Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.119414161C>A | CA435411647 | ARHGAP31 | c.2232C>A (p.Gly744=) c.2139C>A (p.Gly713=) c.2172C>A (p.Gly724=) c.1740C>A (p.Gly580=) | |
3 | g.119414161C>G | CA435411648 | ARHGAP31 | c.2232C>G (p.Gly744=) c.2139C>G (p.Gly713=) c.2172C>G (p.Gly724=) c.1740C>G (p.Gly580=) | |
3 | g.119414161C>T | CA435411649 | ARHGAP31 | c.2232C>T (p.Gly744=) c.2139C>T (p.Gly713=) c.2172C>T (p.Gly724=) c.1740C>T (p.Gly580=) | |
3 | g.119414162C>A | CA354049913 | ARHGAP31 | c.2233C>A (p.Leu745Met) c.2140C>A (p.Leu714Met) c.2173C>A (p.Leu725Met) c.1741C>A (p.Leu581Met) | |
3 | g.119414162C>G | CA354049914 | ARHGAP31 | c.2233C>G (p.Leu745Val) c.2140C>G (p.Leu714Val) c.2173C>G (p.Leu725Val) c.1741C>G (p.Leu581Val) | |
3 | g.119414162C>T | CA435411650 | ARHGAP31 | c.2233C>T (p.Leu745=) c.2140C>T (p.Leu714=) c.2173C>T (p.Leu725=) c.1741C>T (p.Leu581=) | |
3 | g.119414163T>A | CA354049915 | ARHGAP31 | c.2234T>A (p.Leu745Gln) c.2141T>A (p.Leu714Gln) c.2174T>A (p.Leu725Gln) c.1742T>A (p.Leu581Gln) | |
3 | g.119414163T>C | CA354049919 | ARHGAP31 | c.2234T>C (p.Leu745Pro) c.2141T>C (p.Leu714Pro) c.2174T>C (p.Leu725Pro) c.1742T>C (p.Leu581Pro) | |
3 | g.119414163T>G | CA354049918 | ARHGAP31 | c.2234T>G (p.Leu745Arg) c.2141T>G (p.Leu714Arg) c.2174T>G (p.Leu725Arg) c.1742T>G (p.Leu581Arg) | |
3 | g.119414164G>A | CA435411651 | ARHGAP31 | c.2235G>A (p.Leu745=) c.2142G>A (p.Leu714=) c.2175G>A (p.Leu725=) c.1743G>A (p.Leu581=) | |
3 | g.119414164G>C | CA81697478 | ARHGAP31 | c.2235G>C (p.Leu745=) c.2142G>C (p.Leu714=) c.2175G>C (p.Leu725=) c.1743G>C (p.Leu581=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
3 | g.119414164G= | CA1396548577 | ARHGAP31 | c.2235G= (p.Leu745=) c.2142G= (p.Leu714=) c.2175G= (p.Leu725=) c.1743G= (p.Leu581=) | |
3 | g.119414164G>T | CA435411652 | ARHGAP31 | c.2235G>T (p.Leu745=) c.2142G>T (p.Leu714=) c.2175G>T (p.Leu725=) c.1743G>T (p.Leu581=) | |
3 | g.119414165C>A | CA354049930 | ARHGAP31 | c.2236C>A (p.His746Asn) c.2143C>A (p.His715Asn) c.2176C>A (p.His726Asn) c.1744C>A (p.His582Asn) | |
3 | g.119414165C>G | CA354049925 | ARHGAP31 | c.2236C>G (p.His746Asp) c.2143C>G (p.His715Asp) c.2176C>G (p.His726Asp) c.1744C>G (p.His582Asp) | |
3 | g.119414165C>T | CA354049928 | ARHGAP31 | c.2236C>T (p.His746Tyr) c.2143C>T (p.His715Tyr) c.2176C>T (p.His726Tyr) c.1744C>T (p.His582Tyr) | |
3 | g.119414166A>C | CA354049932 | ARHGAP31 | c.2237A>C (p.His746Pro) c.2144A>C (p.His715Pro) c.2177A>C (p.His726Pro) c.1745A>C (p.His582Pro) | |
3 | g.119414166A>G | CA354049935 | ARHGAP31 | c.2237A>G (p.His746Arg) c.2144A>G (p.His715Arg) c.2177A>G (p.His726Arg) c.1745A>G (p.His582Arg) | gnomAD v4 |
3 | g.119414166A>T | CA354049937 | ARHGAP31 | c.2237A>T (p.His746Leu) c.2144A>T (p.His715Leu) c.2177A>T (p.His726Leu) c.1745A>T (p.His582Leu) | |
3 | g.119414167C>A | CA354049940 | ARHGAP31 | c.2238C>A (p.His746Gln) c.2145C>A (p.His715Gln) c.2178C>A (p.His726Gln) c.1746C>A (p.His582Gln) | ClinVar |
3 | g.119414167C= | CA1396548578 | ARHGAP31 | c.2238C= (p.His746=) c.2145C= (p.His715=) c.2178C= (p.His726=) c.1746C= (p.His582=) | |
3 | g.119414167C>G | CA354049948 | ARHGAP31 | c.2238C>G (p.His746Gln) c.2145C>G (p.His715Gln) c.2178C>G (p.His726Gln) c.1746C>G (p.His582Gln) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.119414167C>T | CA435411653 | ARHGAP31 | c.2238C>T (p.His746=) c.2145C>T (p.His715=) c.2178C>T (p.His726=) c.1746C>T (p.His582=) | gnomAD v4 |
3 | g.119414169del | CA2524516268 | ARHGAP31 | c.2240del (p.Pro747GlnfsTer11) c.2147del (p.Pro716GlnfsTer11) c.2180del (p.Pro727GlnfsTer11) c.1748del (p.Pro583GlnfsTer11) | |
3 | g.119414168C>A | CA354049951 | ARHGAP31 | c.2239C>A (p.Pro747Thr) c.2146C>A (p.Pro716Thr) c.2179C>A (p.Pro727Thr) c.1747C>A (p.Pro583Thr) | |
3 | g.119414168C= | CA1396548579 | ARHGAP31 | c.2239C= (p.Pro747=) c.2146C= (p.Pro716=) c.2179C= (p.Pro727=) c.1747C= (p.Pro583=) | |
3 | g.119414168C>G | CA354049953 | ARHGAP31 | c.2239C>G (p.Pro747Ala) c.2146C>G (p.Pro716Ala) c.2179C>G (p.Pro727Ala) c.1747C>G (p.Pro583Ala) | |
3 | g.119414168C>T | CA354049956 | ARHGAP31 | c.2239C>T (p.Pro747Ser) c.2146C>T (p.Pro716Ser) c.2179C>T (p.Pro727Ser) c.1747C>T (p.Pro583Ser) | dbSNP |
3 | g.119414169C>A | CA354049962 | ARHGAP31 | c.2240C>A (p.Pro747Gln) c.2147C>A (p.Pro716Gln) c.2180C>A (p.Pro727Gln) c.1748C>A (p.Pro583Gln) | |
3 | g.119414169C>G | CA354049965 | ARHGAP31 | c.2240C>G (p.Pro747Arg) c.2147C>G (p.Pro716Arg) c.2180C>G (p.Pro727Arg) c.1748C>G (p.Pro583Arg) | |
3 | g.119414169C>T | CA354049970 | ARHGAP31 | c.2240C>T (p.Pro747Leu) c.2147C>T (p.Pro716Leu) c.2180C>T (p.Pro727Leu) c.1748C>T (p.Pro583Leu) | |
3 | g.119414170A= | CA1396548580 | ARHGAP31 | c.2241A= (p.Pro747=) c.2148A= (p.Pro716=) c.2181A= (p.Pro727=) c.1749A= (p.Pro583=) | |
3 | g.119414170A>C | CA2553990 | ARHGAP31 | c.2241A>C (p.Pro747=) c.2148A>C (p.Pro716=) c.2181A>C (p.Pro727=) c.1749A>C (p.Pro583=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.119414170A>G | CA435411654 | ARHGAP31 | c.2241A>G (p.Pro747=) c.2148A>G (p.Pro716=) c.2181A>G (p.Pro727=) c.1749A>G (p.Pro583=) | |
3 | g.119414170A>T | CA435411655 | ARHGAP31 | c.2241A>T (p.Pro747=) c.2148A>T (p.Pro716=) c.2181A>T (p.Pro727=) c.1749A>T (p.Pro583=) | |
3 | g.119414171G>A | CA354049975 | ARHGAP31 | c.2242G>A (p.Asp748Asn) c.2149G>A (p.Asp717Asn) c.2182G>A (p.Asp728Asn) c.1750G>A (p.Asp584Asn) | |
3 | g.119414171G>C | CA354049977 | ARHGAP31 | c.2242G>C (p.Asp748His) c.2149G>C (p.Asp717His) c.2182G>C (p.Asp728His) c.1750G>C (p.Asp584His) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.119414171G= | CA1396548581 | ARHGAP31 | c.2242G= (p.Asp748=) c.2149G= (p.Asp717=) c.2182G= (p.Asp728=) c.1750G= (p.Asp584=) | |
3 | g.119414171G>T | CA354049981 | ARHGAP31 | c.2242G>T (p.Asp748Tyr) c.2149G>T (p.Asp717Tyr) c.2182G>T (p.Asp728Tyr) c.1750G>T (p.Asp584Tyr) | |
3 | g.119414172A= | CA1396548582 | ARHGAP31 | c.2243A= (p.Asp748=) c.2150A= (p.Asp717=) c.2183A= (p.Asp728=) c.1751A= (p.Asp584=) | |
3 | g.119414172A>C | CA354049994 | ARHGAP31 | c.2243A>C (p.Asp748Ala) c.2150A>C (p.Asp717Ala) c.2183A>C (p.Asp728Ala) c.1751A>C (p.Asp584Ala) | |
3 | g.119414172A>G | CA354049997 | ARHGAP31 | c.2243A>G (p.Asp748Gly) c.2150A>G (p.Asp717Gly) c.2183A>G (p.Asp728Gly) c.1751A>G (p.Asp584Gly) | dbSNP gnomAD v2 gnomAD v4 |
3 | g.119414172A>T | CA354049999 | ARHGAP31 | c.2243A>T (p.Asp748Val) c.2150A>T (p.Asp717Val) c.2183A>T (p.Asp728Val) c.1751A>T (p.Asp584Val) | |
3 | g.119414173C>A | CA354050011 | ARHGAP31 | c.2244C>A (p.Asp748Glu) c.2151C>A (p.Asp717Glu) c.2184C>A (p.Asp728Glu) c.1752C>A (p.Asp584Glu) | |
3 | g.119414173C= | CA1396548583 | ARHGAP31 | c.2244C= (p.Asp748=) c.2151C= (p.Asp717=) c.2184C= (p.Asp728=) c.1752C= (p.Asp584=) | |
3 | g.119414173C>G | CA354050018 | ARHGAP31 | c.2244C>G (p.Asp748Glu) c.2151C>G (p.Asp717Glu) c.2184C>G (p.Asp728Glu) c.1752C>G (p.Asp584Glu) | dbSNP |
3 | g.119414173C>T | CA2553991 | ARHGAP31 | c.2244C>T (p.Asp748=) c.2151C>T (p.Asp717=) c.2184C>T (p.Asp728=) c.1752C>T (p.Asp584=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
3 | g.119414174C>A | CA354050023 | ARHGAP31 | c.2245C>A (p.Leu749Ile) c.2152C>A (p.Leu718Ile) c.2185C>A (p.Leu729Ile) c.1753C>A (p.Leu585Ile) | |
3 | g.119414174C= | CA1396548584 | ARHGAP31 | c.2245C= (p.Leu749=) c.2152C= (p.Leu718=) c.2185C= (p.Leu729=) c.1753C= (p.Leu585=) | |
3 | g.119414174C>G | CA354050026 | ARHGAP31 | c.2245C>G (p.Leu749Val) c.2152C>G (p.Leu718Val) c.2185C>G (p.Leu729Val) c.1753C>G (p.Leu585Val) | |
3 | g.119414174C>T | CA2553992 | ARHGAP31 | c.2245C>T (p.Leu749Phe) c.2152C>T (p.Leu718Phe) c.2185C>T (p.Leu729Phe) c.1753C>T (p.Leu585Phe) | dbSNP ExAC gnomAD v2 gnomAD v4 |
3 | g.119414175T>A | CA2553993 | ARHGAP31 | c.2246T>A (p.Leu749His) c.2153T>A (p.Leu718His) c.2186T>A (p.Leu729His) c.1754T>A (p.Leu585His) | dbSNP ExAC gnomAD v2 gnomAD v4 |
3 | g.119414175T>C | CA354050040 | ARHGAP31 | c.2246T>C (p.Leu749Pro) c.2153T>C (p.Leu718Pro) c.2186T>C (p.Leu729Pro) c.1754T>C (p.Leu585Pro) | |
3 | g.119414175T>G | CA354050032 | ARHGAP31 | c.2246T>G (p.Leu749Arg) c.2153T>G (p.Leu718Arg) c.2186T>G (p.Leu729Arg) c.1754T>G (p.Leu585Arg) | |
3 | g.119414175T= | CA1396548585 | ARHGAP31 | c.2246T= (p.Leu749=) c.2153T= (p.Leu718=) c.2186T= (p.Leu729=) c.1754T= (p.Leu585=) | |
3 | g.119414176C>A | CA435411656 | ARHGAP31 | c.2247C>A (p.Leu749=) c.2154C>A (p.Leu718=) c.2187C>A (p.Leu729=) c.1755C>A (p.Leu585=) | dbSNP |
3 | g.119414176C= | CA1396548586 | ARHGAP31 | c.2247C= (p.Leu749=) c.2154C= (p.Leu718=) c.2187C= (p.Leu729=) c.1755C= (p.Leu585=) | |
3 | g.119414176C>G | CA435411657 | ARHGAP31 | c.2247C>G (p.Leu749=) c.2154C>G (p.Leu718=) c.2187C>G (p.Leu729=) c.1755C>G (p.Leu585=) | gnomAD v4 |
3 | g.119414176C>T | CA435411658 | ARHGAP31 | c.2247C>T (p.Leu749=) c.2154C>T (p.Leu718=) c.2187C>T (p.Leu729=) c.1755C>T (p.Leu585=) | dbSNP gnomAD v3 gnomAD v4 |
3 | g.119414177G>A | CA354050043 | ARHGAP31 | c.2248G>A (p.Ala750Thr) c.2155G>A (p.Ala719Thr) c.2188G>A (p.Ala730Thr) c.1756G>A (p.Ala586Thr) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
3 | g.119414177G>C | CA354050046 | ARHGAP31 | c.2248G>C (p.Ala750Pro) c.2155G>C (p.Ala719Pro) c.2188G>C (p.Ala730Pro) c.1756G>C (p.Ala586Pro) | |
3 | g.119414177G= | CA1396548587 | ARHGAP31 | c.2248G= (p.Ala750=) c.2155G= (p.Ala719=) c.2188G= (p.Ala730=) c.1756G= (p.Ala586=) | |
3 | g.119414177G>T | CA354050048 | ARHGAP31 | c.2248G>T (p.Ala750Ser) c.2155G>T (p.Ala719Ser) c.2188G>T (p.Ala730Ser) c.1756G>T (p.Ala586Ser) | |
3 | g.119414178C>A | CA354050050 | ARHGAP31 | c.2249C>A (p.Ala750Asp) c.2156C>A (p.Ala719Asp) c.2189C>A (p.Ala730Asp) c.1757C>A (p.Ala586Asp) | ClinVar dbSNP |
3 | g.119414178C>G | CA354050052 | ARHGAP31 | c.2249C>G (p.Ala750Gly) c.2156C>G (p.Ala719Gly) c.2189C>G (p.Ala730Gly) c.1757C>G (p.Ala586Gly) | |
3 | g.119414178C>T | CA354050055 | ARHGAP31 | c.2249C>T (p.Ala750Val) c.2156C>T (p.Ala719Val) c.2189C>T (p.Ala730Val) c.1757C>T (p.Ala586Val) | |
3 | g.119414179C>A | CA435411659 | ARHGAP31 | c.2250C>A (p.Ala750=) c.2157C>A (p.Ala719=) c.2190C>A (p.Ala730=) c.1758C>A (p.Ala586=) | |
3 | g.119414179C>G | CA435411660 | ARHGAP31 | c.2250C>G (p.Ala750=) c.2157C>G (p.Ala719=) c.2190C>G (p.Ala730=) c.1758C>G (p.Ala586=) | |
3 | g.119414179C>T | CA435411661 | ARHGAP31 | c.2250C>T (p.Ala750=) c.2157C>T (p.Ala719=) c.2190C>T (p.Ala730=) c.1758C>T (p.Ala586=) | |
3 | g.119414180A= | CA1396548588 | ARHGAP31 | c.2251A= (p.Ser751=) c.2158A= (p.Ser720=) c.2191A= (p.Ser731=) c.1759A= (p.Ser587=) | |
3 | g.119414180A>C | CA354050060 | ARHGAP31 | c.2251A>C (p.Ser751Arg) c.2158A>C (p.Ser720Arg) c.2191A>C (p.Ser731Arg) c.1759A>C (p.Ser587Arg) | dbSNP gnomAD v4 |
3 | g.119414180A>G | CA354050061 | ARHGAP31 | c.2251A>G (p.Ser751Gly) c.2158A>G (p.Ser720Gly) c.2191A>G (p.Ser731Gly) c.1759A>G (p.Ser587Gly) | |
3 | g.119414180A>T | CA354050063 | ARHGAP31 | c.2251A>T (p.Ser751Cys) c.2158A>T (p.Ser720Cys) c.2191A>T (p.Ser731Cys) c.1759A>T (p.Ser587Cys) | |
3 | g.119414181G>A | CA354050069 | ARHGAP31 | c.2252G>A (p.Ser751Asn) c.2159G>A (p.Ser720Asn) c.2192G>A (p.Ser731Asn) c.1760G>A (p.Ser587Asn) | dbSNP gnomAD v3 gnomAD v4 |
3 | g.119414181G>C | CA354050070 | ARHGAP31 | c.2252G>C (p.Ser751Thr) c.2159G>C (p.Ser720Thr) c.2192G>C (p.Ser731Thr) c.1760G>C (p.Ser587Thr) | |
3 | g.119414181G= | CA1396548589 | ARHGAP31 | c.2252G= (p.Ser751=) c.2159G= (p.Ser720=) c.2192G= (p.Ser731=) c.1760G= (p.Ser587=) | |
3 | g.119414181G>T | CA354050072 | ARHGAP31 | c.2252G>T (p.Ser751Ile) c.2159G>T (p.Ser720Ile) c.2192G>T (p.Ser731Ile) c.1760G>T (p.Ser587Ile) | dbSNP gnomAD v4 |
3 | g.119414182C>A | CA354050075 | ARHGAP31 | c.2253C>A (p.Ser751Arg) c.2160C>A (p.Ser720Arg) c.2193C>A (p.Ser731Arg) c.1761C>A (p.Ser587Arg) | |
3 | g.119414182C>G | CA354050077 | ARHGAP31 | c.2253C>G (p.Ser751Arg) c.2160C>G (p.Ser720Arg) c.2193C>G (p.Ser731Arg) c.1761C>G (p.Ser587Arg) | |
3 | g.119414182C>T | CA435411662 | ARHGAP31 | c.2253C>T (p.Ser751=) c.2160C>T (p.Ser720=) c.2193C>T (p.Ser731=) c.1761C>T (p.Ser587=) | |
3 | g.119414183C>A | CA354050079 | ARHGAP31 | c.2254C>A (p.Leu752Met) c.2161C>A (p.Leu721Met) c.2194C>A (p.Leu732Met) c.1762C>A (p.Leu588Met) | |
3 | g.119414183C= | CA1396548590 | ARHGAP31 | c.2254C= (p.Leu752=) c.2161C= (p.Leu721=) c.2194C= (p.Leu732=) c.1762C= (p.Leu588=) | |
3 | g.119414183C>G | CA2553994 | ARHGAP31 | c.2254C>G (p.Leu752Val) c.2161C>G (p.Leu721Val) c.2194C>G (p.Leu732Val) c.1762C>G (p.Leu588Val) | dbSNP ExAC gnomAD v2 gnomAD v4 |
3 | g.119414183C>T | CA435411663 | ARHGAP31 | c.2254C>T (p.Leu752=) c.2161C>T (p.Leu721=) c.2194C>T (p.Leu732=) c.1762C>T (p.Leu588=) | |
3 | g.119414184T>A | CA354050084 | ARHGAP31 | c.2255T>A (p.Leu752Gln) c.2162T>A (p.Leu721Gln) c.2195T>A (p.Leu732Gln) c.1763T>A (p.Leu588Gln) | gnomAD v4 |
3 | g.119414184T>C | CA354050088 | ARHGAP31 | c.2255T>C (p.Leu752Pro) c.2162T>C (p.Leu721Pro) c.2195T>C (p.Leu732Pro) c.1763T>C (p.Leu588Pro) | |
3 | g.119414184T>G | CA354050091 | ARHGAP31 | c.2255T>G (p.Leu752Arg) c.2162T>G (p.Leu721Arg) c.2195T>G (p.Leu732Arg) c.1763T>G (p.Leu588Arg) | |
3 | g.119414185G>A | CA435411667 | ARHGAP31 | c.2256G>A (p.Leu752=) c.2163G>A (p.Leu721=) c.2196G>A (p.Leu732=) c.1764G>A (p.Leu588=) | |
3 | g.119414185G>C | CA435411668 | ARHGAP31 | c.2256G>C (p.Leu752=) c.2163G>C (p.Leu721=) c.2196G>C (p.Leu732=) c.1764G>C (p.Leu588=) | |
3 | g.119414185G>T | CA435411669 | ARHGAP31 | c.2256G>T (p.Leu752=) c.2163G>T (p.Leu721=) c.2196G>T (p.Leu732=) c.1764G>T (p.Leu588=) | |
3 | g.119414186G>A | CA354050093 | ARHGAP31 | c.2257G>A (p.Ala753Thr) c.2164G>A (p.Ala722Thr) c.2197G>A (p.Ala733Thr) c.1765G>A (p.Ala589Thr) | COSMIC |
3 | g.119414186G>C | CA81697486 | ARHGAP31 | c.2257G>C (p.Ala753Pro) c.2164G>C (p.Ala722Pro) c.2197G>C (p.Ala733Pro) c.1765G>C (p.Ala589Pro) | dbSNP gnomAD v4 |
3 | g.119414186G= | CA1396548591 | ARHGAP31 | c.2257G= (p.Ala753=) c.2164G= (p.Ala722=) c.2197G= (p.Ala733=) c.1765G= (p.Ala589=) | |
3 | g.119414186G>T | CA354050103 | ARHGAP31 | c.2257G>T (p.Ala753Ser) c.2164G>T (p.Ala722Ser) c.2197G>T (p.Ala733Ser) c.1765G>T (p.Ala589Ser) | |
3 | g.119414187C>A | CA354050106 | ARHGAP31 | c.2258C>A (p.Ala753Asp) c.2165C>A (p.Ala722Asp) c.2198C>A (p.Ala733Asp) c.1766C>A (p.Ala589Asp) | |
3 | g.119414187C>G | CA354050111 | ARHGAP31 | c.2258C>G (p.Ala753Gly) c.2165C>G (p.Ala722Gly) c.2198C>G (p.Ala733Gly) c.1766C>G (p.Ala589Gly) | |
3 | g.119414187C>T | CA354050115 | ARHGAP31 | c.2258C>T (p.Ala753Val) c.2165C>T (p.Ala722Val) c.2198C>T (p.Ala733Val) c.1766C>T (p.Ala589Val) | gnomAD v4 |
3 | g.119414188T>A | CA435411673 | ARHGAP31 | c.2259T>A (p.Ala753=) c.2166T>A (p.Ala722=) c.2199T>A (p.Ala733=) c.1767T>A (p.Ala589=) | |
3 | g.119414188T>C | CA435411671 | ARHGAP31 | c.2259T>C (p.Ala753=) c.2166T>C (p.Ala722=) c.2199T>C (p.Ala733=) c.1767T>C (p.Ala589=) | dbSNP |
3 | g.119414188T>G | CA435411672 | ARHGAP31 | c.2259T>G (p.Ala753=) c.2166T>G (p.Ala722=) c.2199T>G (p.Ala733=) c.1767T>G (p.Ala589=) | gnomAD v4 |
3 | g.119414188T= | CA1396548592 | ARHGAP31 | c.2259T= (p.Ala753=) c.2166T= (p.Ala722=) c.2199T= (p.Ala733=) c.1767T= (p.Ala589=) | |
3 | g.119414189C>A | CA354050119 | ARHGAP31 | c.2260C>A (p.Pro754Thr) c.2167C>A (p.Pro723Thr) c.2200C>A (p.Pro734Thr) c.1768C>A (p.Pro590Thr) | |
3 | g.119414189C>G | CA354050120 | ARHGAP31 | c.2260C>G (p.Pro754Ala) c.2167C>G (p.Pro723Ala) c.2200C>G (p.Pro734Ala) c.1768C>G (p.Pro590Ala) | |
3 | g.119414189C>T | CA354050123 | ARHGAP31 | c.2260C>T (p.Pro754Ser) c.2167C>T (p.Pro723Ser) c.2200C>T (p.Pro734Ser) c.1768C>T (p.Pro590Ser) | gnomAD v4 |
3 | g.119414190C>A | CA2553995 | ARHGAP31 | c.2261C>A (p.Pro754His) c.2168C>A (p.Pro723His) c.2201C>A (p.Pro734His) c.1769C>A (p.Pro590His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
3 | g.119414190C= | CA1396548593 | ARHGAP31 | c.2261C= (p.Pro754=) c.2168C= (p.Pro723=) c.2201C= (p.Pro734=) c.1769C= (p.Pro590=) | |
3 | g.119414190C>G | CA354050137 | ARHGAP31 | c.2261C>G (p.Pro754Arg) c.2168C>G (p.Pro723Arg) c.2201C>G (p.Pro734Arg) c.1769C>G (p.Pro590Arg) | |
3 | g.119414190C>T | CA354050131 | ARHGAP31 | c.2261C>T (p.Pro754Leu) c.2168C>T (p.Pro723Leu) c.2201C>T (p.Pro734Leu) c.1769C>T (p.Pro590Leu) | gnomAD v4 |
3 | g.119414191T>A | CA435411674 | ARHGAP31 | c.2262T>A (p.Pro754=) c.2169T>A (p.Pro723=) c.2202T>A (p.Pro734=) c.1770T>A (p.Pro590=) | |
3 | g.119414191T>C | CA435411675 | ARHGAP31 | c.2262T>C (p.Pro754=) c.2169T>C (p.Pro723=) c.2202T>C (p.Pro734=) c.1770T>C (p.Pro590=) | |
3 | g.119414191T>G | CA435411676 | ARHGAP31 | c.2262T>G (p.Pro754=) c.2169T>G (p.Pro723=) c.2202T>G (p.Pro734=) c.1770T>G (p.Pro590=) | |
3 | g.119414192C>A | CA354050142 | ARHGAP31 | c.2263C>A (p.Leu755Met) c.2170C>A (p.Leu724Met) c.2203C>A (p.Leu735Met) c.1771C>A (p.Leu591Met) | |
3 | g.119414192C>G | CA354050144 | ARHGAP31 | c.2263C>G (p.Leu755Val) c.2170C>G (p.Leu724Val) c.2203C>G (p.Leu735Val) c.1771C>G (p.Leu591Val) | |
3 | g.119414192C>T | CA435411677 | ARHGAP31 | c.2263C>T (p.Leu755=) c.2170C>T (p.Leu724=) c.2203C>T (p.Leu735=) c.1771C>T (p.Leu591=) | COSMIC |
3 | g.119414193T>A | CA354050147 | ARHGAP31 | c.2264T>A (p.Leu755Gln) c.2171T>A (p.Leu724Gln) c.2204T>A (p.Leu735Gln) c.1772T>A (p.Leu591Gln) | |
3 | g.119414193T>C | CA354050152 | ARHGAP31 | c.2264T>C (p.Leu755Pro) c.2171T>C (p.Leu724Pro) c.2204T>C (p.Leu735Pro) c.1772T>C (p.Leu591Pro) | |
3 | g.119414193T>G | CA354050149 | ARHGAP31 | c.2264T>G (p.Leu755Arg) c.2171T>G (p.Leu724Arg) c.2204T>G (p.Leu735Arg) c.1772T>G (p.Leu591Arg) | |
3 | g.119414194G>A | CA435411682 | ARHGAP31 | c.2265G>A (p.Leu755=) c.2172G>A (p.Leu724=) c.2205G>A (p.Leu735=) c.1773G>A (p.Leu591=) | dbSNP gnomAD v2 gnomAD v4 |
3 | g.119414194G>C | CA435411681 | ARHGAP31 | c.2265G>C (p.Leu755=) c.2172G>C (p.Leu724=) c.2205G>C (p.Leu735=) c.1773G>C (p.Leu591=) | |
3 | g.119414194G= | CA1396548594 | ARHGAP31 | c.2265G= (p.Leu755=) c.2172G= (p.Leu724=) c.2205G= (p.Leu735=) c.1773G= (p.Leu591=) | |
3 | g.119414194G>T | CA435411683 | ARHGAP31 | c.2265G>T (p.Leu755=) c.2172G>T (p.Leu724=) c.2205G>T (p.Leu735=) c.1773G>T (p.Leu591=) | |
3 | g.119414195G>A | CA354050155 | ARHGAP31 | c.2266G>A (p.Glu756Lys) c.2173G>A (p.Glu725Lys) c.2206G>A (p.Glu736Lys) c.1774G>A (p.Glu592Lys) | |
3 | g.119414195G>C | CA2553996 | ARHGAP31 | c.2266G>C (p.Glu756Gln) c.2173G>C (p.Glu725Gln) c.2206G>C (p.Glu736Gln) c.1774G>C (p.Glu592Gln) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.119414195G= | CA1396548595 | ARHGAP31 | c.2266G= (p.Glu756=) c.2173G= (p.Glu725=) c.2206G= (p.Glu736=) c.1774G= (p.Glu592=) | |
3 | g.119414195G>T | CA354050158 | ARHGAP31 | c.2266G>T (p.Glu756Ter) c.2173G>T (p.Glu725Ter) c.2206G>T (p.Glu736Ter) c.1774G>T (p.Glu592Ter) | |
3 | g.119414196A>C | CA354050166 | ARHGAP31 | c.2267A>C (p.Glu756Ala) c.2174A>C (p.Glu725Ala) c.2207A>C (p.Glu736Ala) c.1775A>C (p.Glu592Ala) | |
3 | g.119414196A>G | CA354050169 | ARHGAP31 | c.2267A>G (p.Glu756Gly) c.2174A>G (p.Glu725Gly) c.2207A>G (p.Glu736Gly) c.1775A>G (p.Glu592Gly) | |
3 | g.119414196A>T | CA354050175 | ARHGAP31 | c.2267A>T (p.Glu756Val) c.2174A>T (p.Glu725Val) c.2207A>T (p.Glu736Val) c.1775A>T (p.Glu592Val) | |
3 | g.119414197A= | CA1396548596 | ARHGAP31 | c.2268A= (p.Glu756=) c.2175A= (p.Glu725=) c.2208A= (p.Glu736=) c.1776A= (p.Glu592=) | |
3 | g.119414197A>C | CA354050179 | ARHGAP31 | c.2268A>C (p.Glu756Asp) c.2175A>C (p.Glu725Asp) c.2208A>C (p.Glu736Asp) c.1776A>C (p.Glu592Asp) | |
3 | g.119414197A>G | CA435411687 | ARHGAP31 | c.2268A>G (p.Glu756=) c.2175A>G (p.Glu725=) c.2208A>G (p.Glu736=) c.1776A>G (p.Glu592=) | |
3 | g.119414197A>T | CA2553997 | ARHGAP31 | c.2268A>T (p.Glu756Asp) c.2175A>T (p.Glu725Asp) c.2208A>T (p.Glu736Asp) c.1776A>T (p.Glu592Asp) | dbSNP ExAC gnomAD v2 |
3 | g.119414198A>C | CA354050187 | ARHGAP31 | c.2269A>C (p.Ile757Leu) c.2176A>C (p.Ile726Leu) c.2209A>C (p.Ile737Leu) c.1777A>C (p.Ile593Leu) | |
3 | g.119414198A>G | CA354050189 | ARHGAP31 | c.2269A>G (p.Ile757Val) c.2176A>G (p.Ile726Val) c.2209A>G (p.Ile737Val) c.1777A>G (p.Ile593Val) | |
3 | g.119414198A>T | CA354050190 | ARHGAP31 | c.2269A>T (p.Ile757Leu) c.2176A>T (p.Ile726Leu) c.2209A>T (p.Ile737Leu) c.1777A>T (p.Ile593Leu) | |
3 | g.119414199T>A | CA354050193 | ARHGAP31 | c.2270T>A (p.Ile757Lys) c.2177T>A (p.Ile726Lys) c.2210T>A (p.Ile737Lys) c.1778T>A (p.Ile593Lys) | |
3 | g.119414199T>C | CA354050197 | ARHGAP31 | c.2270T>C (p.Ile757Thr) c.2177T>C (p.Ile726Thr) c.2210T>C (p.Ile737Thr) c.1778T>C (p.Ile593Thr) | |
3 | g.119414199T>G | CA354050199 | ARHGAP31 | c.2270T>G (p.Ile757Arg) c.2177T>G (p.Ile726Arg) c.2210T>G (p.Ile737Arg) c.1778T>G (p.Ile593Arg) | |
3 | g.119414200A= | CA1396548597 | ARHGAP31 | c.2271A= (p.Ile757=) c.2178A= (p.Ile726=) c.2211A= (p.Ile737=) c.1779A= (p.Ile593=) | |
3 | g.119414200A>C | CA435411689 | ARHGAP31 | c.2271A>C (p.Ile757=) c.2178A>C (p.Ile726=) c.2211A>C (p.Ile737=) c.1779A>C (p.Ile593=) | |
3 | g.119414200A>G | CA354050215 | ARHGAP31 | c.2271A>G (p.Ile757Met) c.2178A>G (p.Ile726Met) c.2211A>G (p.Ile737Met) c.1779A>G (p.Ile593Met) | |
3 | g.119414200A>T | CA435411690 | ARHGAP31 | c.2271A>T (p.Ile757=) c.2178A>T (p.Ile726=) c.2211A>T (p.Ile737=) c.1779A>T (p.Ile593=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
3 | g.119414201G>A | CA354050218 | ARHGAP31 | c.2272G>A (p.Val758Ile) c.2179G>A (p.Val727Ile) c.2212G>A (p.Val738Ile) c.1780G>A (p.Val594Ile) | |
3 | g.119414201G>C | CA354050223 | ARHGAP31 | c.2272G>C (p.Val758Leu) c.2179G>C (p.Val727Leu) c.2212G>C (p.Val738Leu) c.1780G>C (p.Val594Leu) | |
3 | g.119414201G>T | CA354050220 | ARHGAP31 | c.2272G>T (p.Val758Phe) c.2179G>T (p.Val727Phe) c.2212G>T (p.Val738Phe) c.1780G>T (p.Val594Phe) | |
3 | g.119414202T>A | CA354050226 | ARHGAP31 | c.2273T>A (p.Val758Asp) c.2180T>A (p.Val727Asp) c.2213T>A (p.Val738Asp) c.1781T>A (p.Val594Asp) | |
3 | g.119414202T>C | CA354050229 | ARHGAP31 | c.2273T>C (p.Val758Ala) c.2180T>C (p.Val727Ala) c.2213T>C (p.Val738Ala) c.1781T>C (p.Val594Ala) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.119414202T>G | CA354050232 | ARHGAP31 | c.2273T>G (p.Val758Gly) c.2180T>G (p.Val727Gly) c.2213T>G (p.Val738Gly) c.1781T>G (p.Val594Gly) | |
3 | g.119414202T= | CA1396548598 | ARHGAP31 | c.2273T= (p.Val758=) c.2180T= (p.Val727=) c.2213T= (p.Val738=) c.1781T= (p.Val594=) | |
3 | g.119414203T>A | CA435411694 | ARHGAP31 | c.2274T>A (p.Val758=) c.2181T>A (p.Val727=) c.2214T>A (p.Val738=) c.1782T>A (p.Val594=) | dbSNP gnomAD v2 gnomAD v4 |
3 | g.119414203T>C | CA435411695 | ARHGAP31 | c.2274T>C (p.Val758=) c.2181T>C (p.Val727=) c.2214T>C (p.Val738=) c.1782T>C (p.Val594=) | |
3 | g.119414203T>G | CA435411697 | ARHGAP31 | c.2274T>G (p.Val758=) c.2181T>G (p.Val727=) c.2214T>G (p.Val738=) c.1782T>G (p.Val594=) | |
3 | g.119414203T= | CA1396548599 | ARHGAP31 | c.2274T= (p.Val758=) c.2181T= (p.Val727=) c.2214T= (p.Val738=) c.1782T= (p.Val594=) | |
3 | g.119414204C>A | CA354050236 | ARHGAP31 | c.2275C>A (p.Pro759Thr) c.2182C>A (p.Pro728Thr) c.2215C>A (p.Pro739Thr) c.1783C>A (p.Pro595Thr) | dbSNP gnomAD v2 gnomAD v4 |
3 | g.119414204C= | CA1396548600 | ARHGAP31 | c.2275C= (p.Pro759=) c.2182C= (p.Pro728=) c.2215C= (p.Pro739=) c.1783C= (p.Pro595=) | |
3 | g.119414204C>G | CA354050239 | ARHGAP31 | c.2275C>G (p.Pro759Ala) c.2182C>G (p.Pro728Ala) c.2215C>G (p.Pro739Ala) c.1783C>G (p.Pro595Ala) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.119414204C>T | CA354050241 | ARHGAP31 | c.2275C>T (p.Pro759Ser) c.2182C>T (p.Pro728Ser) c.2215C>T (p.Pro739Ser) c.1783C>T (p.Pro595Ser) | COSMIC |
3 | g.119414205C>A | CA354050243 | ARHGAP31 | c.2276C>A (p.Pro759His) c.2183C>A (p.Pro728His) c.2216C>A (p.Pro739His) c.1784C>A (p.Pro595His) | gnomAD v4 |
3 | g.119414205C>G | CA354050246 | ARHGAP31 | c.2276C>G (p.Pro759Arg) c.2183C>G (p.Pro728Arg) c.2216C>G (p.Pro739Arg) c.1784C>G (p.Pro595Arg) | |
3 | g.119414205C>T | CA354050247 | ARHGAP31 | c.2276C>T (p.Pro759Leu) c.2183C>T (p.Pro728Leu) c.2216C>T (p.Pro739Leu) c.1784C>T (p.Pro595Leu) | |
3 | g.119414206T>A | CA435411700 | ARHGAP31 | c.2277T>A (p.Pro759=) c.2184T>A (p.Pro728=) c.2217T>A (p.Pro739=) c.1785T>A (p.Pro595=) | |
3 | g.119414206T>C | CA435411701 | ARHGAP31 | c.2277T>C (p.Pro759=) c.2184T>C (p.Pro728=) c.2217T>C (p.Pro739=) c.1785T>C (p.Pro595=) | |
3 | g.119414206T>G | CA435411702 | ARHGAP31 | c.2277T>G (p.Pro759=) c.2184T>G (p.Pro728=) c.2217T>G (p.Pro739=) c.1785T>G (p.Pro595=) | |
3 | g.119414207T>A | CA354050257 | ARHGAP31 | c.2278T>A (p.Phe760Ile) c.2185T>A (p.Phe729Ile) c.2218T>A (p.Phe740Ile) c.1786T>A (p.Phe596Ile) | |
3 | g.119414207T>C | CA354050256 | ARHGAP31 | c.2278T>C (p.Phe760Leu) c.2185T>C (p.Phe729Leu) c.2218T>C (p.Phe740Leu) c.1786T>C (p.Phe596Leu) | |
3 | g.119414207T>G | CA354050253 | ARHGAP31 | c.2278T>G (p.Phe760Val) c.2185T>G (p.Phe729Val) c.2218T>G (p.Phe740Val) c.1786T>G (p.Phe596Val) | |
3 | g.119414208T>A | CA354050258 | ARHGAP31 | c.2279T>A (p.Phe760Tyr) c.2186T>A (p.Phe729Tyr) c.2219T>A (p.Phe740Tyr) c.1787T>A (p.Phe596Tyr) | |
3 | g.119414208T>C | CA354050259 | ARHGAP31 | c.2279T>C (p.Phe760Ser) c.2186T>C (p.Phe729Ser) c.2219T>C (p.Phe740Ser) c.1787T>C (p.Phe596Ser) | |
3 | g.119414208T>G | CA354050262 | ARHGAP31 | c.2279T>G (p.Phe760Cys) c.2186T>G (p.Phe729Cys) c.2219T>G (p.Phe740Cys) c.1787T>G (p.Phe596Cys) | |
3 | g.119414209T>A | CA354050266 | ARHGAP31 | c.2280T>A (p.Phe760Leu) c.2187T>A (p.Phe729Leu) c.2220T>A (p.Phe740Leu) c.1788T>A (p.Phe596Leu) | |
3 | g.119414209T>C | CA435411705 | ARHGAP31 | c.2280T>C (p.Phe760=) c.2187T>C (p.Phe729=) c.2220T>C (p.Phe740=) c.1788T>C (p.Phe596=) | |
3 | g.119414209T>G | CA354050270 | ARHGAP31 | c.2280T>G (p.Phe760Leu) c.2187T>G (p.Phe729Leu) c.2220T>G (p.Phe740Leu) c.1788T>G (p.Phe596Leu) | dbSNP |
3 | g.119414209T= | CA1396548601 | ARHGAP31 | c.2280T= (p.Phe760=) c.2187T= (p.Phe729=) c.2220T= (p.Phe740=) c.1788T= (p.Phe596=) | |
3 | g.119414210G>A | CA354050281 | ARHGAP31 | c.2281G>A (p.Glu761Lys) c.2188G>A (p.Glu730Lys) c.2221G>A (p.Glu741Lys) c.1789G>A (p.Glu597Lys) | |
3 | g.119414210G>C | CA354050285 | ARHGAP31 | c.2281G>C (p.Glu761Gln) c.2188G>C (p.Glu730Gln) c.2221G>C (p.Glu741Gln) c.1789G>C (p.Glu597Gln) | |
3 | g.119414210G>T | CA354050289 | ARHGAP31 | c.2281G>T (p.Glu761Ter) c.2188G>T (p.Glu730Ter) c.2221G>T (p.Glu741Ter) c.1789G>T (p.Glu597Ter) | |
3 | g.119414211A>C | CA354050296 | ARHGAP31 | c.2282A>C (p.Glu761Ala) c.2189A>C (p.Glu730Ala) c.2222A>C (p.Glu741Ala) c.1790A>C (p.Glu597Ala) | |
3 | g.119414211A>G | CA354050302 | ARHGAP31 | c.2282A>G (p.Glu761Gly) c.2189A>G (p.Glu730Gly) c.2222A>G (p.Glu741Gly) c.1790A>G (p.Glu597Gly) | |
3 | g.119414211A>T | CA354050303 | ARHGAP31 | c.2282A>T (p.Glu761Val) c.2189A>T (p.Glu730Val) c.2222A>T (p.Glu741Val) c.1790A>T (p.Glu597Val) | |
3 | g.119414212G>A | CA435411710 | ARHGAP31 | c.2283G>A (p.Glu761=) c.2190G>A (p.Glu730=) c.2223G>A (p.Glu741=) c.1791G>A (p.Glu597=) | |
3 | g.119414212G>C | CA354050309 | ARHGAP31 | c.2283G>C (p.Glu761Asp) c.2190G>C (p.Glu730Asp) c.2223G>C (p.Glu741Asp) c.1791G>C (p.Glu597Asp) | |
3 | g.119414212G>T | CA354050310 | ARHGAP31 | c.2283G>T (p.Glu761Asp) c.2190G>T (p.Glu730Asp) c.2223G>T (p.Glu741Asp) c.1791G>T (p.Glu597Asp) | |
3 | g.119414213A>C | CA354050313 | ARHGAP31 | c.2284A>C (p.Lys762Gln) c.2191A>C (p.Lys731Gln) c.2224A>C (p.Lys742Gln) c.1792A>C (p.Lys598Gln) | |
3 | g.119414213A>G | CA354050317 | ARHGAP31 | c.2284A>G (p.Lys762Glu) c.2191A>G (p.Lys731Glu) c.2224A>G (p.Lys742Glu) c.1792A>G (p.Lys598Glu) | |
3 | g.119414213A>T | CA354050315 | ARHGAP31 | c.2284A>T (p.Lys762Ter) c.2191A>T (p.Lys731Ter) c.2224A>T (p.Lys742Ter) c.1792A>T (p.Lys598Ter) | |
3 | g.119414214A= | CA1396548602 | ARHGAP31 | c.2285A= (p.Lys762=) c.2192A= (p.Lys731=) c.2225A= (p.Lys742=) c.1793A= (p.Lys598=) | |
3 | g.119414214A>C | CA2553998 | ARHGAP31 | c.2285A>C (p.Lys762Thr) c.2192A>C (p.Lys731Thr) c.2225A>C (p.Lys742Thr) c.1793A>C (p.Lys598Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.119414214A>G | CA2553999 | ARHGAP31 | c.2285A>G (p.Lys762Arg) c.2192A>G (p.Lys731Arg) c.2225A>G (p.Lys742Arg) c.1793A>G (p.Lys598Arg) | dbSNP ExAC gnomAD v2 gnomAD v4 |
3 | g.119414214A>T | CA354050326 | ARHGAP31 | c.2285A>T (p.Lys762Met) c.2192A>T (p.Lys731Met) c.2225A>T (p.Lys742Met) c.1793A>T (p.Lys598Met) | |
3 | g.119414215G>A | CA435411715 | ARHGAP31 | c.2286G>A (p.Lys762=) c.2193G>A (p.Lys731=) c.2226G>A (p.Lys742=) c.1794G>A (p.Lys598=) | gnomAD v4 |
3 | g.119414215G>C | CA354050329 | ARHGAP31 | c.2286G>C (p.Lys762Asn) c.2193G>C (p.Lys731Asn) c.2226G>C (p.Lys742Asn) c.1794G>C (p.Lys598Asn) | |
3 | g.119414215G>T | CA354050330 | ARHGAP31 | c.2286G>T (p.Lys762Asn) c.2193G>T (p.Lys731Asn) c.2226G>T (p.Lys742Asn) c.1794G>T (p.Lys598Asn) | gnomAD v4 |
3 | g.119414216G>A | CA354050334 | ARHGAP31 | c.2287G>A (p.Ala763Thr) c.2194G>A (p.Ala732Thr) c.2227G>A (p.Ala743Thr) c.1795G>A (p.Ala599Thr) | dbSNP |
3 | g.119414216G>C | CA81697499 | ARHGAP31 | c.2287G>C (p.Ala763Pro) c.2194G>C (p.Ala732Pro) c.2227G>C (p.Ala743Pro) c.1795G>C (p.Ala599Pro) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
3 | g.119414216G= | CA1396548603 | ARHGAP31 | c.2287G= (p.Ala763=) c.2194G= (p.Ala732=) c.2227G= (p.Ala743=) c.1795G= (p.Ala599=) | |
3 | g.119414216G>T | CA354050336 | ARHGAP31 | c.2287G>T (p.Ala763Ser) c.2194G>T (p.Ala732Ser) c.2227G>T (p.Ala743Ser) c.1795G>T (p.Ala599Ser) | gnomAD v4 |
3 | g.119414217C>A | CA354050337 | ARHGAP31 | c.2288C>A (p.Ala763Glu) c.2195C>A (p.Ala732Glu) c.2228C>A (p.Ala743Glu) c.1796C>A (p.Ala599Glu) | |
3 | g.119414217C= | CA1396548604 | ARHGAP31 | c.2288C= (p.Ala763=) c.2195C= (p.Ala732=) c.2228C= (p.Ala743=) c.1796C= (p.Ala599=) | |
3 | g.119414217C>G | CA354050340 | ARHGAP31 | c.2288C>G (p.Ala763Gly) c.2195C>G (p.Ala732Gly) c.2228C>G (p.Ala743Gly) c.1796C>G (p.Ala599Gly) | |
3 | g.119414217C>T | CA2554000 | ARHGAP31 | c.2288C>T (p.Ala763Val) c.2195C>T (p.Ala732Val) c.2228C>T (p.Ala743Val) c.1796C>T (p.Ala599Val) | dbSNP ExAC gnomAD v2 gnomAD v4 |
3 | g.119414218A= | CA1396548605 | ARHGAP31 | c.2289A= (p.Ala763=) c.2196A= (p.Ala732=) c.2229A= (p.Ala743=) c.1797A= (p.Ala599=) | |
3 | g.119414218A>C | CA435411721 | ARHGAP31 | c.2289A>C (p.Ala763=) c.2196A>C (p.Ala732=) c.2229A>C (p.Ala743=) c.1797A>C (p.Ala599=) | |
3 | g.119414218A>G | CA435411720 | ARHGAP31 | c.2289A>G (p.Ala763=) c.2196A>G (p.Ala732=) c.2229A>G (p.Ala743=) c.1797A>G (p.Ala599=) | |
3 | g.119414218A>T | CA435411719 | ARHGAP31 | c.2289A>T (p.Ala763=) c.2196A>T (p.Ala732=) c.2229A>T (p.Ala743=) c.1797A>T (p.Ala599=) | dbSNP gnomAD v3 gnomAD v4 |
3 | g.119414219T>A | CA354050345 | ARHGAP31 | c.2290T>A (p.Ser764Thr) c.2197T>A (p.Ser733Thr) c.2230T>A (p.Ser744Thr) c.1798T>A (p.Ser600Thr) | |
3 | g.119414219T>C | CA354050346 | ARHGAP31 | c.2290T>C (p.Ser764Pro) c.2197T>C (p.Ser733Pro) c.2230T>C (p.Ser744Pro) c.1798T>C (p.Ser600Pro) | |
3 | g.119414219T>G | CA354050344 | ARHGAP31 | c.2290T>G (p.Ser764Ala) c.2197T>G (p.Ser733Ala) c.2230T>G (p.Ser744Ala) c.1798T>G (p.Ser600Ala) | |
3 | g.119414220C>A | CA354050347 | ARHGAP31 | c.2291C>A (p.Ser764Tyr) c.2198C>A (p.Ser733Tyr) c.2231C>A (p.Ser744Tyr) c.1799C>A (p.Ser600Tyr) | |
3 | g.119414220C>G | CA354050349 | ARHGAP31 | c.2291C>G (p.Ser764Cys) c.2198C>G (p.Ser733Cys) c.2231C>G (p.Ser744Cys) c.1799C>G (p.Ser600Cys) | |
3 | g.119414220C>T | CA354050352 | ARHGAP31 | c.2291C>T (p.Ser764Phe) c.2198C>T (p.Ser733Phe) c.2231C>T (p.Ser744Phe) c.1799C>T (p.Ser600Phe) | |
3 | g.119414221T>A | CA435411723 | ARHGAP31 | c.2292T>A (p.Ser764=) c.2199T>A (p.Ser733=) c.2232T>A (p.Ser744=) c.1800T>A (p.Ser600=) | |
3 | g.119414221T>C | CA2554001 | ARHGAP31 | c.2292T>C (p.Ser764=) c.2199T>C (p.Ser733=) c.2232T>C (p.Ser744=) c.1800T>C (p.Ser600=) | dbSNP ExAC gnomAD v4 |
3 | g.119414221T>G | CA435411724 | ARHGAP31 | c.2292T>G (p.Ser764=) c.2199T>G (p.Ser733=) c.2232T>G (p.Ser744=) c.1800T>G (p.Ser600=) | |
3 | g.119414221T= | CA1396548606 | ARHGAP31 | c.2292T= (p.Ser764=) c.2199T= (p.Ser733=) c.2232T= (p.Ser744=) c.1800T= (p.Ser600=) | |
3 | g.119414222C>A | CA354050357 | ARHGAP31 | c.2293C>A (p.Pro765Thr) c.2200C>A (p.Pro734Thr) c.2233C>A (p.Pro745Thr) c.1801C>A (p.Pro601Thr) | |
3 | g.119414222C>G | CA354050358 | ARHGAP31 | c.2293C>G (p.Pro765Ala) c.2200C>G (p.Pro734Ala) c.2233C>G (p.Pro745Ala) c.1801C>G (p.Pro601Ala) | dbSNP |
3 | g.119414222C>T | CA354050360 | ARHGAP31 | c.2293C>T (p.Pro765Ser) c.2200C>T (p.Pro734Ser) c.2233C>T (p.Pro745Ser) c.1801C>T (p.Pro601Ser) | gnomAD v4 |
3 | g.119414223C>A | CA354050363 | ARHGAP31 | c.2294C>A (p.Pro765Gln) c.2201C>A (p.Pro734Gln) c.2234C>A (p.Pro745Gln) c.1802C>A (p.Pro601Gln) | |
3 | g.119414223C>G | CA354050366 | ARHGAP31 | c.2294C>G (p.Pro765Arg) c.2201C>G (p.Pro734Arg) c.2234C>G (p.Pro745Arg) c.1802C>G (p.Pro601Arg) | |
3 | g.119414223C>T | CA354050368 | ARHGAP31 | c.2294C>T (p.Pro765Leu) c.2201C>T (p.Pro734Leu) c.2234C>T (p.Pro745Leu) c.1802C>T (p.Pro601Leu) | gnomAD v4 |
3 | g.119414224A>C | CA435411725 | ARHGAP31 | c.2295A>C (p.Pro765=) c.2202A>C (p.Pro734=) c.2235A>C (p.Pro745=) c.1803A>C (p.Pro601=) | |
3 | g.119414224A>G | CA435411726 | ARHGAP31 | c.2295A>G (p.Pro765=) c.2202A>G (p.Pro734=) c.2235A>G (p.Pro745=) c.1803A>G (p.Pro601=) | |
3 | g.119414224A>T | CA435411727 | ARHGAP31 | c.2295A>T (p.Pro765=) c.2202A>T (p.Pro734=) c.2235A>T (p.Pro745=) c.1803A>T (p.Pro601=) | |
3 | g.119414225C>A | CA354050370 | ARHGAP31 | c.2296C>A (p.Gln766Lys) c.2203C>A (p.Gln735Lys) c.2236C>A (p.Gln746Lys) c.1804C>A (p.Gln602Lys) | dbSNP gnomAD v3 gnomAD v4 |
3 | g.119414225C= | CA1396548607 | ARHGAP31 | c.2296C= (p.Gln766=) c.2203C= (p.Gln735=) c.2236C= (p.Gln746=) c.1804C= (p.Gln602=) | |
3 | g.119414225C>G | CA354050375 | ARHGAP31 | c.2296C>G (p.Gln766Glu) c.2203C>G (p.Gln735Glu) c.2236C>G (p.Gln746Glu) c.1804C>G (p.Gln602Glu) | gnomAD v4 |
3 | g.119414225C>T | CA354050378 | ARHGAP31 | c.2296C>T (p.Gln766Ter) c.2203C>T (p.Gln735Ter) c.2236C>T (p.Gln746Ter) c.1804C>T (p.Gln602Ter) | |
3 | g.119414226A>C | CA354050389 | ARHGAP31 | c.2297A>C (p.Gln766Pro) c.2204A>C (p.Gln735Pro) c.2237A>C (p.Gln746Pro) c.1805A>C (p.Gln602Pro) | |
3 | g.119414226A>G | CA354050383 | ARHGAP31 | c.2297A>G (p.Gln766Arg) c.2204A>G (p.Gln735Arg) c.2237A>G (p.Gln746Arg) c.1805A>G (p.Gln602Arg) | |
3 | g.119414226A>T | CA354050381 | ARHGAP31 | c.2297A>T (p.Gln766Leu) c.2204A>T (p.Gln735Leu) c.2237A>T (p.Gln746Leu) c.1805A>T (p.Gln602Leu) | |
3 | g.119414227A>C | CA354050391 | ARHGAP31 | c.2298A>C (p.Gln766His) c.2205A>C (p.Gln735His) c.2238A>C (p.Gln746His) c.1806A>C (p.Gln602His) | |
3 | g.119414227A>G | CA435411729 | ARHGAP31 | c.2298A>G (p.Gln766=) c.2205A>G (p.Gln735=) c.2238A>G (p.Gln746=) c.1806A>G (p.Gln602=) | |
3 | g.119414227A>T | CA354050393 | ARHGAP31 | c.2298A>T (p.Gln766His) c.2205A>T (p.Gln735His) c.2238A>T (p.Gln746His) c.1806A>T (p.Gln602His) | |
3 | g.119414228G>A | CA354050398 | ARHGAP31 | c.2299G>A (p.Ala767Thr) c.2206G>A (p.Ala736Thr) c.2239G>A (p.Ala747Thr) c.1807G>A (p.Ala603Thr) | dbSNP gnomAD v4 |
3 | g.119414228G>C | CA354050399 | ARHGAP31 | c.2299G>C (p.Ala767Pro) c.2206G>C (p.Ala736Pro) c.2239G>C (p.Ala747Pro) c.1807G>C (p.Ala603Pro) | |
3 | g.119414228G= | CA1396548608 | ARHGAP31 | c.2299G= (p.Ala767=) c.2206G= (p.Ala736=) c.2239G= (p.Ala747=) c.1807G= (p.Ala603=) | |
3 | g.119414228G>T | CA354050402 | ARHGAP31 | c.2299G>T (p.Ala767Ser) c.2206G>T (p.Ala736Ser) c.2239G>T (p.Ala747Ser) c.1807G>T (p.Ala603Ser) | |
3 | g.119414229C>A | CA354050405 | ARHGAP31 | c.2300C>A (p.Ala767Glu) c.2207C>A (p.Ala736Glu) c.2240C>A (p.Ala747Glu) c.1808C>A (p.Ala603Glu) | |
3 | g.119414229C>G | CA354050407 | ARHGAP31 | c.2300C>G (p.Ala767Gly) c.2207C>G (p.Ala736Gly) c.2240C>G (p.Ala747Gly) c.1808C>G (p.Ala603Gly) | |
3 | g.119414229C>T | CA354050408 | ARHGAP31 | c.2300C>T (p.Ala767Val) c.2207C>T (p.Ala736Val) c.2240C>T (p.Ala747Val) c.1808C>T (p.Ala603Val) | |
3 | g.119414230A>C | CA435411732 | ARHGAP31 | c.2301A>C (p.Ala767=) c.2208A>C (p.Ala736=) c.2241A>C (p.Ala747=) c.1809A>C (p.Ala603=) | |
3 | g.119414230A>G | CA435411733 | ARHGAP31 | c.2301A>G (p.Ala767=) c.2208A>G (p.Ala736=) c.2241A>G (p.Ala747=) c.1809A>G (p.Ala603=) | |
3 | g.119414230A>T | CA435411734 | ARHGAP31 | c.2301A>T (p.Ala767=) c.2208A>T (p.Ala736=) c.2241A>T (p.Ala747=) c.1809A>T (p.Ala603=) | |
3 | g.119414231A= | CA1396548609 | ARHGAP31 | c.2302A= (p.Thr768=) c.2209A= (p.Thr737=) c.2242A= (p.Thr748=) c.1810A= (p.Thr604=) | |
3 | g.119414231A>C | CA354050410 | ARHGAP31 | c.2302A>C (p.Thr768Pro) c.2209A>C (p.Thr737Pro) c.2242A>C (p.Thr748Pro) c.1810A>C (p.Thr604Pro) | |
3 | g.119414231A>G | CA354050413 | ARHGAP31 | c.2302A>G (p.Thr768Ala) c.2209A>G (p.Thr737Ala) c.2242A>G (p.Thr748Ala) c.1810A>G (p.Thr604Ala) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
3 | g.119414231A>T | CA354050415 | ARHGAP31 | c.2302A>T (p.Thr768Ser) c.2209A>T (p.Thr737Ser) c.2242A>T (p.Thr748Ser) c.1810A>T (p.Thr604Ser) | |
3 | g.119414232C>A | CA354050418 | ARHGAP31 | c.2303C>A (p.Thr768Lys) c.2210C>A (p.Thr737Lys) c.2243C>A (p.Thr748Lys) c.1811C>A (p.Thr604Lys) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.119414232C= | CA1396548610 | ARHGAP31 | c.2303C= (p.Thr768=) c.2210C= (p.Thr737=) c.2243C= (p.Thr748=) c.1811C= (p.Thr604=) | |
3 | g.119414232C>G | CA354050419 | ARHGAP31 | c.2303C>G (p.Thr768Arg) c.2210C>G (p.Thr737Arg) c.2243C>G (p.Thr748Arg) c.1811C>G (p.Thr604Arg) | |
3 | g.119414232C>T | CA354050421 | ARHGAP31 | c.2303C>T (p.Thr768Ile) c.2210C>T (p.Thr737Ile) c.2243C>T (p.Thr748Ile) c.1811C>T (p.Thr604Ile) | |
3 | g.119414233A>C | CA435411737 | ARHGAP31 | c.2304A>C (p.Thr768=) c.2211A>C (p.Thr737=) c.2244A>C (p.Thr748=) c.1812A>C (p.Thr604=) | |
3 | g.119414233A>G | CA435411739 | ARHGAP31 | c.2304A>G (p.Thr768=) c.2211A>G (p.Thr737=) c.2244A>G (p.Thr748=) c.1812A>G (p.Thr604=) | gnomAD v4 |
3 | g.119414233A>T | CA435411740 | ARHGAP31 | c.2304A>T (p.Thr768=) c.2211A>T (p.Thr737=) c.2244A>T (p.Thr748=) c.1812A>T (p.Thr604=) | |
3 | g.119414234G>A | CA354050427 | ARHGAP31 | c.2305G>A (p.Val769Met) c.2212G>A (p.Val738Met) c.2245G>A (p.Val749Met) c.1813G>A (p.Val605Met) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.119414234G>C | CA354050430 | ARHGAP31 | c.2305G>C (p.Val769Leu) c.2212G>C (p.Val738Leu) c.2245G>C (p.Val749Leu) c.1813G>C (p.Val605Leu) | |
3 | g.119414234G= | CA1396548611 | ARHGAP31 | c.2305G= (p.Val769=) c.2212G= (p.Val738=) c.2245G= (p.Val749=) c.1813G= (p.Val605=) | |
3 | g.119414234G>T | CA354050424 | ARHGAP31 | c.2305G>T (p.Val769Leu) c.2212G>T (p.Val738Leu) c.2245G>T (p.Val749Leu) c.1813G>T (p.Val605Leu) | |
3 | g.119414235T>A | CA354050433 | ARHGAP31 | c.2306T>A (p.Val769Glu) c.2213T>A (p.Val738Glu) c.2246T>A (p.Val749Glu) c.1814T>A (p.Val605Glu) | |
3 | g.119414235T>C | CA2554002 | ARHGAP31 | c.2306T>C (p.Val769Ala) c.2213T>C (p.Val738Ala) c.2246T>C (p.Val749Ala) c.1814T>C (p.Val605Ala) | dbSNP ExAC gnomAD v2 gnomAD v4 |
3 | g.119414235T>G | CA354050436 | ARHGAP31 | c.2306T>G (p.Val769Gly) c.2213T>G (p.Val738Gly) c.2246T>G (p.Val749Gly) c.1814T>G (p.Val605Gly) | |
3 | g.119414235T= | CA1396548612 | ARHGAP31 | c.2306T= (p.Val769=) c.2213T= (p.Val738=) c.2246T= (p.Val749=) c.1814T= (p.Val605=) | |
3 | g.119414236G>A | CA435411744 | ARHGAP31 | c.2307G>A (p.Val769=) c.2214G>A (p.Val738=) c.2247G>A (p.Val749=) c.1815G>A (p.Val605=) | dbSNP gnomAD v4 |
3 | g.119414236G>C | CA435411743 | ARHGAP31 | c.2307G>C (p.Val769=) c.2214G>C (p.Val738=) c.2247G>C (p.Val749=) c.1815G>C (p.Val605=) | gnomAD v4 |
3 | g.119414236G= | CA1396548613 | ARHGAP31 | c.2307G= (p.Val769=) c.2214G= (p.Val738=) c.2247G= (p.Val749=) c.1815G= (p.Val605=) | |
3 | g.119414236G>T | CA435411742 | ARHGAP31 | c.2307G>T (p.Val769=) c.2214G>T (p.Val738=) c.2247G>T (p.Val749=) c.1815G>T (p.Val605=) | |
3 | g.119414237G>A | CA354050437 | ARHGAP31 | c.2308G>A (p.Glu770Lys) c.2215G>A (p.Glu739Lys) c.2248G>A (p.Glu750Lys) c.1816G>A (p.Glu606Lys) | |
3 | g.119414237G>C | CA354050438 | ARHGAP31 | c.2308G>C (p.Glu770Gln) c.2215G>C (p.Glu739Gln) c.2248G>C (p.Glu750Gln) c.1816G>C (p.Glu606Gln) | |
3 | g.119414237G>T | CA354050440 | ARHGAP31 | c.2308G>T (p.Glu770Ter) c.2215G>T (p.Glu739Ter) c.2248G>T (p.Glu750Ter) c.1816G>T (p.Glu606Ter) | |
3 | g.119414238A>C | CA354050450 | ARHGAP31 | c.2309A>C (p.Glu770Ala) c.2216A>C (p.Glu739Ala) c.2249A>C (p.Glu750Ala) c.1817A>C (p.Glu606Ala) | |
3 | g.119414238A>G | CA354050442 | ARHGAP31 | c.2309A>G (p.Glu770Gly) c.2216A>G (p.Glu739Gly) c.2249A>G (p.Glu750Gly) c.1817A>G (p.Glu606Gly) | |
3 | g.119414238A>T | CA354050447 | ARHGAP31 | c.2309A>T (p.Glu770Val) c.2216A>T (p.Glu739Val) c.2249A>T (p.Glu750Val) c.1817A>T (p.Glu606Val) | |
3 | g.119414239A>C | CA354050452 | ARHGAP31 | c.2310A>C (p.Glu770Asp) c.2217A>C (p.Glu739Asp) c.2250A>C (p.Glu750Asp) c.1818A>C (p.Glu606Asp) | |
3 | g.119414239A>G | CA435411749 | ARHGAP31 | c.2310A>G (p.Glu770=) c.2217A>G (p.Glu739=) c.2250A>G (p.Glu750=) c.1818A>G (p.Glu606=) | |
3 | g.119414239A>T | CA354050456 | ARHGAP31 | c.2310A>T (p.Glu770Asp) c.2217A>T (p.Glu739Asp) c.2250A>T (p.Glu750Asp) c.1818A>T (p.Glu606Asp) | |
3 | g.119414240G>A | CA354050458 | ARHGAP31 | c.2311G>A (p.Val771Ile) c.2218G>A (p.Val740Ile) c.2251G>A (p.Val751Ile) c.1819G>A (p.Val607Ile) | |
3 | g.119414240G>C | CA354050460 | ARHGAP31 | c.2311G>C (p.Val771Leu) c.2218G>C (p.Val740Leu) c.2251G>C (p.Val751Leu) c.1819G>C (p.Val607Leu) | |
3 | g.119414240G>T | CA354050462 | ARHGAP31 | c.2311G>T (p.Val771Leu) c.2218G>T (p.Val740Leu) c.2251G>T (p.Val751Leu) c.1819G>T (p.Val607Leu) | |
3 | g.119414241T>A | CA354050466 | ARHGAP31 | c.2312T>A (p.Val771Glu) c.2219T>A (p.Val740Glu) c.2252T>A (p.Val751Glu) c.1820T>A (p.Val607Glu) | |
3 | g.119414241T>C | CA2554003 | ARHGAP31 | c.2312T>C (p.Val771Ala) c.2219T>C (p.Val740Ala) c.2252T>C (p.Val751Ala) c.1820T>C (p.Val607Ala) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.119414241T>G | CA354050469 | ARHGAP31 | c.2312T>G (p.Val771Gly) c.2219T>G (p.Val740Gly) c.2252T>G (p.Val751Gly) c.1820T>G (p.Val607Gly) | |
3 | g.119414241T= | CA1396548614 | ARHGAP31 | c.2312T= (p.Val771=) c.2219T= (p.Val740=) c.2252T= (p.Val751=) c.1820T= (p.Val607=) | |
3 | g.119414242A= | CA1396548615 | ARHGAP31 | c.2313A= (p.Val771=) c.2220A= (p.Val740=) c.2253A= (p.Val751=) c.1821A= (p.Val607=) | |
3 | g.119414242A>C | CA2554004 | ARHGAP31 | c.2313A>C (p.Val771=) c.2220A>C (p.Val740=) c.2253A>C (p.Val751=) c.1821A>C (p.Val607=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.119414242A>G | CA435411753 | ARHGAP31 | c.2313A>G (p.Val771=) c.2220A>G (p.Val740=) c.2253A>G (p.Val751=) c.1821A>G (p.Val607=) | |
3 | g.119414242A>T | CA435411755 | ARHGAP31 | c.2313A>T (p.Val771=) c.2220A>T (p.Val740=) c.2253A>T (p.Val751=) c.1821A>T (p.Val607=) | |
3 | g.119414243G>A | CA2554005 | ARHGAP31 | c.2314G>A (p.Gly772Arg) c.2221G>A (p.Gly741Arg) c.2254G>A (p.Gly752Arg) c.1822G>A (p.Gly608Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.119414243G>C | CA354050479 | ARHGAP31 | c.2314G>C (p.Gly772Arg) c.2221G>C (p.Gly741Arg) c.2254G>C (p.Gly752Arg) c.1822G>C (p.Gly608Arg) | |
3 | g.119414243G= | CA1396548616 | ARHGAP31 | c.2314G= (p.Gly772=) c.2221G= (p.Gly741=) c.2254G= (p.Gly752=) c.1822G= (p.Gly608=) | |
3 | g.119414243G>T | CA354050482 | ARHGAP31 | c.2314G>T (p.Gly772Ter) c.2221G>T (p.Gly741Ter) c.2254G>T (p.Gly752Ter) c.1822G>T (p.Gly608Ter) | |
3 | g.119414244G>A | CA2554006 | ARHGAP31 | c.2315G>A (p.Gly772Glu) c.2222G>A (p.Gly741Glu) c.2255G>A (p.Gly752Glu) c.1823G>A (p.Gly608Glu) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.119414244G>C | CA354050492 | ARHGAP31 | c.2315G>C (p.Gly772Ala) c.2222G>C (p.Gly741Ala) c.2255G>C (p.Gly752Ala) c.1823G>C (p.Gly608Ala) | |
3 | g.119414244G= | CA1396548617 | ARHGAP31 | c.2315G= (p.Gly772=) c.2222G= (p.Gly741=) c.2255G= (p.Gly752=) c.1823G= (p.Gly608=) | |
3 | g.119414244G>T | CA354050494 | ARHGAP31 | c.2315G>T (p.Gly772Val) c.2222G>T (p.Gly741Val) c.2255G>T (p.Gly752Val) c.1823G>T (p.Gly608Val) | |
3 | g.119414245A>C | CA435411758 | ARHGAP31 | c.2316A>C (p.Gly772=) c.2223A>C (p.Gly741=) c.2256A>C (p.Gly752=) c.1824A>C (p.Gly608=) | gnomAD v4 |
3 | g.119414245A>G | CA435411759 | ARHGAP31 | c.2316A>G (p.Gly772=) c.2223A>G (p.Gly741=) c.2256A>G (p.Gly752=) c.1824A>G (p.Gly608=) | |
3 | g.119414245A>T | CA435411761 | ARHGAP31 | c.2316A>T (p.Gly772=) c.2223A>T (p.Gly741=) c.2256A>T (p.Gly752=) c.1824A>T (p.Gly608=) | |
3 | g.119414246G>A | CA354050498 | ARHGAP31 | c.2317G>A (p.Gly773Ser) c.2224G>A (p.Gly742Ser) c.2257G>A (p.Gly753Ser) c.1825G>A (p.Gly609Ser) | |
3 | g.119414246G>C | CA354050499 | ARHGAP31 | c.2317G>C (p.Gly773Arg) c.2224G>C (p.Gly742Arg) c.2257G>C (p.Gly753Arg) c.1825G>C (p.Gly609Arg) | |
3 | g.119414246G>T | CA354050505 | ARHGAP31 | c.2317G>T (p.Gly773Cys) c.2224G>T (p.Gly742Cys) c.2257G>T (p.Gly753Cys) c.1825G>T (p.Gly609Cys) | |
3 | g.119414247G>A | CA354050512 | ARHGAP31 | c.2318G>A (p.Gly773Asp) c.2225G>A (p.Gly742Asp) c.2258G>A (p.Gly753Asp) c.1826G>A (p.Gly609Asp) | gnomAD v4 |
3 | g.119414247G>C | CA354050511 | ARHGAP31 | c.2318G>C (p.Gly773Ala) c.2225G>C (p.Gly742Ala) c.2258G>C (p.Gly753Ala) c.1826G>C (p.Gly609Ala) | |
3 | g.119414247G= | CA1396548618 | ARHGAP31 | c.2318G= (p.Gly773=) c.2225G= (p.Gly742=) c.2258G= (p.Gly753=) c.1826G= (p.Gly609=) | |
3 | g.119414247G>T | CA2554007 | ARHGAP31 | c.2318G>T (p.Gly773Val) c.2225G>T (p.Gly742Val) c.2258G>T (p.Gly753Val) c.1826G>T (p.Gly609Val) | dbSNP ExAC gnomAD v2 |
3 | g.119414248C>A | CA435411767 | ARHGAP31 | c.2319C>A (p.Gly773=) c.2226C>A (p.Gly742=) c.2259C>A (p.Gly753=) c.1827C>A (p.Gly609=) | |
3 | g.119414248C>G | CA435411765 | ARHGAP31 | c.2319C>G (p.Gly773=) c.2226C>G (p.Gly742=) c.2259C>G (p.Gly753=) c.1827C>G (p.Gly609=) | |
3 | g.119414248C>T | CA435411766 | ARHGAP31 | c.2319C>T (p.Gly773=) c.2226C>T (p.Gly742=) c.2259C>T (p.Gly753=) c.1827C>T (p.Gly609=) | |
3 | g.119414249C>A | CA354050513 | ARHGAP31 | c.2320C>A (p.Pro774Thr) c.2227C>A (p.Pro743Thr) c.2260C>A (p.Pro754Thr) c.1828C>A (p.Pro610Thr) | |
3 | g.119414249C>G | CA354050518 | ARHGAP31 | c.2320C>G (p.Pro774Ala) c.2227C>G (p.Pro743Ala) c.2260C>G (p.Pro754Ala) c.1828C>G (p.Pro610Ala) | |
3 | g.119414249C>T | CA354050515 | ARHGAP31 | c.2320C>T (p.Pro774Ser) c.2227C>T (p.Pro743Ser) c.2260C>T (p.Pro754Ser) c.1828C>T (p.Pro610Ser) | |
3 | g.119414250C>A | CA354050521 | ARHGAP31 | c.2321C>A (p.Pro774Gln) c.2228C>A (p.Pro743Gln) c.2261C>A (p.Pro754Gln) c.1829C>A (p.Pro610Gln) | |
3 | g.119414250C>G | CA354050531 | ARHGAP31 | c.2321C>G (p.Pro774Arg) c.2228C>G (p.Pro743Arg) c.2261C>G (p.Pro754Arg) c.1829C>G (p.Pro610Arg) | |
3 | g.119414250C>T | CA354050528 | ARHGAP31 | c.2321C>T (p.Pro774Leu) c.2228C>T (p.Pro743Leu) c.2261C>T (p.Pro754Leu) c.1829C>T (p.Pro610Leu) | |
3 | g.119414251A= | CA1396548619 | ARHGAP31 | c.2322A= (p.Pro774=) c.2229A= (p.Pro743=) c.2262A= (p.Pro754=) c.1830A= (p.Pro610=) | |
3 | g.119414251A>C | CA435411769 | ARHGAP31 | c.2322A>C (p.Pro774=) c.2229A>C (p.Pro743=) c.2262A>C (p.Pro754=) c.1830A>C (p.Pro610=) | |
3 | g.119414251A>G | CA81697519 | ARHGAP31 | c.2322A>G (p.Pro774=) c.2229A>G (p.Pro743=) c.2262A>G (p.Pro754=) c.1830A>G (p.Pro610=) | dbSNP gnomAD v2 gnomAD v4 |
3 | g.119414251A>T | CA435411770 | ARHGAP31 | c.2322A>T (p.Pro774=) c.2229A>T (p.Pro743=) c.2262A>T (p.Pro754=) c.1830A>T (p.Pro610=) | |
3 | g.119414252G>A | CA2554008 | ARHGAP31 | c.2323G>A (p.Gly775Ser) c.2230G>A (p.Gly744Ser) c.2263G>A (p.Gly755Ser) c.1831G>A (p.Gly611Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.119414252G>C | CA354050535 | ARHGAP31 | c.2323G>C (p.Gly775Arg) c.2230G>C (p.Gly744Arg) c.2263G>C (p.Gly755Arg) c.1831G>C (p.Gly611Arg) | |
3 | g.119414252G= | CA1396548620 | ARHGAP31 | c.2323G= (p.Gly775=) c.2230G= (p.Gly744=) c.2263G= (p.Gly755=) c.1831G= (p.Gly611=) | |
3 | g.119414252G>T | CA354050538 | ARHGAP31 | c.2323G>T (p.Gly775Cys) c.2230G>T (p.Gly744Cys) c.2263G>T (p.Gly755Cys) c.1831G>T (p.Gly611Cys) | |
3 | g.119414253G>A | CA354050542 | ARHGAP31 | c.2324G>A (p.Gly775Asp) c.2231G>A (p.Gly744Asp) c.2264G>A (p.Gly755Asp) c.1832G>A (p.Gly611Asp) | |
3 | g.119414253G>C | CA354050545 | ARHGAP31 | c.2324G>C (p.Gly775Ala) c.2231G>C (p.Gly744Ala) c.2264G>C (p.Gly755Ala) c.1832G>C (p.Gly611Ala) | |
3 | g.119414253G>T | CA354050547 | ARHGAP31 | c.2324G>T (p.Gly775Val) c.2231G>T (p.Gly744Val) c.2264G>T (p.Gly755Val) c.1832G>T (p.Gly611Val) | |
3 | g.119414254C>A | CA435411773 | ARHGAP31 | c.2325C>A (p.Gly775=) c.2232C>A (p.Gly744=) c.2265C>A (p.Gly755=) c.1833C>A (p.Gly611=) | |
3 | g.119414254C>G | CA435411774 | ARHGAP31 | c.2325C>G (p.Gly775=) c.2232C>G (p.Gly744=) c.2265C>G (p.Gly755=) c.1833C>G (p.Gly611=) | dbSNP |
3 | g.119414254C>T | CA435411775 | ARHGAP31 | c.2325C>T (p.Gly775=) c.2232C>T (p.Gly744=) c.2265C>T (p.Gly755=) c.1833C>T (p.Gly611=) | gnomAD v4 |
3 | g.119414255A>C | CA354050550 | ARHGAP31 | c.2326A>C (p.Asn776His) c.2233A>C (p.Asn745His) c.2266A>C (p.Asn756His) c.1834A>C (p.Asn612His) | gnomAD v4 |
3 | g.119414255A>G | CA354050552 | ARHGAP31 | c.2326A>G (p.Asn776Asp) c.2233A>G (p.Asn745Asp) c.2266A>G (p.Asn756Asp) c.1834A>G (p.Asn612Asp) | |
3 | g.119414255A>T | CA354050556 | ARHGAP31 | c.2326A>T (p.Asn776Tyr) c.2233A>T (p.Asn745Tyr) c.2266A>T (p.Asn756Tyr) c.1834A>T (p.Asn612Tyr) | |
3 | g.119414256A>C | CA354050558 | ARHGAP31 | c.2327A>C (p.Asn776Thr) c.2234A>C (p.Asn745Thr) c.2267A>C (p.Asn756Thr) c.1835A>C (p.Asn612Thr) | COSMIC |
3 | g.119414256A>G | CA354050560 | ARHGAP31 | c.2327A>G (p.Asn776Ser) c.2234A>G (p.Asn745Ser) c.2267A>G (p.Asn756Ser) c.1835A>G (p.Asn612Ser) | |
3 | g.119414256A>T | CA354050565 | ARHGAP31 | c.2327A>T (p.Asn776Ile) c.2234A>T (p.Asn745Ile) c.2267A>T (p.Asn756Ile) c.1835A>T (p.Asn612Ile) | |
3 | g.119414257T>A | CA354050573 | ARHGAP31 | c.2328T>A (p.Asn776Lys) c.2235T>A (p.Asn745Lys) c.2268T>A (p.Asn756Lys) c.1836T>A (p.Asn612Lys) | |
3 | g.119414257T>C | CA435411778 | ARHGAP31 | c.2328T>C (p.Asn776=) c.2235T>C (p.Asn745=) c.2268T>C (p.Asn756=) c.1836T>C (p.Asn612=) | COSMIC |
3 | g.119414257T>G | CA354050570 | ARHGAP31 | c.2328T>G (p.Asn776Lys) c.2235T>G (p.Asn745Lys) c.2268T>G (p.Asn756Lys) c.1836T>G (p.Asn612Lys) | |
3 | g.119414258C>A | CA354050578 | ARHGAP31 | c.2329C>A (p.Leu777Met) c.2236C>A (p.Leu746Met) c.2269C>A (p.Leu757Met) c.1837C>A (p.Leu613Met) | |
3 | g.119414258C>G | CA354050581 | ARHGAP31 | c.2329C>G (p.Leu777Val) c.2236C>G (p.Leu746Val) c.2269C>G (p.Leu757Val) c.1837C>G (p.Leu613Val) | |
3 | g.119414258C>T | CA435411782 | ARHGAP31 | c.2329C>T (p.Leu777=) c.2236C>T (p.Leu746=) c.2269C>T (p.Leu757=) c.1837C>T (p.Leu613=) | gnomAD v4 |
3 | g.119414259T>A | CA354050584 | ARHGAP31 | c.2330T>A (p.Leu777Gln) c.2237T>A (p.Leu746Gln) c.2270T>A (p.Leu757Gln) c.1838T>A (p.Leu613Gln) | |
3 | g.119414259T>C | CA2554009 | ARHGAP31 | c.2330T>C (p.Leu777Pro) c.2237T>C (p.Leu746Pro) c.2270T>C (p.Leu757Pro) c.1838T>C (p.Leu613Pro) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.119414259T>G | CA354050587 | ARHGAP31 | c.2330T>G (p.Leu777Arg) c.2237T>G (p.Leu746Arg) c.2270T>G (p.Leu757Arg) c.1838T>G (p.Leu613Arg) | |
3 | g.119414259T= | CA1396548621 | ARHGAP31 | c.2330T= (p.Leu777=) c.2237T= (p.Leu746=) c.2270T= (p.Leu757=) c.1838T= (p.Leu613=) | |
3 | g.119414260G>A | CA435411786 | ARHGAP31 | c.2331G>A (p.Leu777=) c.2238G>A (p.Leu746=) c.2271G>A (p.Leu757=) c.1839G>A (p.Leu613=) | gnomAD v4 |
3 | g.119414260G>C | CA435411787 | ARHGAP31 | c.2331G>C (p.Leu777=) c.2238G>C (p.Leu746=) c.2271G>C (p.Leu757=) c.1839G>C (p.Leu613=) | |
3 | g.119414260G>T | CA435411788 | ARHGAP31 | c.2331G>T (p.Leu777=) c.2238G>T (p.Leu746=) c.2271G>T (p.Leu757=) c.1839G>T (p.Leu613=) | |
3 | g.119414261T>A | CA354050592 | ARHGAP31 | c.2332T>A (p.Ser778Thr) c.2239T>A (p.Ser747Thr) c.2272T>A (p.Ser758Thr) c.1840T>A (p.Ser614Thr) | |
3 | g.119414261T>C | CA354050595 | ARHGAP31 | c.2332T>C (p.Ser778Pro) c.2239T>C (p.Ser747Pro) c.2272T>C (p.Ser758Pro) c.1840T>C (p.Ser614Pro) | |
3 | g.119414261T>G | CA354050597 | ARHGAP31 | c.2332T>G (p.Ser778Ala) c.2239T>G (p.Ser747Ala) c.2272T>G (p.Ser758Ala) c.1840T>G (p.Ser614Ala) | |
3 | g.119414261_119414264delinsTCTC | CA1396548622 | ARHGAP31 | c.2332_2335delinsTCTC (p.Ser778=) c.2239_2242delinsTCTC (p.Ser747=) c.2272_2275delinsTCTC (p.Ser758=) c.1840_1843delinsTCTC (p.Ser614=) |