Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.119413919del | CA2667110268 | ARHGAP31 | c.1990del (p.Glu664AsnfsTer14) c.1897del (p.Glu633AsnfsTer14) c.1930del (p.Glu644AsnfsTer14) c.1498del (p.Glu500AsnfsTer14) | gnomAD v4 |
3 | g.119413919G>A | CA354048147 | ARHGAP31 | c.1990G>A (p.Glu664Lys) c.1897G>A (p.Glu633Lys) c.1930G>A (p.Glu644Lys) c.1498G>A (p.Glu500Lys) | |
3 | g.119413919G>C | CA354048144 | ARHGAP31 | c.1990G>C (p.Glu664Gln) c.1897G>C (p.Glu633Gln) c.1930G>C (p.Glu644Gln) c.1498G>C (p.Glu500Gln) | |
3 | g.119413919G>T | CA354048146 | ARHGAP31 | c.1990G>T (p.Glu664Ter) c.1897G>T (p.Glu633Ter) c.1930G>T (p.Glu644Ter) c.1498G>T (p.Glu500Ter) | |
3 | g.119413920A>C | CA354048148 | ARHGAP31 | c.1991A>C (p.Glu664Ala) c.1898A>C (p.Glu633Ala) c.1931A>C (p.Glu644Ala) c.1499A>C (p.Glu500Ala) | |
3 | g.119413920A>G | CA354048149 | ARHGAP31 | c.1991A>G (p.Glu664Gly) c.1898A>G (p.Glu633Gly) c.1931A>G (p.Glu644Gly) c.1499A>G (p.Glu500Gly) | |
3 | g.119413920A>T | CA354048150 | ARHGAP31 | c.1991A>T (p.Glu664Val) c.1898A>T (p.Glu633Val) c.1931A>T (p.Glu644Val) c.1499A>T (p.Glu500Val) | |
3 | g.119413921A>C | CA354048152 | ARHGAP31 | c.1992A>C (p.Glu664Asp) c.1899A>C (p.Glu633Asp) c.1932A>C (p.Glu644Asp) c.1500A>C (p.Glu500Asp) | |
3 | g.119413921A>G | CA435411379 | ARHGAP31 | c.1992A>G (p.Glu664=) c.1899A>G (p.Glu633=) c.1932A>G (p.Glu644=) c.1500A>G (p.Glu500=) | |
3 | g.119413921A>T | CA354048161 | ARHGAP31 | c.1992A>T (p.Glu664Asp) c.1899A>T (p.Glu633Asp) c.1932A>T (p.Glu644Asp) c.1500A>T (p.Glu500Asp) | |
3 | g.119413922T>A | CA354048166 | ARHGAP31 | c.1993T>A (p.Ser665Thr) c.1900T>A (p.Ser634Thr) c.1933T>A (p.Ser645Thr) c.1501T>A (p.Ser501Thr) | |
3 | g.119413922T>C | CA354048169 | ARHGAP31 | c.1993T>C (p.Ser665Pro) c.1900T>C (p.Ser634Pro) c.1933T>C (p.Ser645Pro) c.1501T>C (p.Ser501Pro) | |
3 | g.119413922T>G | CA354048170 | ARHGAP31 | c.1993T>G (p.Ser665Ala) c.1900T>G (p.Ser634Ala) c.1933T>G (p.Ser645Ala) c.1501T>G (p.Ser501Ala) | |
3 | g.119413923C>A | CA354048171 | ARHGAP31 | c.1994C>A (p.Ser665Tyr) c.1901C>A (p.Ser634Tyr) c.1934C>A (p.Ser645Tyr) c.1502C>A (p.Ser501Tyr) | COSMIC |
3 | g.119413923C>G | CA354048172 | ARHGAP31 | c.1994C>G (p.Ser665Cys) c.1901C>G (p.Ser634Cys) c.1934C>G (p.Ser645Cys) c.1502C>G (p.Ser501Cys) | |
3 | g.119413923C>T | CA354048173 | ARHGAP31 | c.1994C>T (p.Ser665Phe) c.1901C>T (p.Ser634Phe) c.1934C>T (p.Ser645Phe) c.1502C>T (p.Ser501Phe) | |
3 | g.119413924T>A | CA435411384 | ARHGAP31 | c.1995T>A (p.Ser665=) c.1902T>A (p.Ser634=) c.1935T>A (p.Ser645=) c.1503T>A (p.Ser501=) | |
3 | g.119413924T>C | CA435411386 | ARHGAP31 | c.1995T>C (p.Ser665=) c.1902T>C (p.Ser634=) c.1935T>C (p.Ser645=) c.1503T>C (p.Ser501=) | |
3 | g.119413924T>G | CA435411387 | ARHGAP31 | c.1995T>G (p.Ser665=) c.1902T>G (p.Ser634=) c.1935T>G (p.Ser645=) c.1503T>G (p.Ser501=) | |
3 | g.119413925G>A | CA354048175 | ARHGAP31 | c.1996G>A (p.Glu666Lys) c.1903G>A (p.Glu635Lys) c.1936G>A (p.Glu646Lys) c.1504G>A (p.Glu502Lys) | |
3 | g.119413925G>C | CA354048177 | ARHGAP31 | c.1996G>C (p.Glu666Gln) c.1903G>C (p.Glu635Gln) c.1936G>C (p.Glu646Gln) c.1504G>C (p.Glu502Gln) | |
3 | g.119413925G>T | CA354048176 | ARHGAP31 | c.1996G>T (p.Glu666Ter) c.1903G>T (p.Glu635Ter) c.1936G>T (p.Glu646Ter) c.1504G>T (p.Glu502Ter) | |
3 | g.119413926A>C | CA354048178 | ARHGAP31 | c.1997A>C (p.Glu666Ala) c.1904A>C (p.Glu635Ala) c.1937A>C (p.Glu646Ala) c.1505A>C (p.Glu502Ala) | |
3 | g.119413926A>G | CA354048180 | ARHGAP31 | c.1997A>G (p.Glu666Gly) c.1904A>G (p.Glu635Gly) c.1937A>G (p.Glu646Gly) c.1505A>G (p.Glu502Gly) | |
3 | g.119413926A>T | CA354048182 | ARHGAP31 | c.1997A>T (p.Glu666Val) c.1904A>T (p.Glu635Val) c.1937A>T (p.Glu646Val) c.1505A>T (p.Glu502Val) | |
3 | g.119413927G>A | CA435411393 | ARHGAP31 | c.1998G>A (p.Glu666=) c.1905G>A (p.Glu635=) c.1938G>A (p.Glu646=) c.1506G>A (p.Glu502=) | |
3 | g.119413927G>C | CA354048185 | ARHGAP31 | c.1998G>C (p.Glu666Asp) c.1905G>C (p.Glu635Asp) c.1938G>C (p.Glu646Asp) c.1506G>C (p.Glu502Asp) | |
3 | g.119413927G>T | CA354048186 | ARHGAP31 | c.1998G>T (p.Glu666Asp) c.1905G>T (p.Glu635Asp) c.1938G>T (p.Glu646Asp) c.1506G>T (p.Glu502Asp) | |
3 | g.119413928G>A | CA354048190 | ARHGAP31 | c.1999G>A (p.Glu667Lys) c.1906G>A (p.Glu636Lys) c.1939G>A (p.Glu647Lys) c.1507G>A (p.Glu503Lys) | |
3 | g.119413928G>C | CA354048193 | ARHGAP31 | c.1999G>C (p.Glu667Gln) c.1906G>C (p.Glu636Gln) c.1939G>C (p.Glu647Gln) c.1507G>C (p.Glu503Gln) | |
3 | g.119413928G>T | CA354048194 | ARHGAP31 | c.1999G>T (p.Glu667Ter) c.1906G>T (p.Glu636Ter) c.1939G>T (p.Glu647Ter) c.1507G>T (p.Glu503Ter) | |
3 | g.119413929A>C | CA354048195 | ARHGAP31 | c.2000A>C (p.Glu667Ala) c.1907A>C (p.Glu636Ala) c.1940A>C (p.Glu647Ala) c.1508A>C (p.Glu503Ala) | |
3 | g.119413929A>G | CA354048196 | ARHGAP31 | c.2000A>G (p.Glu667Gly) c.1907A>G (p.Glu636Gly) c.1940A>G (p.Glu647Gly) c.1508A>G (p.Glu503Gly) | |
3 | g.119413929A>T | CA354048197 | ARHGAP31 | c.2000A>T (p.Glu667Val) c.1907A>T (p.Glu636Val) c.1940A>T (p.Glu647Val) c.1508A>T (p.Glu503Val) | |
3 | g.119413930G>A | CA435411401 | ARHGAP31 | c.2001G>A (p.Glu667=) c.1908G>A (p.Glu636=) c.1941G>A (p.Glu647=) c.1509G>A (p.Glu503=) | |
3 | g.119413930G>C | CA354048201 | ARHGAP31 | c.2001G>C (p.Glu667Asp) c.1908G>C (p.Glu636Asp) c.1941G>C (p.Glu647Asp) c.1509G>C (p.Glu503Asp) | |
3 | g.119413930G>T | CA354048199 | ARHGAP31 | c.2001G>T (p.Glu667Asp) c.1908G>T (p.Glu636Asp) c.1941G>T (p.Glu647Asp) c.1509G>T (p.Glu503Asp) | |
3 | g.119413931G>A | CA354048204 | ARHGAP31 | c.2002G>A (p.Glu668Lys) c.1909G>A (p.Glu637Lys) c.1942G>A (p.Glu648Lys) c.1510G>A (p.Glu504Lys) | |
3 | g.119413931G>C | CA354048208 | ARHGAP31 | c.2002G>C (p.Glu668Gln) c.1909G>C (p.Glu637Gln) c.1942G>C (p.Glu648Gln) c.1510G>C (p.Glu504Gln) | |
3 | g.119413931G>T | CA354048211 | ARHGAP31 | c.2002G>T (p.Glu668Ter) c.1909G>T (p.Glu637Ter) c.1942G>T (p.Glu648Ter) c.1510G>T (p.Glu504Ter) | |
3 | g.119413932A= | CA1396548477 | ARHGAP31 | c.2003A= (p.Glu668=) c.1910A= (p.Glu637=) c.1943A= (p.Glu648=) c.1511A= (p.Glu504=) | |
3 | g.119413932A>C | CA354048214 | ARHGAP31 | c.2003A>C (p.Glu668Ala) c.1910A>C (p.Glu637Ala) c.1943A>C (p.Glu648Ala) c.1511A>C (p.Glu504Ala) | dbSNP |
3 | g.119413932A>G | CA354048216 | ARHGAP31 | c.2003A>G (p.Glu668Gly) c.1910A>G (p.Glu637Gly) c.1943A>G (p.Glu648Gly) c.1511A>G (p.Glu504Gly) | |
3 | g.119413932A>T | CA354048220 | ARHGAP31 | c.2003A>T (p.Glu668Val) c.1910A>T (p.Glu637Val) c.1943A>T (p.Glu648Val) c.1511A>T (p.Glu504Val) | |
3 | g.119413933G>A | CA435411405 | ARHGAP31 | c.2004G>A (p.Glu668=) c.1911G>A (p.Glu637=) c.1944G>A (p.Glu648=) c.1512G>A (p.Glu504=) | |
3 | g.119413933G>C | CA354048232 | ARHGAP31 | c.2004G>C (p.Glu668Asp) c.1911G>C (p.Glu637Asp) c.1944G>C (p.Glu648Asp) c.1512G>C (p.Glu504Asp) | |
3 | g.119413933G>T | CA354048227 | ARHGAP31 | c.2004G>T (p.Glu668Asp) c.1911G>T (p.Glu637Asp) c.1944G>T (p.Glu648Asp) c.1512G>T (p.Glu504Asp) | |
3 | g.119413934C>A | CA354048236 | ARHGAP31 | c.2005C>A (p.Leu669Ile) c.1912C>A (p.Leu638Ile) c.1945C>A (p.Leu649Ile) c.1513C>A (p.Leu505Ile) | |
3 | g.119413934C= | CA1396548478 | ARHGAP31 | c.2005C= (p.Leu669=) c.1912C= (p.Leu638=) c.1945C= (p.Leu649=) c.1513C= (p.Leu505=) | |
3 | g.119413934C>G | CA81697286 | ARHGAP31 | c.2005C>G (p.Leu669Val) c.1912C>G (p.Leu638Val) c.1945C>G (p.Leu649Val) c.1513C>G (p.Leu505Val) | dbSNP |
3 | g.119413934C>T | CA354048242 | ARHGAP31 | c.2005C>T (p.Leu669Phe) c.1912C>T (p.Leu638Phe) c.1945C>T (p.Leu649Phe) c.1513C>T (p.Leu505Phe) | gnomAD v4 |
3 | g.119413935T>A | CA354048246 | ARHGAP31 | c.2006T>A (p.Leu669His) c.1913T>A (p.Leu638His) c.1946T>A (p.Leu649His) c.1514T>A (p.Leu505His) | |
3 | g.119413935T>C | CA354048249 | ARHGAP31 | c.2006T>C (p.Leu669Pro) c.1913T>C (p.Leu638Pro) c.1946T>C (p.Leu649Pro) c.1514T>C (p.Leu505Pro) | |
3 | g.119413935T>G | CA354048252 | ARHGAP31 | c.2006T>G (p.Leu669Arg) c.1913T>G (p.Leu638Arg) c.1946T>G (p.Leu649Arg) c.1514T>G (p.Leu505Arg) | |
3 | g.119413936C>A | CA435411409 | ARHGAP31 | c.2007C>A (p.Leu669=) c.1914C>A (p.Leu638=) c.1947C>A (p.Leu649=) c.1515C>A (p.Leu505=) | |
3 | g.119413936C= | CA1396548479 | ARHGAP31 | c.2007C= (p.Leu669=) c.1914C= (p.Leu638=) c.1947C= (p.Leu649=) c.1515C= (p.Leu505=) | |
3 | g.119413936C>G | CA81697288 | ARHGAP31 | c.2007C>G (p.Leu669=) c.1914C>G (p.Leu638=) c.1947C>G (p.Leu649=) c.1515C>G (p.Leu505=) | dbSNP gnomAD v4 |
3 | g.119413936C>T | CA435411411 | ARHGAP31 | c.2007C>T (p.Leu669=) c.1914C>T (p.Leu638=) c.1947C>T (p.Leu649=) c.1515C>T (p.Leu505=) | dbSNP gnomAD v3 gnomAD v4 |
3 | g.119413937T>A | CA354048263 | ARHGAP31 | c.2008T>A (p.Ser670Thr) c.1915T>A (p.Ser639Thr) c.1948T>A (p.Ser650Thr) c.1516T>A (p.Ser506Thr) | |
3 | g.119413937T>C | CA354048257 | ARHGAP31 | c.2008T>C (p.Ser670Pro) c.1915T>C (p.Ser639Pro) c.1948T>C (p.Ser650Pro) c.1516T>C (p.Ser506Pro) | |
3 | g.119413937T>G | CA354048260 | ARHGAP31 | c.2008T>G (p.Ser670Ala) c.1915T>G (p.Ser639Ala) c.1948T>G (p.Ser650Ala) c.1516T>G (p.Ser506Ala) | |
3 | g.119413938C>A | CA354048266 | ARHGAP31 | c.2009C>A (p.Ser670Ter) c.1916C>A (p.Ser639Ter) c.1949C>A (p.Ser650Ter) c.1517C>A (p.Ser506Ter) | |
3 | g.119413938C>G | CA354048269 | ARHGAP31 | c.2009C>G (p.Ser670Ter) c.1916C>G (p.Ser639Ter) c.1949C>G (p.Ser650Ter) c.1517C>G (p.Ser506Ter) | |
3 | g.119413938C>T | CA354048271 | ARHGAP31 | c.2009C>T (p.Ser670Leu) c.1916C>T (p.Ser639Leu) c.1949C>T (p.Ser650Leu) c.1517C>T (p.Ser506Leu) | |
3 | g.119413939A= | CA1396548480 | ARHGAP31 | c.2010A= (p.Ser670=) c.1917A= (p.Ser639=) c.1950A= (p.Ser650=) c.1518A= (p.Ser506=) | |
3 | g.119413939A>C | CA435411423 | ARHGAP31 | c.2010A>C (p.Ser670=) c.1917A>C (p.Ser639=) c.1950A>C (p.Ser650=) c.1518A>C (p.Ser506=) | gnomAD v4 |
3 | g.119413939A>G | CA435411422 | ARHGAP31 | c.2010A>G (p.Ser670=) c.1917A>G (p.Ser639=) c.1950A>G (p.Ser650=) c.1518A>G (p.Ser506=) | |
3 | g.119413939A>T | CA81697298 | ARHGAP31 | c.2010A>T (p.Ser670=) c.1917A>T (p.Ser639=) c.1950A>T (p.Ser650=) c.1518A>T (p.Ser506=) | dbSNP |
3 | g.119413940T>A | CA354048274 | ARHGAP31 | c.2011T>A (p.Ser671Thr) c.1918T>A (p.Ser640Thr) c.1951T>A (p.Ser651Thr) c.1519T>A (p.Ser507Thr) | |
3 | g.119413940T>C | CA354048275 | ARHGAP31 | c.2011T>C (p.Ser671Pro) c.1918T>C (p.Ser640Pro) c.1951T>C (p.Ser651Pro) c.1519T>C (p.Ser507Pro) | |
3 | g.119413940T>G | CA354048276 | ARHGAP31 | c.2011T>G (p.Ser671Ala) c.1918T>G (p.Ser640Ala) c.1951T>G (p.Ser651Ala) c.1519T>G (p.Ser507Ala) | |
3 | g.119413941C>A | CA354048278 | ARHGAP31 | c.2012C>A (p.Ser671Ter) c.1919C>A (p.Ser640Ter) c.1952C>A (p.Ser651Ter) c.1520C>A (p.Ser507Ter) | |
3 | g.119413941C= | CA1396548481 | ARHGAP31 | c.2012C= (p.Ser671=) c.1919C= (p.Ser640=) c.1952C= (p.Ser651=) c.1520C= (p.Ser507=) | |
3 | g.119413941C>G | CA354048280 | ARHGAP31 | c.2012C>G (p.Ser671Trp) c.1919C>G (p.Ser640Trp) c.1952C>G (p.Ser651Trp) c.1520C>G (p.Ser507Trp) | |
3 | g.119413941C>T | CA354048283 | ARHGAP31 | c.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 |
3 | g.119413942G>A | CA435411432 | ARHGAP31 | c.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 |
3 | g.119413942G>C | CA435411433 | ARHGAP31 | c.2013G>C (p.Ser671=) c.1920G>C (p.Ser640=) c.1953G>C (p.Ser651=) c.1521G>C (p.Ser507=) | |
3 | g.119413942G= | CA1396548482 | ARHGAP31 | c.2013G= (p.Ser671=) c.1920G= (p.Ser640=) c.1953G= (p.Ser651=) c.1521G= (p.Ser507=) | |
3 | g.119413942G>T | CA2553947 | ARHGAP31 | c.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 |
3 | g.119413943T>A | CA354048288 | ARHGAP31 | c.2014T>A (p.Leu672Met) c.1921T>A (p.Leu641Met) c.1954T>A (p.Leu652Met) c.1522T>A (p.Leu508Met) | |
3 | g.119413943T>C | CA435411434 | ARHGAP31 | c.2014T>C (p.Leu672=) c.1921T>C (p.Leu641=) c.1954T>C (p.Leu652=) c.1522T>C (p.Leu508=) | |
3 | g.119413943T>G | CA354048290 | ARHGAP31 | c.2014T>G (p.Leu672Val) c.1921T>G (p.Leu641Val) c.1954T>G (p.Leu652Val) c.1522T>G (p.Leu508Val) | |
3 | g.119413944T>A | CA354048294 | ARHGAP31 | c.2015T>A (p.Leu672Ter) c.1922T>A (p.Leu641Ter) c.1955T>A (p.Leu652Ter) c.1523T>A (p.Leu508Ter) | |
3 | g.119413944T>C | CA354048299 | ARHGAP31 | c.2015T>C (p.Leu672Ser) c.1922T>C (p.Leu641Ser) c.1955T>C (p.Leu652Ser) c.1523T>C (p.Leu508Ser) | |
3 | g.119413944T>G | CA354048295 | ARHGAP31 | c.2015T>G (p.Leu672Trp) c.1922T>G (p.Leu641Trp) c.1955T>G (p.Leu652Trp) c.1523T>G (p.Leu508Trp) | |
3 | g.119413945G>A | CA2553948 | ARHGAP31 | c.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 |
3 | g.119413945G>C | CA354048312 | ARHGAP31 | c.2016G>C (p.Leu672Phe) c.1923G>C (p.Leu641Phe) c.1956G>C (p.Leu652Phe) c.1524G>C (p.Leu508Phe) | |
3 | g.119413945G= | CA1396548483 | ARHGAP31 | c.2016G= (p.Leu672=) c.1923G= (p.Leu641=) c.1956G= (p.Leu652=) c.1524G= (p.Leu508=) | |
3 | g.119413945G>T | CA354048311 | ARHGAP31 | c.2016G>T (p.Leu672Phe) c.1923G>T (p.Leu641Phe) c.1956G>T (p.Leu652Phe) c.1524G>T (p.Leu508Phe) | |
3 | g.119413946C>A | CA354048313 | ARHGAP31 | c.2017C>A (p.Pro673Thr) c.1924C>A (p.Pro642Thr) c.1957C>A (p.Pro653Thr) c.1525C>A (p.Pro509Thr) | |
3 | g.119413946C>G | CA354048318 | ARHGAP31 | c.2017C>G (p.Pro673Ala) c.1924C>G (p.Pro642Ala) c.1957C>G (p.Pro653Ala) c.1525C>G (p.Pro509Ala) | |
3 | g.119413946C>T | CA354048319 | ARHGAP31 | c.2017C>T (p.Pro673Ser) c.1924C>T (p.Pro642Ser) c.1957C>T (p.Pro653Ser) c.1525C>T (p.Pro509Ser) | COSMIC |
3 | g.119413947C>A | CA354048325 | ARHGAP31 | c.2018C>A (p.Pro673Gln) c.1925C>A (p.Pro642Gln) c.1958C>A (p.Pro653Gln) c.1526C>A (p.Pro509Gln) | |
3 | g.119413947C>G | CA354048328 | ARHGAP31 | c.2018C>G (p.Pro673Arg) c.1925C>G (p.Pro642Arg) c.1958C>G (p.Pro653Arg) c.1526C>G (p.Pro509Arg) | |
3 | g.119413947C>T | CA354048330 | ARHGAP31 | c.2018C>T (p.Pro673Leu) c.1925C>T (p.Pro642Leu) c.1958C>T (p.Pro653Leu) c.1526C>T (p.Pro509Leu) | |
3 | g.119413948A= | CA1396548484 | ARHGAP31 | c.2019A= (p.Pro673=) c.1926A= (p.Pro642=) c.1959A= (p.Pro653=) c.1527A= (p.Pro509=) | |
3 | g.119413948A>C | CA435411443 | ARHGAP31 | c.2019A>C (p.Pro673=) c.1926A>C (p.Pro642=) c.1959A>C (p.Pro653=) c.1527A>C (p.Pro509=) | |
3 | g.119413948A>G | CA2553949 | ARHGAP31 | c.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 |
3 | g.119413948A>T | CA435411444 | ARHGAP31 | c.2019A>T (p.Pro673=) c.1926A>T (p.Pro642=) c.1959A>T (p.Pro653=) c.1527A>T (p.Pro509=) | |
3 | g.119413949C>A | CA354048336 | ARHGAP31 | c.2020C>A (p.Pro674Thr) c.1927C>A (p.Pro643Thr) c.1960C>A (p.Pro654Thr) c.1528C>A (p.Pro510Thr) | gnomAD v4 COSMIC |
3 | g.119413949C= | CA1396548485 | ARHGAP31 | c.2020C= (p.Pro674=) c.1927C= (p.Pro643=) c.1960C= (p.Pro654=) c.1528C= (p.Pro510=) | |
3 | g.119413949C>G | CA354048339 | ARHGAP31 | c.2020C>G (p.Pro674Ala) c.1927C>G (p.Pro643Ala) c.1960C>G (p.Pro654Ala) c.1528C>G (p.Pro510Ala) | |
3 | g.119413949C>T | CA81697308 | ARHGAP31 | c.2020C>T (p.Pro674Ser) c.1927C>T (p.Pro643Ser) c.1960C>T (p.Pro654Ser) c.1528C>T (p.Pro510Ser) | dbSNP |
3 | g.119413950C>A | CA354048344 | ARHGAP31 | c.2021C>A (p.Pro674His) c.1928C>A (p.Pro643His) c.1961C>A (p.Pro654His) c.1529C>A (p.Pro510His) | |
3 | g.119413950C>G | CA354048351 | ARHGAP31 | c.2021C>G (p.Pro674Arg) c.1928C>G (p.Pro643Arg) c.1961C>G (p.Pro654Arg) c.1529C>G (p.Pro510Arg) | |
3 | g.119413950C>T | CA354048353 | ARHGAP31 | c.2021C>T (p.Pro674Leu) c.1928C>T (p.Pro643Leu) c.1961C>T (p.Pro654Leu) c.1529C>T (p.Pro510Leu) | ClinVar |
3 | g.119413951T>A | CA435411450 | ARHGAP31 | c.2022T>A (p.Pro674=) c.1929T>A (p.Pro643=) c.1962T>A (p.Pro654=) c.1530T>A (p.Pro510=) | |
3 | g.119413951T>C | CA435411448 | ARHGAP31 | c.2022T>C (p.Pro674=) c.1929T>C (p.Pro643=) c.1962T>C (p.Pro654=) c.1530T>C (p.Pro510=) | |
3 | g.119413951T>G | CA435411449 | ARHGAP31 | c.2022T>G (p.Pro674=) c.1929T>G (p.Pro643=) c.1962T>G (p.Pro654=) c.1530T>G (p.Pro510=) | |
3 | g.119413952C>A | CA354048363 | ARHGAP31 | c.2023C>A (p.Pro675Thr) c.1930C>A (p.Pro644Thr) c.1963C>A (p.Pro655Thr) c.1531C>A (p.Pro511Thr) | |
3 | g.119413952C>G | CA354048373 | ARHGAP31 | c.2023C>G (p.Pro675Ala) c.1930C>G (p.Pro644Ala) c.1963C>G (p.Pro655Ala) c.1531C>G (p.Pro511Ala) | |
3 | g.119413952C>T | CA354048370 | ARHGAP31 | c.2023C>T (p.Pro675Ser) c.1930C>T (p.Pro644Ser) c.1963C>T (p.Pro655Ser) c.1531C>T (p.Pro511Ser) | |
3 | g.119413953C>A | CA354048383 | ARHGAP31 | c.2024C>A (p.Pro675His) c.1931C>A (p.Pro644His) c.1964C>A (p.Pro655His) c.1532C>A (p.Pro511His) | |
3 | g.119413953C>G | CA354048387 | ARHGAP31 | c.2024C>G (p.Pro675Arg) c.1931C>G (p.Pro644Arg) c.1964C>G (p.Pro655Arg) c.1532C>G (p.Pro511Arg) | |
3 | g.119413953C>T | CA354048390 | ARHGAP31 | c.2024C>T (p.Pro675Leu) c.1931C>T (p.Pro644Leu) c.1964C>T (p.Pro655Leu) c.1532C>T (p.Pro511Leu) | |
3 | g.119413954T>A | CA435411455 | ARHGAP31 | c.2025T>A (p.Pro675=) c.1932T>A (p.Pro644=) c.1965T>A (p.Pro655=) c.1533T>A (p.Pro511=) | |
3 | g.119413954T>C | CA435411456 | ARHGAP31 | c.2025T>C (p.Pro675=) c.1932T>C (p.Pro644=) c.1965T>C (p.Pro655=) c.1533T>C (p.Pro511=) | |
3 | g.119413954T>G | CA435411457 | ARHGAP31 | c.2025T>G (p.Pro675=) c.1932T>G (p.Pro644=) c.1965T>G (p.Pro655=) c.1533T>G (p.Pro511=) | |
3 | g.119413955G>A | CA2553950 | ARHGAP31 | c.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 |
3 | g.119413955G>C | CA354048394 | ARHGAP31 | c.2026G>C (p.Ala676Pro) c.1933G>C (p.Ala645Pro) c.1966G>C (p.Ala656Pro) c.1534G>C (p.Ala512Pro) | |
3 | g.119413955G= | CA1396548486 | ARHGAP31 | c.2026G= (p.Ala676=) c.1933G= (p.Ala645=) c.1966G= (p.Ala656=) c.1534G= (p.Ala512=) | |
3 | g.119413955G>T | CA354048398 | ARHGAP31 | c.2026G>T (p.Ala676Ser) c.1933G>T (p.Ala645Ser) c.1966G>T (p.Ala656Ser) c.1534G>T (p.Ala512Ser) | |
3 | g.119413956C>A | CA354048404 | ARHGAP31 | c.2027C>A (p.Ala676Asp) c.1934C>A (p.Ala645Asp) c.1967C>A (p.Ala656Asp) c.1535C>A (p.Ala512Asp) | dbSNP |
3 | g.119413956C>G | CA354048406 | ARHGAP31 | c.2027C>G (p.Ala676Gly) c.1934C>G (p.Ala645Gly) c.1967C>G (p.Ala656Gly) c.1535C>G (p.Ala512Gly) | |
3 | g.119413956C>T | CA354048416 | ARHGAP31 | c.2027C>T (p.Ala676Val) c.1934C>T (p.Ala645Val) c.1967C>T (p.Ala656Val) c.1535C>T (p.Ala512Val) | |
3 | g.119413957T>A | CA2553951 | ARHGAP31 | c.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 |
3 | g.119413957T>C | CA435411463 | ARHGAP31 | c.2028T>C (p.Ala676=) c.1935T>C (p.Ala645=) c.1968T>C (p.Ala656=) c.1536T>C (p.Ala512=) | gnomAD v4 |
3 | g.119413957T>G | CA435411465 | ARHGAP31 | c.2028T>G (p.Ala676=) c.1935T>G (p.Ala645=) c.1968T>G (p.Ala656=) c.1536T>G (p.Ala512=) | |
3 | g.119413957T= | CA1396548487 | ARHGAP31 | c.2028T= (p.Ala676=) c.1935T= (p.Ala645=) c.1968T= (p.Ala656=) c.1536T= (p.Ala512=) | |
3 | g.119413958C>A | CA354048422 | ARHGAP31 | c.2029C>A (p.Leu677Met) c.1936C>A (p.Leu646Met) c.1969C>A (p.Leu657Met) c.1537C>A (p.Leu513Met) | |
3 | g.119413958C>G | CA354048423 | ARHGAP31 | c.2029C>G (p.Leu677Val) c.1936C>G (p.Leu646Val) c.1969C>G (p.Leu657Val) c.1537C>G (p.Leu513Val) | |
3 | g.119413958C>T | CA435411466 | ARHGAP31 | c.2029C>T (p.Leu677=) c.1936C>T (p.Leu646=) c.1969C>T (p.Leu657=) c.1537C>T (p.Leu513=) | COSMIC |
3 | g.119413959T>A | CA354048424 | ARHGAP31 | c.2030T>A (p.Leu677Gln) c.1937T>A (p.Leu646Gln) c.1970T>A (p.Leu657Gln) c.1538T>A (p.Leu513Gln) | |
3 | g.119413959T>C | CA354048425 | ARHGAP31 | c.2030T>C (p.Leu677Pro) c.1937T>C (p.Leu646Pro) c.1970T>C (p.Leu657Pro) c.1538T>C (p.Leu513Pro) | |
3 | g.119413959T>G | CA354048428 | ARHGAP31 | c.2030T>G (p.Leu677Arg) c.1937T>G (p.Leu646Arg) c.1970T>G (p.Leu657Arg) c.1538T>G (p.Leu513Arg) | gnomAD v4 |
3 | g.119413960G>A | CA435411467 | ARHGAP31 | c.2031G>A (p.Leu677=) c.1938G>A (p.Leu646=) c.1971G>A (p.Leu657=) c.1539G>A (p.Leu513=) | |
3 | g.119413960G>C | CA435411468 | ARHGAP31 | c.2031G>C (p.Leu677=) c.1938G>C (p.Leu646=) c.1971G>C (p.Leu657=) c.1539G>C (p.Leu513=) | |
3 | g.119413960G>T | CA435411470 | ARHGAP31 | c.2031G>T (p.Leu677=) c.1938G>T (p.Leu646=) c.1971G>T (p.Leu657=) c.1539G>T (p.Leu513=) | |
3 | g.119413961A>C | CA354048436 | ARHGAP31 | c.2032A>C (p.Lys678Gln) c.1939A>C (p.Lys647Gln) c.1972A>C (p.Lys658Gln) c.1540A>C (p.Lys514Gln) | |
3 | g.119413961A>G | CA354048439 | ARHGAP31 | c.2032A>G (p.Lys678Glu) c.1939A>G (p.Lys647Glu) c.1972A>G (p.Lys658Glu) c.1540A>G (p.Lys514Glu) | |
3 | g.119413961A>T | CA354048443 | ARHGAP31 | c.2032A>T (p.Lys678Ter) c.1939A>T (p.Lys647Ter) c.1972A>T (p.Lys658Ter) c.1540A>T (p.Lys514Ter) | |
3 | g.119413962A>C | CA354048444 | ARHGAP31 | c.2033A>C (p.Lys678Thr) c.1940A>C (p.Lys647Thr) c.1973A>C (p.Lys658Thr) c.1541A>C (p.Lys514Thr) | |
3 | g.119413962A>G | CA354048445 | ARHGAP31 | c.2033A>G (p.Lys678Arg) c.1940A>G (p.Lys647Arg) c.1973A>G (p.Lys658Arg) c.1541A>G (p.Lys514Arg) | |
3 | g.119413962A>T | CA354048446 | ARHGAP31 | c.2033A>T (p.Lys678Met) c.1940A>T (p.Lys647Met) c.1973A>T (p.Lys658Met) c.1541A>T (p.Lys514Met) | |
3 | g.119413963G>A | CA435411472 | ARHGAP31 | c.2034G>A (p.Lys678=) c.1941G>A (p.Lys647=) c.1974G>A (p.Lys658=) c.1542G>A (p.Lys514=) | |
3 | g.119413963G>C | CA354048449 | ARHGAP31 | c.2034G>C (p.Lys678Asn) c.1941G>C (p.Lys647Asn) c.1974G>C (p.Lys658Asn) c.1542G>C (p.Lys514Asn) | dbSNP gnomAD v3 gnomAD v4 |
3 | g.119413963G= | CA1396548488 | ARHGAP31 | c.2034G= (p.Lys678=) c.1941G= (p.Lys647=) c.1974G= (p.Lys658=) c.1542G= (p.Lys514=) | |
3 | g.119413963G>T | CA354048452 | ARHGAP31 | c.2034G>T (p.Lys678Asn) c.1941G>T (p.Lys647Asn) c.1974G>T (p.Lys658Asn) c.1542G>T (p.Lys514Asn) | |
3 | g.119413964A>C | CA354048463 | ARHGAP31 | c.2035A>C (p.Thr679Pro) c.1942A>C (p.Thr648Pro) c.1975A>C (p.Thr659Pro) c.1543A>C (p.Thr515Pro) | |
3 | g.119413964A>G | CA354048461 | ARHGAP31 | c.2035A>G (p.Thr679Ala) c.1942A>G (p.Thr648Ala) c.1975A>G (p.Thr659Ala) c.1543A>G (p.Thr515Ala) | gnomAD v4 |
3 | g.119413964A>T | CA354048458 | ARHGAP31 | c.2035A>T (p.Thr679Ser) c.1942A>T (p.Thr648Ser) c.1975A>T (p.Thr659Ser) c.1543A>T (p.Thr515Ser) | |
3 | g.119413964_119413965delinsAC | CA1396548489 | ARHGAP31 | c.2035_2036delinsAC (p.Thr679=) c.1942_1943delinsAC (p.Thr648=) c.1975_1976delinsAC (p.Thr659=) c.1543_1544delinsAC (p.Thr515=) | |
3 | g.119413965C>A | CA354048467 | ARHGAP31 | c.2036C>A (p.Thr679Asn) c.1943C>A (p.Thr648Asn) c.1976C>A (p.Thr659Asn) c.1544C>A (p.Thr515Asn) | |
3 | g.119413965C= | CA1396548490 | ARHGAP31 | c.2036C= (p.Thr679=) c.1943C= (p.Thr648=) c.1976C= (p.Thr659=) c.1544C= (p.Thr515=) | |
3 | g.119413965C>G | CA354048471 | ARHGAP31 | c.2036C>G (p.Thr679Ser) c.1943C>G (p.Thr648Ser) c.1976C>G (p.Thr659Ser) c.1544C>G (p.Thr515Ser) | gnomAD v4 |
3 | g.119413965C>T | CA2553952 | ARHGAP31 | c.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 |
3 | g.119413966del | CA81697309 | ARHGAP31 | c.2037del (p.Ser680AlafsTer?) c.1944del (p.Ser649AlafsTer?) c.1977del (p.Ser660AlafsTer?) c.1545del (p.Ser516AlafsTer?) | dbSNP |
3 | g.119413966C>A | CA435411476 | ARHGAP31 | c.2037C>A (p.Thr679=) c.1944C>A (p.Thr648=) c.1977C>A (p.Thr659=) c.1545C>A (p.Thr515=) | |
3 | g.119413966C= | CA1396548491 | ARHGAP31 | c.2037C= (p.Thr679=) c.1944C= (p.Thr648=) c.1977C= (p.Thr659=) c.1545C= (p.Thr515=) | |
3 | g.119413966C>G | CA2553953 | ARHGAP31 | c.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 |
3 | g.119413966C>T | CA2553954 | ARHGAP31 | c.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 |
3 | g.119413967A>C | CA354048501 | ARHGAP31 | c.2038A>C (p.Ser680Arg) c.1945A>C (p.Ser649Arg) c.1978A>C (p.Ser660Arg) c.1546A>C (p.Ser516Arg) | |
3 | g.119413967A>G | CA354048505 | ARHGAP31 | c.2038A>G (p.Ser680Gly) c.1945A>G (p.Ser649Gly) c.1978A>G (p.Ser660Gly) c.1546A>G (p.Ser516Gly) | |
3 | g.119413967A>T | CA354048512 | ARHGAP31 | c.2038A>T (p.Ser680Cys) c.1945A>T (p.Ser649Cys) c.1978A>T (p.Ser660Cys) c.1546A>T (p.Ser516Cys) | |
3 | g.119413968G>A | CA2553955 | ARHGAP31 | c.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 |
3 | g.119413968G>C | CA354048518 | ARHGAP31 | c.2039G>C (p.Ser680Thr) c.1946G>C (p.Ser649Thr) c.1979G>C (p.Ser660Thr) c.1547G>C (p.Ser516Thr) | |
3 | g.119413968G= | CA1396548492 | ARHGAP31 | c.2039G= (p.Ser680=) c.1946G= (p.Ser649=) c.1979G= (p.Ser660=) c.1547G= (p.Ser516=) | |
3 | g.119413968G>T | CA354048521 | ARHGAP31 | c.2039G>T (p.Ser680Ile) c.1946G>T (p.Ser649Ile) c.1979G>T (p.Ser660Ile) c.1547G>T (p.Ser516Ile) | |
3 | g.119413969C>A | CA354048531 | ARHGAP31 | c.2040C>A (p.Ser680Arg) c.1947C>A (p.Ser649Arg) c.1980C>A (p.Ser660Arg) c.1548C>A (p.Ser516Arg) | gnomAD v4 |
3 | g.119413969C>G | CA354048532 | ARHGAP31 | c.2040C>G (p.Ser680Arg) c.1947C>G (p.Ser649Arg) c.1980C>G (p.Ser660Arg) c.1548C>G (p.Ser516Arg) | |
3 | g.119413969C>T | CA435411479 | ARHGAP31 | c.2040C>T (p.Ser680=) c.1947C>T (p.Ser649=) c.1980C>T (p.Ser660=) c.1548C>T (p.Ser516=) | |
3 | g.119413970C>A | CA354048537 | ARHGAP31 | c.2041C>A (p.Pro681Thr) c.1948C>A (p.Pro650Thr) c.1981C>A (p.Pro661Thr) c.1549C>A (p.Pro517Thr) | |
3 | g.119413970C= | CA1396548493 | ARHGAP31 | c.2041C= (p.Pro681=) c.1948C= (p.Pro650=) c.1981C= (p.Pro661=) c.1549C= (p.Pro517=) | |
3 | g.119413970C>G | CA354048555 | ARHGAP31 | c.2041C>G (p.Pro681Ala) c.1948C>G (p.Pro650Ala) c.1981C>G (p.Pro661Ala) c.1549C>G (p.Pro517Ala) | |
3 | g.119413970C>T | CA81697334 | ARHGAP31 | c.2041C>T (p.Pro681Ser) c.1948C>T (p.Pro650Ser) c.1981C>T (p.Pro661Ser) c.1549C>T (p.Pro517Ser) | dbSNP gnomAD v3 gnomAD v4 |
3 | g.119413971C>A | CA354048560 | ARHGAP31 | c.2042C>A (p.Pro681Gln) c.1949C>A (p.Pro650Gln) c.1982C>A (p.Pro661Gln) c.1550C>A (p.Pro517Gln) | |
3 | g.119413971C= | CA1396548494 | ARHGAP31 | c.2042C= (p.Pro681=) c.1949C= (p.Pro650=) c.1982C= (p.Pro661=) c.1550C= (p.Pro517=) | |
3 | g.119413971C>G | CA2553956 | ARHGAP31 | c.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 |
3 | g.119413971C>T | CA2553957 | ARHGAP31 | c.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 |
3 | g.119413972A>C | CA435411481 | ARHGAP31 | c.2043A>C (p.Pro681=) c.1950A>C (p.Pro650=) c.1983A>C (p.Pro661=) c.1551A>C (p.Pro517=) | |
3 | g.119413972A>G | CA435411483 | ARHGAP31 | c.2043A>G (p.Pro681=) c.1950A>G (p.Pro650=) c.1983A>G (p.Pro661=) c.1551A>G (p.Pro517=) | |
3 | g.119413972A>T | CA435411482 | ARHGAP31 | c.2043A>T (p.Pro681=) c.1950A>T (p.Pro650=) c.1983A>T (p.Pro661=) c.1551A>T (p.Pro517=) | |
3 | g.119413973A>C | CA354048572 | ARHGAP31 | c.2044A>C (p.Ile682Leu) c.1951A>C (p.Ile651Leu) c.1984A>C (p.Ile662Leu) c.1552A>C (p.Ile518Leu) | |
3 | g.119413973A>G | CA354048585 | ARHGAP31 | c.2044A>G (p.Ile682Val) c.1951A>G (p.Ile651Val) c.1984A>G (p.Ile662Val) c.1552A>G (p.Ile518Val) | gnomAD v4 |
3 | g.119413973A>T | CA354048587 | ARHGAP31 | c.2044A>T (p.Ile682Phe) c.1951A>T (p.Ile651Phe) c.1984A>T (p.Ile662Phe) c.1552A>T (p.Ile518Phe) | |
3 | g.119413974T>A | CA354048589 | ARHGAP31 | c.2045T>A (p.Ile682Asn) c.1952T>A (p.Ile651Asn) c.1985T>A (p.Ile662Asn) c.1553T>A (p.Ile518Asn) | |
3 | g.119413974T>C | CA354048591 | ARHGAP31 | c.2045T>C (p.Ile682Thr) c.1952T>C (p.Ile651Thr) c.1985T>C (p.Ile662Thr) c.1553T>C (p.Ile518Thr) | gnomAD v4 |
3 | g.119413974T>G | CA354048600 | ARHGAP31 | c.2045T>G (p.Ile682Ser) c.1952T>G (p.Ile651Ser) c.1985T>G (p.Ile662Ser) c.1553T>G (p.Ile518Ser) | |
3 | g.119413975T>A | CA435411485 | ARHGAP31 | c.2046T>A (p.Ile682=) c.1953T>A (p.Ile651=) c.1986T>A (p.Ile662=) c.1554T>A (p.Ile518=) | |
3 | g.119413975T>C | CA435411486 | ARHGAP31 | c.2046T>C (p.Ile682=) c.1953T>C (p.Ile651=) c.1986T>C (p.Ile662=) c.1554T>C (p.Ile518=) | |
3 | g.119413975T>G | CA354048603 | ARHGAP31 | c.2046T>G (p.Ile682Met) c.1953T>G (p.Ile651Met) c.1986T>G (p.Ile662Met) c.1554T>G (p.Ile518Met) | |
3 | g.119413976C>A | CA354048606 | ARHGAP31 | c.2047C>A (p.Gln683Lys) c.1954C>A (p.Gln652Lys) c.1987C>A (p.Gln663Lys) c.1555C>A (p.Gln519Lys) | |
3 | g.119413976C= | CA1396548495 | ARHGAP31 | c.2047C= (p.Gln683=) c.1954C= (p.Gln652=) c.1987C= (p.Gln663=) c.1555C= (p.Gln519=) | |
3 | g.119413976C>G | CA354048608 | ARHGAP31 | c.2047C>G (p.Gln683Glu) c.1954C>G (p.Gln652Glu) c.1987C>G (p.Gln663Glu) c.1555C>G (p.Gln519Glu) | |
3 | g.119413976C>T | CA129505 | ARHGAP31 | c.2047C>T (p.Gln683Ter) c.1954C>T (p.Gln652Ter) c.1987C>T (p.Gln663Ter) c.1555C>T (p.Gln519Ter) | ClinVar dbSNP gnomAD v4 |
3 | g.119413977A= | CA1396548496 | ARHGAP31 | c.2048A= (p.Gln683=) c.1955A= (p.Gln652=) c.1988A= (p.Gln663=) c.1556A= (p.Gln519=) | |
3 | g.119413977A>C | CA354048617 | ARHGAP31 | c.2048A>C (p.Gln683Pro) c.1955A>C (p.Gln652Pro) c.1988A>C (p.Gln663Pro) c.1556A>C (p.Gln519Pro) | |
3 | g.119413977A>G | CA81697349 | ARHGAP31 | c.2048A>G (p.Gln683Arg) c.1955A>G (p.Gln652Arg) c.1988A>G (p.Gln663Arg) c.1556A>G (p.Gln519Arg) | ClinVar dbSNP gnomAD v4 |
3 | g.119413977A>T | CA354048612 | ARHGAP31 | c.2048A>T (p.Gln683Leu) c.1955A>T (p.Gln652Leu) c.1988A>T (p.Gln663Leu) c.1556A>T (p.Gln519Leu) | |
3 | g.119413978G>A | CA435411487 | ARHGAP31 | c.2049G>A (p.Gln683=) c.1956G>A (p.Gln652=) c.1989G>A (p.Gln663=) c.1557G>A (p.Gln519=) | dbSNP gnomAD v4 |
3 | g.119413978G>C | CA354048624 | ARHGAP31 | c.2049G>C (p.Gln683His) c.1956G>C (p.Gln652His) c.1989G>C (p.Gln663His) c.1557G>C (p.Gln519His) | |
3 | g.119413978G= | CA1396548497 | ARHGAP31 | c.2049G= (p.Gln683=) c.1956G= (p.Gln652=) c.1989G= (p.Gln663=) c.1557G= (p.Gln519=) | |
3 | g.119413978G>T | CA354048639 | ARHGAP31 | c.2049G>T (p.Gln683His) c.1956G>T (p.Gln652His) c.1989G>T (p.Gln663His) c.1557G>T (p.Gln519His) | |
3 | g.119413979C>A | CA354048644 | ARHGAP31 | c.2050C>A (p.Pro684Thr) c.1957C>A (p.Pro653Thr) c.1990C>A (p.Pro664Thr) c.1558C>A (p.Pro520Thr) | |
3 | g.119413979C= | CA1396548498 | ARHGAP31 | c.2050C= (p.Pro684=) c.1957C= (p.Pro653=) c.1990C= (p.Pro664=) c.1558C= (p.Pro520=) | |
3 | g.119413979C>G | CA354048648 | ARHGAP31 | c.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 |
3 | g.119413979C>T | CA354048650 | ARHGAP31 | c.2050C>T (p.Pro684Ser) c.1957C>T (p.Pro653Ser) c.1990C>T (p.Pro664Ser) c.1558C>T (p.Pro520Ser) | |
3 | g.119413980C>A | CA354048652 | ARHGAP31 | c.2051C>A (p.Pro684His) c.1958C>A (p.Pro653His) c.1991C>A (p.Pro664His) c.1559C>A (p.Pro520His) | |
3 | g.119413980C>G | CA354048653 | ARHGAP31 | c.2051C>G (p.Pro684Arg) c.1958C>G (p.Pro653Arg) c.1991C>G (p.Pro664Arg) c.1559C>G (p.Pro520Arg) | gnomAD v4 |
3 | g.119413980C>T | CA354048655 | ARHGAP31 | c.2051C>T (p.Pro684Leu) c.1958C>T (p.Pro653Leu) c.1991C>T (p.Pro664Leu) c.1559C>T (p.Pro520Leu) | COSMIC |
3 | g.119413981T>A | CA435411488 | ARHGAP31 | c.2052T>A (p.Pro684=) c.1959T>A (p.Pro653=) c.1992T>A (p.Pro664=) c.1560T>A (p.Pro520=) | |
3 | g.119413981T>C | CA435411489 | ARHGAP31 | c.2052T>C (p.Pro684=) c.1959T>C (p.Pro653=) c.1992T>C (p.Pro664=) c.1560T>C (p.Pro520=) | |
3 | g.119413981T>G | CA81697353 | ARHGAP31 | c.2052T>G (p.Pro684=) c.1959T>G (p.Pro653=) c.1992T>G (p.Pro664=) c.1560T>G (p.Pro520=) | dbSNP gnomAD v3 gnomAD v4 |
3 | g.119413981T= | CA1396548499 | ARHGAP31 | c.2052T= (p.Pro684=) c.1959T= (p.Pro653=) c.1992T= (p.Pro664=) c.1560T= (p.Pro520=) | |
3 | g.119413982A= | CA1396548500 | ARHGAP31 | c.2053A= (p.Ile685=) c.1960A= (p.Ile654=) c.1993A= (p.Ile665=) c.1561A= (p.Ile521=) | |
3 | g.119413982A>C | CA354048658 | ARHGAP31 | c.2053A>C (p.Ile685Leu) c.1960A>C (p.Ile654Leu) c.1993A>C (p.Ile665Leu) c.1561A>C (p.Ile521Leu) | |
3 | g.119413982A>G | CA354048661 | ARHGAP31 | c.2053A>G (p.Ile685Val) c.1960A>G (p.Ile654Val) c.1993A>G (p.Ile665Val) c.1561A>G (p.Ile521Val) | dbSNP gnomAD v4 |
3 | g.119413982A>T | CA354048664 | ARHGAP31 | c.2053A>T (p.Ile685Phe) c.1960A>T (p.Ile654Phe) c.1993A>T (p.Ile665Phe) c.1561A>T (p.Ile521Phe) | |
3 | g.119413983T>A | CA354048667 | ARHGAP31 | c.2054T>A (p.Ile685Asn) c.1961T>A (p.Ile654Asn) c.1994T>A (p.Ile665Asn) c.1562T>A (p.Ile521Asn) | |
3 | g.119413983T>C | CA354048672 | ARHGAP31 | c.2054T>C (p.Ile685Thr) c.1961T>C (p.Ile654Thr) c.1994T>C (p.Ile665Thr) c.1562T>C (p.Ile521Thr) | |
3 | g.119413983T>G | CA354048680 | ARHGAP31 | c.2054T>G (p.Ile685Ser) c.1961T>G (p.Ile654Ser) c.1994T>G (p.Ile665Ser) c.1562T>G (p.Ile521Ser) | |
3 | g.119413984T>A | CA435411491 | ARHGAP31 | c.2055T>A (p.Ile685=) c.1962T>A (p.Ile654=) c.1995T>A (p.Ile665=) c.1563T>A (p.Ile521=) | |
3 | g.119413984T>C | CA435411492 | ARHGAP31 | c.2055T>C (p.Ile685=) c.1962T>C (p.Ile654=) c.1995T>C (p.Ile665=) c.1563T>C (p.Ile521=) | |
3 | g.119413984T>G | CA354048692 | ARHGAP31 | c.2055T>G (p.Ile685Met) c.1962T>G (p.Ile654Met) c.1995T>G (p.Ile665Met) c.1563T>G (p.Ile521Met) | |
3 | g.119413985C>A | CA354048700 | ARHGAP31 | c.2056C>A (p.Leu686Ile) c.1963C>A (p.Leu655Ile) c.1996C>A (p.Leu666Ile) c.1564C>A (p.Leu522Ile) | gnomAD v4 COSMIC |
3 | g.119413985C>G | CA354048704 | ARHGAP31 | c.2056C>G (p.Leu686Val) c.1963C>G (p.Leu655Val) c.1996C>G (p.Leu666Val) c.1564C>G (p.Leu522Val) | |
3 | g.119413985C>T | CA354048698 | ARHGAP31 | c.2056C>T (p.Leu686Phe) c.1963C>T (p.Leu655Phe) c.1996C>T (p.Leu666Phe) c.1564C>T (p.Leu522Phe) | |
3 | g.119413986T>A | CA354048707 | ARHGAP31 | c.2057T>A (p.Leu686His) c.1964T>A (p.Leu655His) c.1997T>A (p.Leu666His) c.1565T>A (p.Leu522His) | |
3 | g.119413986T>C | CA354048708 | ARHGAP31 | c.2057T>C (p.Leu686Pro) c.1964T>C (p.Leu655Pro) c.1997T>C (p.Leu666Pro) c.1565T>C (p.Leu522Pro) | |
3 | g.119413986T>G | CA354048709 | ARHGAP31 | c.2057T>G (p.Leu686Arg) c.1964T>G (p.Leu655Arg) c.1997T>G (p.Leu666Arg) c.1565T>G (p.Leu522Arg) | |
3 | g.119413993_119413997del | CA2577942208 | ARHGAP31 | c.2064_2068del (p.Ser689GlyfsTer?) c.1971_1975del (p.Ser658GlyfsTer?) c.2004_2008del (p.Ser669GlyfsTer?) c.1572_1576del (p.Ser525GlyfsTer?) | |
3 | g.119413987C>A | CA435411493 | ARHGAP31 | c.2058C>A (p.Leu686=) c.1965C>A (p.Leu655=) c.1998C>A (p.Leu666=) c.1566C>A (p.Leu522=) | |
3 | g.119413987C= | CA1396548501 | ARHGAP31 | c.2058C= (p.Leu686=) c.1965C= (p.Leu655=) c.1998C= (p.Leu666=) c.1566C= (p.Leu522=) | |
3 | g.119413987C>G | CA2553958 | ARHGAP31 | c.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 |
3 | g.119413987C>T | CA81697356 | ARHGAP31 | c.2058C>T (p.Leu686=) c.1965C>T (p.Leu655=) c.1998C>T (p.Leu666=) c.1566C>T (p.Leu522=) | dbSNP gnomAD v3 gnomAD v4 |
3 | g.119413988G>A | CA2553959 | ARHGAP31 | c.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 |
3 | g.119413988G>C | CA354048724 | ARHGAP31 | c.2059G>C (p.Glu687Gln) c.1966G>C (p.Glu656Gln) c.1999G>C (p.Glu667Gln) c.1567G>C (p.Glu523Gln) | ClinVar dbSNP gnomAD v4 |
3 | g.119413988G= | CA1396548502 | ARHGAP31 | c.2059G= (p.Glu687=) c.1966G= (p.Glu656=) c.1999G= (p.Glu667=) c.1567G= (p.Glu523=) | |
3 | g.119413988G>T | CA354048730 | ARHGAP31 | c.2059G>T (p.Glu687Ter) c.1966G>T (p.Glu656Ter) c.1999G>T (p.Glu667Ter) c.1567G>T (p.Glu523Ter) | |
3 | g.119413989A>C | CA354048737 | ARHGAP31 | c.2060A>C (p.Glu687Ala) c.1967A>C (p.Glu656Ala) c.2000A>C (p.Glu667Ala) c.1568A>C (p.Glu523Ala) | |
3 | g.119413989A>G | CA354048739 | ARHGAP31 | c.2060A>G (p.Glu687Gly) c.1967A>G (p.Glu656Gly) c.2000A>G (p.Glu667Gly) c.1568A>G (p.Glu523Gly) | |
3 | g.119413989A>T | CA354048742 | ARHGAP31 | c.2060A>T (p.Glu687Val) c.1967A>T (p.Glu656Val) c.2000A>T (p.Glu667Val) c.1568A>T (p.Glu523Val) | |
3 | g.119413990G>A | CA435411497 | ARHGAP31 | c.2061G>A (p.Glu687=) c.1968G>A (p.Glu656=) c.2001G>A (p.Glu667=) c.1569G>A (p.Glu523=) | |
3 | g.119413990G>C | CA354048748 | ARHGAP31 | c.2061G>C (p.Glu687Asp) c.1968G>C (p.Glu656Asp) c.2001G>C (p.Glu667Asp) c.1569G>C (p.Glu523Asp) | |
3 | g.119413990G>T | CA354048755 | ARHGAP31 | c.2061G>T (p.Glu687Asp) c.1968G>T (p.Glu656Asp) c.2001G>T (p.Glu667Asp) c.1569G>T (p.Glu523Asp) | COSMIC |
3 | g.119413991T>A | CA354048767 | ARHGAP31 | c.2062T>A (p.Ser688Thr) c.1969T>A (p.Ser657Thr) c.2002T>A (p.Ser668Thr) c.1570T>A (p.Ser524Thr) | |
3 | g.119413991T>C | CA354048761 | ARHGAP31 | c.2062T>C (p.Ser688Pro) c.1969T>C (p.Ser657Pro) c.2002T>C (p.Ser668Pro) c.1570T>C (p.Ser524Pro) | |
3 | g.119413991T>G | CA354048764 | ARHGAP31 | c.2062T>G (p.Ser688Ala) c.1969T>G (p.Ser657Ala) c.2002T>G (p.Ser668Ala) c.1570T>G (p.Ser524Ala) | gnomAD v4 |
3 | g.119413992C>A | CA354048771 | ARHGAP31 | c.2063C>A (p.Ser688Ter) c.1970C>A (p.Ser657Ter) c.2003C>A (p.Ser668Ter) c.1571C>A (p.Ser524Ter) | gnomAD v4 |
3 | g.119413992C= | CA1396548503 | ARHGAP31 | c.2063C= (p.Ser688=) c.1970C= (p.Ser657=) c.2003C= (p.Ser668=) c.1571C= (p.Ser524=) | |
3 | g.119413992C>G | CA2553960 | ARHGAP31 | c.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 |
3 | g.119413992C>T | CA354048776 | ARHGAP31 | c.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 |
3 | g.119413992_119413993insTT | CA2586965849 | ARHGAP31 | c.2063_2064insTT (p.Ser689Ter) c.1970_1971insTT (p.Ser658Ter) c.2003_2004insTT (p.Ser669Ter) c.1571_1572insTT (p.Ser525Ter) | |
3 | g.119413993G>A | CA2553961 | ARHGAP31 | c.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 |
3 | g.119413993G>C | CA435411498 | ARHGAP31 | c.2064G>C (p.Ser688=) c.1971G>C (p.Ser657=) c.2004G>C (p.Ser668=) c.1572G>C (p.Ser524=) | gnomAD v4 |
3 | g.119413993G= | CA1396548504 | ARHGAP31 | c.2064G= (p.Ser688=) c.1971G= (p.Ser657=) c.2004G= (p.Ser668=) c.1572G= (p.Ser524=) | |
3 | g.119413993G>T | CA435411499 | ARHGAP31 | c.2064G>T (p.Ser688=) c.1971G>T (p.Ser657=) c.2004G>T (p.Ser668=) c.1572G>T (p.Ser524=) | |
3 | g.119413994A>C | CA354048785 | ARHGAP31 | c.2065A>C (p.Ser689Arg) c.1972A>C (p.Ser658Arg) c.2005A>C (p.Ser669Arg) c.1573A>C (p.Ser525Arg) | |
3 | g.119413994A>G | CA354048791 | ARHGAP31 | c.2065A>G (p.Ser689Gly) c.1972A>G (p.Ser658Gly) c.2005A>G (p.Ser669Gly) c.1573A>G (p.Ser525Gly) | |
3 | g.119413994A>T | CA354048813 | ARHGAP31 | c.2065A>T (p.Ser689Cys) c.1972A>T (p.Ser658Cys) c.2005A>T (p.Ser669Cys) c.1573A>T (p.Ser525Cys) | |
3 | g.119413995G>A | CA354048818 | ARHGAP31 | c.2066G>A (p.Ser689Asn) c.1973G>A (p.Ser658Asn) c.2006G>A (p.Ser669Asn) c.1574G>A (p.Ser525Asn) | |
3 | g.119413995G>C | CA354048819 | ARHGAP31 | c.2066G>C (p.Ser689Thr) c.1973G>C (p.Ser658Thr) c.2006G>C (p.Ser669Thr) c.1574G>C (p.Ser525Thr) | dbSNP gnomAD v4 |
3 | g.119413995G= | CA1396548505 | ARHGAP31 | c.2066G= (p.Ser689=) c.1973G= (p.Ser658=) c.2006G= (p.Ser669=) c.1574G= (p.Ser525=) | |
3 | g.119413995G>T | CA354048820 | ARHGAP31 | c.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 |
3 | g.119413996T>A | CA354048821 | ARHGAP31 | c.2067T>A (p.Ser689Arg) c.1974T>A (p.Ser658Arg) c.2007T>A (p.Ser669Arg) c.1575T>A (p.Ser525Arg) | dbSNP gnomAD v3 gnomAD v4 |
3 | g.119413996T>C | CA435411500 | ARHGAP31 | c.2067T>C (p.Ser689=) c.1974T>C (p.Ser658=) c.2007T>C (p.Ser669=) c.1575T>C (p.Ser525=) | dbSNP |
3 | g.119413996T>G | CA354048825 | ARHGAP31 | c.2067T>G (p.Ser689Arg) c.1974T>G (p.Ser658Arg) c.2007T>G (p.Ser669Arg) c.1575T>G (p.Ser525Arg) | |
3 | g.119413996T= | CA1396548506 | ARHGAP31 | c.2067T= (p.Ser689=) c.1974T= (p.Ser658=) c.2007T= (p.Ser669=) c.1575T= (p.Ser525=) | |
3 | g.119413996_119413997insG | CA81697371 | ARHGAP31 | c.2067_2068insG (p.Leu690AlafsTer?) c.1974_1975insG (p.Leu659AlafsTer?) c.2007_2008insG (p.Leu670AlafsTer?) c.1575_1576insG (p.Leu526AlafsTer?) | dbSNP |
3 | g.119413997C>A | CA354048849 | ARHGAP31 | c.2068C>A (p.Leu690Met) c.1975C>A (p.Leu659Met) c.2008C>A (p.Leu670Met) c.1576C>A (p.Leu526Met) | |
3 | g.119413997C>G | CA354048847 | ARHGAP31 | c.2068C>G (p.Leu690Val) c.1975C>G (p.Leu659Val) c.2008C>G (p.Leu670Val) c.1576C>G (p.Leu526Val) | |
3 | g.119413997C>T | CA435411503 | ARHGAP31 | c.2068C>T (p.Leu690=) c.1975C>T (p.Leu659=) c.2008C>T (p.Leu670=) c.1576C>T (p.Leu526=) | gnomAD v4 |
3 | g.119413998T>A | CA354048862 | ARHGAP31 | c.2069T>A (p.Leu690Gln) c.1976T>A (p.Leu659Gln) c.2009T>A (p.Leu670Gln) c.1577T>A (p.Leu526Gln) | |
3 | g.119413998T>C | CA354048870 | ARHGAP31 | c.2069T>C (p.Leu690Pro) c.1976T>C (p.Leu659Pro) c.2009T>C (p.Leu670Pro) c.1577T>C (p.Leu526Pro) | dbSNP gnomAD v4 |
3 | g.119413998T>G | CA354048866 | ARHGAP31 | c.2069T>G (p.Leu690Arg) c.1976T>G (p.Leu659Arg) c.2009T>G (p.Leu670Arg) c.1577T>G (p.Leu526Arg) | |
3 | g.119413998T= | CA1396548507 | ARHGAP31 | c.2069T= (p.Leu690=) c.1976T= (p.Leu659=) c.2009T= (p.Leu670=) c.1577T= (p.Leu526=) | |
3 | g.119413999G>A | CA435411504 | ARHGAP31 | c.2070G>A (p.Leu690=) c.1977G>A (p.Leu659=) c.2010G>A (p.Leu670=) c.1578G>A (p.Leu526=) | |
3 | g.119413999G>C | CA2553962 | ARHGAP31 | c.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 |
3 | g.119413999G= | CA1396548508 | ARHGAP31 | c.2070G= (p.Leu690=) c.1977G= (p.Leu659=) c.2010G= (p.Leu670=) c.1578G= (p.Leu526=) | |
3 | g.119413999G>T | CA435411506 | ARHGAP31 | c.2070G>T (p.Leu690=) c.1977G>T (p.Leu659=) c.2010G>T (p.Leu670=) c.1578G>T (p.Leu526=) | |
3 | g.119414000G>A | CA2553963 | ARHGAP31 | c.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 |
3 | g.119414000G>C | CA354048881 | ARHGAP31 | c.2071G>C (p.Gly691Arg) c.1978G>C (p.Gly660Arg) c.2011G>C (p.Gly671Arg) c.1579G>C (p.Gly527Arg) | |
3 | g.119414000G= | CA1396548509 | ARHGAP31 | c.2071G= (p.Gly691=) c.1978G= (p.Gly660=) c.2011G= (p.Gly671=) c.1579G= (p.Gly527=) | |
3 | g.119414000G>T | CA354048884 | ARHGAP31 | c.2071G>T (p.Gly691Trp) c.1978G>T (p.Gly660Trp) c.2011G>T (p.Gly671Trp) c.1579G>T (p.Gly527Trp) | |
3 | g.119414001G>A | CA354048901 | ARHGAP31 | c.2072G>A (p.Gly691Glu) c.1979G>A (p.Gly660Glu) c.2012G>A (p.Gly671Glu) c.1580G>A (p.Gly527Glu) | gnomAD v4 |
3 | g.119414001G>C | CA2553964 | ARHGAP31 | c.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 |
3 | g.119414001G= | CA1396548510 | ARHGAP31 | c.2072G= (p.Gly691=) c.1979G= (p.Gly660=) c.2012G= (p.Gly671=) c.1580G= (p.Gly527=) | |
3 | g.119414001G>T | CA354048905 | ARHGAP31 | c.2072G>T (p.Gly691Val) c.1979G>T (p.Gly660Val) c.2012G>T (p.Gly671Val) c.1580G>T (p.Gly527Val) | |
3 | g.119414002G>A | CA435411510 | ARHGAP31 | c.2073G>A (p.Gly691=) c.1980G>A (p.Gly660=) c.2013G>A (p.Gly671=) c.1581G>A (p.Gly527=) | |
3 | g.119414002G>C | CA435411511 | ARHGAP31 | c.2073G>C (p.Gly691=) c.1980G>C (p.Gly660=) c.2013G>C (p.Gly671=) c.1581G>C (p.Gly527=) | |
3 | g.119414002G>T | CA435411512 | ARHGAP31 | c.2073G>T (p.Gly691=) c.1980G>T (p.Gly660=) c.2013G>T (p.Gly671=) c.1581G>T (p.Gly527=) | |
3 | g.119414003C>A | CA2553965 | ARHGAP31 | c.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 |
3 | g.119414003C= | CA1396548511 | ARHGAP31 | c.2074C= (p.Pro692=) c.1981C= (p.Pro661=) c.2014C= (p.Pro672=) c.1582C= (p.Pro528=) | |
3 | g.119414003C>G | CA354048934 | ARHGAP31 | c.2074C>G (p.Pro692Ala) c.1981C>G (p.Pro661Ala) c.2014C>G (p.Pro672Ala) c.1582C>G (p.Pro528Ala) | |
3 | g.119414003C>T | CA354048938 | ARHGAP31 | c.2074C>T (p.Pro692Ser) c.1981C>T (p.Pro661Ser) c.2014C>T (p.Pro672Ser) c.1582C>T (p.Pro528Ser) | gnomAD v4 |
3 | g.119414004C>A | CA354048945 | ARHGAP31 | c.2075C>A (p.Pro692His) c.1982C>A (p.Pro661His) c.2015C>A (p.Pro672His) c.1583C>A (p.Pro528His) | |
3 | g.119414004C= | CA1396548512 | ARHGAP31 | c.2075C= (p.Pro692=) c.1982C= (p.Pro661=) c.2015C= (p.Pro672=) c.1583C= (p.Pro528=) | |
3 | g.119414004C>G | CA354048948 | ARHGAP31 | c.2075C>G (p.Pro692Arg) c.1982C>G (p.Pro661Arg) c.2015C>G (p.Pro672Arg) c.1583C>G (p.Pro528Arg) | |
3 | g.119414004C>T | CA354048952 | ARHGAP31 | c.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 |
3 | g.119414005C>A | CA2553966 | ARHGAP31 | c.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 |
3 | g.119414005C= | CA1396548513 | ARHGAP31 | c.2076C= (p.Pro692=) c.1983C= (p.Pro661=) c.2016C= (p.Pro672=) c.1584C= (p.Pro528=) | |
3 | g.119414005C>G | CA435411513 | ARHGAP31 | c.2076C>G (p.Pro692=) c.1983C>G (p.Pro661=) c.2016C>G (p.Pro672=) c.1584C>G (p.Pro528=) | |
3 | g.119414005C>T | CA435411514 | ARHGAP31 | c.2076C>T (p.Pro692=) c.1983C>T (p.Pro661=) c.2016C>T (p.Pro672=) c.1584C>T (p.Pro528=) | |
3 | g.119414006T>A | CA354048960 | ARHGAP31 | c.2077T>A (p.Phe693Ile) c.1984T>A (p.Phe662Ile) c.2017T>A (p.Phe673Ile) c.1585T>A (p.Phe529Ile) | |
3 | g.119414006T>C | CA354048964 | ARHGAP31 | c.2077T>C (p.Phe693Leu) c.1984T>C (p.Phe662Leu) c.2017T>C (p.Phe673Leu) c.1585T>C (p.Phe529Leu) | |
3 | g.119414006T>G | CA354048966 | ARHGAP31 | c.2077T>G (p.Phe693Val) c.1984T>G (p.Phe662Val) c.2017T>G (p.Phe673Val) c.1585T>G (p.Phe529Val) | |
3 | g.119414007T>A | CA354048967 | ARHGAP31 | c.2078T>A (p.Phe693Tyr) c.1985T>A (p.Phe662Tyr) c.2018T>A (p.Phe673Tyr) c.1586T>A (p.Phe529Tyr) | |
3 | g.119414007T>C | CA354048968 | ARHGAP31 | c.2078T>C (p.Phe693Ser) c.1985T>C (p.Phe662Ser) c.2018T>C (p.Phe673Ser) c.1586T>C (p.Phe529Ser) | gnomAD v4 |
3 | g.119414007T>G | CA354048969 | ARHGAP31 | c.2078T>G (p.Phe693Cys) c.1985T>G (p.Phe662Cys) c.2018T>G (p.Phe673Cys) c.1586T>G (p.Phe529Cys) | |
3 | g.119414008T>A | CA354048973 | ARHGAP31 | c.2079T>A (p.Phe693Leu) c.1986T>A (p.Phe662Leu) c.2019T>A (p.Phe673Leu) c.1587T>A (p.Phe529Leu) | |
3 | g.119414008T>C | CA2553967 | ARHGAP31 | c.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 |
3 | g.119414008T>G | CA354048977 | ARHGAP31 | c.2079T>G (p.Phe693Leu) c.1986T>G (p.Phe662Leu) c.2019T>G (p.Phe673Leu) c.1587T>G (p.Phe529Leu) | |
3 | g.119414008T= | CA1396548514 | ARHGAP31 | c.2079T= (p.Phe693=) c.1986T= (p.Phe662=) c.2019T= (p.Phe673=) c.1587T= (p.Phe529=) | |
3 | g.119414009A>C | CA354048981 | ARHGAP31 | c.2080A>C (p.Ile694Leu) c.1987A>C (p.Ile663Leu) c.2020A>C (p.Ile674Leu) c.1588A>C (p.Ile530Leu) | |
3 | g.119414009A>G | CA354048984 | ARHGAP31 | c.2080A>G (p.Ile694Val) c.1987A>G (p.Ile663Val) c.2020A>G (p.Ile674Val) c.1588A>G (p.Ile530Val) | |
3 | g.119414009A>T | CA354048989 | ARHGAP31 | c.2080A>T (p.Ile694Phe) c.1987A>T (p.Ile663Phe) c.2020A>T (p.Ile674Phe) c.1588A>T (p.Ile530Phe) | |
3 | g.119414010T>A | CA354049001 | ARHGAP31 | c.2081T>A (p.Ile694Asn) c.1988T>A (p.Ile663Asn) c.2021T>A (p.Ile674Asn) c.1589T>A (p.Ile530Asn) | |
3 | g.119414010T>C | CA354049000 | ARHGAP31 | c.2081T>C (p.Ile694Thr) c.1988T>C (p.Ile663Thr) c.2021T>C (p.Ile674Thr) c.1589T>C (p.Ile530Thr) | dbSNP gnomAD v2 gnomAD v4 |
3 | g.119414010T>G | CA354048993 | ARHGAP31 | c.2081T>G (p.Ile694Ser) c.1988T>G (p.Ile663Ser) c.2021T>G (p.Ile674Ser) c.1589T>G (p.Ile530Ser) | gnomAD v4 |
3 | g.119414010T= | CA1396548515 | ARHGAP31 | c.2081T= (p.Ile694=) c.1988T= (p.Ile663=) c.2021T= (p.Ile674=) c.1589T= (p.Ile530=) | |
3 | g.119414011T>A | CA435411517 | ARHGAP31 | c.2082T>A (p.Ile694=) c.1989T>A (p.Ile663=) c.2022T>A (p.Ile674=) c.1590T>A (p.Ile530=) | dbSNP |
3 | g.119414011T>C | CA435411518 | ARHGAP31 | c.2082T>C (p.Ile694=) c.1989T>C (p.Ile663=) c.2022T>C (p.Ile674=) c.1590T>C (p.Ile530=) | |
3 | g.119414011T>G | CA354049006 | ARHGAP31 | c.2082T>G (p.Ile694Met) c.1989T>G (p.Ile663Met) c.2022T>G (p.Ile674Met) c.1590T>G (p.Ile530Met) | dbSNP |
3 | g.119414011T= | CA1396548516 | ARHGAP31 | c.2082T= (p.Ile694=) c.1989T= (p.Ile663=) c.2022T= (p.Ile674=) c.1590T= (p.Ile530=) | |
3 | g.119414012C>A | CA354049010 | ARHGAP31 | c.2083C>A (p.Pro695Thr) c.1990C>A (p.Pro664Thr) c.2023C>A (p.Pro675Thr) c.1591C>A (p.Pro531Thr) | |
3 | g.119414012C>G | CA354049011 | ARHGAP31 | c.2083C>G (p.Pro695Ala) c.1990C>G (p.Pro664Ala) c.2023C>G (p.Pro675Ala) c.1591C>G (p.Pro531Ala) | |
3 | g.119414012C>T | CA354049013 | ARHGAP31 | c.2083C>T (p.Pro695Ser) c.1990C>T (p.Pro664Ser) c.2023C>T (p.Pro675Ser) c.1591C>T (p.Pro531Ser) | |
3 | g.119414013C>A | CA354049016 | ARHGAP31 | c.2084C>A (p.Pro695His) c.1991C>A (p.Pro664His) c.2024C>A (p.Pro675His) c.1592C>A (p.Pro531His) | |
3 | g.119414013C>G | CA354049018 | ARHGAP31 | c.2084C>G (p.Pro695Arg) c.1991C>G (p.Pro664Arg) c.2024C>G (p.Pro675Arg) c.1592C>G (p.Pro531Arg) | |
3 | g.119414013C>T | CA354049022 | ARHGAP31 | c.2084C>T (p.Pro695Leu) c.1991C>T (p.Pro664Leu) c.2024C>T (p.Pro675Leu) c.1592C>T (p.Pro531Leu) | |
3 | g.119414014C>A | CA435411519 | ARHGAP31 | c.2085C>A (p.Pro695=) c.1992C>A (p.Pro664=) c.2025C>A (p.Pro675=) c.1593C>A (p.Pro531=) | |
3 | g.119414014C>G | CA435411521 | ARHGAP31 | c.2085C>G (p.Pro695=) c.1992C>G (p.Pro664=) c.2025C>G (p.Pro675=) c.1593C>G (p.Pro531=) | |
3 | g.119414014C>T | CA435411520 | ARHGAP31 | c.2085C>T (p.Pro695=) c.1992C>T (p.Pro664=) c.2025C>T (p.Pro675=) c.1593C>T (p.Pro531=) | |
3 | g.119414015T>A | CA354049028 | ARHGAP31 | c.2086T>A (p.Ser696Thr) c.1993T>A (p.Ser665Thr) c.2026T>A (p.Ser676Thr) c.1594T>A (p.Ser532Thr) | |
3 | g.119414015T>C | CA354049031 | ARHGAP31 | c.2086T>C (p.Ser696Pro) c.1993T>C (p.Ser665Pro) c.2026T>C (p.Ser676Pro) c.1594T>C (p.Ser532Pro) | |
3 | g.119414015T>G | CA354049029 | ARHGAP31 | c.2086T>G (p.Ser696Ala) c.1993T>G (p.Ser665Ala) c.2026T>G (p.Ser676Ala) c.1594T>G (p.Ser532Ala) | |
3 | g.119414016C>A | CA354049037 | ARHGAP31 | c.2087C>A (p.Ser696Ter) c.1994C>A (p.Ser665Ter) c.2027C>A (p.Ser676Ter) c.1595C>A (p.Ser532Ter) | |
3 | g.119414016C>G | CA354049042 | ARHGAP31 | c.2087C>G (p.Ser696Ter) c.1994C>G (p.Ser665Ter) c.2027C>G (p.Ser676Ter) c.1595C>G (p.Ser532Ter) | |
3 | g.119414016C>T | CA354049046 | ARHGAP31 | c.2087C>T (p.Ser696Leu) c.1994C>T (p.Ser665Leu) c.2027C>T (p.Ser676Leu) c.1595C>T (p.Ser532Leu) | |
3 | g.119414017A= | CA1396548517 | ARHGAP31 | c.2088A= (p.Ser696=) c.1995A= (p.Ser665=) c.2028A= (p.Ser676=) c.1596A= (p.Ser532=) | |
3 | g.119414017A>C | CA435411523 | ARHGAP31 | c.2088A>C (p.Ser696=) c.1995A>C (p.Ser665=) c.2028A>C (p.Ser676=) c.1596A>C (p.Ser532=) | |
3 | g.119414017A>G | CA2553968 | ARHGAP31 | c.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 |
3 | g.119414017A>T | CA435411524 | ARHGAP31 | c.2088A>T (p.Ser696=) c.1995A>T (p.Ser665=) c.2028A>T (p.Ser676=) c.1596A>T (p.Ser532=) | |
3 | g.119414018G>A | CA354049056 | ARHGAP31 | c.2089G>A (p.Glu697Lys) c.1996G>A (p.Glu666Lys) c.2029G>A (p.Glu677Lys) c.1597G>A (p.Glu533Lys) | |
3 | g.119414018G>C | CA354049065 | ARHGAP31 | c.2089G>C (p.Glu697Gln) c.1996G>C (p.Glu666Gln) c.2029G>C (p.Glu677Gln) c.1597G>C (p.Glu533Gln) | |
3 | g.119414018G>T | CA354049059 | ARHGAP31 | c.2089G>T (p.Glu697Ter) c.1996G>T (p.Glu666Ter) c.2029G>T (p.Glu677Ter) c.1597G>T (p.Glu533Ter) | |
3 | g.119414019A>C | CA354049069 | ARHGAP31 | c.2090A>C (p.Glu697Ala) c.1997A>C (p.Glu666Ala) c.2030A>C (p.Glu677Ala) c.1598A>C (p.Glu533Ala) | |
3 | g.119414019A>G | CA354049073 | ARHGAP31 | c.2090A>G (p.Glu697Gly) c.1997A>G (p.Glu666Gly) c.2030A>G (p.Glu677Gly) c.1598A>G (p.Glu533Gly) | |
3 | g.119414019A>T | CA354049075 | ARHGAP31 | c.2090A>T (p.Glu697Val) c.1997A>T (p.Glu666Val) c.2030A>T (p.Glu677Val) c.1598A>T (p.Glu533Val) |