Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.119414227A>CCA354050391ARHGAP31c.2298A>C (p.Gln766His)
c.2205A>C (p.Gln735His)
c.2238A>C (p.Gln746His)
c.1806A>C (p.Gln602His)
3g.119414227A>GCA435411729ARHGAP31c.2298A>G (p.Gln766=)
c.2205A>G (p.Gln735=)
c.2238A>G (p.Gln746=)
c.1806A>G (p.Gln602=)
3g.119414227A>TCA354050393ARHGAP31c.2298A>T (p.Gln766His)
c.2205A>T (p.Gln735His)
c.2238A>T (p.Gln746His)
c.1806A>T (p.Gln602His)
3g.119414228G>ACA354050398ARHGAP31c.2299G>A (p.Ala767Thr)
c.2206G>A (p.Ala736Thr)
c.2239G>A (p.Ala747Thr)
c.1807G>A (p.Ala603Thr)
 dbSNP gnomAD v4
3g.119414228G>CCA354050399ARHGAP31c.2299G>C (p.Ala767Pro)
c.2206G>C (p.Ala736Pro)
c.2239G>C (p.Ala747Pro)
c.1807G>C (p.Ala603Pro)
3g.119414228G=CA1396548608ARHGAP31c.2299G= (p.Ala767=)
c.2206G= (p.Ala736=)
c.2239G= (p.Ala747=)
c.1807G= (p.Ala603=)
3g.119414228G>TCA354050402ARHGAP31c.2299G>T (p.Ala767Ser)
c.2206G>T (p.Ala736Ser)
c.2239G>T (p.Ala747Ser)
c.1807G>T (p.Ala603Ser)
3g.119414229C>ACA354050405ARHGAP31c.2300C>A (p.Ala767Glu)
c.2207C>A (p.Ala736Glu)
c.2240C>A (p.Ala747Glu)
c.1808C>A (p.Ala603Glu)
3g.119414229C>GCA354050407ARHGAP31c.2300C>G (p.Ala767Gly)
c.2207C>G (p.Ala736Gly)
c.2240C>G (p.Ala747Gly)
c.1808C>G (p.Ala603Gly)
3g.119414229C>TCA354050408ARHGAP31c.2300C>T (p.Ala767Val)
c.2207C>T (p.Ala736Val)
c.2240C>T (p.Ala747Val)
c.1808C>T (p.Ala603Val)
3g.119414230A>CCA435411732ARHGAP31c.2301A>C (p.Ala767=)
c.2208A>C (p.Ala736=)
c.2241A>C (p.Ala747=)
c.1809A>C (p.Ala603=)
3g.119414230A>GCA435411733ARHGAP31c.2301A>G (p.Ala767=)
c.2208A>G (p.Ala736=)
c.2241A>G (p.Ala747=)
c.1809A>G (p.Ala603=)
3g.119414230A>TCA435411734ARHGAP31c.2301A>T (p.Ala767=)
c.2208A>T (p.Ala736=)
c.2241A>T (p.Ala747=)
c.1809A>T (p.Ala603=)
3g.119414231A=CA1396548609ARHGAP31c.2302A= (p.Thr768=)
c.2209A= (p.Thr737=)
c.2242A= (p.Thr748=)
c.1810A= (p.Thr604=)
3g.119414231A>CCA354050410ARHGAP31c.2302A>C (p.Thr768Pro)
c.2209A>C (p.Thr737Pro)
c.2242A>C (p.Thr748Pro)
c.1810A>C (p.Thr604Pro)
3g.119414231A>GCA354050413ARHGAP31c.2302A>G (p.Thr768Ala)
c.2209A>G (p.Thr737Ala)
c.2242A>G (p.Thr748Ala)
c.1810A>G (p.Thr604Ala)
 ClinVar dbSNP gnomAD v3 gnomAD v4
3g.119414231A>TCA354050415ARHGAP31c.2302A>T (p.Thr768Ser)
c.2209A>T (p.Thr737Ser)
c.2242A>T (p.Thr748Ser)
c.1810A>T (p.Thr604Ser)
3g.119414232C>ACA354050418ARHGAP31c.2303C>A (p.Thr768Lys)
c.2210C>A (p.Thr737Lys)
c.2243C>A (p.Thr748Lys)
c.1811C>A (p.Thr604Lys)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.119414232C=CA1396548610ARHGAP31c.2303C= (p.Thr768=)
c.2210C= (p.Thr737=)
c.2243C= (p.Thr748=)
c.1811C= (p.Thr604=)
3g.119414232C>GCA354050419ARHGAP31c.2303C>G (p.Thr768Arg)
c.2210C>G (p.Thr737Arg)
c.2243C>G (p.Thr748Arg)
c.1811C>G (p.Thr604Arg)
3g.119414232C>TCA354050421ARHGAP31c.2303C>T (p.Thr768Ile)
c.2210C>T (p.Thr737Ile)
c.2243C>T (p.Thr748Ile)
c.1811C>T (p.Thr604Ile)
3g.119414233A>CCA435411737ARHGAP31c.2304A>C (p.Thr768=)
c.2211A>C (p.Thr737=)
c.2244A>C (p.Thr748=)
c.1812A>C (p.Thr604=)
3g.119414233A>GCA435411739ARHGAP31c.2304A>G (p.Thr768=)
c.2211A>G (p.Thr737=)
c.2244A>G (p.Thr748=)
c.1812A>G (p.Thr604=)
 gnomAD v4
3g.119414233A>TCA435411740ARHGAP31c.2304A>T (p.Thr768=)
c.2211A>T (p.Thr737=)
c.2244A>T (p.Thr748=)
c.1812A>T (p.Thr604=)
3g.119414234G>ACA354050427ARHGAP31c.2305G>A (p.Val769Met)
c.2212G>A (p.Val738Met)
c.2245G>A (p.Val749Met)
c.1813G>A (p.Val605Met)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.119414234G>CCA354050430ARHGAP31c.2305G>C (p.Val769Leu)
c.2212G>C (p.Val738Leu)
c.2245G>C (p.Val749Leu)
c.1813G>C (p.Val605Leu)
3g.119414234G=CA1396548611ARHGAP31c.2305G= (p.Val769=)
c.2212G= (p.Val738=)
c.2245G= (p.Val749=)
c.1813G= (p.Val605=)
3g.119414234G>TCA354050424ARHGAP31c.2305G>T (p.Val769Leu)
c.2212G>T (p.Val738Leu)
c.2245G>T (p.Val749Leu)
c.1813G>T (p.Val605Leu)
3g.119414235T>ACA354050433ARHGAP31c.2306T>A (p.Val769Glu)
c.2213T>A (p.Val738Glu)
c.2246T>A (p.Val749Glu)
c.1814T>A (p.Val605Glu)
3g.119414235T>CCA2554002ARHGAP31c.2306T>C (p.Val769Ala)
c.2213T>C (p.Val738Ala)
c.2246T>C (p.Val749Ala)
c.1814T>C (p.Val605Ala)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.119414235T>GCA354050436ARHGAP31c.2306T>G (p.Val769Gly)
c.2213T>G (p.Val738Gly)
c.2246T>G (p.Val749Gly)
c.1814T>G (p.Val605Gly)
3g.119414235T=CA1396548612ARHGAP31c.2306T= (p.Val769=)
c.2213T= (p.Val738=)
c.2246T= (p.Val749=)
c.1814T= (p.Val605=)
3g.119414236G>ACA435411744ARHGAP31c.2307G>A (p.Val769=)
c.2214G>A (p.Val738=)
c.2247G>A (p.Val749=)
c.1815G>A (p.Val605=)
 dbSNP gnomAD v4
3g.119414236G>CCA435411743ARHGAP31c.2307G>C (p.Val769=)
c.2214G>C (p.Val738=)
c.2247G>C (p.Val749=)
c.1815G>C (p.Val605=)
 gnomAD v4
3g.119414236G=CA1396548613ARHGAP31c.2307G= (p.Val769=)
c.2214G= (p.Val738=)
c.2247G= (p.Val749=)
c.1815G= (p.Val605=)
3g.119414236G>TCA435411742ARHGAP31c.2307G>T (p.Val769=)
c.2214G>T (p.Val738=)
c.2247G>T (p.Val749=)
c.1815G>T (p.Val605=)
3g.119414237G>ACA354050437ARHGAP31c.2308G>A (p.Glu770Lys)
c.2215G>A (p.Glu739Lys)
c.2248G>A (p.Glu750Lys)
c.1816G>A (p.Glu606Lys)
3g.119414237G>CCA354050438ARHGAP31c.2308G>C (p.Glu770Gln)
c.2215G>C (p.Glu739Gln)
c.2248G>C (p.Glu750Gln)
c.1816G>C (p.Glu606Gln)
3g.119414237G>TCA354050440ARHGAP31c.2308G>T (p.Glu770Ter)
c.2215G>T (p.Glu739Ter)
c.2248G>T (p.Glu750Ter)
c.1816G>T (p.Glu606Ter)
3g.119414238A>CCA354050450ARHGAP31c.2309A>C (p.Glu770Ala)
c.2216A>C (p.Glu739Ala)
c.2249A>C (p.Glu750Ala)
c.1817A>C (p.Glu606Ala)
3g.119414238A>GCA354050442ARHGAP31c.2309A>G (p.Glu770Gly)
c.2216A>G (p.Glu739Gly)
c.2249A>G (p.Glu750Gly)
c.1817A>G (p.Glu606Gly)
3g.119414238A>TCA354050447ARHGAP31c.2309A>T (p.Glu770Val)
c.2216A>T (p.Glu739Val)
c.2249A>T (p.Glu750Val)
c.1817A>T (p.Glu606Val)
3g.119414239A>CCA354050452ARHGAP31c.2310A>C (p.Glu770Asp)
c.2217A>C (p.Glu739Asp)
c.2250A>C (p.Glu750Asp)
c.1818A>C (p.Glu606Asp)
3g.119414239A>GCA435411749ARHGAP31c.2310A>G (p.Glu770=)
c.2217A>G (p.Glu739=)
c.2250A>G (p.Glu750=)
c.1818A>G (p.Glu606=)
3g.119414239A>TCA354050456ARHGAP31c.2310A>T (p.Glu770Asp)
c.2217A>T (p.Glu739Asp)
c.2250A>T (p.Glu750Asp)
c.1818A>T (p.Glu606Asp)
3g.119414240G>ACA354050458ARHGAP31c.2311G>A (p.Val771Ile)
c.2218G>A (p.Val740Ile)
c.2251G>A (p.Val751Ile)
c.1819G>A (p.Val607Ile)
3g.119414240G>CCA354050460ARHGAP31c.2311G>C (p.Val771Leu)
c.2218G>C (p.Val740Leu)
c.2251G>C (p.Val751Leu)
c.1819G>C (p.Val607Leu)
3g.119414240G>TCA354050462ARHGAP31c.2311G>T (p.Val771Leu)
c.2218G>T (p.Val740Leu)
c.2251G>T (p.Val751Leu)
c.1819G>T (p.Val607Leu)
3g.119414241T>ACA354050466ARHGAP31c.2312T>A (p.Val771Glu)
c.2219T>A (p.Val740Glu)
c.2252T>A (p.Val751Glu)
c.1820T>A (p.Val607Glu)
3g.119414241T>CCA2554003ARHGAP31c.2312T>C (p.Val771Ala)
c.2219T>C (p.Val740Ala)
c.2252T>C (p.Val751Ala)
c.1820T>C (p.Val607Ala)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.119414241T>GCA354050469ARHGAP31c.2312T>G (p.Val771Gly)
c.2219T>G (p.Val740Gly)
c.2252T>G (p.Val751Gly)
c.1820T>G (p.Val607Gly)
3g.119414241T=CA1396548614ARHGAP31c.2312T= (p.Val771=)
c.2219T= (p.Val740=)
c.2252T= (p.Val751=)
c.1820T= (p.Val607=)
3g.119414242A=CA1396548615ARHGAP31c.2313A= (p.Val771=)
c.2220A= (p.Val740=)
c.2253A= (p.Val751=)
c.1821A= (p.Val607=)
3g.119414242A>CCA2554004ARHGAP31c.2313A>C (p.Val771=)
c.2220A>C (p.Val740=)
c.2253A>C (p.Val751=)
c.1821A>C (p.Val607=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.119414242A>GCA435411753ARHGAP31c.2313A>G (p.Val771=)
c.2220A>G (p.Val740=)
c.2253A>G (p.Val751=)
c.1821A>G (p.Val607=)
3g.119414242A>TCA435411755ARHGAP31c.2313A>T (p.Val771=)
c.2220A>T (p.Val740=)
c.2253A>T (p.Val751=)
c.1821A>T (p.Val607=)
3g.119414243G>ACA2554005ARHGAP31c.2314G>A (p.Gly772Arg)
c.2221G>A (p.Gly741Arg)
c.2254G>A (p.Gly752Arg)
c.1822G>A (p.Gly608Arg)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.119414243G>CCA354050479ARHGAP31c.2314G>C (p.Gly772Arg)
c.2221G>C (p.Gly741Arg)
c.2254G>C (p.Gly752Arg)
c.1822G>C (p.Gly608Arg)
3g.119414243G=CA1396548616ARHGAP31c.2314G= (p.Gly772=)
c.2221G= (p.Gly741=)
c.2254G= (p.Gly752=)
c.1822G= (p.Gly608=)
3g.119414243G>TCA354050482ARHGAP31c.2314G>T (p.Gly772Ter)
c.2221G>T (p.Gly741Ter)
c.2254G>T (p.Gly752Ter)
c.1822G>T (p.Gly608Ter)
3g.119414244G>ACA2554006ARHGAP31c.2315G>A (p.Gly772Glu)
c.2222G>A (p.Gly741Glu)
c.2255G>A (p.Gly752Glu)
c.1823G>A (p.Gly608Glu)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.119414244G>CCA354050492ARHGAP31c.2315G>C (p.Gly772Ala)
c.2222G>C (p.Gly741Ala)
c.2255G>C (p.Gly752Ala)
c.1823G>C (p.Gly608Ala)
3g.119414244G=CA1396548617ARHGAP31c.2315G= (p.Gly772=)
c.2222G= (p.Gly741=)
c.2255G= (p.Gly752=)
c.1823G= (p.Gly608=)
3g.119414244G>TCA354050494ARHGAP31c.2315G>T (p.Gly772Val)
c.2222G>T (p.Gly741Val)
c.2255G>T (p.Gly752Val)
c.1823G>T (p.Gly608Val)
3g.119414245A>CCA435411758ARHGAP31c.2316A>C (p.Gly772=)
c.2223A>C (p.Gly741=)
c.2256A>C (p.Gly752=)
c.1824A>C (p.Gly608=)
 gnomAD v4
3g.119414245A>GCA435411759ARHGAP31c.2316A>G (p.Gly772=)
c.2223A>G (p.Gly741=)
c.2256A>G (p.Gly752=)
c.1824A>G (p.Gly608=)
3g.119414245A>TCA435411761ARHGAP31c.2316A>T (p.Gly772=)
c.2223A>T (p.Gly741=)
c.2256A>T (p.Gly752=)
c.1824A>T (p.Gly608=)
3g.119414246G>ACA354050498ARHGAP31c.2317G>A (p.Gly773Ser)
c.2224G>A (p.Gly742Ser)
c.2257G>A (p.Gly753Ser)
c.1825G>A (p.Gly609Ser)
3g.119414246G>CCA354050499ARHGAP31c.2317G>C (p.Gly773Arg)
c.2224G>C (p.Gly742Arg)
c.2257G>C (p.Gly753Arg)
c.1825G>C (p.Gly609Arg)
3g.119414246G>TCA354050505ARHGAP31c.2317G>T (p.Gly773Cys)
c.2224G>T (p.Gly742Cys)
c.2257G>T (p.Gly753Cys)
c.1825G>T (p.Gly609Cys)
3g.119414247G>ACA354050512ARHGAP31c.2318G>A (p.Gly773Asp)
c.2225G>A (p.Gly742Asp)
c.2258G>A (p.Gly753Asp)
c.1826G>A (p.Gly609Asp)
 gnomAD v4
3g.119414247G>CCA354050511ARHGAP31c.2318G>C (p.Gly773Ala)
c.2225G>C (p.Gly742Ala)
c.2258G>C (p.Gly753Ala)
c.1826G>C (p.Gly609Ala)
3g.119414247G=CA1396548618ARHGAP31c.2318G= (p.Gly773=)
c.2225G= (p.Gly742=)
c.2258G= (p.Gly753=)
c.1826G= (p.Gly609=)
3g.119414247G>TCA2554007ARHGAP31c.2318G>T (p.Gly773Val)
c.2225G>T (p.Gly742Val)
c.2258G>T (p.Gly753Val)
c.1826G>T (p.Gly609Val)
 dbSNP ExAC gnomAD v2
3g.119414248C>ACA435411767ARHGAP31c.2319C>A (p.Gly773=)
c.2226C>A (p.Gly742=)
c.2259C>A (p.Gly753=)
c.1827C>A (p.Gly609=)
3g.119414248C>GCA435411765ARHGAP31c.2319C>G (p.Gly773=)
c.2226C>G (p.Gly742=)
c.2259C>G (p.Gly753=)
c.1827C>G (p.Gly609=)
3g.119414248C>TCA435411766ARHGAP31c.2319C>T (p.Gly773=)
c.2226C>T (p.Gly742=)
c.2259C>T (p.Gly753=)
c.1827C>T (p.Gly609=)
3g.119414249C>ACA354050513ARHGAP31c.2320C>A (p.Pro774Thr)
c.2227C>A (p.Pro743Thr)
c.2260C>A (p.Pro754Thr)
c.1828C>A (p.Pro610Thr)
3g.119414249C>GCA354050518ARHGAP31c.2320C>G (p.Pro774Ala)
c.2227C>G (p.Pro743Ala)
c.2260C>G (p.Pro754Ala)
c.1828C>G (p.Pro610Ala)
3g.119414249C>TCA354050515ARHGAP31c.2320C>T (p.Pro774Ser)
c.2227C>T (p.Pro743Ser)
c.2260C>T (p.Pro754Ser)
c.1828C>T (p.Pro610Ser)
3g.119414250C>ACA354050521ARHGAP31c.2321C>A (p.Pro774Gln)
c.2228C>A (p.Pro743Gln)
c.2261C>A (p.Pro754Gln)
c.1829C>A (p.Pro610Gln)
3g.119414250C>GCA354050531ARHGAP31c.2321C>G (p.Pro774Arg)
c.2228C>G (p.Pro743Arg)
c.2261C>G (p.Pro754Arg)
c.1829C>G (p.Pro610Arg)
3g.119414250C>TCA354050528ARHGAP31c.2321C>T (p.Pro774Leu)
c.2228C>T (p.Pro743Leu)
c.2261C>T (p.Pro754Leu)
c.1829C>T (p.Pro610Leu)
3g.119414251A=CA1396548619ARHGAP31c.2322A= (p.Pro774=)
c.2229A= (p.Pro743=)
c.2262A= (p.Pro754=)
c.1830A= (p.Pro610=)
3g.119414251A>CCA435411769ARHGAP31c.2322A>C (p.Pro774=)
c.2229A>C (p.Pro743=)
c.2262A>C (p.Pro754=)
c.1830A>C (p.Pro610=)
3g.119414251A>GCA81697519ARHGAP31c.2322A>G (p.Pro774=)
c.2229A>G (p.Pro743=)
c.2262A>G (p.Pro754=)
c.1830A>G (p.Pro610=)
 dbSNP gnomAD v2 gnomAD v4
3g.119414251A>TCA435411770ARHGAP31c.2322A>T (p.Pro774=)
c.2229A>T (p.Pro743=)
c.2262A>T (p.Pro754=)
c.1830A>T (p.Pro610=)
3g.119414252G>ACA2554008ARHGAP31c.2323G>A (p.Gly775Ser)
c.2230G>A (p.Gly744Ser)
c.2263G>A (p.Gly755Ser)
c.1831G>A (p.Gly611Ser)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.119414252G>CCA354050535ARHGAP31c.2323G>C (p.Gly775Arg)
c.2230G>C (p.Gly744Arg)
c.2263G>C (p.Gly755Arg)
c.1831G>C (p.Gly611Arg)
3g.119414252G=CA1396548620ARHGAP31c.2323G= (p.Gly775=)
c.2230G= (p.Gly744=)
c.2263G= (p.Gly755=)
c.1831G= (p.Gly611=)
3g.119414252G>TCA354050538ARHGAP31c.2323G>T (p.Gly775Cys)
c.2230G>T (p.Gly744Cys)
c.2263G>T (p.Gly755Cys)
c.1831G>T (p.Gly611Cys)
3g.119414253G>ACA354050542ARHGAP31c.2324G>A (p.Gly775Asp)
c.2231G>A (p.Gly744Asp)
c.2264G>A (p.Gly755Asp)
c.1832G>A (p.Gly611Asp)
3g.119414253G>CCA354050545ARHGAP31c.2324G>C (p.Gly775Ala)
c.2231G>C (p.Gly744Ala)
c.2264G>C (p.Gly755Ala)
c.1832G>C (p.Gly611Ala)
3g.119414253G>TCA354050547ARHGAP31c.2324G>T (p.Gly775Val)
c.2231G>T (p.Gly744Val)
c.2264G>T (p.Gly755Val)
c.1832G>T (p.Gly611Val)
3g.119414254C>ACA435411773ARHGAP31c.2325C>A (p.Gly775=)
c.2232C>A (p.Gly744=)
c.2265C>A (p.Gly755=)
c.1833C>A (p.Gly611=)
3g.119414254C>GCA435411774ARHGAP31c.2325C>G (p.Gly775=)
c.2232C>G (p.Gly744=)
c.2265C>G (p.Gly755=)
c.1833C>G (p.Gly611=)
 dbSNP
3g.119414254C>TCA435411775ARHGAP31c.2325C>T (p.Gly775=)
c.2232C>T (p.Gly744=)
c.2265C>T (p.Gly755=)
c.1833C>T (p.Gly611=)
 gnomAD v4
3g.119414255A>CCA354050550ARHGAP31c.2326A>C (p.Asn776His)
c.2233A>C (p.Asn745His)
c.2266A>C (p.Asn756His)
c.1834A>C (p.Asn612His)
 gnomAD v4
3g.119414255A>GCA354050552ARHGAP31c.2326A>G (p.Asn776Asp)
c.2233A>G (p.Asn745Asp)
c.2266A>G (p.Asn756Asp)
c.1834A>G (p.Asn612Asp)
3g.119414255A>TCA354050556ARHGAP31c.2326A>T (p.Asn776Tyr)
c.2233A>T (p.Asn745Tyr)
c.2266A>T (p.Asn756Tyr)
c.1834A>T (p.Asn612Tyr)
3g.119414256A>CCA354050558ARHGAP31c.2327A>C (p.Asn776Thr)
c.2234A>C (p.Asn745Thr)
c.2267A>C (p.Asn756Thr)
c.1835A>C (p.Asn612Thr)
 COSMIC
3g.119414256A>GCA354050560ARHGAP31c.2327A>G (p.Asn776Ser)
c.2234A>G (p.Asn745Ser)
c.2267A>G (p.Asn756Ser)
c.1835A>G (p.Asn612Ser)
3g.119414256A>TCA354050565ARHGAP31c.2327A>T (p.Asn776Ile)
c.2234A>T (p.Asn745Ile)
c.2267A>T (p.Asn756Ile)
c.1835A>T (p.Asn612Ile)
3g.119414257T>ACA354050573ARHGAP31c.2328T>A (p.Asn776Lys)
c.2235T>A (p.Asn745Lys)
c.2268T>A (p.Asn756Lys)
c.1836T>A (p.Asn612Lys)
3g.119414257T>CCA435411778ARHGAP31c.2328T>C (p.Asn776=)
c.2235T>C (p.Asn745=)
c.2268T>C (p.Asn756=)
c.1836T>C (p.Asn612=)
 COSMIC
3g.119414257T>GCA354050570ARHGAP31c.2328T>G (p.Asn776Lys)
c.2235T>G (p.Asn745Lys)
c.2268T>G (p.Asn756Lys)
c.1836T>G (p.Asn612Lys)
3g.119414258C>ACA354050578ARHGAP31c.2329C>A (p.Leu777Met)
c.2236C>A (p.Leu746Met)
c.2269C>A (p.Leu757Met)
c.1837C>A (p.Leu613Met)
3g.119414258C>GCA354050581ARHGAP31c.2329C>G (p.Leu777Val)
c.2236C>G (p.Leu746Val)
c.2269C>G (p.Leu757Val)
c.1837C>G (p.Leu613Val)
3g.119414258C>TCA435411782ARHGAP31c.2329C>T (p.Leu777=)
c.2236C>T (p.Leu746=)
c.2269C>T (p.Leu757=)
c.1837C>T (p.Leu613=)
 gnomAD v4
3g.119414259T>ACA354050584ARHGAP31c.2330T>A (p.Leu777Gln)
c.2237T>A (p.Leu746Gln)
c.2270T>A (p.Leu757Gln)
c.1838T>A (p.Leu613Gln)
3g.119414259T>CCA2554009ARHGAP31c.2330T>C (p.Leu777Pro)
c.2237T>C (p.Leu746Pro)
c.2270T>C (p.Leu757Pro)
c.1838T>C (p.Leu613Pro)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.119414259T>GCA354050587ARHGAP31c.2330T>G (p.Leu777Arg)
c.2237T>G (p.Leu746Arg)
c.2270T>G (p.Leu757Arg)
c.1838T>G (p.Leu613Arg)
3g.119414259T=CA1396548621ARHGAP31c.2330T= (p.Leu777=)
c.2237T= (p.Leu746=)
c.2270T= (p.Leu757=)
c.1838T= (p.Leu613=)
3g.119414260G>ACA435411786ARHGAP31c.2331G>A (p.Leu777=)
c.2238G>A (p.Leu746=)
c.2271G>A (p.Leu757=)
c.1839G>A (p.Leu613=)
 gnomAD v4
3g.119414260G>CCA435411787ARHGAP31c.2331G>C (p.Leu777=)
c.2238G>C (p.Leu746=)
c.2271G>C (p.Leu757=)
c.1839G>C (p.Leu613=)
3g.119414260G>TCA435411788ARHGAP31c.2331G>T (p.Leu777=)
c.2238G>T (p.Leu746=)
c.2271G>T (p.Leu757=)
c.1839G>T (p.Leu613=)
3g.119414261T>ACA354050592ARHGAP31c.2332T>A (p.Ser778Thr)
c.2239T>A (p.Ser747Thr)
c.2272T>A (p.Ser758Thr)
c.1840T>A (p.Ser614Thr)
3g.119414261T>CCA354050595ARHGAP31c.2332T>C (p.Ser778Pro)
c.2239T>C (p.Ser747Pro)
c.2272T>C (p.Ser758Pro)
c.1840T>C (p.Ser614Pro)
3g.119414261T>GCA354050597ARHGAP31c.2332T>G (p.Ser778Ala)
c.2239T>G (p.Ser747Ala)
c.2272T>G (p.Ser758Ala)
c.1840T>G (p.Ser614Ala)
3g.119414261_119414264delinsTCTCCA1396548622ARHGAP31c.2332_2335delinsTCTC (p.Ser778=)
c.2239_2242delinsTCTC (p.Ser747=)
c.2272_2275delinsTCTC (p.Ser758=)
c.1840_1843delinsTCTC (p.Ser614=)
3g.119414262C>ACA354050601ARHGAP31c.2333C>A (p.Ser778Tyr)
c.2240C>A (p.Ser747Tyr)
c.2273C>A (p.Ser758Tyr)
c.1841C>A (p.Ser614Tyr)
3g.119414262C>GCA354050604ARHGAP31c.2333C>G (p.Ser778Cys)
c.2240C>G (p.Ser747Cys)
c.2273C>G (p.Ser758Cys)
c.1841C>G (p.Ser614Cys)
 gnomAD v4
3g.119414262C>TCA354050607ARHGAP31c.2333C>T (p.Ser778Phe)
c.2240C>T (p.Ser747Phe)
c.2273C>T (p.Ser758Phe)
c.1841C>T (p.Ser614Phe)
3g.119414266_119414268delCA897779913ARHGAP31c.2337_2339del (p.Pro780del)
c.2244_2246del (p.Pro749del)
c.2277_2279del (p.Pro760del)
c.1845_1847del (p.Pro616del)
 dbSNP
3g.119414263T>ACA435411792ARHGAP31c.2334T>A (p.Ser778=)
c.2241T>A (p.Ser747=)
c.2274T>A (p.Ser758=)
c.1842T>A (p.Ser614=)
 dbSNP gnomAD v3 gnomAD v4
3g.119414263T>CCA435411793ARHGAP31c.2334T>C (p.Ser778=)
c.2241T>C (p.Ser747=)
c.2274T>C (p.Ser758=)
c.1842T>C (p.Ser614=)
3g.119414263T>GCA435411794ARHGAP31c.2334T>G (p.Ser778=)
c.2241T>G (p.Ser747=)
c.2274T>G (p.Ser758=)
c.1842T>G (p.Ser614=)
3g.119414263T=CA1396548623ARHGAP31c.2334T= (p.Ser778=)
c.2241T= (p.Ser747=)
c.2274T= (p.Ser758=)
c.1842T= (p.Ser614=)
3g.119414264C>ACA354050616ARHGAP31c.2335C>A (p.Pro779Thr)
c.2242C>A (p.Pro748Thr)
c.2275C>A (p.Pro759Thr)
c.1843C>A (p.Pro615Thr)
3g.119414264C=CA1396548624ARHGAP31c.2335C= (p.Pro779=)
c.2242C= (p.Pro748=)
c.2275C= (p.Pro759=)
c.1843C= (p.Pro615=)
3g.119414264C>GCA354050613ARHGAP31c.2335C>G (p.Pro779Ala)
c.2242C>G (p.Pro748Ala)
c.2275C>G (p.Pro759Ala)
c.1843C>G (p.Pro615Ala)
3g.119414264C>TCA2554010ARHGAP31c.2335C>T (p.Pro779Ser)
c.2242C>T (p.Pro748Ser)
c.2275C>T (p.Pro759Ser)
c.1843C>T (p.Pro615Ser)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.119414265delCA2667110271ARHGAP31c.2336del (p.Pro779LeufsTer?)
c.2243del (p.Pro748LeufsTer?)
c.2276del (p.Pro759LeufsTer?)
c.1844del (p.Pro615LeufsTer?)
 gnomAD v4
3g.119414265C>ACA354050619ARHGAP31c.2336C>A (p.Pro779His)
c.2243C>A (p.Pro748His)
c.2276C>A (p.Pro759His)
c.1844C>A (p.Pro615His)
3g.119414265C=CA1396548625ARHGAP31c.2336C= (p.Pro779=)
c.2243C= (p.Pro748=)
c.2276C= (p.Pro759=)
c.1844C= (p.Pro615=)
3g.119414265C>GCA354050622ARHGAP31c.2336C>G (p.Pro779Arg)
c.2243C>G (p.Pro748Arg)
c.2276C>G (p.Pro759Arg)
c.1844C>G (p.Pro615Arg)
3g.119414265C>TCA354050625ARHGAP31c.2336C>T (p.Pro779Leu)
c.2243C>T (p.Pro748Leu)
c.2276C>T (p.Pro759Leu)
c.1844C>T (p.Pro615Leu)
 dbSNP gnomAD v2 gnomAD v4
3g.119414266T>ACA435411798ARHGAP31c.2337T>A (p.Pro779=)
c.2244T>A (p.Pro748=)
c.2277T>A (p.Pro759=)
c.1845T>A (p.Pro615=)
3g.119414266T>CCA435411800ARHGAP31c.2337T>C (p.Pro779=)
c.2244T>C (p.Pro748=)
c.2277T>C (p.Pro759=)
c.1845T>C (p.Pro615=)
3g.119414266T>GCA435411801ARHGAP31c.2337T>G (p.Pro779=)
c.2244T>G (p.Pro748=)
c.2277T>G (p.Pro759=)
c.1845T>G (p.Pro615=)
3g.119414267C>ACA354050629ARHGAP31c.2338C>A (p.Pro780Thr)
c.2245C>A (p.Pro749Thr)
c.2278C>A (p.Pro760Thr)
c.1846C>A (p.Pro616Thr)
 gnomAD v4
3g.119414267C=CA1396548626ARHGAP31c.2338C= (p.Pro780=)
c.2245C= (p.Pro749=)
c.2278C= (p.Pro760=)
c.1846C= (p.Pro616=)
3g.119414267C>GCA2554011ARHGAP31c.2338C>G (p.Pro780Ala)
c.2245C>G (p.Pro749Ala)
c.2278C>G (p.Pro760Ala)
c.1846C>G (p.Pro616Ala)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.119414267C>TCA354050636ARHGAP31c.2338C>T (p.Pro780Ser)
c.2245C>T (p.Pro749Ser)
c.2278C>T (p.Pro760Ser)
c.1846C>T (p.Pro616Ser)
3g.119414268C>ACA354050639ARHGAP31c.2339C>A (p.Pro780Gln)
c.2246C>A (p.Pro749Gln)
c.2279C>A (p.Pro760Gln)
c.1847C>A (p.Pro616Gln)
3g.119414268C=CA1396548627ARHGAP31c.2339C= (p.Pro780=)
c.2246C= (p.Pro749=)
c.2279C= (p.Pro760=)
c.1847C= (p.Pro616=)
3g.119414268C>GCA354050640ARHGAP31c.2339C>G (p.Pro780Arg)
c.2246C>G (p.Pro749Arg)
c.2279C>G (p.Pro760Arg)
c.1847C>G (p.Pro616Arg)
3g.119414268C>TCA354050642ARHGAP31c.2339C>T (p.Pro780Leu)
c.2246C>T (p.Pro749Leu)
c.2279C>T (p.Pro760Leu)
c.1847C>T (p.Pro616Leu)
 dbSNP
3g.119414269A>CCA435411805ARHGAP31c.2340A>C (p.Pro780=)
c.2247A>C (p.Pro749=)
c.2280A>C (p.Pro760=)
c.1848A>C (p.Pro616=)
3g.119414269A>GCA435411807ARHGAP31c.2340A>G (p.Pro780=)
c.2247A>G (p.Pro749=)
c.2280A>G (p.Pro760=)
c.1848A>G (p.Pro616=)
3g.119414269A>TCA435411806ARHGAP31c.2340A>T (p.Pro780=)
c.2247A>T (p.Pro749=)
c.2280A>T (p.Pro760=)
c.1848A>T (p.Pro616=)
3g.119414270C>ACA354050645ARHGAP31c.2341C>A (p.Leu781Ile)
c.2248C>A (p.Leu750Ile)
c.2281C>A (p.Leu761Ile)
c.1849C>A (p.Leu617Ile)
3g.119414270C>GCA354050647ARHGAP31c.2341C>G (p.Leu781Val)
c.2248C>G (p.Leu750Val)
c.2281C>G (p.Leu761Val)
c.1849C>G (p.Leu617Val)
3g.119414270C>TCA354050650ARHGAP31c.2341C>T (p.Leu781Phe)
c.2248C>T (p.Leu750Phe)
c.2281C>T (p.Leu761Phe)
c.1849C>T (p.Leu617Phe)
 gnomAD v4
3g.119414271T>ACA354050662ARHGAP31c.2342T>A (p.Leu781His)
c.2249T>A (p.Leu750His)
c.2282T>A (p.Leu761His)
c.1850T>A (p.Leu617His)
3g.119414271T>CCA354050658ARHGAP31c.2342T>C (p.Leu781Pro)
c.2249T>C (p.Leu750Pro)
c.2282T>C (p.Leu761Pro)
c.1850T>C (p.Leu617Pro)
3g.119414271T>GCA354050655ARHGAP31c.2342T>G (p.Leu781Arg)
c.2249T>G (p.Leu750Arg)
c.2282T>G (p.Leu761Arg)
c.1850T>G (p.Leu617Arg)
3g.119414272C>ACA435411811ARHGAP31c.2343C>A (p.Leu781=)
c.2250C>A (p.Leu750=)
c.2283C>A (p.Leu761=)
c.1851C>A (p.Leu617=)
3g.119414272C=CA1396548628ARHGAP31c.2343C= (p.Leu781=)
c.2250C= (p.Leu750=)
c.2283C= (p.Leu761=)
c.1851C= (p.Leu617=)
3g.119414272C>GCA435411812ARHGAP31c.2343C>G (p.Leu781=)
c.2250C>G (p.Leu750=)
c.2283C>G (p.Leu761=)
c.1851C>G (p.Leu617=)
3g.119414272C>TCA435411813ARHGAP31c.2343C>T (p.Leu781=)
c.2250C>T (p.Leu750=)
c.2283C>T (p.Leu761=)
c.1851C>T (p.Leu617=)
 dbSNP gnomAD v3 gnomAD v4
3g.119414273C>ACA2554012ARHGAP31c.2344C>A (p.Pro782Thr)
c.2251C>A (p.Pro751Thr)
c.2284C>A (p.Pro762Thr)
c.1852C>A (p.Pro618Thr)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.119414273C=CA1396548629ARHGAP31c.2344C= (p.Pro782=)
c.2251C= (p.Pro751=)
c.2284C= (p.Pro762=)
c.1852C= (p.Pro618=)
3g.119414273C>GCA354050669ARHGAP31c.2344C>G (p.Pro782Ala)
c.2251C>G (p.Pro751Ala)
c.2284C>G (p.Pro762Ala)
c.1852C>G (p.Pro618Ala)
3g.119414273C>TCA354050671ARHGAP31c.2344C>T (p.Pro782Ser)
c.2251C>T (p.Pro751Ser)
c.2284C>T (p.Pro762Ser)
c.1852C>T (p.Pro618Ser)
 gnomAD v4
3g.119414274C>ACA354050674ARHGAP31c.2345C>A (p.Pro782Gln)
c.2252C>A (p.Pro751Gln)
c.2285C>A (p.Pro762Gln)
c.1853C>A (p.Pro618Gln)
3g.119414274C>GCA354050676ARHGAP31c.2345C>G (p.Pro782Arg)
c.2252C>G (p.Pro751Arg)
c.2285C>G (p.Pro762Arg)
c.1853C>G (p.Pro618Arg)
3g.119414274C>TCA354050677ARHGAP31c.2345C>T (p.Pro782Leu)
c.2252C>T (p.Pro751Leu)
c.2285C>T (p.Pro762Leu)
c.1853C>T (p.Pro618Leu)
3g.119414275A>CCA435411815ARHGAP31c.2346A>C (p.Pro782=)
c.2253A>C (p.Pro751=)
c.2286A>C (p.Pro762=)
c.1854A>C (p.Pro618=)
3g.119414275A>GCA435411817ARHGAP31c.2346A>G (p.Pro782=)
c.2253A>G (p.Pro751=)
c.2286A>G (p.Pro762=)
c.1854A>G (p.Pro618=)
3g.119414275A>TCA435411818ARHGAP31c.2346A>T (p.Pro782=)
c.2253A>T (p.Pro751=)
c.2286A>T (p.Pro762=)
c.1854A>T (p.Pro618=)
3g.119414276C>ACA354050682ARHGAP31c.2347C>A (p.Pro783Thr)
c.2254C>A (p.Pro752Thr)
c.2287C>A (p.Pro763Thr)
c.1855C>A (p.Pro619Thr)
3g.119414276C=CA1396548630ARHGAP31c.2347C= (p.Pro783=)
c.2254C= (p.Pro752=)
c.2287C= (p.Pro763=)
c.1855C= (p.Pro619=)
3g.119414276C>GCA354050686ARHGAP31c.2347C>G (p.Pro783Ala)
c.2254C>G (p.Pro752Ala)
c.2287C>G (p.Pro763Ala)
c.1855C>G (p.Pro619Ala)
3g.119414276C>TCA354050689ARHGAP31c.2347C>T (p.Pro783Ser)
c.2254C>T (p.Pro752Ser)
c.2287C>T (p.Pro763Ser)
c.1855C>T (p.Pro619Ser)
 dbSNP gnomAD v2 gnomAD v4
3g.119414277C>ACA354050693ARHGAP31c.2348C>A (p.Pro783His)
c.2255C>A (p.Pro752His)
c.2288C>A (p.Pro763His)
c.1856C>A (p.Pro619His)
3g.119414277C>GCA354050697ARHGAP31c.2348C>G (p.Pro783Arg)
c.2255C>G (p.Pro752Arg)
c.2288C>G (p.Pro763Arg)
c.1856C>G (p.Pro619Arg)
 COSMIC
3g.119414277C>TCA354050701ARHGAP31c.2348C>T (p.Pro783Leu)
c.2255C>T (p.Pro752Leu)
c.2288C>T (p.Pro763Leu)
c.1856C>T (p.Pro619Leu)
3g.119414278T>ACA435411823ARHGAP31c.2349T>A (p.Pro783=)
c.2256T>A (p.Pro752=)
c.2289T>A (p.Pro763=)
c.1857T>A (p.Pro619=)
3g.119414278T>CCA435411824ARHGAP31c.2349T>C (p.Pro783=)
c.2256T>C (p.Pro752=)
c.2289T>C (p.Pro763=)
c.1857T>C (p.Pro619=)
3g.119414278T>GCA435411826ARHGAP31c.2349T>G (p.Pro783=)
c.2256T>G (p.Pro752=)
c.2289T>G (p.Pro763=)
c.1857T>G (p.Pro619=)
 gnomAD v4
3g.119414279G>ACA354050712ARHGAP31c.2350G>A (p.Ala784Thr)
c.2257G>A (p.Ala753Thr)
c.2290G>A (p.Ala764Thr)
c.1858G>A (p.Ala620Thr)
3g.119414279G>CCA354050708ARHGAP31c.2350G>C (p.Ala784Pro)
c.2257G>C (p.Ala753Pro)
c.2290G>C (p.Ala764Pro)
c.1858G>C (p.Ala620Pro)
3g.119414279G>TCA354050705ARHGAP31c.2350G>T (p.Ala784Ser)
c.2257G>T (p.Ala753Ser)
c.2290G>T (p.Ala764Ser)
c.1858G>T (p.Ala620Ser)
3g.119414280C>ACA354050717ARHGAP31c.2351C>A (p.Ala784Asp)
c.2258C>A (p.Ala753Asp)
c.2291C>A (p.Ala764Asp)
c.1859C>A (p.Ala620Asp)
3g.119414280C=CA1396548631ARHGAP31c.2351C= (p.Ala784=)
c.2258C= (p.Ala753=)
c.2291C= (p.Ala764=)
c.1859C= (p.Ala620=)
3g.119414280C>GCA354050731ARHGAP31c.2351C>G (p.Ala784Gly)
c.2258C>G (p.Ala753Gly)
c.2291C>G (p.Ala764Gly)
c.1859C>G (p.Ala620Gly)
3g.119414280C>TCA81697573ARHGAP31c.2351C>T (p.Ala784Val)
c.2258C>T (p.Ala753Val)
c.2291C>T (p.Ala764Val)
c.1859C>T (p.Ala620Val)
 dbSNP gnomAD v4
3g.119414281T>ACA435411830ARHGAP31c.2352T>A (p.Ala784=)
c.2259T>A (p.Ala753=)
c.2292T>A (p.Ala764=)
c.1860T>A (p.Ala620=)
3g.119414281T>CCA435411832ARHGAP31c.2352T>C (p.Ala784=)
c.2259T>C (p.Ala753=)
c.2292T>C (p.Ala764=)
c.1860T>C (p.Ala620=)
3g.119414281T>GCA435411831ARHGAP31c.2352T>G (p.Ala784=)
c.2259T>G (p.Ala753=)
c.2292T>G (p.Ala764=)
c.1860T>G (p.Ala620=)
3g.119414282C>ACA354050736ARHGAP31c.2353C>A (p.Pro785Thr)
c.2260C>A (p.Pro754Thr)
c.2293C>A (p.Pro765Thr)
c.1861C>A (p.Pro621Thr)
 gnomAD v4
3g.119414282C>GCA354050739ARHGAP31c.2353C>G (p.Pro785Ala)
c.2260C>G (p.Pro754Ala)
c.2293C>G (p.Pro765Ala)
c.1861C>G (p.Pro621Ala)
3g.119414282C>TCA354050743ARHGAP31c.2353C>T (p.Pro785Ser)
c.2260C>T (p.Pro754Ser)
c.2293C>T (p.Pro765Ser)
c.1861C>T (p.Pro621Ser)
3g.119414283C>ACA354050748ARHGAP31c.2354C>A (p.Pro785His)
c.2261C>A (p.Pro754His)
c.2294C>A (p.Pro765His)
c.1862C>A (p.Pro621His)
3g.119414283C>GCA354050749ARHGAP31c.2354C>G (p.Pro785Arg)
c.2261C>G (p.Pro754Arg)
c.2294C>G (p.Pro765Arg)
c.1862C>G (p.Pro621Arg)
3g.119414283C>TCA354050751ARHGAP31c.2354C>T (p.Pro785Leu)
c.2261C>T (p.Pro754Leu)
c.2294C>T (p.Pro765Leu)
c.1862C>T (p.Pro621Leu)
3g.119414284T>ACA435411835ARHGAP31c.2355T>A (p.Pro785=)
c.2262T>A (p.Pro754=)
c.2295T>A (p.Pro765=)
c.1863T>A (p.Pro621=)
3g.119414284T>CCA435411836ARHGAP31c.2355T>C (p.Pro785=)
c.2262T>C (p.Pro754=)
c.2295T>C (p.Pro765=)
c.1863T>C (p.Pro621=)
3g.119414284T>GCA2554013ARHGAP31c.2355T>G (p.Pro785=)
c.2262T>G (p.Pro754=)
c.2295T>G (p.Pro765=)
c.1863T>G (p.Pro621=)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.119414284T=CA1396548632ARHGAP31c.2355T= (p.Pro785=)
c.2262T= (p.Pro754=)
c.2295T= (p.Pro765=)
c.1863T= (p.Pro621=)
3g.119414285C>ACA354050760ARHGAP31c.2356C>A (p.Pro786Thr)
c.2263C>A (p.Pro755Thr)
c.2296C>A (p.Pro766Thr)
c.1864C>A (p.Pro622Thr)
3g.119414285C=CA1396548633ARHGAP31c.2356C= (p.Pro786=)
c.2263C= (p.Pro755=)
c.2296C= (p.Pro766=)
c.1864C= (p.Pro622=)
3g.119414285C>GCA354050764ARHGAP31c.2356C>G (p.Pro786Ala)
c.2263C>G (p.Pro755Ala)
c.2296C>G (p.Pro766Ala)
c.1864C>G (p.Pro622Ala)
3g.119414285C>TCA354050766ARHGAP31c.2356C>T (p.Pro786Ser)
c.2263C>T (p.Pro755Ser)
c.2296C>T (p.Pro766Ser)
c.1864C>T (p.Pro622Ser)
 ClinVar dbSNP gnomAD v3 gnomAD v4
3g.119414286C>ACA354050771ARHGAP31c.2357C>A (p.Pro786His)
c.2264C>A (p.Pro755His)
c.2297C>A (p.Pro766His)
c.1865C>A (p.Pro622His)
 gnomAD v4
3g.119414286C=CA1396548634ARHGAP31c.2357C= (p.Pro786=)
c.2264C= (p.Pro755=)
c.2297C= (p.Pro766=)
c.1865C= (p.Pro622=)
3g.119414286C>GCA354050774ARHGAP31c.2357C>G (p.Pro786Arg)
c.2264C>G (p.Pro755Arg)
c.2297C>G (p.Pro766Arg)
c.1865C>G (p.Pro622Arg)
3g.119414286C>TCA354050776ARHGAP31c.2357C>T (p.Pro786Leu)
c.2264C>T (p.Pro755Leu)
c.2297C>T (p.Pro766Leu)
c.1865C>T (p.Pro622Leu)
 dbSNP gnomAD v2 gnomAD v4
3g.119414287C>ACA435411846ARHGAP31c.2358C>A (p.Pro786=)
c.2265C>A (p.Pro755=)
c.2298C>A (p.Pro766=)
c.1866C>A (p.Pro622=)
3g.119414287C=CA1396548635ARHGAP31c.2358C= (p.Pro786=)
c.2265C= (p.Pro755=)
c.2298C= (p.Pro766=)
c.1866C= (p.Pro622=)
3g.119414287C>GCA435411840ARHGAP31c.2358C>G (p.Pro786=)
c.2265C>G (p.Pro755=)
c.2298C>G (p.Pro766=)
c.1866C>G (p.Pro622=)
 gnomAD v4
3g.119414287C>TCA435411843ARHGAP31c.2358C>T (p.Pro786=)
c.2265C>T (p.Pro755=)
c.2298C>T (p.Pro766=)
c.1866C>T (p.Pro622=)
 dbSNP
3g.119414288C>ACA354050781ARHGAP31c.2359C>A (p.Pro787Thr)
c.2266C>A (p.Pro756Thr)
c.2299C>A (p.Pro767Thr)
c.1867C>A (p.Pro623Thr)
3g.119414288C=CA1396548636ARHGAP31c.2359C= (p.Pro787=)
c.2266C= (p.Pro756=)
c.2299C= (p.Pro767=)
c.1867C= (p.Pro623=)
3g.119414288C>GCA2554014ARHGAP31c.2359C>G (p.Pro787Ala)
c.2266C>G (p.Pro756Ala)
c.2299C>G (p.Pro767Ala)
c.1867C>G (p.Pro623Ala)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.119414288C>TCA2554015ARHGAP31c.2359C>T (p.Pro787Ser)
c.2266C>T (p.Pro756Ser)
c.2299C>T (p.Pro767Ser)
c.1867C>T (p.Pro623Ser)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.119414289C>ACA354050788ARHGAP31c.2360C>A (p.Pro787His)
c.2267C>A (p.Pro756His)
c.2300C>A (p.Pro767His)
c.1868C>A (p.Pro623His)
3g.119414289C=CA1396548637ARHGAP31c.2360C= (p.Pro787=)
c.2267C= (p.Pro756=)
c.2300C= (p.Pro767=)
c.1868C= (p.Pro623=)
3g.119414289C>GCA2554016ARHGAP31c.2360C>G (p.Pro787Arg)
c.2267C>G (p.Pro756Arg)
c.2300C>G (p.Pro767Arg)
c.1868C>G (p.Pro623Arg)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.119414289C>TCA354050794ARHGAP31c.2360C>T (p.Pro787Leu)
c.2267C>T (p.Pro756Leu)
c.2300C>T (p.Pro767Leu)
c.1868C>T (p.Pro623Leu)
 dbSNP gnomAD v2 gnomAD v4
3g.119414290T>ACA435411853ARHGAP31c.2361T>A (p.Pro787=)
c.2268T>A (p.Pro756=)
c.2301T>A (p.Pro767=)
c.1869T>A (p.Pro623=)
3g.119414290T>CCA435411854ARHGAP31c.2361T>C (p.Pro787=)
c.2268T>C (p.Pro756=)
c.2301T>C (p.Pro767=)
c.1869T>C (p.Pro623=)
3g.119414290T>GCA435411855ARHGAP31c.2361T>G (p.Pro787=)
c.2268T>G (p.Pro756=)
c.2301T>G (p.Pro767=)
c.1869T>G (p.Pro623=)
3g.119414291C>ACA354050798ARHGAP31c.2362C>A (p.Pro788Thr)
c.2269C>A (p.Pro757Thr)
c.2302C>A (p.Pro768Thr)
c.1870C>A (p.Pro624Thr)
3g.119414291C>GCA354050801ARHGAP31c.2362C>G (p.Pro788Ala)
c.2269C>G (p.Pro757Ala)
c.2302C>G (p.Pro768Ala)
c.1870C>G (p.Pro624Ala)
3g.119414291C>TCA354050804ARHGAP31c.2362C>T (p.Pro788Ser)
c.2269C>T (p.Pro757Ser)
c.2302C>T (p.Pro768Ser)
c.1870C>T (p.Pro624Ser)
3g.119414292C>ACA354050814ARHGAP31c.2363C>A (p.Pro788Gln)
c.2270C>A (p.Pro757Gln)
c.2303C>A (p.Pro768Gln)
c.1871C>A (p.Pro624Gln)
3g.119414292C>GCA354050816ARHGAP31c.2363C>G (p.Pro788Arg)
c.2270C>G (p.Pro757Arg)
c.2303C>G (p.Pro768Arg)
c.1871C>G (p.Pro624Arg)
3g.119414292C>TCA354050819ARHGAP31c.2363C>T (p.Pro788Leu)
c.2270C>T (p.Pro757Leu)
c.2303C>T (p.Pro768Leu)
c.1871C>T (p.Pro624Leu)
3g.119414293A=CA1396548638ARHGAP31c.2364A= (p.Pro788=)
c.2271A= (p.Pro757=)
c.2304A= (p.Pro768=)
c.1872A= (p.Pro624=)
3g.119414293A>CCA435411862ARHGAP31c.2364A>C (p.Pro788=)
c.2271A>C (p.Pro757=)
c.2304A>C (p.Pro768=)
c.1872A>C (p.Pro624=)
3g.119414293A>GCA435411861ARHGAP31c.2364A>G (p.Pro788=)
c.2271A>G (p.Pro757=)
c.2304A>G (p.Pro768=)
c.1872A>G (p.Pro624=)
3g.119414293A>TCA2554017ARHGAP31c.2364A>T (p.Pro788=)
c.2271A>T (p.Pro757=)
c.2304A>T (p.Pro768=)
c.1872A>T (p.Pro624=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.119414294A=CA1396548639ARHGAP31c.2365A= (p.Thr789=)
c.2272A= (p.Thr758=)
c.2305A= (p.Thr769=)
c.1873A= (p.Thr625=)
3g.119414294A>CCA2554018ARHGAP31c.2365A>C (p.Thr789Pro)
c.2272A>C (p.Thr758Pro)
c.2305A>C (p.Thr769Pro)
c.1873A>C (p.Thr625Pro)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.119414294A>GCA2554019ARHGAP31c.2365A>G (p.Thr789Ala)
c.2272A>G (p.Thr758Ala)
c.2305A>G (p.Thr769Ala)
c.1873A>G (p.Thr625Ala)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.119414294A>TCA354050828ARHGAP31c.2365A>T (p.Thr789Ser)
c.2272A>T (p.Thr758Ser)
c.2305A>T (p.Thr769Ser)
c.1873A>T (p.Thr625Ser)
3g.119414295C>ACA354050839ARHGAP31c.2366C>A (p.Thr789Asn)
c.2273C>A (p.Thr758Asn)
c.2306C>A (p.Thr769Asn)
c.1874C>A (p.Thr625Asn)
3g.119414295C>GCA354050846ARHGAP31c.2366C>G (p.Thr789Ser)
c.2273C>G (p.Thr758Ser)
c.2306C>G (p.Thr769Ser)
c.1874C>G (p.Thr625Ser)
 gnomAD v4
3g.119414295C>TCA354050849ARHGAP31c.2366C>T (p.Thr789Ile)
c.2273C>T (p.Thr758Ile)
c.2306C>T (p.Thr769Ile)
c.1874C>T (p.Thr625Ile)
 gnomAD v4
3g.119414296T>ACA435411867ARHGAP31c.2367T>A (p.Thr789=)
c.2274T>A (p.Thr758=)
c.2307T>A (p.Thr769=)
c.1875T>A (p.Thr625=)
3g.119414296T>CCA2554020ARHGAP31c.2367T>C (p.Thr789=)
c.2274T>C (p.Thr758=)
c.2307T>C (p.Thr769=)
c.1875T>C (p.Thr625=)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.119414296T>GCA435411868ARHGAP31c.2367T>G (p.Thr789=)
c.2274T>G (p.Thr758=)
c.2307T>G (p.Thr769=)
c.1875T>G (p.Thr625=)
3g.119414296T=CA1396548640ARHGAP31c.2367T= (p.Thr789=)
c.2274T= (p.Thr758=)
c.2307T= (p.Thr769=)
c.1875T= (p.Thr625=)
3g.119414297C>ACA354050855ARHGAP31c.2368C>A (p.Pro790Thr)
c.2275C>A (p.Pro759Thr)
c.2308C>A (p.Pro770Thr)
c.1876C>A (p.Pro626Thr)
3g.119414297C>GCA354050859ARHGAP31c.2368C>G (p.Pro790Ala)
c.2275C>G (p.Pro759Ala)
c.2308C>G (p.Pro770Ala)
c.1876C>G (p.Pro626Ala)
3g.119414297C>TCA354050862ARHGAP31c.2368C>T (p.Pro790Ser)
c.2275C>T (p.Pro759Ser)
c.2308C>T (p.Pro770Ser)
c.1876C>T (p.Pro626Ser)
3g.119414298C>ACA354050868ARHGAP31c.2369C>A (p.Pro790His)
c.2276C>A (p.Pro759His)
c.2309C>A (p.Pro770His)
c.1877C>A (p.Pro626His)
3g.119414298C=CA1396548641ARHGAP31c.2369C= (p.Pro790=)
c.2276C= (p.Pro759=)
c.2309C= (p.Pro770=)
c.1877C= (p.Pro626=)
3g.119414298C>GCA354050870ARHGAP31c.2369C>G (p.Pro790Arg)
c.2276C>G (p.Pro759Arg)
c.2309C>G (p.Pro770Arg)
c.1877C>G (p.Pro626Arg)
 dbSNP gnomAD v4
3g.119414298C>TCA354050874ARHGAP31c.2369C>T (p.Pro790Leu)
c.2276C>T (p.Pro759Leu)
c.2309C>T (p.Pro770Leu)
c.1877C>T (p.Pro626Leu)
 gnomAD v4
3g.119414299T>ACA435411873ARHGAP31c.2370T>A (p.Pro790=)
c.2277T>A (p.Pro759=)
c.2310T>A (p.Pro770=)
c.1878T>A (p.Pro626=)
3g.119414299T>CCA435411874ARHGAP31c.2370T>C (p.Pro790=)
c.2277T>C (p.Pro759=)
c.2310T>C (p.Pro770=)
c.1878T>C (p.Pro626=)
3g.119414299T>GCA435411877ARHGAP31c.2370T>G (p.Pro790=)
c.2277T>G (p.Pro759=)
c.2310T>G (p.Pro770=)
c.1878T>G (p.Pro626=)
3g.119414300C>ACA354050876ARHGAP31c.2371C>A (p.Leu791Met)
c.2278C>A (p.Leu760Met)
c.2311C>A (p.Leu771Met)
c.1879C>A (p.Leu627Met)
3g.119414300C>GCA354050878ARHGAP31c.2371C>G (p.Leu791Val)
c.2278C>G (p.Leu760Val)
c.2311C>G (p.Leu771Val)
c.1879C>G (p.Leu627Val)
3g.119414300C>TCA435411906ARHGAP31c.2371C>T (p.Leu791=)
c.2278C>T (p.Leu760=)
c.2311C>T (p.Leu771=)
c.1879C>T (p.Leu627=)
3g.119414301T>ACA354050892ARHGAP31c.2372T>A (p.Leu791Gln)
c.2279T>A (p.Leu760Gln)
c.2312T>A (p.Leu771Gln)
c.1880T>A (p.Leu627Gln)
3g.119414301T>CCA354050893ARHGAP31c.2372T>C (p.Leu791Pro)
c.2279T>C (p.Leu760Pro)
c.2312T>C (p.Leu771Pro)
c.1880T>C (p.Leu627Pro)
 gnomAD v4
3g.119414301T>GCA354050891ARHGAP31c.2372T>G (p.Leu791Arg)
c.2279T>G (p.Leu760Arg)
c.2312T>G (p.Leu771Arg)
c.1880T>G (p.Leu627Arg)
 dbSNP gnomAD v2 gnomAD v4
3g.119414301T=CA1396548642ARHGAP31c.2372T= (p.Leu791=)
c.2279T= (p.Leu760=)
c.2312T= (p.Leu771=)
c.1880T= (p.Leu627=)
3g.119414302G>ACA435411910ARHGAP31c.2373G>A (p.Leu791=)
c.2280G>A (p.Leu760=)
c.2313G>A (p.Leu771=)
c.1881G>A (p.Leu627=)
3g.119414302G>CCA435411912ARHGAP31c.2373G>C (p.Leu791=)
c.2280G>C (p.Leu760=)
c.2313G>C (p.Leu771=)
c.1881G>C (p.Leu627=)
3g.119414302G>TCA435411913ARHGAP31c.2373G>T (p.Leu791=)
c.2280G>T (p.Leu760=)
c.2313G>T (p.Leu771=)
c.1881G>T (p.Leu627=)
3g.119414303G>ACA2554021ARHGAP31c.2374G>A (p.Glu792Lys)
c.2281G>A (p.Glu761Lys)
c.2314G>A (p.Glu772Lys)
c.1882G>A (p.Glu628Lys)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.119414303G>CCA354050899ARHGAP31c.2374G>C (p.Glu792Gln)
c.2281G>C (p.Glu761Gln)
c.2314G>C (p.Glu772Gln)
c.1882G>C (p.Glu628Gln)
3g.119414303G=CA1396548643ARHGAP31c.2374G= (p.Glu792=)
c.2281G= (p.Glu761=)
c.2314G= (p.Glu772=)
c.1882G= (p.Glu628=)
3g.119414303G>TCA354050901ARHGAP31c.2374G>T (p.Glu792Ter)
c.2281G>T (p.Glu761Ter)
c.2314G>T (p.Glu772Ter)
c.1882G>T (p.Glu628Ter)
3g.119414304A>CCA354050904ARHGAP31c.2375A>C (p.Glu792Ala)
c.2282A>C (p.Glu761Ala)
c.2315A>C (p.Glu772Ala)
c.1883A>C (p.Glu628Ala)
3g.119414304A>GCA354050906ARHGAP31c.2375A>G (p.Glu792Gly)
c.2282A>G (p.Glu761Gly)
c.2315A>G (p.Glu772Gly)
c.1883A>G (p.Glu628Gly)
3g.119414304A>TCA354050908ARHGAP31c.2375A>T (p.Glu792Val)
c.2282A>T (p.Glu761Val)
c.2315A>T (p.Glu772Val)
c.1883A>T (p.Glu628Val)
3g.119414305G>ACA435411918ARHGAP31c.2376G>A (p.Glu792=)
c.2283G>A (p.Glu761=)
c.2316G>A (p.Glu772=)
c.1884G>A (p.Glu628=)
3g.119414305G>CCA354050911ARHGAP31c.2376G>C (p.Glu792Asp)
c.2283G>C (p.Glu761Asp)
c.2316G>C (p.Glu772Asp)
c.1884G>C (p.Glu628Asp)
3g.119414305G>TCA354050913ARHGAP31c.2376G>T (p.Glu792Asp)
c.2283G>T (p.Glu761Asp)
c.2316G>T (p.Glu772Asp)
c.1884G>T (p.Glu628Asp)
3g.119414306G>ACA354050917ARHGAP31c.2377G>A (p.Glu793Lys)
c.2284G>A (p.Glu762Lys)
c.2317G>A (p.Glu773Lys)
c.1885G>A (p.Glu629Lys)
3g.119414306G>CCA354050920ARHGAP31c.2377G>C (p.Glu793Gln)
c.2284G>C (p.Glu762Gln)
c.2317G>C (p.Glu773Gln)
c.1885G>C (p.Glu629Gln)
3g.119414306G>TCA354050922ARHGAP31c.2377G>T (p.Glu793Ter)
c.2284G>T (p.Glu762Ter)
c.2317G>T (p.Glu773Ter)
c.1885G>T (p.Glu629Ter)
3g.119414307A>CCA354050926ARHGAP31c.2378A>C (p.Glu793Ala)
c.2285A>C (p.Glu762Ala)
c.2318A>C (p.Glu773Ala)
c.1886A>C (p.Glu629Ala)
3g.119414307A>GCA354050929ARHGAP31c.2378A>G (p.Glu793Gly)
c.2285A>G (p.Glu762Gly)
c.2318A>G (p.Glu773Gly)
c.1886A>G (p.Glu629Gly)
 gnomAD v4
3g.119414307A>TCA354050931ARHGAP31c.2378A>T (p.Glu793Val)
c.2285A>T (p.Glu762Val)
c.2318A>T (p.Glu773Val)
c.1886A>T (p.Glu629Val)
3g.119414308G>ACA435411924ARHGAP31c.2379G>A (p.Glu793=)
c.2286G>A (p.Glu762=)
c.2319G>A (p.Glu773=)
c.1887G>A (p.Glu629=)
3g.119414308G>CCA354050935ARHGAP31c.2379G>C (p.Glu793Asp)
c.2286G>C (p.Glu762Asp)
c.2319G>C (p.Glu773Asp)
c.1887G>C (p.Glu629Asp)
3g.119414308G>TCA354050937ARHGAP31c.2379G>T (p.Glu793Asp)
c.2286G>T (p.Glu762Asp)
c.2319G>T (p.Glu773Asp)
c.1887G>T (p.Glu629Asp)
3g.119414309T>ACA354050940ARHGAP31c.2380T>A (p.Ser794Thr)
c.2287T>A (p.Ser763Thr)
c.2320T>A (p.Ser774Thr)
c.1888T>A (p.Ser630Thr)
3g.119414309T>CCA354050945ARHGAP31c.2380T>C (p.Ser794Pro)
c.2287T>C (p.Ser763Pro)
c.2320T>C (p.Ser774Pro)
c.1888T>C (p.Ser630Pro)
3g.119414309T>GCA354050943ARHGAP31c.2380T>G (p.Ser794Ala)
c.2287T>G (p.Ser763Ala)
c.2320T>G (p.Ser774Ala)
c.1888T>G (p.Ser630Ala)
 dbSNP
3g.119414309T=CA1396548644ARHGAP31c.2380T= (p.Ser794=)
c.2287T= (p.Ser763=)
c.2320T= (p.Ser774=)
c.1888T= (p.Ser630=)
3g.119414310C>ACA354050949ARHGAP31c.2381C>A (p.Ser794Ter)
c.2288C>A (p.Ser763Ter)
c.2321C>A (p.Ser774Ter)
c.1889C>A (p.Ser630Ter)
3g.119414310C=CA1396548645ARHGAP31c.2381C= (p.Ser794=)
c.2288C= (p.Ser763=)
c.2321C= (p.Ser774=)
c.1889C= (p.Ser630=)
3g.119414310C>GCA354050953ARHGAP31c.2381C>G (p.Ser794Ter)
c.2288C>G (p.Ser763Ter)
c.2321C>G (p.Ser774Ter)
c.1889C>G (p.Ser630Ter)
3g.119414310C>TCA2554022ARHGAP31c.2381C>T (p.Ser794Leu)
c.2288C>T (p.Ser763Leu)
c.2321C>T (p.Ser774Leu)
c.1889C>T (p.Ser630Leu)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.119414311A>CCA435411928ARHGAP31c.2382A>C (p.Ser794=)
c.2289A>C (p.Ser763=)
c.2322A>C (p.Ser774=)
c.1890A>C (p.Ser630=)
3g.119414311A>GCA435411929ARHGAP31c.2382A>G (p.Ser794=)
c.2289A>G (p.Ser763=)
c.2322A>G (p.Ser774=)
c.1890A>G (p.Ser630=)
 gnomAD v4
3g.119414311A>TCA435411930ARHGAP31c.2382A>T (p.Ser794=)
c.2289A>T (p.Ser763=)
c.2322A>T (p.Ser774=)
c.1890A>T (p.Ser630=)
3g.119414312A=CA1396548646ARHGAP31c.2383A= (p.Thr795=)
c.2290A= (p.Thr764=)
c.2323A= (p.Thr775=)
c.1891A= (p.Thr631=)
3g.119414312A>CCA354050956ARHGAP31c.2383A>C (p.Thr795Pro)
c.2290A>C (p.Thr764Pro)
c.2323A>C (p.Thr775Pro)
c.1891A>C (p.Thr631Pro)
3g.119414312A>GCA354050961ARHGAP31c.2383A>G (p.Thr795Ala)
c.2290A>G (p.Thr764Ala)
c.2323A>G (p.Thr775Ala)
c.1891A>G (p.Thr631Ala)
 dbSNP gnomAD v3 gnomAD v4
3g.119414312A>TCA354050959ARHGAP31c.2383A>T (p.Thr795Ser)
c.2290A>T (p.Thr764Ser)
c.2323A>T (p.Thr775Ser)
c.1891A>T (p.Thr631Ser)
3g.119414313C>ACA354050963ARHGAP31c.2384C>A (p.Thr795Asn)
c.2291C>A (p.Thr764Asn)
c.2324C>A (p.Thr775Asn)
c.1892C>A (p.Thr631Asn)
3g.119414313C>GCA354050969ARHGAP31c.2384C>G (p.Thr795Ser)
c.2291C>G (p.Thr764Ser)
c.2324C>G (p.Thr775Ser)
c.1892C>G (p.Thr631Ser)
3g.119414313C>TCA354050966ARHGAP31c.2384C>T (p.Thr795Ile)
c.2291C>T (p.Thr764Ile)
c.2324C>T (p.Thr775Ile)
c.1892C>T (p.Thr631Ile)
3g.119414314T>ACA435411939ARHGAP31c.2385T>A (p.Thr795=)
c.2292T>A (p.Thr764=)
c.2325T>A (p.Thr775=)
c.1893T>A (p.Thr631=)
3g.119414314T>CCA435411941ARHGAP31c.2385T>C (p.Thr795=)
c.2292T>C (p.Thr764=)
c.2325T>C (p.Thr775=)
c.1893T>C (p.Thr631=)
3g.119414314T>GCA435411940ARHGAP31c.2385T>G (p.Thr795=)
c.2292T>G (p.Thr764=)
c.2325T>G (p.Thr775=)
c.1893T>G (p.Thr631=)
3g.119414315C>ACA354050972ARHGAP31c.2386C>A (p.Pro796Thr)
c.2293C>A (p.Pro765Thr)
c.2326C>A (p.Pro776Thr)
c.1894C>A (p.Pro632Thr)
3g.119414315C=CA1396548647ARHGAP31c.2386C= (p.Pro796=)
c.2293C= (p.Pro765=)
c.2326C= (p.Pro776=)
c.1894C= (p.Pro632=)
3g.119414315C>GCA354050978ARHGAP31c.2386C>G (p.Pro796Ala)
c.2293C>G (p.Pro765Ala)
c.2326C>G (p.Pro776Ala)
c.1894C>G (p.Pro632Ala)
 dbSNP gnomAD v2 gnomAD v4
3g.119414315C>TCA354050975ARHGAP31c.2386C>T (p.Pro796Ser)
c.2293C>T (p.Pro765Ser)
c.2326C>T (p.Pro776Ser)
c.1894C>T (p.Pro632Ser)
3g.119414316C>ACA354050981ARHGAP31c.2387C>A (p.Pro796Gln)
c.2294C>A (p.Pro765Gln)
c.2327C>A (p.Pro776Gln)
c.1895C>A (p.Pro632Gln)
3g.119414316C>GCA354050983ARHGAP31c.2387C>G (p.Pro796Arg)
c.2294C>G (p.Pro765Arg)
c.2327C>G (p.Pro776Arg)
c.1895C>G (p.Pro632Arg)
3g.119414316C>TCA354050984ARHGAP31c.2387C>T (p.Pro796Leu)
c.2294C>T (p.Pro765Leu)
c.2327C>T (p.Pro776Leu)
c.1895C>T (p.Pro632Leu)
3g.119414317A=CA1396548648ARHGAP31c.2388A= (p.Pro796=)
c.2295A= (p.Pro765=)
c.2328A= (p.Pro776=)
c.1896A= (p.Pro632=)
3g.119414317A>CCA435411950ARHGAP31c.2388A>C (p.Pro796=)
c.2295A>C (p.Pro765=)
c.2328A>C (p.Pro776=)
c.1896A>C (p.Pro632=)
3g.119414317A>GCA435411951ARHGAP31c.2388A>G (p.Pro796=)
c.2295A>G (p.Pro765=)
c.2328A>G (p.Pro776=)
c.1896A>G (p.Pro632=)
 dbSNP gnomAD v3 gnomAD v4
3g.119414317A>TCA435411953ARHGAP31c.2388A>T (p.Pro796=)
c.2295A>T (p.Pro765=)
c.2328A>T (p.Pro776=)
c.1896A>T (p.Pro632=)
3g.119414318G>ACA354050987ARHGAP31c.2389G>A (p.Val797Ile)
c.2296G>A (p.Val766Ile)
c.2329G>A (p.Val777Ile)
c.1897G>A (p.Val633Ile)
3g.119414318G>CCA2554023ARHGAP31c.2389G>C (p.Val797Leu)
c.2296G>C (p.Val766Leu)
c.2329G>C (p.Val777Leu)
c.1897G>C (p.Val633Leu)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.119414318G=CA1396548649ARHGAP31c.2389G= (p.Val797=)
c.2296G= (p.Val766=)
c.2329G= (p.Val777=)
c.1897G= (p.Val633=)
3g.119414318G>TCA354050989ARHGAP31c.2389G>T (p.Val797Phe)
c.2296G>T (p.Val766Phe)
c.2329G>T (p.Val777Phe)
c.1897G>T (p.Val633Phe)
3g.119414319T>ACA2554024ARHGAP31c.2390T>A (p.Val797Asp)
c.2297T>A (p.Val766Asp)
c.2330T>A (p.Val777Asp)
c.1898T>A (p.Val633Asp)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.119414319T>CCA354050995ARHGAP31c.2390T>C (p.Val797Ala)
c.2297T>C (p.Val766Ala)
c.2330T>C (p.Val777Ala)
c.1898T>C (p.Val633Ala)
 dbSNP
3g.119414319T>GCA354050997ARHGAP31c.2390T>G (p.Val797Gly)
c.2297T>G (p.Val766Gly)
c.2330T>G (p.Val777Gly)
c.1898T>G (p.Val633Gly)
3g.119414319T=CA1396548650ARHGAP31c.2390T= (p.Val797=)
c.2297T= (p.Val766=)
c.2330T= (p.Val777=)
c.1898T= (p.Val633=)
3g.119414320C>ACA435411959ARHGAP31c.2391C>A (p.Val797=)
c.2298C>A (p.Val766=)
c.2331C>A (p.Val777=)
c.1899C>A (p.Val633=)
3g.119414320C=CA1396548651ARHGAP31c.2391C= (p.Val797=)
c.2298C= (p.Val766=)
c.2331C= (p.Val777=)
c.1899C= (p.Val633=)
3g.119414320C>GCA435411960ARHGAP31c.2391C>G (p.Val797=)
c.2298C>G (p.Val766=)
c.2331C>G (p.Val777=)
c.1899C>G (p.Val633=)
 dbSNP gnomAD v3 gnomAD v4
3g.119414320C>TCA2554025ARHGAP31c.2391C>T (p.Val797=)
c.2298C>T (p.Val766=)
c.2331C>T (p.Val777=)
c.1899C>T (p.Val633=)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.119414321C>ACA354051000ARHGAP31c.2392C>A (p.Leu798Met)
c.2299C>A (p.Leu767Met)
c.2332C>A (p.Leu778Met)
c.1900C>A (p.Leu634Met)
3g.119414321C>GCA354051001ARHGAP31c.2392C>G (p.Leu798Val)
c.2299C>G (p.Leu767Val)
c.2332C>G (p.Leu778Val)
c.1900C>G (p.Leu634Val)
3g.119414321C>TCA435411965ARHGAP31c.2392C>T (p.Leu798=)
c.2299C>T (p.Leu767=)
c.2332C>T (p.Leu778=)
c.1900C>T (p.Leu634=)
3g.119414322T>ACA354051003ARHGAP31c.2393T>A (p.Leu798Gln)
c.2300T>A (p.Leu767Gln)
c.2333T>A (p.Leu778Gln)
c.1901T>A (p.Leu634Gln)
3g.119414322T>CCA2554026ARHGAP31c.2393T>C (p.Leu798Pro)
c.2300T>C (p.Leu767Pro)
c.2333T>C (p.Leu778Pro)
c.1901T>C (p.Leu634Pro)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.119414322T>GCA354051004ARHGAP31c.2393T>G (p.Leu798Arg)
c.2300T>G (p.Leu767Arg)
c.2333T>G (p.Leu778Arg)
c.1901T>G (p.Leu634Arg)
3g.119414322T=CA1396548652ARHGAP31c.2393T= (p.Leu798=)
c.2300T= (p.Leu767=)
c.2333T= (p.Leu778=)
c.1901T= (p.Leu634=)
3g.119414323G>ACA435411969ARHGAP31c.2394G>A (p.Leu798=)
c.2301G>A (p.Leu767=)
c.2334G>A (p.Leu778=)
c.1902G>A (p.Leu634=)
3g.119414323G>CCA435411970ARHGAP31c.2394G>C (p.Leu798=)
c.2301G>C (p.Leu767=)
c.2334G>C (p.Leu778=)
c.1902G>C (p.Leu634=)
3g.119414323G>TCA435411972ARHGAP31c.2394G>T (p.Leu798=)
c.2301G>T (p.Leu767=)
c.2334G>T (p.Leu778=)
c.1902G>T (p.Leu634=)
3g.119414324C>ACA354051006ARHGAP31c.2395C>A (p.Leu799Ile)
c.2302C>A (p.Leu768Ile)
c.2335C>A (p.Leu779Ile)
c.1903C>A (p.Leu635Ile)
3g.119414324C>GCA354051007ARHGAP31c.2395C>G (p.Leu799Val)
c.2302C>G (p.Leu768Val)
c.2335C>G (p.Leu779Val)
c.1903C>G (p.Leu635Val)
 gnomAD v4
3g.119414324C>TCA354051009ARHGAP31c.2395C>T (p.Leu799Phe)
c.2302C>T (p.Leu768Phe)
c.2335C>T (p.Leu779Phe)
c.1903C>T (p.Leu635Phe)
3g.119414325T>ACA354051011ARHGAP31c.2396T>A (p.Leu799His)
c.2303T>A (p.Leu768His)
c.2336T>A (p.Leu779His)
c.1904T>A (p.Leu635His)
3g.119414325T>CCA354051013ARHGAP31c.2396T>C (p.Leu799Pro)
c.2303T>C (p.Leu768Pro)
c.2336T>C (p.Leu779Pro)
c.1904T>C (p.Leu635Pro)
3g.119414325T>GCA354051014ARHGAP31c.2396T>G (p.Leu799Arg)
c.2303T>G (p.Leu768Arg)
c.2336T>G (p.Leu779Arg)
c.1904T>G (p.Leu635Arg)
3g.119414326T>ACA435411981ARHGAP31c.2397T>A (p.Leu799=)
c.2304T>A (p.Leu768=)
c.2337T>A (p.Leu779=)
c.1905T>A (p.Leu635=)
3g.119414326T>CCA435411984ARHGAP31c.2397T>C (p.Leu799=)
c.2304T>C (p.Leu768=)
c.2337T>C (p.Leu779=)
c.1905T>C (p.Leu635=)
3g.119414326T>GCA435411983ARHGAP31c.2397T>G (p.Leu799=)
c.2304T>G (p.Leu768=)
c.2337T>G (p.Leu779=)
c.1905T>G (p.Leu635=)
3g.119414327T>ACA354051016ARHGAP31c.2398T>A (p.Ser800Thr)
c.2305T>A (p.Ser769Thr)
c.2338T>A (p.Ser780Thr)
c.1906T>A (p.Ser636Thr)
3g.119414327T>CCA354051017ARHGAP31c.2398T>C (p.Ser800Pro)
c.2305T>C (p.Ser769Pro)
c.2338T>C (p.Ser780Pro)
c.1906T>C (p.Ser636Pro)
3g.119414327T>GCA354051019ARHGAP31c.2398T>G (p.Ser800Ala)
c.2305T>G (p.Ser769Ala)
c.2338T>G (p.Ser780Ala)
c.1906T>G (p.Ser636Ala)

Number of alleles fetched