Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.119414034T>ACA354049161ARHGAP31c.2105T>A (p.Leu702Ter)
c.2012T>A (p.Leu671Ter)
c.2045T>A (p.Leu682Ter)
c.1613T>A (p.Leu538Ter)
3g.119414034T>CCA354049163ARHGAP31c.2105T>C (p.Leu702Ser)
c.2012T>C (p.Leu671Ser)
c.2045T>C (p.Leu682Ser)
c.1613T>C (p.Leu538Ser)
3g.119414034T>GCA354049165ARHGAP31c.2105T>G (p.Leu702Trp)
c.2012T>G (p.Leu671Trp)
c.2045T>G (p.Leu682Trp)
c.1613T>G (p.Leu538Trp)
3g.119414035G>ACA81697392ARHGAP31c.2106G>A (p.Leu702=)
c.2013G>A (p.Leu671=)
c.2046G>A (p.Leu682=)
c.1614G>A (p.Leu538=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.119414035G>CCA354049172ARHGAP31c.2106G>C (p.Leu702Phe)
c.2013G>C (p.Leu671Phe)
c.2046G>C (p.Leu682Phe)
c.1614G>C (p.Leu538Phe)
3g.119414035G=CA1396548520ARHGAP31c.2106G= (p.Leu702=)
c.2013G= (p.Leu671=)
c.2046G= (p.Leu682=)
c.1614G= (p.Leu538=)
3g.119414035G>TCA354049169ARHGAP31c.2106G>T (p.Leu702Phe)
c.2013G>T (p.Leu671Phe)
c.2046G>T (p.Leu682Phe)
c.1614G>T (p.Leu538Phe)
3g.119414036C>ACA354049176ARHGAP31c.2107C>A (p.Pro703Thr)
c.2014C>A (p.Pro672Thr)
c.2047C>A (p.Pro683Thr)
c.1615C>A (p.Pro539Thr)
3g.119414036C>GCA354049179ARHGAP31c.2107C>G (p.Pro703Ala)
c.2014C>G (p.Pro672Ala)
c.2047C>G (p.Pro683Ala)
c.1615C>G (p.Pro539Ala)
3g.119414036C>TCA354049182ARHGAP31c.2107C>T (p.Pro703Ser)
c.2014C>T (p.Pro672Ser)
c.2047C>T (p.Pro683Ser)
c.1615C>T (p.Pro539Ser)
3g.119414037C>ACA354049187ARHGAP31c.2108C>A (p.Pro703His)
c.2015C>A (p.Pro672His)
c.2048C>A (p.Pro683His)
c.1616C>A (p.Pro539His)
3g.119414037C>GCA354049188ARHGAP31c.2108C>G (p.Pro703Arg)
c.2015C>G (p.Pro672Arg)
c.2048C>G (p.Pro683Arg)
c.1616C>G (p.Pro539Arg)
3g.119414037C>TCA354049190ARHGAP31c.2108C>T (p.Pro703Leu)
c.2015C>T (p.Pro672Leu)
c.2048C>T (p.Pro683Leu)
c.1616C>T (p.Pro539Leu)
3g.119414038T>ACA435411547ARHGAP31c.2109T>A (p.Pro703=)
c.2016T>A (p.Pro672=)
c.2049T>A (p.Pro683=)
c.1617T>A (p.Pro539=)
3g.119414038T>CCA435411548ARHGAP31c.2109T>C (p.Pro703=)
c.2016T>C (p.Pro672=)
c.2049T>C (p.Pro683=)
c.1617T>C (p.Pro539=)
 dbSNP gnomAD v2 gnomAD v4
3g.119414038T>GCA435411549ARHGAP31c.2109T>G (p.Pro703=)
c.2016T>G (p.Pro672=)
c.2049T>G (p.Pro683=)
c.1617T>G (p.Pro539=)
3g.119414038T=CA1396548521ARHGAP31c.2109T= (p.Pro703=)
c.2016T= (p.Pro672=)
c.2049T= (p.Pro683=)
c.1617T= (p.Pro539=)
3g.119414039T>ACA354049200ARHGAP31c.2110T>A (p.Cys704Ser)
c.2017T>A (p.Cys673Ser)
c.2050T>A (p.Cys684Ser)
c.1618T>A (p.Cys540Ser)
3g.119414039T>CCA354049205ARHGAP31c.2110T>C (p.Cys704Arg)
c.2017T>C (p.Cys673Arg)
c.2050T>C (p.Cys684Arg)
c.1618T>C (p.Cys540Arg)
3g.119414039T>GCA354049203ARHGAP31c.2110T>G (p.Cys704Gly)
c.2017T>G (p.Cys673Gly)
c.2050T>G (p.Cys684Gly)
c.1618T>G (p.Cys540Gly)
3g.119414040G>ACA354049209ARHGAP31c.2111G>A (p.Cys704Tyr)
c.2018G>A (p.Cys673Tyr)
c.2051G>A (p.Cys684Tyr)
c.1619G>A (p.Cys540Tyr)
 gnomAD v4
3g.119414040G>CCA354049212ARHGAP31c.2111G>C (p.Cys704Ser)
c.2018G>C (p.Cys673Ser)
c.2051G>C (p.Cys684Ser)
c.1619G>C (p.Cys540Ser)
 dbSNP gnomAD v4
3g.119414040G=CA1396548522ARHGAP31c.2111G= (p.Cys704=)
c.2018G= (p.Cys673=)
c.2051G= (p.Cys684=)
c.1619G= (p.Cys540=)
3g.119414040G>TCA354049213ARHGAP31c.2111G>T (p.Cys704Phe)
c.2018G>T (p.Cys673Phe)
c.2051G>T (p.Cys684Phe)
c.1619G>T (p.Cys540Phe)
3g.119414041T>ACA354049215ARHGAP31c.2112T>A (p.Cys704Ter)
c.2019T>A (p.Cys673Ter)
c.2052T>A (p.Cys684Ter)
c.1620T>A (p.Cys540Ter)
3g.119414041T>CCA435411552ARHGAP31c.2112T>C (p.Cys704=)
c.2019T>C (p.Cys673=)
c.2052T>C (p.Cys684=)
c.1620T>C (p.Cys540=)
3g.119414041T>GCA354049217ARHGAP31c.2112T>G (p.Cys704Trp)
c.2019T>G (p.Cys673Trp)
c.2052T>G (p.Cys684Trp)
c.1620T>G (p.Cys540Trp)
3g.119414042G>ACA354049223ARHGAP31c.2113G>A (p.Gly705Ser)
c.2020G>A (p.Gly674Ser)
c.2053G>A (p.Gly685Ser)
c.1621G>A (p.Gly541Ser)
3g.119414042G>CCA354049222ARHGAP31c.2113G>C (p.Gly705Arg)
c.2020G>C (p.Gly674Arg)
c.2053G>C (p.Gly685Arg)
c.1621G>C (p.Gly541Arg)
3g.119414042G>TCA354049219ARHGAP31c.2113G>T (p.Gly705Cys)
c.2020G>T (p.Gly674Cys)
c.2053G>T (p.Gly685Cys)
c.1621G>T (p.Gly541Cys)
3g.119414043G>ACA354049226ARHGAP31c.2114G>A (p.Gly705Asp)
c.2021G>A (p.Gly674Asp)
c.2054G>A (p.Gly685Asp)
c.1622G>A (p.Gly541Asp)
 gnomAD v4
3g.119414043G>CCA354049228ARHGAP31c.2114G>C (p.Gly705Ala)
c.2021G>C (p.Gly674Ala)
c.2054G>C (p.Gly685Ala)
c.1622G>C (p.Gly541Ala)
3g.119414043G>TCA354049232ARHGAP31c.2114G>T (p.Gly705Val)
c.2021G>T (p.Gly674Val)
c.2054G>T (p.Gly685Val)
c.1622G>T (p.Gly541Val)
3g.119414044C>ACA435411553ARHGAP31c.2115C>A (p.Gly705=)
c.2022C>A (p.Gly674=)
c.2055C>A (p.Gly685=)
c.1623C>A (p.Gly541=)
3g.119414044C>GCA435411554ARHGAP31c.2115C>G (p.Gly705=)
c.2022C>G (p.Gly674=)
c.2055C>G (p.Gly685=)
c.1623C>G (p.Gly541=)
3g.119414044C>TCA435411555ARHGAP31c.2115C>T (p.Gly705=)
c.2022C>T (p.Gly674=)
c.2055C>T (p.Gly685=)
c.1623C>T (p.Gly541=)
3g.119414045T>ACA354049236ARHGAP31c.2116T>A (p.Ser706Thr)
c.2023T>A (p.Ser675Thr)
c.2056T>A (p.Ser686Thr)
c.1624T>A (p.Ser542Thr)
3g.119414045T>CCA354049238ARHGAP31c.2116T>C (p.Ser706Pro)
c.2023T>C (p.Ser675Pro)
c.2056T>C (p.Ser686Pro)
c.1624T>C (p.Ser542Pro)
3g.119414045T>GCA354049239ARHGAP31c.2116T>G (p.Ser706Ala)
c.2023T>G (p.Ser675Ala)
c.2056T>G (p.Ser686Ala)
c.1624T>G (p.Ser542Ala)
 gnomAD v4 COSMIC
3g.119414046C>ACA354049244ARHGAP31c.2117C>A (p.Ser706Tyr)
c.2024C>A (p.Ser675Tyr)
c.2057C>A (p.Ser686Tyr)
c.1625C>A (p.Ser542Tyr)
3g.119414046C=CA1396548523ARHGAP31c.2117C= (p.Ser706=)
c.2024C= (p.Ser675=)
c.2057C= (p.Ser686=)
c.1625C= (p.Ser542=)
3g.119414046C>GCA354049248ARHGAP31c.2117C>G (p.Ser706Cys)
c.2024C>G (p.Ser675Cys)
c.2057C>G (p.Ser686Cys)
c.1625C>G (p.Ser542Cys)
3g.119414046C>TCA354049245ARHGAP31c.2117C>T (p.Ser706Phe)
c.2024C>T (p.Ser675Phe)
c.2057C>T (p.Ser686Phe)
c.1625C>T (p.Ser542Phe)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.119414047C>ACA435411557ARHGAP31c.2118C>A (p.Ser706=)
c.2025C>A (p.Ser675=)
c.2058C>A (p.Ser686=)
c.1626C>A (p.Ser542=)
3g.119414047C>GCA435411559ARHGAP31c.2118C>G (p.Ser706=)
c.2025C>G (p.Ser675=)
c.2058C>G (p.Ser686=)
c.1626C>G (p.Ser542=)
3g.119414047C>TCA435411558ARHGAP31c.2118C>T (p.Ser706=)
c.2025C>T (p.Ser675=)
c.2058C>T (p.Ser686=)
c.1626C>T (p.Ser542=)
3g.119414048T>ACA354049250ARHGAP31c.2119T>A (p.Phe707Ile)
c.2026T>A (p.Phe676Ile)
c.2059T>A (p.Phe687Ile)
c.1627T>A (p.Phe543Ile)
3g.119414048T>CCA2553971ARHGAP31c.2119T>C (p.Phe707Leu)
c.2026T>C (p.Phe676Leu)
c.2059T>C (p.Phe687Leu)
c.1627T>C (p.Phe543Leu)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.119414048T>GCA354049253ARHGAP31c.2119T>G (p.Phe707Val)
c.2026T>G (p.Phe676Val)
c.2059T>G (p.Phe687Val)
c.1627T>G (p.Phe543Val)
3g.119414048T=CA1396548524ARHGAP31c.2119T= (p.Phe707=)
c.2026T= (p.Phe676=)
c.2059T= (p.Phe687=)
c.1627T= (p.Phe543=)
3g.119414049T>ACA354049255ARHGAP31c.2120T>A (p.Phe707Tyr)
c.2027T>A (p.Phe676Tyr)
c.2060T>A (p.Phe687Tyr)
c.1628T>A (p.Phe543Tyr)
3g.119414049T>CCA354049257ARHGAP31c.2120T>C (p.Phe707Ser)
c.2027T>C (p.Phe676Ser)
c.2060T>C (p.Phe687Ser)
c.1628T>C (p.Phe543Ser)
3g.119414049T>GCA354049259ARHGAP31c.2120T>G (p.Phe707Cys)
c.2027T>G (p.Phe676Cys)
c.2060T>G (p.Phe687Cys)
c.1628T>G (p.Phe543Cys)
3g.119414050C>ACA354049266ARHGAP31c.2121C>A (p.Phe707Leu)
c.2028C>A (p.Phe676Leu)
c.2061C>A (p.Phe687Leu)
c.1629C>A (p.Phe543Leu)
3g.119414050C>GCA354049268ARHGAP31c.2121C>G (p.Phe707Leu)
c.2028C>G (p.Phe676Leu)
c.2061C>G (p.Phe687Leu)
c.1629C>G (p.Phe543Leu)
3g.119414050C>TCA435411563ARHGAP31c.2121C>T (p.Phe707=)
c.2028C>T (p.Phe676=)
c.2061C>T (p.Phe687=)
c.1629C>T (p.Phe543=)
3g.119414051C>ACA354049274ARHGAP31c.2122C>A (p.Pro708Thr)
c.2029C>A (p.Pro677Thr)
c.2062C>A (p.Pro688Thr)
c.1630C>A (p.Pro544Thr)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.119414051C=CA1396548525ARHGAP31c.2122C= (p.Pro708=)
c.2029C= (p.Pro677=)
c.2062C= (p.Pro688=)
c.1630C= (p.Pro544=)
3g.119414051C>GCA354049276ARHGAP31c.2122C>G (p.Pro708Ala)
c.2029C>G (p.Pro677Ala)
c.2062C>G (p.Pro688Ala)
c.1630C>G (p.Pro544Ala)
3g.119414051C>TCA354049279ARHGAP31c.2122C>T (p.Pro708Ser)
c.2029C>T (p.Pro677Ser)
c.2062C>T (p.Pro688Ser)
c.1630C>T (p.Pro544Ser)
3g.119414052C>ACA354049282ARHGAP31c.2123C>A (p.Pro708His)
c.2030C>A (p.Pro677His)
c.2063C>A (p.Pro688His)
c.1631C>A (p.Pro544His)
3g.119414052C>GCA354049288ARHGAP31c.2123C>G (p.Pro708Arg)
c.2030C>G (p.Pro677Arg)
c.2063C>G (p.Pro688Arg)
c.1631C>G (p.Pro544Arg)
3g.119414052C>TCA354049284ARHGAP31c.2123C>T (p.Pro708Leu)
c.2030C>T (p.Pro677Leu)
c.2063C>T (p.Pro688Leu)
c.1631C>T (p.Pro544Leu)
3g.119414053T>ACA435411564ARHGAP31c.2124T>A (p.Pro708=)
c.2031T>A (p.Pro677=)
c.2064T>A (p.Pro688=)
c.1632T>A (p.Pro544=)
3g.119414053T>CCA435411565ARHGAP31c.2124T>C (p.Pro708=)
c.2031T>C (p.Pro677=)
c.2064T>C (p.Pro688=)
c.1632T>C (p.Pro544=)
 gnomAD v4
3g.119414053T>GCA435411566ARHGAP31c.2124T>G (p.Pro708=)
c.2031T>G (p.Pro677=)
c.2064T>G (p.Pro688=)
c.1632T>G (p.Pro544=)
3g.119414054G>ACA2553972ARHGAP31c.2125G>A (p.Ala709Thr)
c.2032G>A (p.Ala678Thr)
c.2065G>A (p.Ala689Thr)
c.1633G>A (p.Ala545Thr)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.119414054G>CCA354049293ARHGAP31c.2125G>C (p.Ala709Pro)
c.2032G>C (p.Ala678Pro)
c.2065G>C (p.Ala689Pro)
c.1633G>C (p.Ala545Pro)
3g.119414054G=CA1396548526ARHGAP31c.2125G= (p.Ala709=)
c.2032G= (p.Ala678=)
c.2065G= (p.Ala689=)
c.1633G= (p.Ala545=)
3g.119414054G>TCA354049296ARHGAP31c.2125G>T (p.Ala709Ser)
c.2032G>T (p.Ala678Ser)
c.2065G>T (p.Ala689Ser)
c.1633G>T (p.Ala545Ser)
3g.119414055C>ACA354049301ARHGAP31c.2126C>A (p.Ala709Asp)
c.2033C>A (p.Ala678Asp)
c.2066C>A (p.Ala689Asp)
c.1634C>A (p.Ala545Asp)
3g.119414055C>GCA354049304ARHGAP31c.2126C>G (p.Ala709Gly)
c.2033C>G (p.Ala678Gly)
c.2066C>G (p.Ala689Gly)
c.1634C>G (p.Ala545Gly)
3g.119414055C>TCA354049305ARHGAP31c.2126C>T (p.Ala709Val)
c.2033C>T (p.Ala678Val)
c.2066C>T (p.Ala689Val)
c.1634C>T (p.Ala545Val)
3g.119414056T>ACA435411569ARHGAP31c.2127T>A (p.Ala709=)
c.2034T>A (p.Ala678=)
c.2067T>A (p.Ala689=)
c.1635T>A (p.Ala545=)
3g.119414056T>CCA435411570ARHGAP31c.2127T>C (p.Ala709=)
c.2034T>C (p.Ala678=)
c.2067T>C (p.Ala689=)
c.1635T>C (p.Ala545=)
 gnomAD v4
3g.119414056T>GCA435411568ARHGAP31c.2127T>G (p.Ala709=)
c.2034T>G (p.Ala678=)
c.2067T>G (p.Ala689=)
c.1635T>G (p.Ala545=)
3g.119414057C>ACA354049313ARHGAP31c.2128C>A (p.Pro710Thr)
c.2035C>A (p.Pro679Thr)
c.2068C>A (p.Pro690Thr)
c.1636C>A (p.Pro546Thr)
3g.119414057C>GCA354049312ARHGAP31c.2128C>G (p.Pro710Ala)
c.2035C>G (p.Pro679Ala)
c.2068C>G (p.Pro690Ala)
c.1636C>G (p.Pro546Ala)
3g.119414057C>TCA354049309ARHGAP31c.2128C>T (p.Pro710Ser)
c.2035C>T (p.Pro679Ser)
c.2068C>T (p.Pro690Ser)
c.1636C>T (p.Pro546Ser)
 COSMIC
3g.119414058C>ACA354049314ARHGAP31c.2129C>A (p.Pro710Gln)
c.2036C>A (p.Pro679Gln)
c.2069C>A (p.Pro690Gln)
c.1637C>A (p.Pro546Gln)
3g.119414058C>GCA354049315ARHGAP31c.2129C>G (p.Pro710Arg)
c.2036C>G (p.Pro679Arg)
c.2069C>G (p.Pro690Arg)
c.1637C>G (p.Pro546Arg)
3g.119414058C>TCA354049317ARHGAP31c.2129C>T (p.Pro710Leu)
c.2036C>T (p.Pro679Leu)
c.2069C>T (p.Pro690Leu)
c.1637C>T (p.Pro546Leu)
3g.119414059A=CA1396548527ARHGAP31c.2130A= (p.Pro710=)
c.2037A= (p.Pro679=)
c.2070A= (p.Pro690=)
c.1638A= (p.Pro546=)
3g.119414059A>CCA435411571ARHGAP31c.2130A>C (p.Pro710=)
c.2037A>C (p.Pro679=)
c.2070A>C (p.Pro690=)
c.1638A>C (p.Pro546=)
 dbSNP
3g.119414059A>GCA435411573ARHGAP31c.2130A>G (p.Pro710=)
c.2037A>G (p.Pro679=)
c.2070A>G (p.Pro690=)
c.1638A>G (p.Pro546=)
 dbSNP gnomAD v3 gnomAD v4
3g.119414059A>TCA435411575ARHGAP31c.2130A>T (p.Pro710=)
c.2037A>T (p.Pro679=)
c.2070A>T (p.Pro690=)
c.1638A>T (p.Pro546=)
3g.119414060G>ACA354049319ARHGAP31c.2131G>A (p.Val711Ile)
c.2038G>A (p.Val680Ile)
c.2071G>A (p.Val691Ile)
c.1639G>A (p.Val547Ile)
3g.119414060G>CCA354049321ARHGAP31c.2131G>C (p.Val711Leu)
c.2038G>C (p.Val680Leu)
c.2071G>C (p.Val691Leu)
c.1639G>C (p.Val547Leu)
3g.119414060G>TCA354049325ARHGAP31c.2131G>T (p.Val711Phe)
c.2038G>T (p.Val680Phe)
c.2071G>T (p.Val691Phe)
c.1639G>T (p.Val547Phe)
3g.119414061T>ACA354049327ARHGAP31c.2132T>A (p.Val711Asp)
c.2039T>A (p.Val680Asp)
c.2072T>A (p.Val691Asp)
c.1640T>A (p.Val547Asp)
3g.119414061T>CCA354049332ARHGAP31c.2132T>C (p.Val711Ala)
c.2039T>C (p.Val680Ala)
c.2072T>C (p.Val691Ala)
c.1640T>C (p.Val547Ala)
3g.119414061T>GCA354049329ARHGAP31c.2132T>G (p.Val711Gly)
c.2039T>G (p.Val680Gly)
c.2072T>G (p.Val691Gly)
c.1640T>G (p.Val547Gly)
3g.119414061_119414067delinsTCTCCACCA1396548528ARHGAP31c.2132_2138delinsTCTCCAC (p.Val711=)
c.2039_2045delinsTCTCCAC (p.Val680=)
c.2072_2078delinsTCTCCAC (p.Val691=)
c.1640_1646delinsTCTCCAC (p.Val547=)
3g.119414062C>ACA435411577ARHGAP31c.2133C>A (p.Val711=)
c.2040C>A (p.Val680=)
c.2073C>A (p.Val691=)
c.1641C>A (p.Val547=)
3g.119414062C>GCA435411578ARHGAP31c.2133C>G (p.Val711=)
c.2040C>G (p.Val680=)
c.2073C>G (p.Val691=)
c.1641C>G (p.Val547=)
3g.119414062C>TCA435411579ARHGAP31c.2133C>T (p.Val711=)
c.2040C>T (p.Val680=)
c.2073C>T (p.Val691=)
c.1641C>T (p.Val547=)
3g.119414063_119414068delCA2553973ARHGAP31c.2134_2139del (p.Ser712_Thr713del)
c.2041_2046del (p.Ser681_Thr682del)
c.2074_2079del (p.Ser692_Thr693del)
c.1642_1647del (p.Ser548_Thr549del)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.119414063T>ACA354049344ARHGAP31c.2134T>A (p.Ser712Thr)
c.2041T>A (p.Ser681Thr)
c.2074T>A (p.Ser692Thr)
c.1642T>A (p.Ser548Thr)
3g.119414063T>CCA354049346ARHGAP31c.2134T>C (p.Ser712Pro)
c.2041T>C (p.Ser681Pro)
c.2074T>C (p.Ser692Pro)
c.1642T>C (p.Ser548Pro)
 dbSNP gnomAD v2 gnomAD v4
3g.119414063T>GCA354049348ARHGAP31c.2134T>G (p.Ser712Ala)
c.2041T>G (p.Ser681Ala)
c.2074T>G (p.Ser692Ala)
c.1642T>G (p.Ser548Ala)
3g.119414063T=CA1396548529ARHGAP31c.2134T= (p.Ser712=)
c.2041T= (p.Ser681=)
c.2074T= (p.Ser692=)
c.1642T= (p.Ser548=)
3g.119414064C>ACA354049352ARHGAP31c.2135C>A (p.Ser712Tyr)
c.2042C>A (p.Ser681Tyr)
c.2075C>A (p.Ser692Tyr)
c.1643C>A (p.Ser548Tyr)
3g.119414064C=CA1396548530ARHGAP31c.2135C= (p.Ser712=)
c.2042C= (p.Ser681=)
c.2075C= (p.Ser692=)
c.1643C= (p.Ser548=)
3g.119414064C>GCA354049355ARHGAP31c.2135C>G (p.Ser712Cys)
c.2042C>G (p.Ser681Cys)
c.2075C>G (p.Ser692Cys)
c.1643C>G (p.Ser548Cys)
 gnomAD v4
3g.119414064C>TCA81697411ARHGAP31c.2135C>T (p.Ser712Phe)
c.2042C>T (p.Ser681Phe)
c.2075C>T (p.Ser692Phe)
c.1643C>T (p.Ser548Phe)
 dbSNP gnomAD v2 gnomAD v4
3g.119414065C>ACA435411583ARHGAP31c.2136C>A (p.Ser712=)
c.2043C>A (p.Ser681=)
c.2076C>A (p.Ser692=)
c.1644C>A (p.Ser548=)
3g.119414065C>GCA435411584ARHGAP31c.2136C>G (p.Ser712=)
c.2043C>G (p.Ser681=)
c.2076C>G (p.Ser692=)
c.1644C>G (p.Ser548=)
3g.119414065C>TCA435411585ARHGAP31c.2136C>T (p.Ser712=)
c.2043C>T (p.Ser681=)
c.2076C>T (p.Ser692=)
c.1644C>T (p.Ser548=)
3g.119414066A=CA1396548531ARHGAP31c.2137A= (p.Thr713=)
c.2044A= (p.Thr682=)
c.2077A= (p.Thr693=)
c.1645A= (p.Thr549=)
3g.119414066A>CCA354049359ARHGAP31c.2137A>C (p.Thr713Pro)
c.2044A>C (p.Thr682Pro)
c.2077A>C (p.Thr693Pro)
c.1645A>C (p.Thr549Pro)
 dbSNP
3g.119414066A>GCA354049361ARHGAP31c.2137A>G (p.Thr713Ala)
c.2044A>G (p.Thr682Ala)
c.2077A>G (p.Thr693Ala)
c.1645A>G (p.Thr549Ala)
 dbSNP
3g.119414066A>TCA354049368ARHGAP31c.2137A>T (p.Thr713Ser)
c.2044A>T (p.Thr682Ser)
c.2077A>T (p.Thr693Ser)
c.1645A>T (p.Thr549Ser)
3g.119414067C>ACA354049373ARHGAP31c.2138C>A (p.Thr713Asn)
c.2045C>A (p.Thr682Asn)
c.2078C>A (p.Thr693Asn)
c.1646C>A (p.Thr549Asn)
 dbSNP gnomAD v3 gnomAD v4
3g.119414067C=CA1396548532ARHGAP31c.2138C= (p.Thr713=)
c.2045C= (p.Thr682=)
c.2078C= (p.Thr693=)
c.1646C= (p.Thr549=)
3g.119414067C>GCA354049379ARHGAP31c.2138C>G (p.Thr713Ser)
c.2045C>G (p.Thr682Ser)
c.2078C>G (p.Thr693Ser)
c.1646C>G (p.Thr549Ser)
3g.119414067C>TCA354049376ARHGAP31c.2138C>T (p.Thr713Ile)
c.2045C>T (p.Thr682Ile)
c.2078C>T (p.Thr693Ile)
c.1646C>T (p.Thr549Ile)
3g.119414068C>ACA435411587ARHGAP31c.2139C>A (p.Thr713=)
c.2046C>A (p.Thr682=)
c.2079C>A (p.Thr693=)
c.1647C>A (p.Thr549=)
3g.119414068C=CA1396548533ARHGAP31c.2139C= (p.Thr713=)
c.2046C= (p.Thr682=)
c.2079C= (p.Thr693=)
c.1647C= (p.Thr549=)
3g.119414068C>GCA435411589ARHGAP31c.2139C>G (p.Thr713=)
c.2046C>G (p.Thr682=)
c.2079C>G (p.Thr693=)
c.1647C>G (p.Thr549=)
 gnomAD v4
3g.119414068C>TCA435411588ARHGAP31c.2139C>T (p.Thr713=)
c.2046C>T (p.Thr682=)
c.2079C>T (p.Thr693=)
c.1647C>T (p.Thr549=)
 dbSNP gnomAD v3 gnomAD v4
3g.119414069C>ACA354049382ARHGAP31c.2140C>A (p.Pro714Thr)
c.2047C>A (p.Pro683Thr)
c.2080C>A (p.Pro694Thr)
c.1648C>A (p.Pro550Thr)
3g.119414069C=CA1396548534ARHGAP31c.2140C= (p.Pro714=)
c.2047C= (p.Pro683=)
c.2080C= (p.Pro694=)
c.1648C= (p.Pro550=)
3g.119414069C>GCA354049383ARHGAP31c.2140C>G (p.Pro714Ala)
c.2047C>G (p.Pro683Ala)
c.2080C>G (p.Pro694Ala)
c.1648C>G (p.Pro550Ala)
3g.119414069C>TCA2553974ARHGAP31c.2140C>T (p.Pro714Ser)
c.2047C>T (p.Pro683Ser)
c.2080C>T (p.Pro694Ser)
c.1648C>T (p.Pro550Ser)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.119414070C>ACA81697424ARHGAP31c.2141C>A (p.Pro714His)
c.2048C>A (p.Pro683His)
c.2081C>A (p.Pro694His)
c.1649C>A (p.Pro550His)
 dbSNP gnomAD v4
3g.119414070C=CA1396548535ARHGAP31c.2141C= (p.Pro714=)
c.2048C= (p.Pro683=)
c.2081C= (p.Pro694=)
c.1649C= (p.Pro550=)
3g.119414070C>GCA354049391ARHGAP31c.2141C>G (p.Pro714Arg)
c.2048C>G (p.Pro683Arg)
c.2081C>G (p.Pro694Arg)
c.1649C>G (p.Pro550Arg)
3g.119414070C>TCA354049394ARHGAP31c.2141C>T (p.Pro714Leu)
c.2048C>T (p.Pro683Leu)
c.2081C>T (p.Pro694Leu)
c.1649C>T (p.Pro550Leu)
3g.119414072_119414073delCA2839816717ARHGAP31c.2143_2144del (p.Leu715GlyfsTer5)
c.2050_2051del (p.Leu684GlyfsTer5)
c.2083_2084del (p.Leu695GlyfsTer5)
c.1651_1652del (p.Leu551GlyfsTer5)
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.119414098dupCA2840618632ARHGAP31c.2169dup (p.Asn724GlnfsTer19)
c.2076dup (p.Asn693GlnfsTer19)
c.2109dup (p.Asn704GlnfsTer19)
c.1677dup (p.Asn560GlnfsTer19)
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=)

Number of alleles fetched