Chr Mutation (hg38) CAid Gene Transcript Linkouts
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)
3g.119414077G>ACA2553977ARHGAP31c.2148G>A (p.Glu716=)
c.2055G>A (p.Glu685=)
c.2088G>A (p.Glu696=)
c.1656G>A (p.Glu552=)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.119414077G>CCA354049432ARHGAP31c.2148G>C (p.Glu716Asp)
c.2055G>C (p.Glu685Asp)
c.2088G>C (p.Glu696Asp)
c.1656G>C (p.Glu552Asp)
3g.119414077G=CA1396548539ARHGAP31c.2148G= (p.Glu716=)
c.2055G= (p.Glu685=)
c.2088G= (p.Glu696=)
c.1656G= (p.Glu552=)
3g.119414077G>TCA354049435ARHGAP31c.2148G>T (p.Glu716Asp)
c.2055G>T (p.Glu685Asp)
c.2088G>T (p.Glu696Asp)
c.1656G>T (p.Glu552Asp)
3g.119414078G>ACA354049437ARHGAP31c.2149G>A (p.Val717Met)
c.2056G>A (p.Val686Met)
c.2089G>A (p.Val697Met)
c.1657G>A (p.Val553Met)
3g.119414078G>CCA354049440ARHGAP31c.2149G>C (p.Val717Leu)
c.2056G>C (p.Val686Leu)
c.2089G>C (p.Val697Leu)
c.1657G>C (p.Val553Leu)
3g.119414078G=CA1396548540ARHGAP31c.2149G= (p.Val717=)
c.2056G= (p.Val686=)
c.2089G= (p.Val697=)
c.1657G= (p.Val553=)
3g.119414078G>TCA81697436ARHGAP31c.2149G>T (p.Val717Leu)
c.2056G>T (p.Val686Leu)
c.2089G>T (p.Val697Leu)
c.1657G>T (p.Val553Leu)
 dbSNP gnomAD v4
3g.119414079T>ACA354049444ARHGAP31c.2150T>A (p.Val717Glu)
c.2057T>A (p.Val686Glu)
c.2090T>A (p.Val697Glu)
c.1658T>A (p.Val553Glu)
3g.119414079T>CCA354049447ARHGAP31c.2150T>C (p.Val717Ala)
c.2057T>C (p.Val686Ala)
c.2090T>C (p.Val697Ala)
c.1658T>C (p.Val553Ala)
3g.119414079T>GCA354049449ARHGAP31c.2150T>G (p.Val717Gly)
c.2057T>G (p.Val686Gly)
c.2090T>G (p.Val697Gly)
c.1658T>G (p.Val553Gly)
 dbSNP
3g.119414079T=CA1396548541ARHGAP31c.2150T= (p.Val717=)
c.2057T= (p.Val686=)
c.2090T= (p.Val697=)
c.1658T= (p.Val553=)
3g.119414080G>ACA435411597ARHGAP31c.2151G>A (p.Val717=)
c.2058G>A (p.Val686=)
c.2091G>A (p.Val697=)
c.1659G>A (p.Val553=)
3g.119414080G>CCA435411598ARHGAP31c.2151G>C (p.Val717=)
c.2058G>C (p.Val686=)
c.2091G>C (p.Val697=)
c.1659G>C (p.Val553=)
3g.119414080G>TCA435411599ARHGAP31c.2151G>T (p.Val717=)
c.2058G>T (p.Val686=)
c.2091G>T (p.Val697=)
c.1659G>T (p.Val553=)
3g.119414081T>ACA354049455ARHGAP31c.2152T>A (p.Trp718Arg)
c.2059T>A (p.Trp687Arg)
c.2092T>A (p.Trp698Arg)
c.1660T>A (p.Trp554Arg)
3g.119414081T>CCA2553978ARHGAP31c.2152T>C (p.Trp718Arg)
c.2059T>C (p.Trp687Arg)
c.2092T>C (p.Trp698Arg)
c.1660T>C (p.Trp554Arg)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.119414081T>GCA2553979ARHGAP31c.2152T>G (p.Trp718Gly)
c.2059T>G (p.Trp687Gly)
c.2092T>G (p.Trp698Gly)
c.1660T>G (p.Trp554Gly)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.119414081T=CA1396548542ARHGAP31c.2152T= (p.Trp718=)
c.2059T= (p.Trp687=)
c.2092T= (p.Trp698=)
c.1660T= (p.Trp554=)
3g.119414082G>ACA354049462ARHGAP31c.2153G>A (p.Trp718Ter)
c.2060G>A (p.Trp687Ter)
c.2093G>A (p.Trp698Ter)
c.1661G>A (p.Trp554Ter)
3g.119414082G>CCA354049460ARHGAP31c.2153G>C (p.Trp718Ser)
c.2060G>C (p.Trp687Ser)
c.2093G>C (p.Trp698Ser)
c.1661G>C (p.Trp554Ser)
3g.119414082G>TCA354049465ARHGAP31c.2153G>T (p.Trp718Leu)
c.2060G>T (p.Trp687Leu)
c.2093G>T (p.Trp698Leu)
c.1661G>T (p.Trp554Leu)
3g.119414083G>ACA354049468ARHGAP31c.2154G>A (p.Trp718Ter)
c.2061G>A (p.Trp687Ter)
c.2094G>A (p.Trp698Ter)
c.1662G>A (p.Trp554Ter)
3g.119414083G>CCA354049474ARHGAP31c.2154G>C (p.Trp718Cys)
c.2061G>C (p.Trp687Cys)
c.2094G>C (p.Trp698Cys)
c.1662G>C (p.Trp554Cys)
3g.119414083G>TCA354049472ARHGAP31c.2154G>T (p.Trp718Cys)
c.2061G>T (p.Trp687Cys)
c.2094G>T (p.Trp698Cys)
c.1662G>T (p.Trp554Cys)
3g.119414084A>CCA354049477ARHGAP31c.2155A>C (p.Thr719Pro)
c.2062A>C (p.Thr688Pro)
c.2095A>C (p.Thr699Pro)
c.1663A>C (p.Thr555Pro)
3g.119414084A>GCA354049482ARHGAP31c.2155A>G (p.Thr719Ala)
c.2062A>G (p.Thr688Ala)
c.2095A>G (p.Thr699Ala)
c.1663A>G (p.Thr555Ala)
3g.119414084A>TCA354049479ARHGAP31c.2155A>T (p.Thr719Ser)
c.2062A>T (p.Thr688Ser)
c.2095A>T (p.Thr699Ser)
c.1663A>T (p.Thr555Ser)
3g.119414085C>ACA354049484ARHGAP31c.2156C>A (p.Thr719Asn)
c.2063C>A (p.Thr688Asn)
c.2096C>A (p.Thr699Asn)
c.1664C>A (p.Thr555Asn)
3g.119414085C>GCA354049486ARHGAP31c.2156C>G (p.Thr719Ser)
c.2063C>G (p.Thr688Ser)
c.2096C>G (p.Thr699Ser)
c.1664C>G (p.Thr555Ser)
3g.119414085C>TCA354049489ARHGAP31c.2156C>T (p.Thr719Ile)
c.2063C>T (p.Thr688Ile)
c.2096C>T (p.Thr699Ile)
c.1664C>T (p.Thr555Ile)
3g.119414086T>ACA435411600ARHGAP31c.2157T>A (p.Thr719=)
c.2064T>A (p.Thr688=)
c.2097T>A (p.Thr699=)
c.1665T>A (p.Thr555=)
3g.119414086T>CCA435411601ARHGAP31c.2157T>C (p.Thr719=)
c.2064T>C (p.Thr688=)
c.2097T>C (p.Thr699=)
c.1665T>C (p.Thr555=)
3g.119414086T>GCA435411602ARHGAP31c.2157T>G (p.Thr719=)
c.2064T>G (p.Thr688=)
c.2097T>G (p.Thr699=)
c.1665T>G (p.Thr555=)
3g.119414087A>CCA435411603ARHGAP31c.2158A>C (p.Arg720=)
c.2065A>C (p.Arg689=)
c.2098A>C (p.Arg700=)
c.1666A>C (p.Arg556=)
3g.119414087A>GCA354049491ARHGAP31c.2158A>G (p.Arg720Gly)
c.2065A>G (p.Arg689Gly)
c.2098A>G (p.Arg700Gly)
c.1666A>G (p.Arg556Gly)
3g.119414087A>TCA354049494ARHGAP31c.2158A>T (p.Arg720Trp)
c.2065A>T (p.Arg689Trp)
c.2098A>T (p.Arg700Trp)
c.1666A>T (p.Arg556Trp)
3g.119414088G>ACA354049497ARHGAP31c.2159G>A (p.Arg720Lys)
c.2066G>A (p.Arg689Lys)
c.2099G>A (p.Arg700Lys)
c.1667G>A (p.Arg556Lys)
3g.119414088G>CCA354049500ARHGAP31c.2159G>C (p.Arg720Thr)
c.2066G>C (p.Arg689Thr)
c.2099G>C (p.Arg700Thr)
c.1667G>C (p.Arg556Thr)
 gnomAD v4
3g.119414088G>TCA354049503ARHGAP31c.2159G>T (p.Arg720Met)
c.2066G>T (p.Arg689Met)
c.2099G>T (p.Arg700Met)
c.1667G>T (p.Arg556Met)
3g.119414089G>ACA2553980ARHGAP31c.2160G>A (p.Arg720=)
c.2067G>A (p.Arg689=)
c.2100G>A (p.Arg700=)
c.1668G>A (p.Arg556=)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.119414089G>CCA354049508ARHGAP31c.2160G>C (p.Arg720Ser)
c.2067G>C (p.Arg689Ser)
c.2100G>C (p.Arg700Ser)
c.1668G>C (p.Arg556Ser)
 gnomAD v4
3g.119414089G=CA1396548543ARHGAP31c.2160G= (p.Arg720=)
c.2067G= (p.Arg689=)
c.2100G= (p.Arg700=)
c.1668G= (p.Arg556=)
3g.119414089G>TCA354049511ARHGAP31c.2160G>T (p.Arg720Ser)
c.2067G>T (p.Arg689Ser)
c.2100G>T (p.Arg700Ser)
c.1668G>T (p.Arg556Ser)
3g.119414090G>ACA354049519ARHGAP31c.2161G>A (p.Asp721Asn)
c.2068G>A (p.Asp690Asn)
c.2101G>A (p.Asp701Asn)
c.1669G>A (p.Asp557Asn)
3g.119414090G>CCA354049516ARHGAP31c.2161G>C (p.Asp721His)
c.2068G>C (p.Asp690His)
c.2101G>C (p.Asp701His)
c.1669G>C (p.Asp557His)
3g.119414090G>TCA354049513ARHGAP31c.2161G>T (p.Asp721Tyr)
c.2068G>T (p.Asp690Tyr)
c.2101G>T (p.Asp701Tyr)
c.1669G>T (p.Asp557Tyr)
3g.119414091A>CCA354049521ARHGAP31c.2162A>C (p.Asp721Ala)
c.2069A>C (p.Asp690Ala)
c.2102A>C (p.Asp701Ala)
c.1670A>C (p.Asp557Ala)
3g.119414091A>GCA354049523ARHGAP31c.2162A>G (p.Asp721Gly)
c.2069A>G (p.Asp690Gly)
c.2102A>G (p.Asp701Gly)
c.1670A>G (p.Asp557Gly)
3g.119414091A>TCA354049526ARHGAP31c.2162A>T (p.Asp721Val)
c.2069A>T (p.Asp690Val)
c.2102A>T (p.Asp701Val)
c.1670A>T (p.Asp557Val)
3g.119414092T>ACA354049529ARHGAP31c.2163T>A (p.Asp721Glu)
c.2070T>A (p.Asp690Glu)
c.2103T>A (p.Asp701Glu)
c.1671T>A (p.Asp557Glu)
3g.119414092T>CCA435411604ARHGAP31c.2163T>C (p.Asp721=)
c.2070T>C (p.Asp690=)
c.2103T>C (p.Asp701=)
c.1671T>C (p.Asp557=)
 dbSNP
3g.119414092T>GCA354049530ARHGAP31c.2163T>G (p.Asp721Glu)
c.2070T>G (p.Asp690Glu)
c.2103T>G (p.Asp701Glu)
c.1671T>G (p.Asp557Glu)
 gnomAD v4
3g.119414092T=CA1396548544ARHGAP31c.2163T= (p.Asp721=)
c.2070T= (p.Asp690=)
c.2103T= (p.Asp701=)
c.1671T= (p.Asp557=)
3g.119414093C>ACA354049534ARHGAP31c.2164C>A (p.Pro722Thr)
c.2071C>A (p.Pro691Thr)
c.2104C>A (p.Pro702Thr)
c.1672C>A (p.Pro558Thr)
3g.119414093C=CA1396548545ARHGAP31c.2164C= (p.Pro722=)
c.2071C= (p.Pro691=)
c.2104C= (p.Pro702=)
c.1672C= (p.Pro558=)
3g.119414093C>GCA354049538ARHGAP31c.2164C>G (p.Pro722Ala)
c.2071C>G (p.Pro691Ala)
c.2104C>G (p.Pro702Ala)
c.1672C>G (p.Pro558Ala)
3g.119414093C>TCA354049539ARHGAP31c.2164C>T (p.Pro722Ser)
c.2071C>T (p.Pro691Ser)
c.2104C>T (p.Pro702Ser)
c.1672C>T (p.Pro558Ser)
 dbSNP gnomAD v3 gnomAD v4 COSMIC
3g.119414094C>ACA354049541ARHGAP31c.2165C>A (p.Pro722Gln)
c.2072C>A (p.Pro691Gln)
c.2105C>A (p.Pro702Gln)
c.1673C>A (p.Pro558Gln)
 dbSNP
3g.119414094C=CA1396548546ARHGAP31c.2165C= (p.Pro722=)
c.2072C= (p.Pro691=)
c.2105C= (p.Pro702=)
c.1673C= (p.Pro558=)
3g.119414094C>GCA354049544ARHGAP31c.2165C>G (p.Pro722Arg)
c.2072C>G (p.Pro691Arg)
c.2105C>G (p.Pro702Arg)
c.1673C>G (p.Pro558Arg)
3g.119414094C>TCA2553981ARHGAP31c.2165C>T (p.Pro722Leu)
c.2072C>T (p.Pro691Leu)
c.2105C>T (p.Pro702Leu)
c.1673C>T (p.Pro558Leu)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.119414095A>CCA435411605ARHGAP31c.2166A>C (p.Pro722=)
c.2073A>C (p.Pro691=)
c.2106A>C (p.Pro702=)
c.1674A>C (p.Pro558=)
3g.119414095A>GCA435411606ARHGAP31c.2166A>G (p.Pro722=)
c.2073A>G (p.Pro691=)
c.2106A>G (p.Pro702=)
c.1674A>G (p.Pro558=)
3g.119414095A>TCA435411607ARHGAP31c.2166A>T (p.Pro722=)
c.2073A>T (p.Pro691=)
c.2106A>T (p.Pro702=)
c.1674A>T (p.Pro558=)
3g.119414096G>ACA354049557ARHGAP31c.2167G>A (p.Ala723Thr)
c.2074G>A (p.Ala692Thr)
c.2107G>A (p.Ala703Thr)
c.1675G>A (p.Ala559Thr)
3g.119414096G>CCA354049555ARHGAP31c.2167G>C (p.Ala723Pro)
c.2074G>C (p.Ala692Pro)
c.2107G>C (p.Ala703Pro)
c.1675G>C (p.Ala559Pro)
3g.119414096G>TCA354049550ARHGAP31c.2167G>T (p.Ala723Ser)
c.2074G>T (p.Ala692Ser)
c.2107G>T (p.Ala703Ser)
c.1675G>T (p.Ala559Ser)
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)

Number of alleles fetched