Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.119413925G>ACA354048175ARHGAP31c.1996G>A (p.Glu666Lys)
c.1903G>A (p.Glu635Lys)
c.1936G>A (p.Glu646Lys)
c.1504G>A (p.Glu502Lys)
3g.119413925G>CCA354048177ARHGAP31c.1996G>C (p.Glu666Gln)
c.1903G>C (p.Glu635Gln)
c.1936G>C (p.Glu646Gln)
c.1504G>C (p.Glu502Gln)
3g.119413925G>TCA354048176ARHGAP31c.1996G>T (p.Glu666Ter)
c.1903G>T (p.Glu635Ter)
c.1936G>T (p.Glu646Ter)
c.1504G>T (p.Glu502Ter)
3g.119413926A>CCA354048178ARHGAP31c.1997A>C (p.Glu666Ala)
c.1904A>C (p.Glu635Ala)
c.1937A>C (p.Glu646Ala)
c.1505A>C (p.Glu502Ala)
3g.119413926A>GCA354048180ARHGAP31c.1997A>G (p.Glu666Gly)
c.1904A>G (p.Glu635Gly)
c.1937A>G (p.Glu646Gly)
c.1505A>G (p.Glu502Gly)
3g.119413926A>TCA354048182ARHGAP31c.1997A>T (p.Glu666Val)
c.1904A>T (p.Glu635Val)
c.1937A>T (p.Glu646Val)
c.1505A>T (p.Glu502Val)
3g.119413927G>ACA435411393ARHGAP31c.1998G>A (p.Glu666=)
c.1905G>A (p.Glu635=)
c.1938G>A (p.Glu646=)
c.1506G>A (p.Glu502=)
3g.119413927G>CCA354048185ARHGAP31c.1998G>C (p.Glu666Asp)
c.1905G>C (p.Glu635Asp)
c.1938G>C (p.Glu646Asp)
c.1506G>C (p.Glu502Asp)
3g.119413927G>TCA354048186ARHGAP31c.1998G>T (p.Glu666Asp)
c.1905G>T (p.Glu635Asp)
c.1938G>T (p.Glu646Asp)
c.1506G>T (p.Glu502Asp)
3g.119413928G>ACA354048190ARHGAP31c.1999G>A (p.Glu667Lys)
c.1906G>A (p.Glu636Lys)
c.1939G>A (p.Glu647Lys)
c.1507G>A (p.Glu503Lys)
3g.119413928G>CCA354048193ARHGAP31c.1999G>C (p.Glu667Gln)
c.1906G>C (p.Glu636Gln)
c.1939G>C (p.Glu647Gln)
c.1507G>C (p.Glu503Gln)
3g.119413928G>TCA354048194ARHGAP31c.1999G>T (p.Glu667Ter)
c.1906G>T (p.Glu636Ter)
c.1939G>T (p.Glu647Ter)
c.1507G>T (p.Glu503Ter)
3g.119413929A>CCA354048195ARHGAP31c.2000A>C (p.Glu667Ala)
c.1907A>C (p.Glu636Ala)
c.1940A>C (p.Glu647Ala)
c.1508A>C (p.Glu503Ala)
3g.119413929A>GCA354048196ARHGAP31c.2000A>G (p.Glu667Gly)
c.1907A>G (p.Glu636Gly)
c.1940A>G (p.Glu647Gly)
c.1508A>G (p.Glu503Gly)
3g.119413929A>TCA354048197ARHGAP31c.2000A>T (p.Glu667Val)
c.1907A>T (p.Glu636Val)
c.1940A>T (p.Glu647Val)
c.1508A>T (p.Glu503Val)
3g.119413930G>ACA435411401ARHGAP31c.2001G>A (p.Glu667=)
c.1908G>A (p.Glu636=)
c.1941G>A (p.Glu647=)
c.1509G>A (p.Glu503=)
3g.119413930G>CCA354048201ARHGAP31c.2001G>C (p.Glu667Asp)
c.1908G>C (p.Glu636Asp)
c.1941G>C (p.Glu647Asp)
c.1509G>C (p.Glu503Asp)
3g.119413930G>TCA354048199ARHGAP31c.2001G>T (p.Glu667Asp)
c.1908G>T (p.Glu636Asp)
c.1941G>T (p.Glu647Asp)
c.1509G>T (p.Glu503Asp)
3g.119413931G>ACA354048204ARHGAP31c.2002G>A (p.Glu668Lys)
c.1909G>A (p.Glu637Lys)
c.1942G>A (p.Glu648Lys)
c.1510G>A (p.Glu504Lys)
3g.119413931G>CCA354048208ARHGAP31c.2002G>C (p.Glu668Gln)
c.1909G>C (p.Glu637Gln)
c.1942G>C (p.Glu648Gln)
c.1510G>C (p.Glu504Gln)
3g.119413931G>TCA354048211ARHGAP31c.2002G>T (p.Glu668Ter)
c.1909G>T (p.Glu637Ter)
c.1942G>T (p.Glu648Ter)
c.1510G>T (p.Glu504Ter)
3g.119413932A=CA1396548477ARHGAP31c.2003A= (p.Glu668=)
c.1910A= (p.Glu637=)
c.1943A= (p.Glu648=)
c.1511A= (p.Glu504=)
3g.119413932A>CCA354048214ARHGAP31c.2003A>C (p.Glu668Ala)
c.1910A>C (p.Glu637Ala)
c.1943A>C (p.Glu648Ala)
c.1511A>C (p.Glu504Ala)
 dbSNP
3g.119413932A>GCA354048216ARHGAP31c.2003A>G (p.Glu668Gly)
c.1910A>G (p.Glu637Gly)
c.1943A>G (p.Glu648Gly)
c.1511A>G (p.Glu504Gly)
3g.119413932A>TCA354048220ARHGAP31c.2003A>T (p.Glu668Val)
c.1910A>T (p.Glu637Val)
c.1943A>T (p.Glu648Val)
c.1511A>T (p.Glu504Val)
3g.119413933G>ACA435411405ARHGAP31c.2004G>A (p.Glu668=)
c.1911G>A (p.Glu637=)
c.1944G>A (p.Glu648=)
c.1512G>A (p.Glu504=)
3g.119413933G>CCA354048232ARHGAP31c.2004G>C (p.Glu668Asp)
c.1911G>C (p.Glu637Asp)
c.1944G>C (p.Glu648Asp)
c.1512G>C (p.Glu504Asp)
3g.119413933G>TCA354048227ARHGAP31c.2004G>T (p.Glu668Asp)
c.1911G>T (p.Glu637Asp)
c.1944G>T (p.Glu648Asp)
c.1512G>T (p.Glu504Asp)
3g.119413934C>ACA354048236ARHGAP31c.2005C>A (p.Leu669Ile)
c.1912C>A (p.Leu638Ile)
c.1945C>A (p.Leu649Ile)
c.1513C>A (p.Leu505Ile)
3g.119413934C=CA1396548478ARHGAP31c.2005C= (p.Leu669=)
c.1912C= (p.Leu638=)
c.1945C= (p.Leu649=)
c.1513C= (p.Leu505=)
3g.119413934C>GCA81697286ARHGAP31c.2005C>G (p.Leu669Val)
c.1912C>G (p.Leu638Val)
c.1945C>G (p.Leu649Val)
c.1513C>G (p.Leu505Val)
 dbSNP
3g.119413934C>TCA354048242ARHGAP31c.2005C>T (p.Leu669Phe)
c.1912C>T (p.Leu638Phe)
c.1945C>T (p.Leu649Phe)
c.1513C>T (p.Leu505Phe)
 gnomAD v4
3g.119413935T>ACA354048246ARHGAP31c.2006T>A (p.Leu669His)
c.1913T>A (p.Leu638His)
c.1946T>A (p.Leu649His)
c.1514T>A (p.Leu505His)
3g.119413935T>CCA354048249ARHGAP31c.2006T>C (p.Leu669Pro)
c.1913T>C (p.Leu638Pro)
c.1946T>C (p.Leu649Pro)
c.1514T>C (p.Leu505Pro)
3g.119413935T>GCA354048252ARHGAP31c.2006T>G (p.Leu669Arg)
c.1913T>G (p.Leu638Arg)
c.1946T>G (p.Leu649Arg)
c.1514T>G (p.Leu505Arg)
3g.119413936C>ACA435411409ARHGAP31c.2007C>A (p.Leu669=)
c.1914C>A (p.Leu638=)
c.1947C>A (p.Leu649=)
c.1515C>A (p.Leu505=)
3g.119413936C=CA1396548479ARHGAP31c.2007C= (p.Leu669=)
c.1914C= (p.Leu638=)
c.1947C= (p.Leu649=)
c.1515C= (p.Leu505=)
3g.119413936C>GCA81697288ARHGAP31c.2007C>G (p.Leu669=)
c.1914C>G (p.Leu638=)
c.1947C>G (p.Leu649=)
c.1515C>G (p.Leu505=)
 dbSNP gnomAD v4
3g.119413936C>TCA435411411ARHGAP31c.2007C>T (p.Leu669=)
c.1914C>T (p.Leu638=)
c.1947C>T (p.Leu649=)
c.1515C>T (p.Leu505=)
 dbSNP gnomAD v3 gnomAD v4
3g.119413937T>ACA354048263ARHGAP31c.2008T>A (p.Ser670Thr)
c.1915T>A (p.Ser639Thr)
c.1948T>A (p.Ser650Thr)
c.1516T>A (p.Ser506Thr)
3g.119413937T>CCA354048257ARHGAP31c.2008T>C (p.Ser670Pro)
c.1915T>C (p.Ser639Pro)
c.1948T>C (p.Ser650Pro)
c.1516T>C (p.Ser506Pro)
3g.119413937T>GCA354048260ARHGAP31c.2008T>G (p.Ser670Ala)
c.1915T>G (p.Ser639Ala)
c.1948T>G (p.Ser650Ala)
c.1516T>G (p.Ser506Ala)
3g.119413938C>ACA354048266ARHGAP31c.2009C>A (p.Ser670Ter)
c.1916C>A (p.Ser639Ter)
c.1949C>A (p.Ser650Ter)
c.1517C>A (p.Ser506Ter)
3g.119413938C>GCA354048269ARHGAP31c.2009C>G (p.Ser670Ter)
c.1916C>G (p.Ser639Ter)
c.1949C>G (p.Ser650Ter)
c.1517C>G (p.Ser506Ter)
3g.119413938C>TCA354048271ARHGAP31c.2009C>T (p.Ser670Leu)
c.1916C>T (p.Ser639Leu)
c.1949C>T (p.Ser650Leu)
c.1517C>T (p.Ser506Leu)
3g.119413939A=CA1396548480ARHGAP31c.2010A= (p.Ser670=)
c.1917A= (p.Ser639=)
c.1950A= (p.Ser650=)
c.1518A= (p.Ser506=)
3g.119413939A>CCA435411423ARHGAP31c.2010A>C (p.Ser670=)
c.1917A>C (p.Ser639=)
c.1950A>C (p.Ser650=)
c.1518A>C (p.Ser506=)
 gnomAD v4
3g.119413939A>GCA435411422ARHGAP31c.2010A>G (p.Ser670=)
c.1917A>G (p.Ser639=)
c.1950A>G (p.Ser650=)
c.1518A>G (p.Ser506=)
3g.119413939A>TCA81697298ARHGAP31c.2010A>T (p.Ser670=)
c.1917A>T (p.Ser639=)
c.1950A>T (p.Ser650=)
c.1518A>T (p.Ser506=)
 dbSNP
3g.119413940T>ACA354048274ARHGAP31c.2011T>A (p.Ser671Thr)
c.1918T>A (p.Ser640Thr)
c.1951T>A (p.Ser651Thr)
c.1519T>A (p.Ser507Thr)
3g.119413940T>CCA354048275ARHGAP31c.2011T>C (p.Ser671Pro)
c.1918T>C (p.Ser640Pro)
c.1951T>C (p.Ser651Pro)
c.1519T>C (p.Ser507Pro)
3g.119413940T>GCA354048276ARHGAP31c.2011T>G (p.Ser671Ala)
c.1918T>G (p.Ser640Ala)
c.1951T>G (p.Ser651Ala)
c.1519T>G (p.Ser507Ala)
3g.119413941C>ACA354048278ARHGAP31c.2012C>A (p.Ser671Ter)
c.1919C>A (p.Ser640Ter)
c.1952C>A (p.Ser651Ter)
c.1520C>A (p.Ser507Ter)
3g.119413941C=CA1396548481ARHGAP31c.2012C= (p.Ser671=)
c.1919C= (p.Ser640=)
c.1952C= (p.Ser651=)
c.1520C= (p.Ser507=)
3g.119413941C>GCA354048280ARHGAP31c.2012C>G (p.Ser671Trp)
c.1919C>G (p.Ser640Trp)
c.1952C>G (p.Ser651Trp)
c.1520C>G (p.Ser507Trp)
3g.119413941C>TCA354048283ARHGAP31c.2012C>T (p.Ser671Leu)
c.1919C>T (p.Ser640Leu)
c.1952C>T (p.Ser651Leu)
c.1520C>T (p.Ser507Leu)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.119413942G>ACA435411432ARHGAP31c.2013G>A (p.Ser671=)
c.1920G>A (p.Ser640=)
c.1953G>A (p.Ser651=)
c.1521G>A (p.Ser507=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
3g.119413942G>CCA435411433ARHGAP31c.2013G>C (p.Ser671=)
c.1920G>C (p.Ser640=)
c.1953G>C (p.Ser651=)
c.1521G>C (p.Ser507=)
3g.119413942G=CA1396548482ARHGAP31c.2013G= (p.Ser671=)
c.1920G= (p.Ser640=)
c.1953G= (p.Ser651=)
c.1521G= (p.Ser507=)
3g.119413942G>TCA2553947ARHGAP31c.2013G>T (p.Ser671=)
c.1920G>T (p.Ser640=)
c.1953G>T (p.Ser651=)
c.1521G>T (p.Ser507=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.119413943T>ACA354048288ARHGAP31c.2014T>A (p.Leu672Met)
c.1921T>A (p.Leu641Met)
c.1954T>A (p.Leu652Met)
c.1522T>A (p.Leu508Met)
3g.119413943T>CCA435411434ARHGAP31c.2014T>C (p.Leu672=)
c.1921T>C (p.Leu641=)
c.1954T>C (p.Leu652=)
c.1522T>C (p.Leu508=)
3g.119413943T>GCA354048290ARHGAP31c.2014T>G (p.Leu672Val)
c.1921T>G (p.Leu641Val)
c.1954T>G (p.Leu652Val)
c.1522T>G (p.Leu508Val)
3g.119413944T>ACA354048294ARHGAP31c.2015T>A (p.Leu672Ter)
c.1922T>A (p.Leu641Ter)
c.1955T>A (p.Leu652Ter)
c.1523T>A (p.Leu508Ter)
3g.119413944T>CCA354048299ARHGAP31c.2015T>C (p.Leu672Ser)
c.1922T>C (p.Leu641Ser)
c.1955T>C (p.Leu652Ser)
c.1523T>C (p.Leu508Ser)
3g.119413944T>GCA354048295ARHGAP31c.2015T>G (p.Leu672Trp)
c.1922T>G (p.Leu641Trp)
c.1955T>G (p.Leu652Trp)
c.1523T>G (p.Leu508Trp)
3g.119413945G>ACA2553948ARHGAP31c.2016G>A (p.Leu672=)
c.1923G>A (p.Leu641=)
c.1956G>A (p.Leu652=)
c.1524G>A (p.Leu508=)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.119413945G>CCA354048312ARHGAP31c.2016G>C (p.Leu672Phe)
c.1923G>C (p.Leu641Phe)
c.1956G>C (p.Leu652Phe)
c.1524G>C (p.Leu508Phe)
3g.119413945G=CA1396548483ARHGAP31c.2016G= (p.Leu672=)
c.1923G= (p.Leu641=)
c.1956G= (p.Leu652=)
c.1524G= (p.Leu508=)
3g.119413945G>TCA354048311ARHGAP31c.2016G>T (p.Leu672Phe)
c.1923G>T (p.Leu641Phe)
c.1956G>T (p.Leu652Phe)
c.1524G>T (p.Leu508Phe)
3g.119413946C>ACA354048313ARHGAP31c.2017C>A (p.Pro673Thr)
c.1924C>A (p.Pro642Thr)
c.1957C>A (p.Pro653Thr)
c.1525C>A (p.Pro509Thr)
3g.119413946C>GCA354048318ARHGAP31c.2017C>G (p.Pro673Ala)
c.1924C>G (p.Pro642Ala)
c.1957C>G (p.Pro653Ala)
c.1525C>G (p.Pro509Ala)
3g.119413946C>TCA354048319ARHGAP31c.2017C>T (p.Pro673Ser)
c.1924C>T (p.Pro642Ser)
c.1957C>T (p.Pro653Ser)
c.1525C>T (p.Pro509Ser)
 COSMIC
3g.119413947C>ACA354048325ARHGAP31c.2018C>A (p.Pro673Gln)
c.1925C>A (p.Pro642Gln)
c.1958C>A (p.Pro653Gln)
c.1526C>A (p.Pro509Gln)
3g.119413947C>GCA354048328ARHGAP31c.2018C>G (p.Pro673Arg)
c.1925C>G (p.Pro642Arg)
c.1958C>G (p.Pro653Arg)
c.1526C>G (p.Pro509Arg)
3g.119413947C>TCA354048330ARHGAP31c.2018C>T (p.Pro673Leu)
c.1925C>T (p.Pro642Leu)
c.1958C>T (p.Pro653Leu)
c.1526C>T (p.Pro509Leu)
3g.119413948A=CA1396548484ARHGAP31c.2019A= (p.Pro673=)
c.1926A= (p.Pro642=)
c.1959A= (p.Pro653=)
c.1527A= (p.Pro509=)
3g.119413948A>CCA435411443ARHGAP31c.2019A>C (p.Pro673=)
c.1926A>C (p.Pro642=)
c.1959A>C (p.Pro653=)
c.1527A>C (p.Pro509=)
3g.119413948A>GCA2553949ARHGAP31c.2019A>G (p.Pro673=)
c.1926A>G (p.Pro642=)
c.1959A>G (p.Pro653=)
c.1527A>G (p.Pro509=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.119413948A>TCA435411444ARHGAP31c.2019A>T (p.Pro673=)
c.1926A>T (p.Pro642=)
c.1959A>T (p.Pro653=)
c.1527A>T (p.Pro509=)
3g.119413949C>ACA354048336ARHGAP31c.2020C>A (p.Pro674Thr)
c.1927C>A (p.Pro643Thr)
c.1960C>A (p.Pro654Thr)
c.1528C>A (p.Pro510Thr)
 gnomAD v4 COSMIC
3g.119413949C=CA1396548485ARHGAP31c.2020C= (p.Pro674=)
c.1927C= (p.Pro643=)
c.1960C= (p.Pro654=)
c.1528C= (p.Pro510=)
3g.119413949C>GCA354048339ARHGAP31c.2020C>G (p.Pro674Ala)
c.1927C>G (p.Pro643Ala)
c.1960C>G (p.Pro654Ala)
c.1528C>G (p.Pro510Ala)
3g.119413949C>TCA81697308ARHGAP31c.2020C>T (p.Pro674Ser)
c.1927C>T (p.Pro643Ser)
c.1960C>T (p.Pro654Ser)
c.1528C>T (p.Pro510Ser)
 dbSNP
3g.119413950C>ACA354048344ARHGAP31c.2021C>A (p.Pro674His)
c.1928C>A (p.Pro643His)
c.1961C>A (p.Pro654His)
c.1529C>A (p.Pro510His)
3g.119413950C>GCA354048351ARHGAP31c.2021C>G (p.Pro674Arg)
c.1928C>G (p.Pro643Arg)
c.1961C>G (p.Pro654Arg)
c.1529C>G (p.Pro510Arg)
3g.119413950C>TCA354048353ARHGAP31c.2021C>T (p.Pro674Leu)
c.1928C>T (p.Pro643Leu)
c.1961C>T (p.Pro654Leu)
c.1529C>T (p.Pro510Leu)
 ClinVar
3g.119413951T>ACA435411450ARHGAP31c.2022T>A (p.Pro674=)
c.1929T>A (p.Pro643=)
c.1962T>A (p.Pro654=)
c.1530T>A (p.Pro510=)
3g.119413951T>CCA435411448ARHGAP31c.2022T>C (p.Pro674=)
c.1929T>C (p.Pro643=)
c.1962T>C (p.Pro654=)
c.1530T>C (p.Pro510=)
3g.119413951T>GCA435411449ARHGAP31c.2022T>G (p.Pro674=)
c.1929T>G (p.Pro643=)
c.1962T>G (p.Pro654=)
c.1530T>G (p.Pro510=)
3g.119413952C>ACA354048363ARHGAP31c.2023C>A (p.Pro675Thr)
c.1930C>A (p.Pro644Thr)
c.1963C>A (p.Pro655Thr)
c.1531C>A (p.Pro511Thr)
3g.119413952C>GCA354048373ARHGAP31c.2023C>G (p.Pro675Ala)
c.1930C>G (p.Pro644Ala)
c.1963C>G (p.Pro655Ala)
c.1531C>G (p.Pro511Ala)
3g.119413952C>TCA354048370ARHGAP31c.2023C>T (p.Pro675Ser)
c.1930C>T (p.Pro644Ser)
c.1963C>T (p.Pro655Ser)
c.1531C>T (p.Pro511Ser)
3g.119413953C>ACA354048383ARHGAP31c.2024C>A (p.Pro675His)
c.1931C>A (p.Pro644His)
c.1964C>A (p.Pro655His)
c.1532C>A (p.Pro511His)
3g.119413953C>GCA354048387ARHGAP31c.2024C>G (p.Pro675Arg)
c.1931C>G (p.Pro644Arg)
c.1964C>G (p.Pro655Arg)
c.1532C>G (p.Pro511Arg)
3g.119413953C>TCA354048390ARHGAP31c.2024C>T (p.Pro675Leu)
c.1931C>T (p.Pro644Leu)
c.1964C>T (p.Pro655Leu)
c.1532C>T (p.Pro511Leu)
3g.119413954T>ACA435411455ARHGAP31c.2025T>A (p.Pro675=)
c.1932T>A (p.Pro644=)
c.1965T>A (p.Pro655=)
c.1533T>A (p.Pro511=)
3g.119413954T>CCA435411456ARHGAP31c.2025T>C (p.Pro675=)
c.1932T>C (p.Pro644=)
c.1965T>C (p.Pro655=)
c.1533T>C (p.Pro511=)
3g.119413954T>GCA435411457ARHGAP31c.2025T>G (p.Pro675=)
c.1932T>G (p.Pro644=)
c.1965T>G (p.Pro655=)
c.1533T>G (p.Pro511=)
3g.119413955G>ACA2553950ARHGAP31c.2026G>A (p.Ala676Thr)
c.1933G>A (p.Ala645Thr)
c.1966G>A (p.Ala656Thr)
c.1534G>A (p.Ala512Thr)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.119413955G>CCA354048394ARHGAP31c.2026G>C (p.Ala676Pro)
c.1933G>C (p.Ala645Pro)
c.1966G>C (p.Ala656Pro)
c.1534G>C (p.Ala512Pro)
3g.119413955G=CA1396548486ARHGAP31c.2026G= (p.Ala676=)
c.1933G= (p.Ala645=)
c.1966G= (p.Ala656=)
c.1534G= (p.Ala512=)
3g.119413955G>TCA354048398ARHGAP31c.2026G>T (p.Ala676Ser)
c.1933G>T (p.Ala645Ser)
c.1966G>T (p.Ala656Ser)
c.1534G>T (p.Ala512Ser)
3g.119413956C>ACA354048404ARHGAP31c.2027C>A (p.Ala676Asp)
c.1934C>A (p.Ala645Asp)
c.1967C>A (p.Ala656Asp)
c.1535C>A (p.Ala512Asp)
 dbSNP
3g.119413956C>GCA354048406ARHGAP31c.2027C>G (p.Ala676Gly)
c.1934C>G (p.Ala645Gly)
c.1967C>G (p.Ala656Gly)
c.1535C>G (p.Ala512Gly)
3g.119413956C>TCA354048416ARHGAP31c.2027C>T (p.Ala676Val)
c.1934C>T (p.Ala645Val)
c.1967C>T (p.Ala656Val)
c.1535C>T (p.Ala512Val)
3g.119413957T>ACA2553951ARHGAP31c.2028T>A (p.Ala676=)
c.1935T>A (p.Ala645=)
c.1968T>A (p.Ala656=)
c.1536T>A (p.Ala512=)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.119413957T>CCA435411463ARHGAP31c.2028T>C (p.Ala676=)
c.1935T>C (p.Ala645=)
c.1968T>C (p.Ala656=)
c.1536T>C (p.Ala512=)
 gnomAD v4
3g.119413957T>GCA435411465ARHGAP31c.2028T>G (p.Ala676=)
c.1935T>G (p.Ala645=)
c.1968T>G (p.Ala656=)
c.1536T>G (p.Ala512=)
3g.119413957T=CA1396548487ARHGAP31c.2028T= (p.Ala676=)
c.1935T= (p.Ala645=)
c.1968T= (p.Ala656=)
c.1536T= (p.Ala512=)
3g.119413958C>ACA354048422ARHGAP31c.2029C>A (p.Leu677Met)
c.1936C>A (p.Leu646Met)
c.1969C>A (p.Leu657Met)
c.1537C>A (p.Leu513Met)
3g.119413958C>GCA354048423ARHGAP31c.2029C>G (p.Leu677Val)
c.1936C>G (p.Leu646Val)
c.1969C>G (p.Leu657Val)
c.1537C>G (p.Leu513Val)
3g.119413958C>TCA435411466ARHGAP31c.2029C>T (p.Leu677=)
c.1936C>T (p.Leu646=)
c.1969C>T (p.Leu657=)
c.1537C>T (p.Leu513=)
 COSMIC
3g.119413959T>ACA354048424ARHGAP31c.2030T>A (p.Leu677Gln)
c.1937T>A (p.Leu646Gln)
c.1970T>A (p.Leu657Gln)
c.1538T>A (p.Leu513Gln)
3g.119413959T>CCA354048425ARHGAP31c.2030T>C (p.Leu677Pro)
c.1937T>C (p.Leu646Pro)
c.1970T>C (p.Leu657Pro)
c.1538T>C (p.Leu513Pro)
3g.119413959T>GCA354048428ARHGAP31c.2030T>G (p.Leu677Arg)
c.1937T>G (p.Leu646Arg)
c.1970T>G (p.Leu657Arg)
c.1538T>G (p.Leu513Arg)
 gnomAD v4
3g.119413960G>ACA435411467ARHGAP31c.2031G>A (p.Leu677=)
c.1938G>A (p.Leu646=)
c.1971G>A (p.Leu657=)
c.1539G>A (p.Leu513=)
3g.119413960G>CCA435411468ARHGAP31c.2031G>C (p.Leu677=)
c.1938G>C (p.Leu646=)
c.1971G>C (p.Leu657=)
c.1539G>C (p.Leu513=)
3g.119413960G>TCA435411470ARHGAP31c.2031G>T (p.Leu677=)
c.1938G>T (p.Leu646=)
c.1971G>T (p.Leu657=)
c.1539G>T (p.Leu513=)
3g.119413961A>CCA354048436ARHGAP31c.2032A>C (p.Lys678Gln)
c.1939A>C (p.Lys647Gln)
c.1972A>C (p.Lys658Gln)
c.1540A>C (p.Lys514Gln)
3g.119413961A>GCA354048439ARHGAP31c.2032A>G (p.Lys678Glu)
c.1939A>G (p.Lys647Glu)
c.1972A>G (p.Lys658Glu)
c.1540A>G (p.Lys514Glu)
3g.119413961A>TCA354048443ARHGAP31c.2032A>T (p.Lys678Ter)
c.1939A>T (p.Lys647Ter)
c.1972A>T (p.Lys658Ter)
c.1540A>T (p.Lys514Ter)
3g.119413962A>CCA354048444ARHGAP31c.2033A>C (p.Lys678Thr)
c.1940A>C (p.Lys647Thr)
c.1973A>C (p.Lys658Thr)
c.1541A>C (p.Lys514Thr)
3g.119413962A>GCA354048445ARHGAP31c.2033A>G (p.Lys678Arg)
c.1940A>G (p.Lys647Arg)
c.1973A>G (p.Lys658Arg)
c.1541A>G (p.Lys514Arg)
3g.119413962A>TCA354048446ARHGAP31c.2033A>T (p.Lys678Met)
c.1940A>T (p.Lys647Met)
c.1973A>T (p.Lys658Met)
c.1541A>T (p.Lys514Met)
3g.119413963G>ACA435411472ARHGAP31c.2034G>A (p.Lys678=)
c.1941G>A (p.Lys647=)
c.1974G>A (p.Lys658=)
c.1542G>A (p.Lys514=)
3g.119413963G>CCA354048449ARHGAP31c.2034G>C (p.Lys678Asn)
c.1941G>C (p.Lys647Asn)
c.1974G>C (p.Lys658Asn)
c.1542G>C (p.Lys514Asn)
 dbSNP gnomAD v3 gnomAD v4
3g.119413963G=CA1396548488ARHGAP31c.2034G= (p.Lys678=)
c.1941G= (p.Lys647=)
c.1974G= (p.Lys658=)
c.1542G= (p.Lys514=)
3g.119413963G>TCA354048452ARHGAP31c.2034G>T (p.Lys678Asn)
c.1941G>T (p.Lys647Asn)
c.1974G>T (p.Lys658Asn)
c.1542G>T (p.Lys514Asn)
3g.119413964A>CCA354048463ARHGAP31c.2035A>C (p.Thr679Pro)
c.1942A>C (p.Thr648Pro)
c.1975A>C (p.Thr659Pro)
c.1543A>C (p.Thr515Pro)
3g.119413964A>GCA354048461ARHGAP31c.2035A>G (p.Thr679Ala)
c.1942A>G (p.Thr648Ala)
c.1975A>G (p.Thr659Ala)
c.1543A>G (p.Thr515Ala)
 gnomAD v4
3g.119413964A>TCA354048458ARHGAP31c.2035A>T (p.Thr679Ser)
c.1942A>T (p.Thr648Ser)
c.1975A>T (p.Thr659Ser)
c.1543A>T (p.Thr515Ser)
3g.119413964_119413965delinsACCA1396548489ARHGAP31c.2035_2036delinsAC (p.Thr679=)
c.1942_1943delinsAC (p.Thr648=)
c.1975_1976delinsAC (p.Thr659=)
c.1543_1544delinsAC (p.Thr515=)
3g.119413965C>ACA354048467ARHGAP31c.2036C>A (p.Thr679Asn)
c.1943C>A (p.Thr648Asn)
c.1976C>A (p.Thr659Asn)
c.1544C>A (p.Thr515Asn)
3g.119413965C=CA1396548490ARHGAP31c.2036C= (p.Thr679=)
c.1943C= (p.Thr648=)
c.1976C= (p.Thr659=)
c.1544C= (p.Thr515=)
3g.119413965C>GCA354048471ARHGAP31c.2036C>G (p.Thr679Ser)
c.1943C>G (p.Thr648Ser)
c.1976C>G (p.Thr659Ser)
c.1544C>G (p.Thr515Ser)
 gnomAD v4
3g.119413965C>TCA2553952ARHGAP31c.2036C>T (p.Thr679Ile)
c.1943C>T (p.Thr648Ile)
c.1976C>T (p.Thr659Ile)
c.1544C>T (p.Thr515Ile)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.119413966delCA81697309ARHGAP31c.2037del (p.Ser680AlafsTer?)
c.1944del (p.Ser649AlafsTer?)
c.1977del (p.Ser660AlafsTer?)
c.1545del (p.Ser516AlafsTer?)
 dbSNP
3g.119413966C>ACA435411476ARHGAP31c.2037C>A (p.Thr679=)
c.1944C>A (p.Thr648=)
c.1977C>A (p.Thr659=)
c.1545C>A (p.Thr515=)
3g.119413966C=CA1396548491ARHGAP31c.2037C= (p.Thr679=)
c.1944C= (p.Thr648=)
c.1977C= (p.Thr659=)
c.1545C= (p.Thr515=)
3g.119413966C>GCA2553953ARHGAP31c.2037C>G (p.Thr679=)
c.1944C>G (p.Thr648=)
c.1977C>G (p.Thr659=)
c.1545C>G (p.Thr515=)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.119413966C>TCA2553954ARHGAP31c.2037C>T (p.Thr679=)
c.1944C>T (p.Thr648=)
c.1977C>T (p.Thr659=)
c.1545C>T (p.Thr515=)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.119413967A>CCA354048501ARHGAP31c.2038A>C (p.Ser680Arg)
c.1945A>C (p.Ser649Arg)
c.1978A>C (p.Ser660Arg)
c.1546A>C (p.Ser516Arg)
3g.119413967A>GCA354048505ARHGAP31c.2038A>G (p.Ser680Gly)
c.1945A>G (p.Ser649Gly)
c.1978A>G (p.Ser660Gly)
c.1546A>G (p.Ser516Gly)
3g.119413967A>TCA354048512ARHGAP31c.2038A>T (p.Ser680Cys)
c.1945A>T (p.Ser649Cys)
c.1978A>T (p.Ser660Cys)
c.1546A>T (p.Ser516Cys)
3g.119413968G>ACA2553955ARHGAP31c.2039G>A (p.Ser680Asn)
c.1946G>A (p.Ser649Asn)
c.1979G>A (p.Ser660Asn)
c.1547G>A (p.Ser516Asn)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.119413968G>CCA354048518ARHGAP31c.2039G>C (p.Ser680Thr)
c.1946G>C (p.Ser649Thr)
c.1979G>C (p.Ser660Thr)
c.1547G>C (p.Ser516Thr)
3g.119413968G=CA1396548492ARHGAP31c.2039G= (p.Ser680=)
c.1946G= (p.Ser649=)
c.1979G= (p.Ser660=)
c.1547G= (p.Ser516=)
3g.119413968G>TCA354048521ARHGAP31c.2039G>T (p.Ser680Ile)
c.1946G>T (p.Ser649Ile)
c.1979G>T (p.Ser660Ile)
c.1547G>T (p.Ser516Ile)
3g.119413969C>ACA354048531ARHGAP31c.2040C>A (p.Ser680Arg)
c.1947C>A (p.Ser649Arg)
c.1980C>A (p.Ser660Arg)
c.1548C>A (p.Ser516Arg)
 gnomAD v4
3g.119413969C>GCA354048532ARHGAP31c.2040C>G (p.Ser680Arg)
c.1947C>G (p.Ser649Arg)
c.1980C>G (p.Ser660Arg)
c.1548C>G (p.Ser516Arg)
3g.119413969C>TCA435411479ARHGAP31c.2040C>T (p.Ser680=)
c.1947C>T (p.Ser649=)
c.1980C>T (p.Ser660=)
c.1548C>T (p.Ser516=)
3g.119413970C>ACA354048537ARHGAP31c.2041C>A (p.Pro681Thr)
c.1948C>A (p.Pro650Thr)
c.1981C>A (p.Pro661Thr)
c.1549C>A (p.Pro517Thr)
3g.119413970C=CA1396548493ARHGAP31c.2041C= (p.Pro681=)
c.1948C= (p.Pro650=)
c.1981C= (p.Pro661=)
c.1549C= (p.Pro517=)
3g.119413970C>GCA354048555ARHGAP31c.2041C>G (p.Pro681Ala)
c.1948C>G (p.Pro650Ala)
c.1981C>G (p.Pro661Ala)
c.1549C>G (p.Pro517Ala)
3g.119413970C>TCA81697334ARHGAP31c.2041C>T (p.Pro681Ser)
c.1948C>T (p.Pro650Ser)
c.1981C>T (p.Pro661Ser)
c.1549C>T (p.Pro517Ser)
 dbSNP gnomAD v3 gnomAD v4
3g.119413971C>ACA354048560ARHGAP31c.2042C>A (p.Pro681Gln)
c.1949C>A (p.Pro650Gln)
c.1982C>A (p.Pro661Gln)
c.1550C>A (p.Pro517Gln)
3g.119413971C=CA1396548494ARHGAP31c.2042C= (p.Pro681=)
c.1949C= (p.Pro650=)
c.1982C= (p.Pro661=)
c.1550C= (p.Pro517=)
3g.119413971C>GCA2553956ARHGAP31c.2042C>G (p.Pro681Arg)
c.1949C>G (p.Pro650Arg)
c.1982C>G (p.Pro661Arg)
c.1550C>G (p.Pro517Arg)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.119413971C>TCA2553957ARHGAP31c.2042C>T (p.Pro681Leu)
c.1949C>T (p.Pro650Leu)
c.1982C>T (p.Pro661Leu)
c.1550C>T (p.Pro517Leu)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.119413972A>CCA435411481ARHGAP31c.2043A>C (p.Pro681=)
c.1950A>C (p.Pro650=)
c.1983A>C (p.Pro661=)
c.1551A>C (p.Pro517=)
3g.119413972A>GCA435411483ARHGAP31c.2043A>G (p.Pro681=)
c.1950A>G (p.Pro650=)
c.1983A>G (p.Pro661=)
c.1551A>G (p.Pro517=)
3g.119413972A>TCA435411482ARHGAP31c.2043A>T (p.Pro681=)
c.1950A>T (p.Pro650=)
c.1983A>T (p.Pro661=)
c.1551A>T (p.Pro517=)
3g.119413973A>CCA354048572ARHGAP31c.2044A>C (p.Ile682Leu)
c.1951A>C (p.Ile651Leu)
c.1984A>C (p.Ile662Leu)
c.1552A>C (p.Ile518Leu)
3g.119413973A>GCA354048585ARHGAP31c.2044A>G (p.Ile682Val)
c.1951A>G (p.Ile651Val)
c.1984A>G (p.Ile662Val)
c.1552A>G (p.Ile518Val)
 gnomAD v4
3g.119413973A>TCA354048587ARHGAP31c.2044A>T (p.Ile682Phe)
c.1951A>T (p.Ile651Phe)
c.1984A>T (p.Ile662Phe)
c.1552A>T (p.Ile518Phe)
3g.119413974T>ACA354048589ARHGAP31c.2045T>A (p.Ile682Asn)
c.1952T>A (p.Ile651Asn)
c.1985T>A (p.Ile662Asn)
c.1553T>A (p.Ile518Asn)
3g.119413974T>CCA354048591ARHGAP31c.2045T>C (p.Ile682Thr)
c.1952T>C (p.Ile651Thr)
c.1985T>C (p.Ile662Thr)
c.1553T>C (p.Ile518Thr)
 gnomAD v4
3g.119413974T>GCA354048600ARHGAP31c.2045T>G (p.Ile682Ser)
c.1952T>G (p.Ile651Ser)
c.1985T>G (p.Ile662Ser)
c.1553T>G (p.Ile518Ser)
3g.119413975T>ACA435411485ARHGAP31c.2046T>A (p.Ile682=)
c.1953T>A (p.Ile651=)
c.1986T>A (p.Ile662=)
c.1554T>A (p.Ile518=)
3g.119413975T>CCA435411486ARHGAP31c.2046T>C (p.Ile682=)
c.1953T>C (p.Ile651=)
c.1986T>C (p.Ile662=)
c.1554T>C (p.Ile518=)
3g.119413975T>GCA354048603ARHGAP31c.2046T>G (p.Ile682Met)
c.1953T>G (p.Ile651Met)
c.1986T>G (p.Ile662Met)
c.1554T>G (p.Ile518Met)
3g.119413976C>ACA354048606ARHGAP31c.2047C>A (p.Gln683Lys)
c.1954C>A (p.Gln652Lys)
c.1987C>A (p.Gln663Lys)
c.1555C>A (p.Gln519Lys)
3g.119413976C=CA1396548495ARHGAP31c.2047C= (p.Gln683=)
c.1954C= (p.Gln652=)
c.1987C= (p.Gln663=)
c.1555C= (p.Gln519=)
3g.119413976C>GCA354048608ARHGAP31c.2047C>G (p.Gln683Glu)
c.1954C>G (p.Gln652Glu)
c.1987C>G (p.Gln663Glu)
c.1555C>G (p.Gln519Glu)
3g.119413976C>TCA129505ARHGAP31c.2047C>T (p.Gln683Ter)
c.1954C>T (p.Gln652Ter)
c.1987C>T (p.Gln663Ter)
c.1555C>T (p.Gln519Ter)
 ClinVar dbSNP gnomAD v4
3g.119413977A=CA1396548496ARHGAP31c.2048A= (p.Gln683=)
c.1955A= (p.Gln652=)
c.1988A= (p.Gln663=)
c.1556A= (p.Gln519=)
3g.119413977A>CCA354048617ARHGAP31c.2048A>C (p.Gln683Pro)
c.1955A>C (p.Gln652Pro)
c.1988A>C (p.Gln663Pro)
c.1556A>C (p.Gln519Pro)
3g.119413977A>GCA81697349ARHGAP31c.2048A>G (p.Gln683Arg)
c.1955A>G (p.Gln652Arg)
c.1988A>G (p.Gln663Arg)
c.1556A>G (p.Gln519Arg)
 ClinVar dbSNP gnomAD v4
3g.119413977A>TCA354048612ARHGAP31c.2048A>T (p.Gln683Leu)
c.1955A>T (p.Gln652Leu)
c.1988A>T (p.Gln663Leu)
c.1556A>T (p.Gln519Leu)
3g.119413978G>ACA435411487ARHGAP31c.2049G>A (p.Gln683=)
c.1956G>A (p.Gln652=)
c.1989G>A (p.Gln663=)
c.1557G>A (p.Gln519=)
 dbSNP gnomAD v4
3g.119413978G>CCA354048624ARHGAP31c.2049G>C (p.Gln683His)
c.1956G>C (p.Gln652His)
c.1989G>C (p.Gln663His)
c.1557G>C (p.Gln519His)
3g.119413978G=CA1396548497ARHGAP31c.2049G= (p.Gln683=)
c.1956G= (p.Gln652=)
c.1989G= (p.Gln663=)
c.1557G= (p.Gln519=)
3g.119413978G>TCA354048639ARHGAP31c.2049G>T (p.Gln683His)
c.1956G>T (p.Gln652His)
c.1989G>T (p.Gln663His)
c.1557G>T (p.Gln519His)
3g.119413979C>ACA354048644ARHGAP31c.2050C>A (p.Pro684Thr)
c.1957C>A (p.Pro653Thr)
c.1990C>A (p.Pro664Thr)
c.1558C>A (p.Pro520Thr)
3g.119413979C=CA1396548498ARHGAP31c.2050C= (p.Pro684=)
c.1957C= (p.Pro653=)
c.1990C= (p.Pro664=)
c.1558C= (p.Pro520=)
3g.119413979C>GCA354048648ARHGAP31c.2050C>G (p.Pro684Ala)
c.1957C>G (p.Pro653Ala)
c.1990C>G (p.Pro664Ala)
c.1558C>G (p.Pro520Ala)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.119413979C>TCA354048650ARHGAP31c.2050C>T (p.Pro684Ser)
c.1957C>T (p.Pro653Ser)
c.1990C>T (p.Pro664Ser)
c.1558C>T (p.Pro520Ser)
3g.119413980C>ACA354048652ARHGAP31c.2051C>A (p.Pro684His)
c.1958C>A (p.Pro653His)
c.1991C>A (p.Pro664His)
c.1559C>A (p.Pro520His)
3g.119413980C>GCA354048653ARHGAP31c.2051C>G (p.Pro684Arg)
c.1958C>G (p.Pro653Arg)
c.1991C>G (p.Pro664Arg)
c.1559C>G (p.Pro520Arg)
 gnomAD v4
3g.119413980C>TCA354048655ARHGAP31c.2051C>T (p.Pro684Leu)
c.1958C>T (p.Pro653Leu)
c.1991C>T (p.Pro664Leu)
c.1559C>T (p.Pro520Leu)
 COSMIC
3g.119413981T>ACA435411488ARHGAP31c.2052T>A (p.Pro684=)
c.1959T>A (p.Pro653=)
c.1992T>A (p.Pro664=)
c.1560T>A (p.Pro520=)
3g.119413981T>CCA435411489ARHGAP31c.2052T>C (p.Pro684=)
c.1959T>C (p.Pro653=)
c.1992T>C (p.Pro664=)
c.1560T>C (p.Pro520=)
3g.119413981T>GCA81697353ARHGAP31c.2052T>G (p.Pro684=)
c.1959T>G (p.Pro653=)
c.1992T>G (p.Pro664=)
c.1560T>G (p.Pro520=)
 dbSNP gnomAD v3 gnomAD v4
3g.119413981T=CA1396548499ARHGAP31c.2052T= (p.Pro684=)
c.1959T= (p.Pro653=)
c.1992T= (p.Pro664=)
c.1560T= (p.Pro520=)
3g.119413982A=CA1396548500ARHGAP31c.2053A= (p.Ile685=)
c.1960A= (p.Ile654=)
c.1993A= (p.Ile665=)
c.1561A= (p.Ile521=)
3g.119413982A>CCA354048658ARHGAP31c.2053A>C (p.Ile685Leu)
c.1960A>C (p.Ile654Leu)
c.1993A>C (p.Ile665Leu)
c.1561A>C (p.Ile521Leu)
3g.119413982A>GCA354048661ARHGAP31c.2053A>G (p.Ile685Val)
c.1960A>G (p.Ile654Val)
c.1993A>G (p.Ile665Val)
c.1561A>G (p.Ile521Val)
 dbSNP gnomAD v4
3g.119413982A>TCA354048664ARHGAP31c.2053A>T (p.Ile685Phe)
c.1960A>T (p.Ile654Phe)
c.1993A>T (p.Ile665Phe)
c.1561A>T (p.Ile521Phe)
3g.119413983T>ACA354048667ARHGAP31c.2054T>A (p.Ile685Asn)
c.1961T>A (p.Ile654Asn)
c.1994T>A (p.Ile665Asn)
c.1562T>A (p.Ile521Asn)
3g.119413983T>CCA354048672ARHGAP31c.2054T>C (p.Ile685Thr)
c.1961T>C (p.Ile654Thr)
c.1994T>C (p.Ile665Thr)
c.1562T>C (p.Ile521Thr)
3g.119413983T>GCA354048680ARHGAP31c.2054T>G (p.Ile685Ser)
c.1961T>G (p.Ile654Ser)
c.1994T>G (p.Ile665Ser)
c.1562T>G (p.Ile521Ser)
3g.119413984T>ACA435411491ARHGAP31c.2055T>A (p.Ile685=)
c.1962T>A (p.Ile654=)
c.1995T>A (p.Ile665=)
c.1563T>A (p.Ile521=)
3g.119413984T>CCA435411492ARHGAP31c.2055T>C (p.Ile685=)
c.1962T>C (p.Ile654=)
c.1995T>C (p.Ile665=)
c.1563T>C (p.Ile521=)
3g.119413984T>GCA354048692ARHGAP31c.2055T>G (p.Ile685Met)
c.1962T>G (p.Ile654Met)
c.1995T>G (p.Ile665Met)
c.1563T>G (p.Ile521Met)
3g.119413985C>ACA354048700ARHGAP31c.2056C>A (p.Leu686Ile)
c.1963C>A (p.Leu655Ile)
c.1996C>A (p.Leu666Ile)
c.1564C>A (p.Leu522Ile)
 gnomAD v4 COSMIC
3g.119413985C>GCA354048704ARHGAP31c.2056C>G (p.Leu686Val)
c.1963C>G (p.Leu655Val)
c.1996C>G (p.Leu666Val)
c.1564C>G (p.Leu522Val)
3g.119413985C>TCA354048698ARHGAP31c.2056C>T (p.Leu686Phe)
c.1963C>T (p.Leu655Phe)
c.1996C>T (p.Leu666Phe)
c.1564C>T (p.Leu522Phe)
3g.119413986T>ACA354048707ARHGAP31c.2057T>A (p.Leu686His)
c.1964T>A (p.Leu655His)
c.1997T>A (p.Leu666His)
c.1565T>A (p.Leu522His)
3g.119413986T>CCA354048708ARHGAP31c.2057T>C (p.Leu686Pro)
c.1964T>C (p.Leu655Pro)
c.1997T>C (p.Leu666Pro)
c.1565T>C (p.Leu522Pro)
3g.119413986T>GCA354048709ARHGAP31c.2057T>G (p.Leu686Arg)
c.1964T>G (p.Leu655Arg)
c.1997T>G (p.Leu666Arg)
c.1565T>G (p.Leu522Arg)
3g.119413993_119413997delCA2577942208ARHGAP31c.2064_2068del (p.Ser689GlyfsTer?)
c.1971_1975del (p.Ser658GlyfsTer?)
c.2004_2008del (p.Ser669GlyfsTer?)
c.1572_1576del (p.Ser525GlyfsTer?)
3g.119413987C>ACA435411493ARHGAP31c.2058C>A (p.Leu686=)
c.1965C>A (p.Leu655=)
c.1998C>A (p.Leu666=)
c.1566C>A (p.Leu522=)
3g.119413987C=CA1396548501ARHGAP31c.2058C= (p.Leu686=)
c.1965C= (p.Leu655=)
c.1998C= (p.Leu666=)
c.1566C= (p.Leu522=)
3g.119413987C>GCA2553958ARHGAP31c.2058C>G (p.Leu686=)
c.1965C>G (p.Leu655=)
c.1998C>G (p.Leu666=)
c.1566C>G (p.Leu522=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.119413987C>TCA81697356ARHGAP31c.2058C>T (p.Leu686=)
c.1965C>T (p.Leu655=)
c.1998C>T (p.Leu666=)
c.1566C>T (p.Leu522=)
 dbSNP gnomAD v3 gnomAD v4
3g.119413988G>ACA2553959ARHGAP31c.2059G>A (p.Glu687Lys)
c.1966G>A (p.Glu656Lys)
c.1999G>A (p.Glu667Lys)
c.1567G>A (p.Glu523Lys)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.119413988G>CCA354048724ARHGAP31c.2059G>C (p.Glu687Gln)
c.1966G>C (p.Glu656Gln)
c.1999G>C (p.Glu667Gln)
c.1567G>C (p.Glu523Gln)
 ClinVar dbSNP gnomAD v4
3g.119413988G=CA1396548502ARHGAP31c.2059G= (p.Glu687=)
c.1966G= (p.Glu656=)
c.1999G= (p.Glu667=)
c.1567G= (p.Glu523=)
3g.119413988G>TCA354048730ARHGAP31c.2059G>T (p.Glu687Ter)
c.1966G>T (p.Glu656Ter)
c.1999G>T (p.Glu667Ter)
c.1567G>T (p.Glu523Ter)
3g.119413989A>CCA354048737ARHGAP31c.2060A>C (p.Glu687Ala)
c.1967A>C (p.Glu656Ala)
c.2000A>C (p.Glu667Ala)
c.1568A>C (p.Glu523Ala)
3g.119413989A>GCA354048739ARHGAP31c.2060A>G (p.Glu687Gly)
c.1967A>G (p.Glu656Gly)
c.2000A>G (p.Glu667Gly)
c.1568A>G (p.Glu523Gly)
3g.119413989A>TCA354048742ARHGAP31c.2060A>T (p.Glu687Val)
c.1967A>T (p.Glu656Val)
c.2000A>T (p.Glu667Val)
c.1568A>T (p.Glu523Val)
3g.119413990G>ACA435411497ARHGAP31c.2061G>A (p.Glu687=)
c.1968G>A (p.Glu656=)
c.2001G>A (p.Glu667=)
c.1569G>A (p.Glu523=)
3g.119413990G>CCA354048748ARHGAP31c.2061G>C (p.Glu687Asp)
c.1968G>C (p.Glu656Asp)
c.2001G>C (p.Glu667Asp)
c.1569G>C (p.Glu523Asp)
3g.119413990G>TCA354048755ARHGAP31c.2061G>T (p.Glu687Asp)
c.1968G>T (p.Glu656Asp)
c.2001G>T (p.Glu667Asp)
c.1569G>T (p.Glu523Asp)
 COSMIC
3g.119413991T>ACA354048767ARHGAP31c.2062T>A (p.Ser688Thr)
c.1969T>A (p.Ser657Thr)
c.2002T>A (p.Ser668Thr)
c.1570T>A (p.Ser524Thr)
3g.119413991T>CCA354048761ARHGAP31c.2062T>C (p.Ser688Pro)
c.1969T>C (p.Ser657Pro)
c.2002T>C (p.Ser668Pro)
c.1570T>C (p.Ser524Pro)
3g.119413991T>GCA354048764ARHGAP31c.2062T>G (p.Ser688Ala)
c.1969T>G (p.Ser657Ala)
c.2002T>G (p.Ser668Ala)
c.1570T>G (p.Ser524Ala)
 gnomAD v4
3g.119413992C>ACA354048771ARHGAP31c.2063C>A (p.Ser688Ter)
c.1970C>A (p.Ser657Ter)
c.2003C>A (p.Ser668Ter)
c.1571C>A (p.Ser524Ter)
 gnomAD v4
3g.119413992C=CA1396548503ARHGAP31c.2063C= (p.Ser688=)
c.1970C= (p.Ser657=)
c.2003C= (p.Ser668=)
c.1571C= (p.Ser524=)
3g.119413992C>GCA2553960ARHGAP31c.2063C>G (p.Ser688Trp)
c.1970C>G (p.Ser657Trp)
c.2003C>G (p.Ser668Trp)
c.1571C>G (p.Ser524Trp)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.119413992C>TCA354048776ARHGAP31c.2063C>T (p.Ser688Leu)
c.1970C>T (p.Ser657Leu)
c.2003C>T (p.Ser668Leu)
c.1571C>T (p.Ser524Leu)
 dbSNP gnomAD v3 gnomAD v4 COSMIC
3g.119413992_119413993insTTCA2586965849ARHGAP31c.2063_2064insTT (p.Ser689Ter)
c.1970_1971insTT (p.Ser658Ter)
c.2003_2004insTT (p.Ser669Ter)
c.1571_1572insTT (p.Ser525Ter)
3g.119413993G>ACA2553961ARHGAP31c.2064G>A (p.Ser688=)
c.1971G>A (p.Ser657=)
c.2004G>A (p.Ser668=)
c.1572G>A (p.Ser524=)
 dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
3g.119413993G>CCA435411498ARHGAP31c.2064G>C (p.Ser688=)
c.1971G>C (p.Ser657=)
c.2004G>C (p.Ser668=)
c.1572G>C (p.Ser524=)
 gnomAD v4
3g.119413993G=CA1396548504ARHGAP31c.2064G= (p.Ser688=)
c.1971G= (p.Ser657=)
c.2004G= (p.Ser668=)
c.1572G= (p.Ser524=)
3g.119413993G>TCA435411499ARHGAP31c.2064G>T (p.Ser688=)
c.1971G>T (p.Ser657=)
c.2004G>T (p.Ser668=)
c.1572G>T (p.Ser524=)
3g.119413994A>CCA354048785ARHGAP31c.2065A>C (p.Ser689Arg)
c.1972A>C (p.Ser658Arg)
c.2005A>C (p.Ser669Arg)
c.1573A>C (p.Ser525Arg)
3g.119413994A>GCA354048791ARHGAP31c.2065A>G (p.Ser689Gly)
c.1972A>G (p.Ser658Gly)
c.2005A>G (p.Ser669Gly)
c.1573A>G (p.Ser525Gly)
3g.119413994A>TCA354048813ARHGAP31c.2065A>T (p.Ser689Cys)
c.1972A>T (p.Ser658Cys)
c.2005A>T (p.Ser669Cys)
c.1573A>T (p.Ser525Cys)
3g.119413995G>ACA354048818ARHGAP31c.2066G>A (p.Ser689Asn)
c.1973G>A (p.Ser658Asn)
c.2006G>A (p.Ser669Asn)
c.1574G>A (p.Ser525Asn)
3g.119413995G>CCA354048819ARHGAP31c.2066G>C (p.Ser689Thr)
c.1973G>C (p.Ser658Thr)
c.2006G>C (p.Ser669Thr)
c.1574G>C (p.Ser525Thr)
 dbSNP gnomAD v4
3g.119413995G=CA1396548505ARHGAP31c.2066G= (p.Ser689=)
c.1973G= (p.Ser658=)
c.2006G= (p.Ser669=)
c.1574G= (p.Ser525=)
3g.119413995G>TCA354048820ARHGAP31c.2066G>T (p.Ser689Ile)
c.1973G>T (p.Ser658Ile)
c.2006G>T (p.Ser669Ile)
c.1574G>T (p.Ser525Ile)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.119413996T>ACA354048821ARHGAP31c.2067T>A (p.Ser689Arg)
c.1974T>A (p.Ser658Arg)
c.2007T>A (p.Ser669Arg)
c.1575T>A (p.Ser525Arg)
 dbSNP gnomAD v3 gnomAD v4
3g.119413996T>CCA435411500ARHGAP31c.2067T>C (p.Ser689=)
c.1974T>C (p.Ser658=)
c.2007T>C (p.Ser669=)
c.1575T>C (p.Ser525=)
 dbSNP
3g.119413996T>GCA354048825ARHGAP31c.2067T>G (p.Ser689Arg)
c.1974T>G (p.Ser658Arg)
c.2007T>G (p.Ser669Arg)
c.1575T>G (p.Ser525Arg)
3g.119413996T=CA1396548506ARHGAP31c.2067T= (p.Ser689=)
c.1974T= (p.Ser658=)
c.2007T= (p.Ser669=)
c.1575T= (p.Ser525=)
3g.119413996_119413997insGCA81697371ARHGAP31c.2067_2068insG (p.Leu690AlafsTer?)
c.1974_1975insG (p.Leu659AlafsTer?)
c.2007_2008insG (p.Leu670AlafsTer?)
c.1575_1576insG (p.Leu526AlafsTer?)
 dbSNP
3g.119413997C>ACA354048849ARHGAP31c.2068C>A (p.Leu690Met)
c.1975C>A (p.Leu659Met)
c.2008C>A (p.Leu670Met)
c.1576C>A (p.Leu526Met)
3g.119413997C>GCA354048847ARHGAP31c.2068C>G (p.Leu690Val)
c.1975C>G (p.Leu659Val)
c.2008C>G (p.Leu670Val)
c.1576C>G (p.Leu526Val)
3g.119413997C>TCA435411503ARHGAP31c.2068C>T (p.Leu690=)
c.1975C>T (p.Leu659=)
c.2008C>T (p.Leu670=)
c.1576C>T (p.Leu526=)
 gnomAD v4
3g.119413998T>ACA354048862ARHGAP31c.2069T>A (p.Leu690Gln)
c.1976T>A (p.Leu659Gln)
c.2009T>A (p.Leu670Gln)
c.1577T>A (p.Leu526Gln)
3g.119413998T>CCA354048870ARHGAP31c.2069T>C (p.Leu690Pro)
c.1976T>C (p.Leu659Pro)
c.2009T>C (p.Leu670Pro)
c.1577T>C (p.Leu526Pro)
 dbSNP gnomAD v4
3g.119413998T>GCA354048866ARHGAP31c.2069T>G (p.Leu690Arg)
c.1976T>G (p.Leu659Arg)
c.2009T>G (p.Leu670Arg)
c.1577T>G (p.Leu526Arg)
3g.119413998T=CA1396548507ARHGAP31c.2069T= (p.Leu690=)
c.1976T= (p.Leu659=)
c.2009T= (p.Leu670=)
c.1577T= (p.Leu526=)
3g.119413999G>ACA435411504ARHGAP31c.2070G>A (p.Leu690=)
c.1977G>A (p.Leu659=)
c.2010G>A (p.Leu670=)
c.1578G>A (p.Leu526=)
3g.119413999G>CCA2553962ARHGAP31c.2070G>C (p.Leu690=)
c.1977G>C (p.Leu659=)
c.2010G>C (p.Leu670=)
c.1578G>C (p.Leu526=)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.119413999G=CA1396548508ARHGAP31c.2070G= (p.Leu690=)
c.1977G= (p.Leu659=)
c.2010G= (p.Leu670=)
c.1578G= (p.Leu526=)
3g.119413999G>TCA435411506ARHGAP31c.2070G>T (p.Leu690=)
c.1977G>T (p.Leu659=)
c.2010G>T (p.Leu670=)
c.1578G>T (p.Leu526=)
3g.119414000G>ACA2553963ARHGAP31c.2071G>A (p.Gly691Arg)
c.1978G>A (p.Gly660Arg)
c.2011G>A (p.Gly671Arg)
c.1579G>A (p.Gly527Arg)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.119414000G>CCA354048881ARHGAP31c.2071G>C (p.Gly691Arg)
c.1978G>C (p.Gly660Arg)
c.2011G>C (p.Gly671Arg)
c.1579G>C (p.Gly527Arg)
3g.119414000G=CA1396548509ARHGAP31c.2071G= (p.Gly691=)
c.1978G= (p.Gly660=)
c.2011G= (p.Gly671=)
c.1579G= (p.Gly527=)
3g.119414000G>TCA354048884ARHGAP31c.2071G>T (p.Gly691Trp)
c.1978G>T (p.Gly660Trp)
c.2011G>T (p.Gly671Trp)
c.1579G>T (p.Gly527Trp)
3g.119414001G>ACA354048901ARHGAP31c.2072G>A (p.Gly691Glu)
c.1979G>A (p.Gly660Glu)
c.2012G>A (p.Gly671Glu)
c.1580G>A (p.Gly527Glu)
 gnomAD v4
3g.119414001G>CCA2553964ARHGAP31c.2072G>C (p.Gly691Ala)
c.1979G>C (p.Gly660Ala)
c.2012G>C (p.Gly671Ala)
c.1580G>C (p.Gly527Ala)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.119414001G=CA1396548510ARHGAP31c.2072G= (p.Gly691=)
c.1979G= (p.Gly660=)
c.2012G= (p.Gly671=)
c.1580G= (p.Gly527=)
3g.119414001G>TCA354048905ARHGAP31c.2072G>T (p.Gly691Val)
c.1979G>T (p.Gly660Val)
c.2012G>T (p.Gly671Val)
c.1580G>T (p.Gly527Val)
3g.119414002G>ACA435411510ARHGAP31c.2073G>A (p.Gly691=)
c.1980G>A (p.Gly660=)
c.2013G>A (p.Gly671=)
c.1581G>A (p.Gly527=)
3g.119414002G>CCA435411511ARHGAP31c.2073G>C (p.Gly691=)
c.1980G>C (p.Gly660=)
c.2013G>C (p.Gly671=)
c.1581G>C (p.Gly527=)
3g.119414002G>TCA435411512ARHGAP31c.2073G>T (p.Gly691=)
c.1980G>T (p.Gly660=)
c.2013G>T (p.Gly671=)
c.1581G>T (p.Gly527=)
3g.119414003C>ACA2553965ARHGAP31c.2074C>A (p.Pro692Thr)
c.1981C>A (p.Pro661Thr)
c.2014C>A (p.Pro672Thr)
c.1582C>A (p.Pro528Thr)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.119414003C=CA1396548511ARHGAP31c.2074C= (p.Pro692=)
c.1981C= (p.Pro661=)
c.2014C= (p.Pro672=)
c.1582C= (p.Pro528=)
3g.119414003C>GCA354048934ARHGAP31c.2074C>G (p.Pro692Ala)
c.1981C>G (p.Pro661Ala)
c.2014C>G (p.Pro672Ala)
c.1582C>G (p.Pro528Ala)
3g.119414003C>TCA354048938ARHGAP31c.2074C>T (p.Pro692Ser)
c.1981C>T (p.Pro661Ser)
c.2014C>T (p.Pro672Ser)
c.1582C>T (p.Pro528Ser)
 gnomAD v4
3g.119414004C>ACA354048945ARHGAP31c.2075C>A (p.Pro692His)
c.1982C>A (p.Pro661His)
c.2015C>A (p.Pro672His)
c.1583C>A (p.Pro528His)
3g.119414004C=CA1396548512ARHGAP31c.2075C= (p.Pro692=)
c.1982C= (p.Pro661=)
c.2015C= (p.Pro672=)
c.1583C= (p.Pro528=)
3g.119414004C>GCA354048948ARHGAP31c.2075C>G (p.Pro692Arg)
c.1982C>G (p.Pro661Arg)
c.2015C>G (p.Pro672Arg)
c.1583C>G (p.Pro528Arg)
3g.119414004C>TCA354048952ARHGAP31c.2075C>T (p.Pro692Leu)
c.1982C>T (p.Pro661Leu)
c.2015C>T (p.Pro672Leu)
c.1583C>T (p.Pro528Leu)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.119414005C>ACA2553966ARHGAP31c.2076C>A (p.Pro692=)
c.1983C>A (p.Pro661=)
c.2016C>A (p.Pro672=)
c.1584C>A (p.Pro528=)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.119414005C=CA1396548513ARHGAP31c.2076C= (p.Pro692=)
c.1983C= (p.Pro661=)
c.2016C= (p.Pro672=)
c.1584C= (p.Pro528=)
3g.119414005C>GCA435411513ARHGAP31c.2076C>G (p.Pro692=)
c.1983C>G (p.Pro661=)
c.2016C>G (p.Pro672=)
c.1584C>G (p.Pro528=)
3g.119414005C>TCA435411514ARHGAP31c.2076C>T (p.Pro692=)
c.1983C>T (p.Pro661=)
c.2016C>T (p.Pro672=)
c.1584C>T (p.Pro528=)
3g.119414006T>ACA354048960ARHGAP31c.2077T>A (p.Phe693Ile)
c.1984T>A (p.Phe662Ile)
c.2017T>A (p.Phe673Ile)
c.1585T>A (p.Phe529Ile)
3g.119414006T>CCA354048964ARHGAP31c.2077T>C (p.Phe693Leu)
c.1984T>C (p.Phe662Leu)
c.2017T>C (p.Phe673Leu)
c.1585T>C (p.Phe529Leu)
3g.119414006T>GCA354048966ARHGAP31c.2077T>G (p.Phe693Val)
c.1984T>G (p.Phe662Val)
c.2017T>G (p.Phe673Val)
c.1585T>G (p.Phe529Val)
3g.119414007T>ACA354048967ARHGAP31c.2078T>A (p.Phe693Tyr)
c.1985T>A (p.Phe662Tyr)
c.2018T>A (p.Phe673Tyr)
c.1586T>A (p.Phe529Tyr)
3g.119414007T>CCA354048968ARHGAP31c.2078T>C (p.Phe693Ser)
c.1985T>C (p.Phe662Ser)
c.2018T>C (p.Phe673Ser)
c.1586T>C (p.Phe529Ser)
 gnomAD v4
3g.119414007T>GCA354048969ARHGAP31c.2078T>G (p.Phe693Cys)
c.1985T>G (p.Phe662Cys)
c.2018T>G (p.Phe673Cys)
c.1586T>G (p.Phe529Cys)
3g.119414008T>ACA354048973ARHGAP31c.2079T>A (p.Phe693Leu)
c.1986T>A (p.Phe662Leu)
c.2019T>A (p.Phe673Leu)
c.1587T>A (p.Phe529Leu)
3g.119414008T>CCA2553967ARHGAP31c.2079T>C (p.Phe693=)
c.1986T>C (p.Phe662=)
c.2019T>C (p.Phe673=)
c.1587T>C (p.Phe529=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.119414008T>GCA354048977ARHGAP31c.2079T>G (p.Phe693Leu)
c.1986T>G (p.Phe662Leu)
c.2019T>G (p.Phe673Leu)
c.1587T>G (p.Phe529Leu)
3g.119414008T=CA1396548514ARHGAP31c.2079T= (p.Phe693=)
c.1986T= (p.Phe662=)
c.2019T= (p.Phe673=)
c.1587T= (p.Phe529=)
3g.119414009A>CCA354048981ARHGAP31c.2080A>C (p.Ile694Leu)
c.1987A>C (p.Ile663Leu)
c.2020A>C (p.Ile674Leu)
c.1588A>C (p.Ile530Leu)
3g.119414009A>GCA354048984ARHGAP31c.2080A>G (p.Ile694Val)
c.1987A>G (p.Ile663Val)
c.2020A>G (p.Ile674Val)
c.1588A>G (p.Ile530Val)
3g.119414009A>TCA354048989ARHGAP31c.2080A>T (p.Ile694Phe)
c.1987A>T (p.Ile663Phe)
c.2020A>T (p.Ile674Phe)
c.1588A>T (p.Ile530Phe)
3g.119414010T>ACA354049001ARHGAP31c.2081T>A (p.Ile694Asn)
c.1988T>A (p.Ile663Asn)
c.2021T>A (p.Ile674Asn)
c.1589T>A (p.Ile530Asn)
3g.119414010T>CCA354049000ARHGAP31c.2081T>C (p.Ile694Thr)
c.1988T>C (p.Ile663Thr)
c.2021T>C (p.Ile674Thr)
c.1589T>C (p.Ile530Thr)
 dbSNP gnomAD v2 gnomAD v4
3g.119414010T>GCA354048993ARHGAP31c.2081T>G (p.Ile694Ser)
c.1988T>G (p.Ile663Ser)
c.2021T>G (p.Ile674Ser)
c.1589T>G (p.Ile530Ser)
 gnomAD v4
3g.119414010T=CA1396548515ARHGAP31c.2081T= (p.Ile694=)
c.1988T= (p.Ile663=)
c.2021T= (p.Ile674=)
c.1589T= (p.Ile530=)
3g.119414011T>ACA435411517ARHGAP31c.2082T>A (p.Ile694=)
c.1989T>A (p.Ile663=)
c.2022T>A (p.Ile674=)
c.1590T>A (p.Ile530=)
 dbSNP
3g.119414011T>CCA435411518ARHGAP31c.2082T>C (p.Ile694=)
c.1989T>C (p.Ile663=)
c.2022T>C (p.Ile674=)
c.1590T>C (p.Ile530=)
3g.119414011T>GCA354049006ARHGAP31c.2082T>G (p.Ile694Met)
c.1989T>G (p.Ile663Met)
c.2022T>G (p.Ile674Met)
c.1590T>G (p.Ile530Met)
 dbSNP
3g.119414011T=CA1396548516ARHGAP31c.2082T= (p.Ile694=)
c.1989T= (p.Ile663=)
c.2022T= (p.Ile674=)
c.1590T= (p.Ile530=)
3g.119414012C>ACA354049010ARHGAP31c.2083C>A (p.Pro695Thr)
c.1990C>A (p.Pro664Thr)
c.2023C>A (p.Pro675Thr)
c.1591C>A (p.Pro531Thr)
3g.119414012C>GCA354049011ARHGAP31c.2083C>G (p.Pro695Ala)
c.1990C>G (p.Pro664Ala)
c.2023C>G (p.Pro675Ala)
c.1591C>G (p.Pro531Ala)
3g.119414012C>TCA354049013ARHGAP31c.2083C>T (p.Pro695Ser)
c.1990C>T (p.Pro664Ser)
c.2023C>T (p.Pro675Ser)
c.1591C>T (p.Pro531Ser)
3g.119414013C>ACA354049016ARHGAP31c.2084C>A (p.Pro695His)
c.1991C>A (p.Pro664His)
c.2024C>A (p.Pro675His)
c.1592C>A (p.Pro531His)
3g.119414013C>GCA354049018ARHGAP31c.2084C>G (p.Pro695Arg)
c.1991C>G (p.Pro664Arg)
c.2024C>G (p.Pro675Arg)
c.1592C>G (p.Pro531Arg)
3g.119414013C>TCA354049022ARHGAP31c.2084C>T (p.Pro695Leu)
c.1991C>T (p.Pro664Leu)
c.2024C>T (p.Pro675Leu)
c.1592C>T (p.Pro531Leu)
3g.119414014C>ACA435411519ARHGAP31c.2085C>A (p.Pro695=)
c.1992C>A (p.Pro664=)
c.2025C>A (p.Pro675=)
c.1593C>A (p.Pro531=)
3g.119414014C>GCA435411521ARHGAP31c.2085C>G (p.Pro695=)
c.1992C>G (p.Pro664=)
c.2025C>G (p.Pro675=)
c.1593C>G (p.Pro531=)
3g.119414014C>TCA435411520ARHGAP31c.2085C>T (p.Pro695=)
c.1992C>T (p.Pro664=)
c.2025C>T (p.Pro675=)
c.1593C>T (p.Pro531=)
3g.119414015T>ACA354049028ARHGAP31c.2086T>A (p.Ser696Thr)
c.1993T>A (p.Ser665Thr)
c.2026T>A (p.Ser676Thr)
c.1594T>A (p.Ser532Thr)
3g.119414015T>CCA354049031ARHGAP31c.2086T>C (p.Ser696Pro)
c.1993T>C (p.Ser665Pro)
c.2026T>C (p.Ser676Pro)
c.1594T>C (p.Ser532Pro)
3g.119414015T>GCA354049029ARHGAP31c.2086T>G (p.Ser696Ala)
c.1993T>G (p.Ser665Ala)
c.2026T>G (p.Ser676Ala)
c.1594T>G (p.Ser532Ala)
3g.119414016C>ACA354049037ARHGAP31c.2087C>A (p.Ser696Ter)
c.1994C>A (p.Ser665Ter)
c.2027C>A (p.Ser676Ter)
c.1595C>A (p.Ser532Ter)
3g.119414016C>GCA354049042ARHGAP31c.2087C>G (p.Ser696Ter)
c.1994C>G (p.Ser665Ter)
c.2027C>G (p.Ser676Ter)
c.1595C>G (p.Ser532Ter)
3g.119414016C>TCA354049046ARHGAP31c.2087C>T (p.Ser696Leu)
c.1994C>T (p.Ser665Leu)
c.2027C>T (p.Ser676Leu)
c.1595C>T (p.Ser532Leu)
3g.119414017A=CA1396548517ARHGAP31c.2088A= (p.Ser696=)
c.1995A= (p.Ser665=)
c.2028A= (p.Ser676=)
c.1596A= (p.Ser532=)
3g.119414017A>CCA435411523ARHGAP31c.2088A>C (p.Ser696=)
c.1995A>C (p.Ser665=)
c.2028A>C (p.Ser676=)
c.1596A>C (p.Ser532=)
3g.119414017A>GCA2553968ARHGAP31c.2088A>G (p.Ser696=)
c.1995A>G (p.Ser665=)
c.2028A>G (p.Ser676=)
c.1596A>G (p.Ser532=)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.119414017A>TCA435411524ARHGAP31c.2088A>T (p.Ser696=)
c.1995A>T (p.Ser665=)
c.2028A>T (p.Ser676=)
c.1596A>T (p.Ser532=)
3g.119414018G>ACA354049056ARHGAP31c.2089G>A (p.Glu697Lys)
c.1996G>A (p.Glu666Lys)
c.2029G>A (p.Glu677Lys)
c.1597G>A (p.Glu533Lys)
3g.119414018G>CCA354049065ARHGAP31c.2089G>C (p.Glu697Gln)
c.1996G>C (p.Glu666Gln)
c.2029G>C (p.Glu677Gln)
c.1597G>C (p.Glu533Gln)
3g.119414018G>TCA354049059ARHGAP31c.2089G>T (p.Glu697Ter)
c.1996G>T (p.Glu666Ter)
c.2029G>T (p.Glu677Ter)
c.1597G>T (p.Glu533Ter)
3g.119414019A>CCA354049069ARHGAP31c.2090A>C (p.Glu697Ala)
c.1997A>C (p.Glu666Ala)
c.2030A>C (p.Glu677Ala)
c.1598A>C (p.Glu533Ala)
3g.119414019A>GCA354049073ARHGAP31c.2090A>G (p.Glu697Gly)
c.1997A>G (p.Glu666Gly)
c.2030A>G (p.Glu677Gly)
c.1598A>G (p.Glu533Gly)
3g.119414019A>TCA354049075ARHGAP31c.2090A>T (p.Glu697Val)
c.1997A>T (p.Glu666Val)
c.2030A>T (p.Glu677Val)
c.1598A>T (p.Glu533Val)
3g.119414020G>ACA435411526ARHGAP31c.2091G>A (p.Glu697=)
c.1998G>A (p.Glu666=)
c.2031G>A (p.Glu677=)
c.1599G>A (p.Glu533=)
3g.119414020G>CCA354049079ARHGAP31c.2091G>C (p.Glu697Asp)
c.1998G>C (p.Glu666Asp)
c.2031G>C (p.Glu677Asp)
c.1599G>C (p.Glu533Asp)
3g.119414020G>TCA354049082ARHGAP31c.2091G>T (p.Glu697Asp)
c.1998G>T (p.Glu666Asp)
c.2031G>T (p.Glu677Asp)
c.1599G>T (p.Glu533Asp)
3g.119414021C>ACA354049087ARHGAP31c.2092C>A (p.Pro698Thr)
c.1999C>A (p.Pro667Thr)
c.2032C>A (p.Pro678Thr)
c.1600C>A (p.Pro534Thr)
3g.119414021C>GCA354049088ARHGAP31c.2092C>G (p.Pro698Ala)
c.1999C>G (p.Pro667Ala)
c.2032C>G (p.Pro678Ala)
c.1600C>G (p.Pro534Ala)
3g.119414021C>TCA354049089ARHGAP31c.2092C>T (p.Pro698Ser)
c.1999C>T (p.Pro667Ser)
c.2032C>T (p.Pro678Ser)
c.1600C>T (p.Pro534Ser)
 gnomAD v4
3g.119414022C>ACA354049090ARHGAP31c.2093C>A (p.Pro698His)
c.2000C>A (p.Pro667His)
c.2033C>A (p.Pro678His)
c.1601C>A (p.Pro534His)
3g.119414022C=CA1396548518ARHGAP31c.2093C= (p.Pro698=)
c.2000C= (p.Pro667=)
c.2033C= (p.Pro678=)
c.1601C= (p.Pro534=)
3g.119414022C>GCA2553969ARHGAP31c.2093C>G (p.Pro698Arg)
c.2000C>G (p.Pro667Arg)
c.2033C>G (p.Pro678Arg)
c.1601C>G (p.Pro534Arg)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.119414022C>TCA354049094ARHGAP31c.2093C>T (p.Pro698Leu)
c.2000C>T (p.Pro667Leu)
c.2033C>T (p.Pro678Leu)
c.1601C>T (p.Pro534Leu)
3g.119414023T>ACA435411530ARHGAP31c.2094T>A (p.Pro698=)
c.2001T>A (p.Pro667=)
c.2034T>A (p.Pro678=)
c.1602T>A (p.Pro534=)
3g.119414023T>CCA435411531ARHGAP31c.2094T>C (p.Pro698=)
c.2001T>C (p.Pro667=)
c.2034T>C (p.Pro678=)
c.1602T>C (p.Pro534=)
3g.119414023T>GCA435411532ARHGAP31c.2094T>G (p.Pro698=)
c.2001T>G (p.Pro667=)
c.2034T>G (p.Pro678=)
c.1602T>G (p.Pro534=)
3g.119414024C>ACA354049097ARHGAP31c.2095C>A (p.Pro699Thr)
c.2002C>A (p.Pro668Thr)
c.2035C>A (p.Pro679Thr)
c.1603C>A (p.Pro535Thr)
3g.119414024C>GCA354049102ARHGAP31c.2095C>G (p.Pro699Ala)
c.2002C>G (p.Pro668Ala)
c.2035C>G (p.Pro679Ala)
c.1603C>G (p.Pro535Ala)
 gnomAD v4
3g.119414024C>TCA354049100ARHGAP31c.2095C>T (p.Pro699Ser)
c.2002C>T (p.Pro668Ser)
c.2035C>T (p.Pro679Ser)
c.1603C>T (p.Pro535Ser)
3g.119414025C>ACA354049106ARHGAP31c.2096C>A (p.Pro699His)
c.2003C>A (p.Pro668His)
c.2036C>A (p.Pro679His)
c.1604C>A (p.Pro535His)
3g.119414025C>GCA354049123ARHGAP31c.2096C>G (p.Pro699Arg)
c.2003C>G (p.Pro668Arg)
c.2036C>G (p.Pro679Arg)
c.1604C>G (p.Pro535Arg)
3g.119414025C>TCA354049119ARHGAP31c.2096C>T (p.Pro699Leu)
c.2003C>T (p.Pro668Leu)
c.2036C>T (p.Pro679Leu)
c.1604C>T (p.Pro535Leu)
 gnomAD v4

Number of alleles fetched