Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.119414184T>ACA354050084ARHGAP31c.2255T>A (p.Leu752Gln)
c.2162T>A (p.Leu721Gln)
c.2195T>A (p.Leu732Gln)
c.1763T>A (p.Leu588Gln)
 gnomAD v4
3g.119414184T>CCA354050088ARHGAP31c.2255T>C (p.Leu752Pro)
c.2162T>C (p.Leu721Pro)
c.2195T>C (p.Leu732Pro)
c.1763T>C (p.Leu588Pro)
3g.119414184T>GCA354050091ARHGAP31c.2255T>G (p.Leu752Arg)
c.2162T>G (p.Leu721Arg)
c.2195T>G (p.Leu732Arg)
c.1763T>G (p.Leu588Arg)
3g.119414185G>ACA435411667ARHGAP31c.2256G>A (p.Leu752=)
c.2163G>A (p.Leu721=)
c.2196G>A (p.Leu732=)
c.1764G>A (p.Leu588=)
3g.119414185G>CCA435411668ARHGAP31c.2256G>C (p.Leu752=)
c.2163G>C (p.Leu721=)
c.2196G>C (p.Leu732=)
c.1764G>C (p.Leu588=)
3g.119414185G>TCA435411669ARHGAP31c.2256G>T (p.Leu752=)
c.2163G>T (p.Leu721=)
c.2196G>T (p.Leu732=)
c.1764G>T (p.Leu588=)
3g.119414186G>ACA354050093ARHGAP31c.2257G>A (p.Ala753Thr)
c.2164G>A (p.Ala722Thr)
c.2197G>A (p.Ala733Thr)
c.1765G>A (p.Ala589Thr)
 COSMIC
3g.119414186G>CCA81697486ARHGAP31c.2257G>C (p.Ala753Pro)
c.2164G>C (p.Ala722Pro)
c.2197G>C (p.Ala733Pro)
c.1765G>C (p.Ala589Pro)
 dbSNP gnomAD v4
3g.119414186G=CA1396548591ARHGAP31c.2257G= (p.Ala753=)
c.2164G= (p.Ala722=)
c.2197G= (p.Ala733=)
c.1765G= (p.Ala589=)
3g.119414186G>TCA354050103ARHGAP31c.2257G>T (p.Ala753Ser)
c.2164G>T (p.Ala722Ser)
c.2197G>T (p.Ala733Ser)
c.1765G>T (p.Ala589Ser)
3g.119414187C>ACA354050106ARHGAP31c.2258C>A (p.Ala753Asp)
c.2165C>A (p.Ala722Asp)
c.2198C>A (p.Ala733Asp)
c.1766C>A (p.Ala589Asp)
3g.119414187C>GCA354050111ARHGAP31c.2258C>G (p.Ala753Gly)
c.2165C>G (p.Ala722Gly)
c.2198C>G (p.Ala733Gly)
c.1766C>G (p.Ala589Gly)
3g.119414187C>TCA354050115ARHGAP31c.2258C>T (p.Ala753Val)
c.2165C>T (p.Ala722Val)
c.2198C>T (p.Ala733Val)
c.1766C>T (p.Ala589Val)
 gnomAD v4
3g.119414188T>ACA435411673ARHGAP31c.2259T>A (p.Ala753=)
c.2166T>A (p.Ala722=)
c.2199T>A (p.Ala733=)
c.1767T>A (p.Ala589=)
3g.119414188T>CCA435411671ARHGAP31c.2259T>C (p.Ala753=)
c.2166T>C (p.Ala722=)
c.2199T>C (p.Ala733=)
c.1767T>C (p.Ala589=)
 dbSNP
3g.119414188T>GCA435411672ARHGAP31c.2259T>G (p.Ala753=)
c.2166T>G (p.Ala722=)
c.2199T>G (p.Ala733=)
c.1767T>G (p.Ala589=)
 gnomAD v4
3g.119414188T=CA1396548592ARHGAP31c.2259T= (p.Ala753=)
c.2166T= (p.Ala722=)
c.2199T= (p.Ala733=)
c.1767T= (p.Ala589=)
3g.119414189C>ACA354050119ARHGAP31c.2260C>A (p.Pro754Thr)
c.2167C>A (p.Pro723Thr)
c.2200C>A (p.Pro734Thr)
c.1768C>A (p.Pro590Thr)
3g.119414189C>GCA354050120ARHGAP31c.2260C>G (p.Pro754Ala)
c.2167C>G (p.Pro723Ala)
c.2200C>G (p.Pro734Ala)
c.1768C>G (p.Pro590Ala)
3g.119414189C>TCA354050123ARHGAP31c.2260C>T (p.Pro754Ser)
c.2167C>T (p.Pro723Ser)
c.2200C>T (p.Pro734Ser)
c.1768C>T (p.Pro590Ser)
 gnomAD v4
3g.119414190C>ACA2553995ARHGAP31c.2261C>A (p.Pro754His)
c.2168C>A (p.Pro723His)
c.2201C>A (p.Pro734His)
c.1769C>A (p.Pro590His)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.119414190C=CA1396548593ARHGAP31c.2261C= (p.Pro754=)
c.2168C= (p.Pro723=)
c.2201C= (p.Pro734=)
c.1769C= (p.Pro590=)
3g.119414190C>GCA354050137ARHGAP31c.2261C>G (p.Pro754Arg)
c.2168C>G (p.Pro723Arg)
c.2201C>G (p.Pro734Arg)
c.1769C>G (p.Pro590Arg)
3g.119414190C>TCA354050131ARHGAP31c.2261C>T (p.Pro754Leu)
c.2168C>T (p.Pro723Leu)
c.2201C>T (p.Pro734Leu)
c.1769C>T (p.Pro590Leu)
 gnomAD v4
3g.119414191T>ACA435411674ARHGAP31c.2262T>A (p.Pro754=)
c.2169T>A (p.Pro723=)
c.2202T>A (p.Pro734=)
c.1770T>A (p.Pro590=)
3g.119414191T>CCA435411675ARHGAP31c.2262T>C (p.Pro754=)
c.2169T>C (p.Pro723=)
c.2202T>C (p.Pro734=)
c.1770T>C (p.Pro590=)
3g.119414191T>GCA435411676ARHGAP31c.2262T>G (p.Pro754=)
c.2169T>G (p.Pro723=)
c.2202T>G (p.Pro734=)
c.1770T>G (p.Pro590=)
3g.119414192C>ACA354050142ARHGAP31c.2263C>A (p.Leu755Met)
c.2170C>A (p.Leu724Met)
c.2203C>A (p.Leu735Met)
c.1771C>A (p.Leu591Met)
3g.119414192C>GCA354050144ARHGAP31c.2263C>G (p.Leu755Val)
c.2170C>G (p.Leu724Val)
c.2203C>G (p.Leu735Val)
c.1771C>G (p.Leu591Val)
3g.119414192C>TCA435411677ARHGAP31c.2263C>T (p.Leu755=)
c.2170C>T (p.Leu724=)
c.2203C>T (p.Leu735=)
c.1771C>T (p.Leu591=)
 COSMIC
3g.119414193T>ACA354050147ARHGAP31c.2264T>A (p.Leu755Gln)
c.2171T>A (p.Leu724Gln)
c.2204T>A (p.Leu735Gln)
c.1772T>A (p.Leu591Gln)
3g.119414193T>CCA354050152ARHGAP31c.2264T>C (p.Leu755Pro)
c.2171T>C (p.Leu724Pro)
c.2204T>C (p.Leu735Pro)
c.1772T>C (p.Leu591Pro)
3g.119414193T>GCA354050149ARHGAP31c.2264T>G (p.Leu755Arg)
c.2171T>G (p.Leu724Arg)
c.2204T>G (p.Leu735Arg)
c.1772T>G (p.Leu591Arg)
3g.119414194G>ACA435411682ARHGAP31c.2265G>A (p.Leu755=)
c.2172G>A (p.Leu724=)
c.2205G>A (p.Leu735=)
c.1773G>A (p.Leu591=)
 dbSNP gnomAD v2 gnomAD v4
3g.119414194G>CCA435411681ARHGAP31c.2265G>C (p.Leu755=)
c.2172G>C (p.Leu724=)
c.2205G>C (p.Leu735=)
c.1773G>C (p.Leu591=)
3g.119414194G=CA1396548594ARHGAP31c.2265G= (p.Leu755=)
c.2172G= (p.Leu724=)
c.2205G= (p.Leu735=)
c.1773G= (p.Leu591=)
3g.119414194G>TCA435411683ARHGAP31c.2265G>T (p.Leu755=)
c.2172G>T (p.Leu724=)
c.2205G>T (p.Leu735=)
c.1773G>T (p.Leu591=)
3g.119414195G>ACA354050155ARHGAP31c.2266G>A (p.Glu756Lys)
c.2173G>A (p.Glu725Lys)
c.2206G>A (p.Glu736Lys)
c.1774G>A (p.Glu592Lys)
3g.119414195G>CCA2553996ARHGAP31c.2266G>C (p.Glu756Gln)
c.2173G>C (p.Glu725Gln)
c.2206G>C (p.Glu736Gln)
c.1774G>C (p.Glu592Gln)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.119414195G=CA1396548595ARHGAP31c.2266G= (p.Glu756=)
c.2173G= (p.Glu725=)
c.2206G= (p.Glu736=)
c.1774G= (p.Glu592=)
3g.119414195G>TCA354050158ARHGAP31c.2266G>T (p.Glu756Ter)
c.2173G>T (p.Glu725Ter)
c.2206G>T (p.Glu736Ter)
c.1774G>T (p.Glu592Ter)
3g.119414196A>CCA354050166ARHGAP31c.2267A>C (p.Glu756Ala)
c.2174A>C (p.Glu725Ala)
c.2207A>C (p.Glu736Ala)
c.1775A>C (p.Glu592Ala)
3g.119414196A>GCA354050169ARHGAP31c.2267A>G (p.Glu756Gly)
c.2174A>G (p.Glu725Gly)
c.2207A>G (p.Glu736Gly)
c.1775A>G (p.Glu592Gly)
3g.119414196A>TCA354050175ARHGAP31c.2267A>T (p.Glu756Val)
c.2174A>T (p.Glu725Val)
c.2207A>T (p.Glu736Val)
c.1775A>T (p.Glu592Val)
3g.119414197A=CA1396548596ARHGAP31c.2268A= (p.Glu756=)
c.2175A= (p.Glu725=)
c.2208A= (p.Glu736=)
c.1776A= (p.Glu592=)
3g.119414197A>CCA354050179ARHGAP31c.2268A>C (p.Glu756Asp)
c.2175A>C (p.Glu725Asp)
c.2208A>C (p.Glu736Asp)
c.1776A>C (p.Glu592Asp)
3g.119414197A>GCA435411687ARHGAP31c.2268A>G (p.Glu756=)
c.2175A>G (p.Glu725=)
c.2208A>G (p.Glu736=)
c.1776A>G (p.Glu592=)
3g.119414197A>TCA2553997ARHGAP31c.2268A>T (p.Glu756Asp)
c.2175A>T (p.Glu725Asp)
c.2208A>T (p.Glu736Asp)
c.1776A>T (p.Glu592Asp)
 dbSNP ExAC gnomAD v2
3g.119414198A>CCA354050187ARHGAP31c.2269A>C (p.Ile757Leu)
c.2176A>C (p.Ile726Leu)
c.2209A>C (p.Ile737Leu)
c.1777A>C (p.Ile593Leu)
3g.119414198A>GCA354050189ARHGAP31c.2269A>G (p.Ile757Val)
c.2176A>G (p.Ile726Val)
c.2209A>G (p.Ile737Val)
c.1777A>G (p.Ile593Val)
3g.119414198A>TCA354050190ARHGAP31c.2269A>T (p.Ile757Leu)
c.2176A>T (p.Ile726Leu)
c.2209A>T (p.Ile737Leu)
c.1777A>T (p.Ile593Leu)
3g.119414199T>ACA354050193ARHGAP31c.2270T>A (p.Ile757Lys)
c.2177T>A (p.Ile726Lys)
c.2210T>A (p.Ile737Lys)
c.1778T>A (p.Ile593Lys)
3g.119414199T>CCA354050197ARHGAP31c.2270T>C (p.Ile757Thr)
c.2177T>C (p.Ile726Thr)
c.2210T>C (p.Ile737Thr)
c.1778T>C (p.Ile593Thr)
3g.119414199T>GCA354050199ARHGAP31c.2270T>G (p.Ile757Arg)
c.2177T>G (p.Ile726Arg)
c.2210T>G (p.Ile737Arg)
c.1778T>G (p.Ile593Arg)
3g.119414200A=CA1396548597ARHGAP31c.2271A= (p.Ile757=)
c.2178A= (p.Ile726=)
c.2211A= (p.Ile737=)
c.1779A= (p.Ile593=)
3g.119414200A>CCA435411689ARHGAP31c.2271A>C (p.Ile757=)
c.2178A>C (p.Ile726=)
c.2211A>C (p.Ile737=)
c.1779A>C (p.Ile593=)
3g.119414200A>GCA354050215ARHGAP31c.2271A>G (p.Ile757Met)
c.2178A>G (p.Ile726Met)
c.2211A>G (p.Ile737Met)
c.1779A>G (p.Ile593Met)
3g.119414200A>TCA435411690ARHGAP31c.2271A>T (p.Ile757=)
c.2178A>T (p.Ile726=)
c.2211A>T (p.Ile737=)
c.1779A>T (p.Ile593=)
 ClinVar dbSNP gnomAD v3 gnomAD v4
3g.119414201G>ACA354050218ARHGAP31c.2272G>A (p.Val758Ile)
c.2179G>A (p.Val727Ile)
c.2212G>A (p.Val738Ile)
c.1780G>A (p.Val594Ile)
3g.119414201G>CCA354050223ARHGAP31c.2272G>C (p.Val758Leu)
c.2179G>C (p.Val727Leu)
c.2212G>C (p.Val738Leu)
c.1780G>C (p.Val594Leu)
3g.119414201G>TCA354050220ARHGAP31c.2272G>T (p.Val758Phe)
c.2179G>T (p.Val727Phe)
c.2212G>T (p.Val738Phe)
c.1780G>T (p.Val594Phe)
3g.119414202T>ACA354050226ARHGAP31c.2273T>A (p.Val758Asp)
c.2180T>A (p.Val727Asp)
c.2213T>A (p.Val738Asp)
c.1781T>A (p.Val594Asp)
3g.119414202T>CCA354050229ARHGAP31c.2273T>C (p.Val758Ala)
c.2180T>C (p.Val727Ala)
c.2213T>C (p.Val738Ala)
c.1781T>C (p.Val594Ala)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.119414202T>GCA354050232ARHGAP31c.2273T>G (p.Val758Gly)
c.2180T>G (p.Val727Gly)
c.2213T>G (p.Val738Gly)
c.1781T>G (p.Val594Gly)
3g.119414202T=CA1396548598ARHGAP31c.2273T= (p.Val758=)
c.2180T= (p.Val727=)
c.2213T= (p.Val738=)
c.1781T= (p.Val594=)
3g.119414203T>ACA435411694ARHGAP31c.2274T>A (p.Val758=)
c.2181T>A (p.Val727=)
c.2214T>A (p.Val738=)
c.1782T>A (p.Val594=)
 dbSNP gnomAD v2 gnomAD v4
3g.119414203T>CCA435411695ARHGAP31c.2274T>C (p.Val758=)
c.2181T>C (p.Val727=)
c.2214T>C (p.Val738=)
c.1782T>C (p.Val594=)
3g.119414203T>GCA435411697ARHGAP31c.2274T>G (p.Val758=)
c.2181T>G (p.Val727=)
c.2214T>G (p.Val738=)
c.1782T>G (p.Val594=)
3g.119414203T=CA1396548599ARHGAP31c.2274T= (p.Val758=)
c.2181T= (p.Val727=)
c.2214T= (p.Val738=)
c.1782T= (p.Val594=)
3g.119414204C>ACA354050236ARHGAP31c.2275C>A (p.Pro759Thr)
c.2182C>A (p.Pro728Thr)
c.2215C>A (p.Pro739Thr)
c.1783C>A (p.Pro595Thr)
 dbSNP gnomAD v2 gnomAD v4
3g.119414204C=CA1396548600ARHGAP31c.2275C= (p.Pro759=)
c.2182C= (p.Pro728=)
c.2215C= (p.Pro739=)
c.1783C= (p.Pro595=)
3g.119414204C>GCA354050239ARHGAP31c.2275C>G (p.Pro759Ala)
c.2182C>G (p.Pro728Ala)
c.2215C>G (p.Pro739Ala)
c.1783C>G (p.Pro595Ala)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.119414204C>TCA354050241ARHGAP31c.2275C>T (p.Pro759Ser)
c.2182C>T (p.Pro728Ser)
c.2215C>T (p.Pro739Ser)
c.1783C>T (p.Pro595Ser)
 COSMIC
3g.119414205C>ACA354050243ARHGAP31c.2276C>A (p.Pro759His)
c.2183C>A (p.Pro728His)
c.2216C>A (p.Pro739His)
c.1784C>A (p.Pro595His)
 gnomAD v4
3g.119414205C>GCA354050246ARHGAP31c.2276C>G (p.Pro759Arg)
c.2183C>G (p.Pro728Arg)
c.2216C>G (p.Pro739Arg)
c.1784C>G (p.Pro595Arg)
3g.119414205C>TCA354050247ARHGAP31c.2276C>T (p.Pro759Leu)
c.2183C>T (p.Pro728Leu)
c.2216C>T (p.Pro739Leu)
c.1784C>T (p.Pro595Leu)
3g.119414206T>ACA435411700ARHGAP31c.2277T>A (p.Pro759=)
c.2184T>A (p.Pro728=)
c.2217T>A (p.Pro739=)
c.1785T>A (p.Pro595=)
3g.119414206T>CCA435411701ARHGAP31c.2277T>C (p.Pro759=)
c.2184T>C (p.Pro728=)
c.2217T>C (p.Pro739=)
c.1785T>C (p.Pro595=)
3g.119414206T>GCA435411702ARHGAP31c.2277T>G (p.Pro759=)
c.2184T>G (p.Pro728=)
c.2217T>G (p.Pro739=)
c.1785T>G (p.Pro595=)
3g.119414207T>ACA354050257ARHGAP31c.2278T>A (p.Phe760Ile)
c.2185T>A (p.Phe729Ile)
c.2218T>A (p.Phe740Ile)
c.1786T>A (p.Phe596Ile)
3g.119414207T>CCA354050256ARHGAP31c.2278T>C (p.Phe760Leu)
c.2185T>C (p.Phe729Leu)
c.2218T>C (p.Phe740Leu)
c.1786T>C (p.Phe596Leu)
3g.119414207T>GCA354050253ARHGAP31c.2278T>G (p.Phe760Val)
c.2185T>G (p.Phe729Val)
c.2218T>G (p.Phe740Val)
c.1786T>G (p.Phe596Val)
3g.119414208T>ACA354050258ARHGAP31c.2279T>A (p.Phe760Tyr)
c.2186T>A (p.Phe729Tyr)
c.2219T>A (p.Phe740Tyr)
c.1787T>A (p.Phe596Tyr)
3g.119414208T>CCA354050259ARHGAP31c.2279T>C (p.Phe760Ser)
c.2186T>C (p.Phe729Ser)
c.2219T>C (p.Phe740Ser)
c.1787T>C (p.Phe596Ser)
3g.119414208T>GCA354050262ARHGAP31c.2279T>G (p.Phe760Cys)
c.2186T>G (p.Phe729Cys)
c.2219T>G (p.Phe740Cys)
c.1787T>G (p.Phe596Cys)
3g.119414209T>ACA354050266ARHGAP31c.2280T>A (p.Phe760Leu)
c.2187T>A (p.Phe729Leu)
c.2220T>A (p.Phe740Leu)
c.1788T>A (p.Phe596Leu)
3g.119414209T>CCA435411705ARHGAP31c.2280T>C (p.Phe760=)
c.2187T>C (p.Phe729=)
c.2220T>C (p.Phe740=)
c.1788T>C (p.Phe596=)
3g.119414209T>GCA354050270ARHGAP31c.2280T>G (p.Phe760Leu)
c.2187T>G (p.Phe729Leu)
c.2220T>G (p.Phe740Leu)
c.1788T>G (p.Phe596Leu)
 dbSNP
3g.119414209T=CA1396548601ARHGAP31c.2280T= (p.Phe760=)
c.2187T= (p.Phe729=)
c.2220T= (p.Phe740=)
c.1788T= (p.Phe596=)
3g.119414210G>ACA354050281ARHGAP31c.2281G>A (p.Glu761Lys)
c.2188G>A (p.Glu730Lys)
c.2221G>A (p.Glu741Lys)
c.1789G>A (p.Glu597Lys)
3g.119414210G>CCA354050285ARHGAP31c.2281G>C (p.Glu761Gln)
c.2188G>C (p.Glu730Gln)
c.2221G>C (p.Glu741Gln)
c.1789G>C (p.Glu597Gln)
3g.119414210G>TCA354050289ARHGAP31c.2281G>T (p.Glu761Ter)
c.2188G>T (p.Glu730Ter)
c.2221G>T (p.Glu741Ter)
c.1789G>T (p.Glu597Ter)
3g.119414211A>CCA354050296ARHGAP31c.2282A>C (p.Glu761Ala)
c.2189A>C (p.Glu730Ala)
c.2222A>C (p.Glu741Ala)
c.1790A>C (p.Glu597Ala)
3g.119414211A>GCA354050302ARHGAP31c.2282A>G (p.Glu761Gly)
c.2189A>G (p.Glu730Gly)
c.2222A>G (p.Glu741Gly)
c.1790A>G (p.Glu597Gly)
3g.119414211A>TCA354050303ARHGAP31c.2282A>T (p.Glu761Val)
c.2189A>T (p.Glu730Val)
c.2222A>T (p.Glu741Val)
c.1790A>T (p.Glu597Val)
3g.119414212G>ACA435411710ARHGAP31c.2283G>A (p.Glu761=)
c.2190G>A (p.Glu730=)
c.2223G>A (p.Glu741=)
c.1791G>A (p.Glu597=)
3g.119414212G>CCA354050309ARHGAP31c.2283G>C (p.Glu761Asp)
c.2190G>C (p.Glu730Asp)
c.2223G>C (p.Glu741Asp)
c.1791G>C (p.Glu597Asp)
3g.119414212G>TCA354050310ARHGAP31c.2283G>T (p.Glu761Asp)
c.2190G>T (p.Glu730Asp)
c.2223G>T (p.Glu741Asp)
c.1791G>T (p.Glu597Asp)
3g.119414213A>CCA354050313ARHGAP31c.2284A>C (p.Lys762Gln)
c.2191A>C (p.Lys731Gln)
c.2224A>C (p.Lys742Gln)
c.1792A>C (p.Lys598Gln)
3g.119414213A>GCA354050317ARHGAP31c.2284A>G (p.Lys762Glu)
c.2191A>G (p.Lys731Glu)
c.2224A>G (p.Lys742Glu)
c.1792A>G (p.Lys598Glu)
3g.119414213A>TCA354050315ARHGAP31c.2284A>T (p.Lys762Ter)
c.2191A>T (p.Lys731Ter)
c.2224A>T (p.Lys742Ter)
c.1792A>T (p.Lys598Ter)
3g.119414214A=CA1396548602ARHGAP31c.2285A= (p.Lys762=)
c.2192A= (p.Lys731=)
c.2225A= (p.Lys742=)
c.1793A= (p.Lys598=)
3g.119414214A>CCA2553998ARHGAP31c.2285A>C (p.Lys762Thr)
c.2192A>C (p.Lys731Thr)
c.2225A>C (p.Lys742Thr)
c.1793A>C (p.Lys598Thr)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.119414214A>GCA2553999ARHGAP31c.2285A>G (p.Lys762Arg)
c.2192A>G (p.Lys731Arg)
c.2225A>G (p.Lys742Arg)
c.1793A>G (p.Lys598Arg)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.119414214A>TCA354050326ARHGAP31c.2285A>T (p.Lys762Met)
c.2192A>T (p.Lys731Met)
c.2225A>T (p.Lys742Met)
c.1793A>T (p.Lys598Met)
3g.119414215G>ACA435411715ARHGAP31c.2286G>A (p.Lys762=)
c.2193G>A (p.Lys731=)
c.2226G>A (p.Lys742=)
c.1794G>A (p.Lys598=)
 gnomAD v4
3g.119414215G>CCA354050329ARHGAP31c.2286G>C (p.Lys762Asn)
c.2193G>C (p.Lys731Asn)
c.2226G>C (p.Lys742Asn)
c.1794G>C (p.Lys598Asn)
3g.119414215G>TCA354050330ARHGAP31c.2286G>T (p.Lys762Asn)
c.2193G>T (p.Lys731Asn)
c.2226G>T (p.Lys742Asn)
c.1794G>T (p.Lys598Asn)
 gnomAD v4
3g.119414216G>ACA354050334ARHGAP31c.2287G>A (p.Ala763Thr)
c.2194G>A (p.Ala732Thr)
c.2227G>A (p.Ala743Thr)
c.1795G>A (p.Ala599Thr)
 dbSNP
3g.119414216G>CCA81697499ARHGAP31c.2287G>C (p.Ala763Pro)
c.2194G>C (p.Ala732Pro)
c.2227G>C (p.Ala743Pro)
c.1795G>C (p.Ala599Pro)
 ClinVar dbSNP gnomAD v3 gnomAD v4
3g.119414216G=CA1396548603ARHGAP31c.2287G= (p.Ala763=)
c.2194G= (p.Ala732=)
c.2227G= (p.Ala743=)
c.1795G= (p.Ala599=)
3g.119414216G>TCA354050336ARHGAP31c.2287G>T (p.Ala763Ser)
c.2194G>T (p.Ala732Ser)
c.2227G>T (p.Ala743Ser)
c.1795G>T (p.Ala599Ser)
 gnomAD v4
3g.119414217C>ACA354050337ARHGAP31c.2288C>A (p.Ala763Glu)
c.2195C>A (p.Ala732Glu)
c.2228C>A (p.Ala743Glu)
c.1796C>A (p.Ala599Glu)
3g.119414217C=CA1396548604ARHGAP31c.2288C= (p.Ala763=)
c.2195C= (p.Ala732=)
c.2228C= (p.Ala743=)
c.1796C= (p.Ala599=)
3g.119414217C>GCA354050340ARHGAP31c.2288C>G (p.Ala763Gly)
c.2195C>G (p.Ala732Gly)
c.2228C>G (p.Ala743Gly)
c.1796C>G (p.Ala599Gly)
3g.119414217C>TCA2554000ARHGAP31c.2288C>T (p.Ala763Val)
c.2195C>T (p.Ala732Val)
c.2228C>T (p.Ala743Val)
c.1796C>T (p.Ala599Val)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.119414218A=CA1396548605ARHGAP31c.2289A= (p.Ala763=)
c.2196A= (p.Ala732=)
c.2229A= (p.Ala743=)
c.1797A= (p.Ala599=)
3g.119414218A>CCA435411721ARHGAP31c.2289A>C (p.Ala763=)
c.2196A>C (p.Ala732=)
c.2229A>C (p.Ala743=)
c.1797A>C (p.Ala599=)
3g.119414218A>GCA435411720ARHGAP31c.2289A>G (p.Ala763=)
c.2196A>G (p.Ala732=)
c.2229A>G (p.Ala743=)
c.1797A>G (p.Ala599=)
3g.119414218A>TCA435411719ARHGAP31c.2289A>T (p.Ala763=)
c.2196A>T (p.Ala732=)
c.2229A>T (p.Ala743=)
c.1797A>T (p.Ala599=)
 dbSNP gnomAD v3 gnomAD v4
3g.119414219T>ACA354050345ARHGAP31c.2290T>A (p.Ser764Thr)
c.2197T>A (p.Ser733Thr)
c.2230T>A (p.Ser744Thr)
c.1798T>A (p.Ser600Thr)
3g.119414219T>CCA354050346ARHGAP31c.2290T>C (p.Ser764Pro)
c.2197T>C (p.Ser733Pro)
c.2230T>C (p.Ser744Pro)
c.1798T>C (p.Ser600Pro)
3g.119414219T>GCA354050344ARHGAP31c.2290T>G (p.Ser764Ala)
c.2197T>G (p.Ser733Ala)
c.2230T>G (p.Ser744Ala)
c.1798T>G (p.Ser600Ala)
3g.119414220C>ACA354050347ARHGAP31c.2291C>A (p.Ser764Tyr)
c.2198C>A (p.Ser733Tyr)
c.2231C>A (p.Ser744Tyr)
c.1799C>A (p.Ser600Tyr)
3g.119414220C>GCA354050349ARHGAP31c.2291C>G (p.Ser764Cys)
c.2198C>G (p.Ser733Cys)
c.2231C>G (p.Ser744Cys)
c.1799C>G (p.Ser600Cys)
3g.119414220C>TCA354050352ARHGAP31c.2291C>T (p.Ser764Phe)
c.2198C>T (p.Ser733Phe)
c.2231C>T (p.Ser744Phe)
c.1799C>T (p.Ser600Phe)
3g.119414221T>ACA435411723ARHGAP31c.2292T>A (p.Ser764=)
c.2199T>A (p.Ser733=)
c.2232T>A (p.Ser744=)
c.1800T>A (p.Ser600=)
3g.119414221T>CCA2554001ARHGAP31c.2292T>C (p.Ser764=)
c.2199T>C (p.Ser733=)
c.2232T>C (p.Ser744=)
c.1800T>C (p.Ser600=)
 dbSNP ExAC gnomAD v4
3g.119414221T>GCA435411724ARHGAP31c.2292T>G (p.Ser764=)
c.2199T>G (p.Ser733=)
c.2232T>G (p.Ser744=)
c.1800T>G (p.Ser600=)
3g.119414221T=CA1396548606ARHGAP31c.2292T= (p.Ser764=)
c.2199T= (p.Ser733=)
c.2232T= (p.Ser744=)
c.1800T= (p.Ser600=)
3g.119414222C>ACA354050357ARHGAP31c.2293C>A (p.Pro765Thr)
c.2200C>A (p.Pro734Thr)
c.2233C>A (p.Pro745Thr)
c.1801C>A (p.Pro601Thr)
3g.119414222C>GCA354050358ARHGAP31c.2293C>G (p.Pro765Ala)
c.2200C>G (p.Pro734Ala)
c.2233C>G (p.Pro745Ala)
c.1801C>G (p.Pro601Ala)
 dbSNP
3g.119414222C>TCA354050360ARHGAP31c.2293C>T (p.Pro765Ser)
c.2200C>T (p.Pro734Ser)
c.2233C>T (p.Pro745Ser)
c.1801C>T (p.Pro601Ser)
 gnomAD v4
3g.119414223C>ACA354050363ARHGAP31c.2294C>A (p.Pro765Gln)
c.2201C>A (p.Pro734Gln)
c.2234C>A (p.Pro745Gln)
c.1802C>A (p.Pro601Gln)
3g.119414223C>GCA354050366ARHGAP31c.2294C>G (p.Pro765Arg)
c.2201C>G (p.Pro734Arg)
c.2234C>G (p.Pro745Arg)
c.1802C>G (p.Pro601Arg)
3g.119414223C>TCA354050368ARHGAP31c.2294C>T (p.Pro765Leu)
c.2201C>T (p.Pro734Leu)
c.2234C>T (p.Pro745Leu)
c.1802C>T (p.Pro601Leu)
 gnomAD v4
3g.119414224A>CCA435411725ARHGAP31c.2295A>C (p.Pro765=)
c.2202A>C (p.Pro734=)
c.2235A>C (p.Pro745=)
c.1803A>C (p.Pro601=)
3g.119414224A>GCA435411726ARHGAP31c.2295A>G (p.Pro765=)
c.2202A>G (p.Pro734=)
c.2235A>G (p.Pro745=)
c.1803A>G (p.Pro601=)
3g.119414224A>TCA435411727ARHGAP31c.2295A>T (p.Pro765=)
c.2202A>T (p.Pro734=)
c.2235A>T (p.Pro745=)
c.1803A>T (p.Pro601=)
3g.119414225C>ACA354050370ARHGAP31c.2296C>A (p.Gln766Lys)
c.2203C>A (p.Gln735Lys)
c.2236C>A (p.Gln746Lys)
c.1804C>A (p.Gln602Lys)
 dbSNP gnomAD v3 gnomAD v4
3g.119414225C=CA1396548607ARHGAP31c.2296C= (p.Gln766=)
c.2203C= (p.Gln735=)
c.2236C= (p.Gln746=)
c.1804C= (p.Gln602=)
3g.119414225C>GCA354050375ARHGAP31c.2296C>G (p.Gln766Glu)
c.2203C>G (p.Gln735Glu)
c.2236C>G (p.Gln746Glu)
c.1804C>G (p.Gln602Glu)
 gnomAD v4
3g.119414225C>TCA354050378ARHGAP31c.2296C>T (p.Gln766Ter)
c.2203C>T (p.Gln735Ter)
c.2236C>T (p.Gln746Ter)
c.1804C>T (p.Gln602Ter)
3g.119414226A>CCA354050389ARHGAP31c.2297A>C (p.Gln766Pro)
c.2204A>C (p.Gln735Pro)
c.2237A>C (p.Gln746Pro)
c.1805A>C (p.Gln602Pro)
3g.119414226A>GCA354050383ARHGAP31c.2297A>G (p.Gln766Arg)
c.2204A>G (p.Gln735Arg)
c.2237A>G (p.Gln746Arg)
c.1805A>G (p.Gln602Arg)
3g.119414226A>TCA354050381ARHGAP31c.2297A>T (p.Gln766Leu)
c.2204A>T (p.Gln735Leu)
c.2237A>T (p.Gln746Leu)
c.1805A>T (p.Gln602Leu)
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=)

Number of alleles fetched