACA354050155ARHGAP31c.2266G>A (p.Glu756Lys)
c.2173G>A (p.Glu725Lys)
c.2206G>A (p.Glu736Lys)
c.1774G>A (p.Glu592Lys)
3g.119414195G>CCA2553996ARHGAP31c.2266G>C (p.Glu756Gln)
c.2173G>C (p.Glu725Gln)
c.2206G>C (p.Glu736Gln)
c.1774G>C (p.Glu592Gln)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.119414195G=CA1396548595ARHGAP31c.2266G= (p.Glu756=)
c.2173G= (p.Glu725=)
c.2206G= (p.Glu736=)
c.1774G= (p.Glu592=)
3g.119414195G>TCA354050158ARHGAP31c.2266G>T (p.Glu756Ter)
c.2173G>T (p.Glu725Ter)
c.2206G>T (p.Glu736Ter)
c.1774G>T (p.Glu592Ter)
3g.119414196A>CCA354050166ARHGAP31c.2267A>C (p.Glu756Ala)
c.2174A>C (p.Glu725Ala)
c.2207A>C (p.Glu736Ala)
c.1775A>C (p.Glu592Ala)
3g.119414196A>GCA354050169ARHGAP31c.2267A>G (p.Glu756Gly)
c.2174A>G (p.Glu725Gly)
c.2207A>G (p.Glu736Gly)
c.1775A>G (p.Glu592Gly)
3g.119414196A>TCA354050175ARHGAP31c.2267A>T (p.Glu756Val)
c.2174A>T (p.Glu725Val)
c.2207A>T (p.Glu736Val)
c.1775A>T (p.Glu592Val)
3g.119414197A=CA1396548596ARHGAP31c.2268A= (p.Glu756=)
c.2175A= (p.Glu725=)
c.2208A= (p.Glu736=)
c.1776A= (p.Glu592=)
3g.119414197A>CCA354050179ARHGAP31c.2268A>C (p.Glu756Asp)
c.2175A>C (p.Glu725Asp)
c.2208A>C (p.Glu736Asp)
c.1776A>C (p.Glu592Asp)
3g.119414197A>GCA435411687ARHGAP31c.2268A>G (p.Glu756=)
c.2175A>G (p.Glu725=)
c.2208A>G (p.Glu736=)
c.1776A>G (p.Glu592=)
3g.119414197A>TCA2553997ARHGAP31c.2268A>T (p.Glu756Asp)
c.2175A>T (p.Glu725Asp)
c.2208A>T (p.Glu736Asp)
c.1776A>T (p.Glu592Asp)
 dbSNP ExAC gnomAD v2

Number of alleles fetched