Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
5 | g.56881730T>A | CA359785996 | MAP3K1 | c.2530T>A (p.Ser844Thr) c.2152T>A (p.Ser718Thr) c.2275T>A (p.Ser759Thr) c.2251T>A (p.Ser751Thr) c.2119T>A (p.Ser707Thr) c.2041T>A (p.Ser681Thr) n.2561T>A | |
5 | g.56881730T>C | CA359785997 | MAP3K1 | c.2530T>C (p.Ser844Pro) c.2152T>C (p.Ser718Pro) c.2275T>C (p.Ser759Pro) c.2251T>C (p.Ser751Pro) c.2119T>C (p.Ser707Pro) c.2041T>C (p.Ser681Pro) n.2561T>C | |
5 | g.56881730T>G | CA359785998 | MAP3K1 | c.2530T>G (p.Ser844Ala) c.2152T>G (p.Ser718Ala) c.2275T>G (p.Ser759Ala) c.2251T>G (p.Ser751Ala) c.2119T>G (p.Ser707Ala) c.2041T>G (p.Ser681Ala) n.2561T>G | dbSNP gnomAD v4 |
5 | g.56881730T= | CA1548139275 | MAP3K1 | c.2530T= (p.Ser844=) c.2152T= (p.Ser718=) c.2275T= (p.Ser759=) c.2251T= (p.Ser751=) c.2119T= (p.Ser707=) c.2041T= (p.Ser681=) n.2561T= | |
5 | g.56881731C>A | CA359786001 | MAP3K1 | c.2531C>A (p.Ser844Tyr) c.2153C>A (p.Ser718Tyr) c.2276C>A (p.Ser759Tyr) c.2252C>A (p.Ser751Tyr) c.2120C>A (p.Ser707Tyr) c.2042C>A (p.Ser681Tyr) n.2562C>A | gnomAD v4 |
5 | g.56881731C>G | CA359786000 | MAP3K1 | c.2531C>G (p.Ser844Cys) c.2153C>G (p.Ser718Cys) c.2276C>G (p.Ser759Cys) c.2252C>G (p.Ser751Cys) c.2120C>G (p.Ser707Cys) c.2042C>G (p.Ser681Cys) n.2562C>G | gnomAD v4 |
5 | g.56881731C>T | CA359785999 | MAP3K1 | c.2531C>T (p.Ser844Phe) c.2153C>T (p.Ser718Phe) c.2276C>T (p.Ser759Phe) c.2252C>T (p.Ser751Phe) c.2120C>T (p.Ser707Phe) c.2042C>T (p.Ser681Phe) n.2562C>T | |
5 | g.56881732C>A | CA444399140 | MAP3K1 | c.2532C>A (p.Ser844=) c.2154C>A (p.Ser718=) c.2277C>A (p.Ser759=) c.2253C>A (p.Ser751=) c.2121C>A (p.Ser707=) c.2043C>A (p.Ser681=) n.2563C>A | |
5 | g.56881732C>G | CA444399141 | MAP3K1 | c.2532C>G (p.Ser844=) c.2154C>G (p.Ser718=) c.2277C>G (p.Ser759=) c.2253C>G (p.Ser751=) c.2121C>G (p.Ser707=) c.2043C>G (p.Ser681=) n.2563C>G | |
5 | g.56881732C>T | CA444399142 | MAP3K1 | c.2532C>T (p.Ser844=) c.2154C>T (p.Ser718=) c.2277C>T (p.Ser759=) c.2253C>T (p.Ser751=) c.2121C>T (p.Ser707=) c.2043C>T (p.Ser681=) n.2563C>T | gnomAD v4 |
5 | g.56881733A= | CA1548139276 | MAP3K1 | c.2533A= (p.Ser845=) c.2155A= (p.Ser719=) c.2278A= (p.Ser760=) c.2254A= (p.Ser752=) c.2122A= (p.Ser708=) c.2044A= (p.Ser682=) n.2564A= | |
5 | g.56881733A>C | CA359786002 | MAP3K1 | c.2533A>C (p.Ser845Arg) c.2155A>C (p.Ser719Arg) c.2278A>C (p.Ser760Arg) c.2254A>C (p.Ser752Arg) c.2122A>C (p.Ser708Arg) c.2044A>C (p.Ser682Arg) n.2564A>C | gnomAD v4 |
5 | g.56881733A>G | CA359786003 | MAP3K1 | c.2533A>G (p.Ser845Gly) c.2155A>G (p.Ser719Gly) c.2278A>G (p.Ser760Gly) c.2254A>G (p.Ser752Gly) c.2122A>G (p.Ser708Gly) c.2044A>G (p.Ser682Gly) n.2564A>G | dbSNP gnomAD v3 gnomAD v4 |
5 | g.56881733A>T | CA359786004 | MAP3K1 | c.2533A>T (p.Ser845Cys) c.2155A>T (p.Ser719Cys) c.2278A>T (p.Ser760Cys) c.2254A>T (p.Ser752Cys) c.2122A>T (p.Ser708Cys) c.2044A>T (p.Ser682Cys) n.2564A>T | gnomAD v4 |
5 | g.56881734G>A | CA3273012 | MAP3K1 | c.2534G>A (p.Ser845Asn) c.2156G>A (p.Ser719Asn) c.2279G>A (p.Ser760Asn) c.2255G>A (p.Ser752Asn) c.2123G>A (p.Ser708Asn) c.2045G>A (p.Ser682Asn) n.2565G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.56881734G>C | CA3273013 | MAP3K1 | c.2534G>C (p.Ser845Thr) c.2156G>C (p.Ser719Thr) c.2279G>C (p.Ser760Thr) c.2255G>C (p.Ser752Thr) c.2123G>C (p.Ser708Thr) c.2045G>C (p.Ser682Thr) n.2565G>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
5 | g.56881734G= | CA1548139277 | MAP3K1 | c.2534G= (p.Ser845=) c.2156G= (p.Ser719=) c.2279G= (p.Ser760=) c.2255G= (p.Ser752=) c.2123G= (p.Ser708=) c.2045G= (p.Ser682=) n.2565G= | |
5 | g.56881734G>T | CA359786005 | MAP3K1 | c.2534G>T (p.Ser845Ile) c.2156G>T (p.Ser719Ile) c.2279G>T (p.Ser760Ile) c.2255G>T (p.Ser752Ile) c.2123G>T (p.Ser708Ile) c.2045G>T (p.Ser682Ile) n.2565G>T | dbSNP |
5 | g.56881735T>A | CA359786006 | MAP3K1 | c.2535T>A (p.Ser845Arg) c.2157T>A (p.Ser719Arg) c.2280T>A (p.Ser760Arg) c.2256T>A (p.Ser752Arg) c.2124T>A (p.Ser708Arg) c.2046T>A (p.Ser682Arg) n.2566T>A | |
5 | g.56881735T>C | CA444399143 | MAP3K1 | c.2535T>C (p.Ser845=) c.2157T>C (p.Ser719=) c.2280T>C (p.Ser760=) c.2256T>C (p.Ser752=) c.2124T>C (p.Ser708=) c.2046T>C (p.Ser682=) n.2566T>C | |
5 | g.56881735T>G | CA359786007 | MAP3K1 | c.2535T>G (p.Ser845Arg) c.2157T>G (p.Ser719Arg) c.2280T>G (p.Ser760Arg) c.2256T>G (p.Ser752Arg) c.2124T>G (p.Ser708Arg) c.2046T>G (p.Ser682Arg) n.2566T>G | |
5 | g.56881736T>A | CA359786008 | MAP3K1 | c.2536T>A (p.Ser846Thr) c.2158T>A (p.Ser720Thr) c.2281T>A (p.Ser761Thr) c.2257T>A (p.Ser753Thr) c.2125T>A (p.Ser709Thr) c.2047T>A (p.Ser683Thr) n.2567T>A | |
5 | g.56881736T>C | CA359786009 | MAP3K1 | c.2536T>C (p.Ser846Pro) c.2158T>C (p.Ser720Pro) c.2281T>C (p.Ser761Pro) c.2257T>C (p.Ser753Pro) c.2125T>C (p.Ser709Pro) c.2047T>C (p.Ser683Pro) n.2567T>C | |
5 | g.56881736T>G | CA359786010 | MAP3K1 | c.2536T>G (p.Ser846Ala) c.2158T>G (p.Ser720Ala) c.2281T>G (p.Ser761Ala) c.2257T>G (p.Ser753Ala) c.2125T>G (p.Ser709Ala) c.2047T>G (p.Ser683Ala) n.2567T>G | |
5 | g.56881737C>A | CA359786013 | MAP3K1 | c.2537C>A (p.Ser846Tyr) c.2159C>A (p.Ser720Tyr) c.2282C>A (p.Ser761Tyr) c.2258C>A (p.Ser753Tyr) c.2126C>A (p.Ser709Tyr) c.2048C>A (p.Ser683Tyr) n.2568C>A | dbSNP gnomAD v3 gnomAD v4 |
5 | g.56881737C= | CA1548139278 | MAP3K1 | c.2537C= (p.Ser846=) c.2159C= (p.Ser720=) c.2282C= (p.Ser761=) c.2258C= (p.Ser753=) c.2126C= (p.Ser709=) c.2048C= (p.Ser683=) n.2568C= | |
5 | g.56881737C>G | CA359786012 | MAP3K1 | c.2537C>G (p.Ser846Cys) c.2159C>G (p.Ser720Cys) c.2282C>G (p.Ser761Cys) c.2258C>G (p.Ser753Cys) c.2126C>G (p.Ser709Cys) c.2048C>G (p.Ser683Cys) n.2568C>G | gnomAD v4 |
5 | g.56881737C>T | CA359786011 | MAP3K1 | c.2537C>T (p.Ser846Phe) c.2159C>T (p.Ser720Phe) c.2282C>T (p.Ser761Phe) c.2258C>T (p.Ser753Phe) c.2126C>T (p.Ser709Phe) c.2048C>T (p.Ser683Phe) n.2568C>T | gnomAD v4 |
5 | g.56881738del | CA645557008 | MAP3K1 | c.2538del (p.Thr847LeufsTer10) c.2160del (p.Thr721LeufsTer10) c.2283del (p.Thr762LeufsTer10) c.2259del (p.Thr754LeufsTer10) c.2127del (p.Thr710LeufsTer10) c.2049del (p.Thr684LeufsTer10) n.2569del | COSMIC |
5 | g.56881738C>A | CA444399144 | MAP3K1 | c.2538C>A (p.Ser846=) c.2160C>A (p.Ser720=) c.2283C>A (p.Ser761=) c.2259C>A (p.Ser753=) c.2127C>A (p.Ser709=) c.2049C>A (p.Ser683=) n.2569C>A | |
5 | g.56881738C= | CA1548139279 | MAP3K1 | c.2538C= (p.Ser846=) c.2160C= (p.Ser720=) c.2283C= (p.Ser761=) c.2259C= (p.Ser753=) c.2127C= (p.Ser709=) c.2049C= (p.Ser683=) n.2569C= | |
5 | g.56881738C>G | CA444399145 | MAP3K1 | c.2538C>G (p.Ser846=) c.2160C>G (p.Ser720=) c.2283C>G (p.Ser761=) c.2259C>G (p.Ser753=) c.2127C>G (p.Ser709=) c.2049C>G (p.Ser683=) n.2569C>G | dbSNP |
5 | g.56881738C>T | CA444399146 | MAP3K1 | c.2538C>T (p.Ser846=) c.2160C>T (p.Ser720=) c.2283C>T (p.Ser761=) c.2259C>T (p.Ser753=) c.2127C>T (p.Ser709=) c.2049C>T (p.Ser683=) n.2569C>T | |
5 | g.56881739A>C | CA359786014 | MAP3K1 | c.2539A>C (p.Thr847Pro) c.2161A>C (p.Thr721Pro) c.2284A>C (p.Thr762Pro) c.2260A>C (p.Thr754Pro) c.2128A>C (p.Thr710Pro) c.2050A>C (p.Thr684Pro) n.2570A>C | |
5 | g.56881739A>G | CA359786015 | MAP3K1 | c.2539A>G (p.Thr847Ala) c.2161A>G (p.Thr721Ala) c.2284A>G (p.Thr762Ala) c.2260A>G (p.Thr754Ala) c.2128A>G (p.Thr710Ala) c.2050A>G (p.Thr684Ala) n.2570A>G | ClinVar |
5 | g.56881739A>T | CA359786016 | MAP3K1 | c.2539A>T (p.Thr847Ser) c.2161A>T (p.Thr721Ser) c.2284A>T (p.Thr762Ser) c.2260A>T (p.Thr754Ser) c.2128A>T (p.Thr710Ser) c.2050A>T (p.Thr684Ser) n.2570A>T | |
5 | g.56881740C>A | CA359786017 | MAP3K1 | c.2540C>A (p.Thr847Asn) c.2162C>A (p.Thr721Asn) c.2285C>A (p.Thr762Asn) c.2261C>A (p.Thr754Asn) c.2129C>A (p.Thr710Asn) c.2051C>A (p.Thr684Asn) n.2571C>A | |
5 | g.56881740C>G | CA359786018 | MAP3K1 | c.2540C>G (p.Thr847Ser) c.2162C>G (p.Thr721Ser) c.2285C>G (p.Thr762Ser) c.2261C>G (p.Thr754Ser) c.2129C>G (p.Thr710Ser) c.2051C>G (p.Thr684Ser) n.2571C>G | |
5 | g.56881740C>T | CA359786019 | MAP3K1 | c.2540C>T (p.Thr847Ile) c.2162C>T (p.Thr721Ile) c.2285C>T (p.Thr762Ile) c.2261C>T (p.Thr754Ile) c.2129C>T (p.Thr710Ile) c.2051C>T (p.Thr684Ile) n.2571C>T | dbSNP COSMIC |
5 | g.56881741T>A | CA444399147 | MAP3K1 | c.2541T>A (p.Thr847=) c.2163T>A (p.Thr721=) c.2286T>A (p.Thr762=) c.2262T>A (p.Thr754=) c.2130T>A (p.Thr710=) c.2052T>A (p.Thr684=) n.2572T>A | |
5 | g.56881741T>C | CA444399148 | MAP3K1 | c.2541T>C (p.Thr847=) c.2163T>C (p.Thr721=) c.2286T>C (p.Thr762=) c.2262T>C (p.Thr754=) c.2130T>C (p.Thr710=) c.2052T>C (p.Thr684=) n.2572T>C | |
5 | g.56881741T>G | CA444399149 | MAP3K1 | c.2541T>G (p.Thr847=) c.2163T>G (p.Thr721=) c.2286T>G (p.Thr762=) c.2262T>G (p.Thr754=) c.2130T>G (p.Thr710=) c.2052T>G (p.Thr684=) n.2572T>G | |
5 | g.56881742C>A | CA359786020 | MAP3K1 | c.2542C>A (p.His848Asn) c.2164C>A (p.His722Asn) c.2287C>A (p.His763Asn) c.2263C>A (p.His755Asn) c.2131C>A (p.His711Asn) c.2053C>A (p.His685Asn) n.2573C>A | |
5 | g.56881742C= | CA1548139280 | MAP3K1 | c.2542C= (p.His848=) c.2164C= (p.His722=) c.2287C= (p.His763=) c.2263C= (p.His755=) c.2131C= (p.His711=) c.2053C= (p.His685=) n.2573C= | |
5 | g.56881742C>G | CA359786021 | MAP3K1 | c.2542C>G (p.His848Asp) c.2164C>G (p.His722Asp) c.2287C>G (p.His763Asp) c.2263C>G (p.His755Asp) c.2131C>G (p.His711Asp) c.2053C>G (p.His685Asp) n.2573C>G | dbSNP gnomAD v2 |
5 | g.56881742C>T | CA359786022 | MAP3K1 | c.2542C>T (p.His848Tyr) c.2164C>T (p.His722Tyr) c.2287C>T (p.His763Tyr) c.2263C>T (p.His755Tyr) c.2131C>T (p.His711Tyr) c.2053C>T (p.His685Tyr) n.2573C>T | |
5 | g.56881743A>C | CA359786023 | MAP3K1 | c.2543A>C (p.His848Pro) c.2165A>C (p.His722Pro) c.2288A>C (p.His763Pro) c.2264A>C (p.His755Pro) c.2132A>C (p.His711Pro) c.2054A>C (p.His685Pro) n.2574A>C | dbSNP |
5 | g.56881743A>G | CA359786024 | MAP3K1 | c.2543A>G (p.His848Arg) c.2165A>G (p.His722Arg) c.2288A>G (p.His763Arg) c.2264A>G (p.His755Arg) c.2132A>G (p.His711Arg) c.2054A>G (p.His685Arg) n.2574A>G | |
5 | g.56881743A>T | CA359786025 | MAP3K1 | c.2543A>T (p.His848Leu) c.2165A>T (p.His722Leu) c.2288A>T (p.His763Leu) c.2264A>T (p.His755Leu) c.2132A>T (p.His711Leu) c.2054A>T (p.His685Leu) n.2574A>T | |
5 | g.56881744C>A | CA359786027 | MAP3K1 | c.2544C>A (p.His848Gln) c.2166C>A (p.His722Gln) c.2289C>A (p.His763Gln) c.2265C>A (p.His755Gln) c.2133C>A (p.His711Gln) c.2055C>A (p.His685Gln) n.2575C>A | COSMIC |
5 | g.56881744C= | CA1548139281 | MAP3K1 | c.2544C= (p.His848=) c.2166C= (p.His722=) c.2289C= (p.His763=) c.2265C= (p.His755=) c.2133C= (p.His711=) c.2055C= (p.His685=) n.2575C= | |
5 | g.56881744C>G | CA359786026 | MAP3K1 | c.2544C>G (p.His848Gln) c.2166C>G (p.His722Gln) c.2289C>G (p.His763Gln) c.2265C>G (p.His755Gln) c.2133C>G (p.His711Gln) c.2055C>G (p.His685Gln) n.2575C>G | |
5 | g.56881744C>T | CA119079090 | MAP3K1 | c.2544C>T (p.His848=) c.2166C>T (p.His722=) c.2289C>T (p.His763=) c.2265C>T (p.His755=) c.2133C>T (p.His711=) c.2055C>T (p.His685=) n.2575C>T | dbSNP gnomAD v4 |
5 | g.56881745T>A | CA359786028 | MAP3K1 | c.2545T>A (p.Phe849Ile) c.2167T>A (p.Phe723Ile) c.2290T>A (p.Phe764Ile) c.2266T>A (p.Phe756Ile) c.2134T>A (p.Phe712Ile) c.2056T>A (p.Phe686Ile) n.2576T>A | |
5 | g.56881745T>C | CA359786030 | MAP3K1 | c.2545T>C (p.Phe849Leu) c.2167T>C (p.Phe723Leu) c.2290T>C (p.Phe764Leu) c.2266T>C (p.Phe756Leu) c.2134T>C (p.Phe712Leu) c.2056T>C (p.Phe686Leu) n.2576T>C | |
5 | g.56881745T>G | CA359786029 | MAP3K1 | c.2545T>G (p.Phe849Val) c.2167T>G (p.Phe723Val) c.2290T>G (p.Phe764Val) c.2266T>G (p.Phe756Val) c.2134T>G (p.Phe712Val) c.2056T>G (p.Phe686Val) n.2576T>G | |
5 | g.56881746T>A | CA359786031 | MAP3K1 | c.2546T>A (p.Phe849Tyr) c.2168T>A (p.Phe723Tyr) c.2291T>A (p.Phe764Tyr) c.2267T>A (p.Phe756Tyr) c.2135T>A (p.Phe712Tyr) c.2057T>A (p.Phe686Tyr) n.2577T>A | |
5 | g.56881746T>C | CA359786032 | MAP3K1 | c.2546T>C (p.Phe849Ser) c.2168T>C (p.Phe723Ser) c.2291T>C (p.Phe764Ser) c.2267T>C (p.Phe756Ser) c.2135T>C (p.Phe712Ser) c.2057T>C (p.Phe686Ser) n.2577T>C | gnomAD v4 |
5 | g.56881746T>G | CA359786033 | MAP3K1 | c.2546T>G (p.Phe849Cys) c.2168T>G (p.Phe723Cys) c.2291T>G (p.Phe764Cys) c.2267T>G (p.Phe756Cys) c.2135T>G (p.Phe712Cys) c.2057T>G (p.Phe686Cys) n.2577T>G | |
5 | g.56881747C>A | CA359786034 | MAP3K1 | c.2547C>A (p.Phe849Leu) c.2169C>A (p.Phe723Leu) c.2292C>A (p.Phe764Leu) c.2268C>A (p.Phe756Leu) c.2136C>A (p.Phe712Leu) c.2058C>A (p.Phe686Leu) n.2578C>A | |
5 | g.56881747C= | CA1548139282 | MAP3K1 | c.2547C= (p.Phe849=) c.2169C= (p.Phe723=) c.2292C= (p.Phe764=) c.2268C= (p.Phe756=) c.2136C= (p.Phe712=) c.2058C= (p.Phe686=) n.2578C= | |
5 | g.56881747C>G | CA119079093 | MAP3K1 | c.2547C>G (p.Phe849Leu) c.2169C>G (p.Phe723Leu) c.2292C>G (p.Phe764Leu) c.2268C>G (p.Phe756Leu) c.2136C>G (p.Phe712Leu) c.2058C>G (p.Phe686Leu) n.2578C>G | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.56881747C>T | CA444399150 | MAP3K1 | c.2547C>T (p.Phe849=) c.2169C>T (p.Phe723=) c.2292C>T (p.Phe764=) c.2268C>T (p.Phe756=) c.2136C>T (p.Phe712=) c.2058C>T (p.Phe686=) n.2578C>T | dbSNP |
5 | g.56881748A= | CA1548139283 | MAP3K1 | c.2548A= (p.Thr850=) c.2170A= (p.Thr724=) c.2293A= (p.Thr765=) c.2269A= (p.Thr757=) c.2137A= (p.Thr713=) c.2059A= (p.Thr687=) n.2579A= | |
5 | g.56881748A>C | CA359786035 | MAP3K1 | c.2548A>C (p.Thr850Pro) c.2170A>C (p.Thr724Pro) c.2293A>C (p.Thr765Pro) c.2269A>C (p.Thr757Pro) c.2137A>C (p.Thr713Pro) c.2059A>C (p.Thr687Pro) n.2579A>C | |
5 | g.56881748A>G | CA3273014 | MAP3K1 | c.2548A>G (p.Thr850Ala) c.2170A>G (p.Thr724Ala) c.2293A>G (p.Thr765Ala) c.2269A>G (p.Thr757Ala) c.2137A>G (p.Thr713Ala) c.2059A>G (p.Thr687Ala) n.2579A>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.56881748A>T | CA359786036 | MAP3K1 | c.2548A>T (p.Thr850Ser) c.2170A>T (p.Thr724Ser) c.2293A>T (p.Thr765Ser) c.2269A>T (p.Thr757Ser) c.2137A>T (p.Thr713Ser) c.2059A>T (p.Thr687Ser) n.2579A>T | |
5 | g.56881749C>A | CA359786037 | MAP3K1 | c.2549C>A (p.Thr850Asn) c.2171C>A (p.Thr724Asn) c.2294C>A (p.Thr765Asn) c.2270C>A (p.Thr757Asn) c.2138C>A (p.Thr713Asn) c.2060C>A (p.Thr687Asn) n.2580C>A | |
5 | g.56881749C= | CA1548139284 | MAP3K1 | c.2549C= (p.Thr850=) c.2171C= (p.Thr724=) c.2294C= (p.Thr765=) c.2270C= (p.Thr757=) c.2138C= (p.Thr713=) c.2060C= (p.Thr687=) n.2580C= | |
5 | g.56881749C>G | CA359786038 | MAP3K1 | c.2549C>G (p.Thr850Ser) c.2171C>G (p.Thr724Ser) c.2294C>G (p.Thr765Ser) c.2270C>G (p.Thr757Ser) c.2138C>G (p.Thr713Ser) c.2060C>G (p.Thr687Ser) n.2580C>G | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.56881749C>T | CA359786039 | MAP3K1 | c.2549C>T (p.Thr850Ile) c.2171C>T (p.Thr724Ile) c.2294C>T (p.Thr765Ile) c.2270C>T (p.Thr757Ile) c.2138C>T (p.Thr713Ile) c.2060C>T (p.Thr687Ile) n.2580C>T | gnomAD v4 |
5 | g.56881750C>A | CA444399151 | MAP3K1 | c.2550C>A (p.Thr850=) c.2172C>A (p.Thr724=) c.2295C>A (p.Thr765=) c.2271C>A (p.Thr757=) c.2139C>A (p.Thr713=) c.2061C>A (p.Thr687=) n.2581C>A | |
5 | g.56881750C= | CA1548139285 | MAP3K1 | c.2550C= (p.Thr850=) c.2172C= (p.Thr724=) c.2295C= (p.Thr765=) c.2271C= (p.Thr757=) c.2139C= (p.Thr713=) c.2061C= (p.Thr687=) n.2581C= | |
5 | g.56881750C>G | CA444399152 | MAP3K1 | c.2550C>G (p.Thr850=) c.2172C>G (p.Thr724=) c.2295C>G (p.Thr765=) c.2271C>G (p.Thr757=) c.2139C>G (p.Thr713=) c.2061C>G (p.Thr687=) n.2581C>G | dbSNP |
5 | g.56881750C>T | CA3273015 | MAP3K1 | c.2550C>T (p.Thr850=) c.2172C>T (p.Thr724=) c.2295C>T (p.Thr765=) c.2271C>T (p.Thr757=) c.2139C>T (p.Thr713=) c.2061C>T (p.Thr687=) n.2581C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.56881751A= | CA1548139286 | MAP3K1 | c.2551A= (p.Arg851=) c.2173A= (p.Arg725=) c.2296A= (p.Arg766=) c.2272A= (p.Arg758=) c.2140A= (p.Arg714=) c.2062A= (p.Arg688=) n.2582A= | |
5 | g.56881751A>C | CA444399153 | MAP3K1 | c.2551A>C (p.Arg851=) c.2173A>C (p.Arg725=) c.2296A>C (p.Arg766=) c.2272A>C (p.Arg758=) c.2140A>C (p.Arg714=) c.2062A>C (p.Arg688=) n.2582A>C | dbSNP gnomAD v3 gnomAD v4 |
5 | g.56881751A>G | CA359786040 | MAP3K1 | c.2551A>G (p.Arg851Gly) c.2173A>G (p.Arg725Gly) c.2296A>G (p.Arg766Gly) c.2272A>G (p.Arg758Gly) c.2140A>G (p.Arg714Gly) c.2062A>G (p.Arg688Gly) n.2582A>G | gnomAD v4 |
5 | g.56881751A>T | CA359786041 | MAP3K1 | c.2551A>T (p.Arg851Trp) c.2173A>T (p.Arg725Trp) c.2296A>T (p.Arg766Trp) c.2272A>T (p.Arg758Trp) c.2140A>T (p.Arg714Trp) c.2062A>T (p.Arg688Trp) n.2582A>T | |
5 | g.56881752G>A | CA359786042 | MAP3K1 | c.2552G>A (p.Arg851Lys) c.2174G>A (p.Arg725Lys) c.2297G>A (p.Arg766Lys) c.2273G>A (p.Arg758Lys) c.2141G>A (p.Arg714Lys) c.2063G>A (p.Arg688Lys) n.2583G>A | |
5 | g.56881752G>C | CA359786043 | MAP3K1 | c.2552G>C (p.Arg851Thr) c.2174G>C (p.Arg725Thr) c.2297G>C (p.Arg766Thr) c.2273G>C (p.Arg758Thr) c.2141G>C (p.Arg714Thr) c.2063G>C (p.Arg688Thr) n.2583G>C | dbSNP gnomAD v3 gnomAD v4 |
5 | g.56881752G= | CA1548139287 | MAP3K1 | c.2552G= (p.Arg851=) c.2174G= (p.Arg725=) c.2297G= (p.Arg766=) c.2273G= (p.Arg758=) c.2141G= (p.Arg714=) c.2063G= (p.Arg688=) n.2583G= | |
5 | g.56881752G>T | CA359786044 | MAP3K1 | c.2552G>T (p.Arg851Met) c.2174G>T (p.Arg725Met) c.2297G>T (p.Arg766Met) c.2273G>T (p.Arg758Met) c.2141G>T (p.Arg714Met) c.2063G>T (p.Arg688Met) n.2583G>T | |
5 | g.56881753G>A | CA444399154 | MAP3K1 | c.2553G>A (p.Arg851=) c.2175G>A (p.Arg725=) c.2298G>A (p.Arg766=) c.2274G>A (p.Arg758=) c.2142G>A (p.Arg714=) c.2064G>A (p.Arg688=) n.2584G>A | dbSNP |
5 | g.56881753G>C | CA359786045 | MAP3K1 | c.2553G>C (p.Arg851Ser) c.2175G>C (p.Arg725Ser) c.2298G>C (p.Arg766Ser) c.2274G>C (p.Arg758Ser) c.2142G>C (p.Arg714Ser) c.2064G>C (p.Arg688Ser) n.2584G>C | |
5 | g.56881753G>T | CA359786046 | MAP3K1 | c.2553G>T (p.Arg851Ser) c.2175G>T (p.Arg725Ser) c.2298G>T (p.Arg766Ser) c.2274G>T (p.Arg758Ser) c.2142G>T (p.Arg714Ser) c.2064G>T (p.Arg688Ser) n.2584G>T | gnomAD v4 |
5 | g.56881754A>C | CA359786047 | MAP3K1 | c.2554A>C (p.Met852Leu) c.2176A>C (p.Met726Leu) c.2299A>C (p.Met767Leu) c.2275A>C (p.Met759Leu) c.2143A>C (p.Met715Leu) c.2065A>C (p.Met689Leu) n.2585A>C | |
5 | g.56881754A>G | CA359786048 | MAP3K1 | c.2554A>G (p.Met852Val) c.2176A>G (p.Met726Val) c.2299A>G (p.Met767Val) c.2275A>G (p.Met759Val) c.2143A>G (p.Met715Val) c.2065A>G (p.Met689Val) n.2585A>G | |
5 | g.56881754A>T | CA359786049 | MAP3K1 | c.2554A>T (p.Met852Leu) c.2176A>T (p.Met726Leu) c.2299A>T (p.Met767Leu) c.2275A>T (p.Met759Leu) c.2143A>T (p.Met715Leu) c.2065A>T (p.Met689Leu) n.2585A>T | |
5 | g.56881755T>A | CA359786050 | MAP3K1 | c.2555T>A (p.Met852Lys) c.2177T>A (p.Met726Lys) c.2300T>A (p.Met767Lys) c.2276T>A (p.Met759Lys) c.2144T>A (p.Met715Lys) c.2066T>A (p.Met689Lys) n.2586T>A | dbSNP gnomAD v4 |
5 | g.56881755T>C | CA3273016 | MAP3K1 | c.2555T>C (p.Met852Thr) c.2177T>C (p.Met726Thr) c.2300T>C (p.Met767Thr) c.2276T>C (p.Met759Thr) c.2144T>C (p.Met715Thr) c.2066T>C (p.Met689Thr) n.2586T>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.56881755T>G | CA359786051 | MAP3K1 | c.2555T>G (p.Met852Arg) c.2177T>G (p.Met726Arg) c.2300T>G (p.Met767Arg) c.2276T>G (p.Met759Arg) c.2144T>G (p.Met715Arg) c.2066T>G (p.Met689Arg) n.2586T>G | |
5 | g.56881755T= | CA1548139288 | MAP3K1 | c.2555T= (p.Met852=) c.2177T= (p.Met726=) c.2300T= (p.Met767=) c.2276T= (p.Met759=) c.2144T= (p.Met715=) c.2066T= (p.Met689=) n.2586T= | |
5 | g.56881756G>A | CA359786053 | MAP3K1 | c.2556G>A (p.Met852Ile) c.2178G>A (p.Met726Ile) c.2301G>A (p.Met767Ile) c.2277G>A (p.Met759Ile) c.2145G>A (p.Met715Ile) c.2067G>A (p.Met689Ile) n.2587G>A | dbSNP |
5 | g.56881756G>C | CA359786054 | MAP3K1 | c.2556G>C (p.Met852Ile) c.2178G>C (p.Met726Ile) c.2301G>C (p.Met767Ile) c.2277G>C (p.Met759Ile) c.2145G>C (p.Met715Ile) c.2067G>C (p.Met689Ile) n.2587G>C | |
5 | g.56881756G>T | CA359786052 | MAP3K1 | c.2556G>T (p.Met852Ile) c.2178G>T (p.Met726Ile) c.2301G>T (p.Met767Ile) c.2277G>T (p.Met759Ile) c.2145G>T (p.Met715Ile) c.2067G>T (p.Met689Ile) n.2587G>T | |
5 | g.56881758_56881762dup | CA2708984055 | MAP3K1 | c.2558_2562dup (p.Arg855ValfsTer4) c.2180_2184dup (p.Arg729ValfsTer4) c.2303_2307dup (p.Arg770ValfsTer4) c.2279_2283dup (p.Arg762ValfsTer4) c.2147_2151dup (p.Arg718ValfsTer4) c.2069_2073dup (p.Arg692ValfsTer4) n.2589_2593dup | dbSNP |
5 | g.56881757C>A | CA3273018 | MAP3K1 | c.2557C>A (p.Arg853Ser) c.2179C>A (p.Arg727Ser) c.2302C>A (p.Arg768Ser) c.2278C>A (p.Arg760Ser) c.2146C>A (p.Arg716Ser) c.2068C>A (p.Arg690Ser) n.2588C>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
5 | g.56881757C= | CA1548139289 | MAP3K1 | c.2557C= (p.Arg853=) c.2179C= (p.Arg727=) c.2302C= (p.Arg768=) c.2278C= (p.Arg760=) c.2146C= (p.Arg716=) c.2068C= (p.Arg690=) n.2588C= | |
5 | g.56881757C>G | CA359786055 | MAP3K1 | c.2557C>G (p.Arg853Gly) c.2179C>G (p.Arg727Gly) c.2302C>G (p.Arg768Gly) c.2278C>G (p.Arg760Gly) c.2146C>G (p.Arg716Gly) c.2068C>G (p.Arg690Gly) n.2588C>G | |
5 | g.56881757C>T | CA3273017 | MAP3K1 | c.2557C>T (p.Arg853Cys) c.2179C>T (p.Arg727Cys) c.2302C>T (p.Arg768Cys) c.2278C>T (p.Arg760Cys) c.2146C>T (p.Arg716Cys) c.2068C>T (p.Arg690Cys) n.2588C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
5 | g.56881758G>A | CA3273019 | MAP3K1 | c.2558G>A (p.Arg853His) c.2180G>A (p.Arg727His) c.2303G>A (p.Arg768His) c.2279G>A (p.Arg760His) c.2147G>A (p.Arg716His) c.2069G>A (p.Arg690His) n.2589G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.56881758G>C | CA359786056 | MAP3K1 | c.2558G>C (p.Arg853Pro) c.2180G>C (p.Arg727Pro) c.2303G>C (p.Arg768Pro) c.2279G>C (p.Arg760Pro) c.2147G>C (p.Arg716Pro) c.2069G>C (p.Arg690Pro) n.2589G>C | |
5 | g.56881758G= | CA1548139290 | MAP3K1 | c.2558G= (p.Arg853=) c.2180G= (p.Arg727=) c.2303G= (p.Arg768=) c.2279G= (p.Arg760=) c.2147G= (p.Arg716=) c.2069G= (p.Arg690=) n.2589G= | |
5 | g.56881758G>T | CA359786057 | MAP3K1 | c.2558G>T (p.Arg853Leu) c.2180G>T (p.Arg727Leu) c.2303G>T (p.Arg768Leu) c.2279G>T (p.Arg760Leu) c.2147G>T (p.Arg716Leu) c.2069G>T (p.Arg690Leu) n.2589G>T | COSMIC |
5 | g.56881759T>A | CA444399155 | MAP3K1 | c.2559T>A (p.Arg853=) c.2181T>A (p.Arg727=) c.2304T>A (p.Arg768=) c.2280T>A (p.Arg760=) c.2148T>A (p.Arg716=) c.2070T>A (p.Arg690=) n.2590T>A | |
5 | g.56881759T>C | CA444399156 | MAP3K1 | c.2559T>C (p.Arg853=) c.2181T>C (p.Arg727=) c.2304T>C (p.Arg768=) c.2280T>C (p.Arg760=) c.2148T>C (p.Arg716=) c.2070T>C (p.Arg690=) n.2590T>C | dbSNP |
5 | g.56881759T>G | CA444399157 | MAP3K1 | c.2559T>G (p.Arg853=) c.2181T>G (p.Arg727=) c.2304T>G (p.Arg768=) c.2280T>G (p.Arg760=) c.2148T>G (p.Arg716=) c.2070T>G (p.Arg690=) n.2590T>G | |
5 | g.56881760C>A | CA359786058 | MAP3K1 | c.2560C>A (p.Arg854Ser) c.2182C>A (p.Arg728Ser) c.2305C>A (p.Arg769Ser) c.2281C>A (p.Arg761Ser) c.2149C>A (p.Arg717Ser) c.2071C>A (p.Arg691Ser) n.2591C>A | dbSNP |
5 | g.56881760C= | CA1548139291 | MAP3K1 | c.2560C= (p.Arg854=) c.2182C= (p.Arg728=) c.2305C= (p.Arg769=) c.2281C= (p.Arg761=) c.2149C= (p.Arg717=) c.2071C= (p.Arg691=) n.2591C= | |
5 | g.56881760C>G | CA359786059 | MAP3K1 | c.2560C>G (p.Arg854Gly) c.2182C>G (p.Arg728Gly) c.2305C>G (p.Arg769Gly) c.2281C>G (p.Arg761Gly) c.2149C>G (p.Arg717Gly) c.2071C>G (p.Arg691Gly) n.2591C>G | dbSNP |
5 | g.56881760C>T | CA3273020 | MAP3K1 | c.2560C>T (p.Arg854Cys) c.2182C>T (p.Arg728Cys) c.2305C>T (p.Arg769Cys) c.2281C>T (p.Arg761Cys) c.2149C>T (p.Arg717Cys) c.2071C>T (p.Arg691Cys) n.2591C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.56881761G>A | CA359786060 | MAP3K1 | c.2561G>A (p.Arg854His) c.2183G>A (p.Arg728His) c.2306G>A (p.Arg769His) c.2282G>A (p.Arg761His) c.2150G>A (p.Arg717His) c.2072G>A (p.Arg691His) n.2592G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
5 | g.56881761G>C | CA359786061 | MAP3K1 | c.2561G>C (p.Arg854Pro) c.2183G>C (p.Arg728Pro) c.2306G>C (p.Arg769Pro) c.2282G>C (p.Arg761Pro) c.2150G>C (p.Arg717Pro) c.2072G>C (p.Arg691Pro) n.2592G>C | |
5 | g.56881761G= | CA1548139292 | MAP3K1 | c.2561G= (p.Arg854=) c.2183G= (p.Arg728=) c.2306G= (p.Arg769=) c.2282G= (p.Arg761=) c.2150G= (p.Arg717=) c.2072G= (p.Arg691=) n.2592G= | |
5 | g.56881761G>T | CA359786062 | MAP3K1 | c.2561G>T (p.Arg854Leu) c.2183G>T (p.Arg728Leu) c.2306G>T (p.Arg769Leu) c.2282G>T (p.Arg761Leu) c.2150G>T (p.Arg717Leu) c.2072G>T (p.Arg691Leu) n.2592G>T | |
5 | g.56881762C>A | CA444399158 | MAP3K1 | c.2562C>A (p.Arg854=) c.2184C>A (p.Arg728=) c.2307C>A (p.Arg769=) c.2283C>A (p.Arg761=) c.2151C>A (p.Arg717=) c.2073C>A (p.Arg691=) n.2593C>A | |
5 | g.56881762C>G | CA444399159 | MAP3K1 | c.2562C>G (p.Arg854=) c.2184C>G (p.Arg728=) c.2307C>G (p.Arg769=) c.2283C>G (p.Arg761=) c.2151C>G (p.Arg717=) c.2073C>G (p.Arg691=) n.2593C>G | |
5 | g.56881762C>T | CA444399160 | MAP3K1 | c.2562C>T (p.Arg854=) c.2184C>T (p.Arg728=) c.2307C>T (p.Arg769=) c.2283C>T (p.Arg761=) c.2151C>T (p.Arg717=) c.2073C>T (p.Arg691=) n.2593C>T | |
5 | g.56881763C>A | CA359786063 | MAP3K1 | c.2563C>A (p.Arg855Ser) c.2185C>A (p.Arg729Ser) c.2308C>A (p.Arg770Ser) c.2284C>A (p.Arg762Ser) c.2152C>A (p.Arg718Ser) c.2074C>A (p.Arg692Ser) n.2594C>A | |
5 | g.56881763C= | CA1548139293 | MAP3K1 | c.2563C= (p.Arg855=) c.2185C= (p.Arg729=) c.2308C= (p.Arg770=) c.2284C= (p.Arg762=) c.2152C= (p.Arg718=) c.2074C= (p.Arg692=) n.2594C= | |
5 | g.56881763C>G | CA359786064 | MAP3K1 | c.2563C>G (p.Arg855Gly) c.2185C>G (p.Arg729Gly) c.2308C>G (p.Arg770Gly) c.2284C>G (p.Arg762Gly) c.2152C>G (p.Arg718Gly) c.2074C>G (p.Arg692Gly) n.2594C>G | |
5 | g.56881763C>T | CA3273021 | MAP3K1 | c.2563C>T (p.Arg855Cys) c.2185C>T (p.Arg729Cys) c.2308C>T (p.Arg770Cys) c.2284C>T (p.Arg762Cys) c.2152C>T (p.Arg718Cys) c.2074C>T (p.Arg692Cys) n.2594C>T | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
5 | g.56881764G>A | CA119079184 | MAP3K1 | c.2564G>A (p.Arg855His) c.2186G>A (p.Arg729His) c.2309G>A (p.Arg770His) c.2285G>A (p.Arg762His) c.2153G>A (p.Arg718His) c.2075G>A (p.Arg692His) n.2595G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.56881764G>C | CA359786065 | MAP3K1 | c.2564G>C (p.Arg855Pro) c.2186G>C (p.Arg729Pro) c.2309G>C (p.Arg770Pro) c.2285G>C (p.Arg762Pro) c.2153G>C (p.Arg718Pro) c.2075G>C (p.Arg692Pro) n.2595G>C | dbSNP |
5 | g.56881764G= | CA1548139294 | MAP3K1 | c.2564G= (p.Arg855=) c.2186G= (p.Arg729=) c.2309G= (p.Arg770=) c.2285G= (p.Arg762=) c.2153G= (p.Arg718=) c.2075G= (p.Arg692=) n.2595G= | |
5 | g.56881764G>T | CA359786066 | MAP3K1 | c.2564G>T (p.Arg855Leu) c.2186G>T (p.Arg729Leu) c.2309G>T (p.Arg770Leu) c.2285G>T (p.Arg762Leu) c.2153G>T (p.Arg718Leu) c.2075G>T (p.Arg692Leu) n.2595G>T | |
5 | g.56881765T>A | CA444399161 | MAP3K1 | c.2565T>A (p.Arg855=) c.2187T>A (p.Arg729=) c.2310T>A (p.Arg770=) c.2286T>A (p.Arg762=) c.2154T>A (p.Arg718=) c.2076T>A (p.Arg692=) n.2596T>A | |
5 | g.56881765T>C | CA444399162 | MAP3K1 | c.2565T>C (p.Arg855=) c.2187T>C (p.Arg729=) c.2310T>C (p.Arg770=) c.2286T>C (p.Arg762=) c.2154T>C (p.Arg718=) c.2076T>C (p.Arg692=) n.2596T>C | |
5 | g.56881765T>G | CA444399163 | MAP3K1 | c.2565T>G (p.Arg855=) c.2187T>G (p.Arg729=) c.2310T>G (p.Arg770=) c.2286T>G (p.Arg762=) c.2154T>G (p.Arg718=) c.2076T>G (p.Arg692=) n.2596T>G | |
5 | g.56881766T>A | CA359786067 | MAP3K1 | c.2566T>A (p.Leu856Met) c.2188T>A (p.Leu730Met) c.2311T>A (p.Leu771Met) c.2287T>A (p.Leu763Met) c.2155T>A (p.Leu719Met) c.2077T>A (p.Leu693Met) n.2597T>A | |
5 | g.56881766T>C | CA444399164 | MAP3K1 | c.2566T>C (p.Leu856=) c.2188T>C (p.Leu730=) c.2311T>C (p.Leu771=) c.2287T>C (p.Leu763=) c.2155T>C (p.Leu719=) c.2077T>C (p.Leu693=) n.2597T>C | |
5 | g.56881766T>G | CA359786068 | MAP3K1 | c.2566T>G (p.Leu856Val) c.2188T>G (p.Leu730Val) c.2311T>G (p.Leu771Val) c.2287T>G (p.Leu763Val) c.2155T>G (p.Leu719Val) c.2077T>G (p.Leu693Val) n.2597T>G | |
5 | g.56881767T>A | CA359786071 | MAP3K1 | c.2567T>A (p.Leu856Ter) c.2189T>A (p.Leu730Ter) c.2312T>A (p.Leu771Ter) c.2288T>A (p.Leu763Ter) c.2156T>A (p.Leu719Ter) c.2078T>A (p.Leu693Ter) n.2598T>A | |
5 | g.56881767T>C | CA359786069 | MAP3K1 | c.2567T>C (p.Leu856Ser) c.2189T>C (p.Leu730Ser) c.2312T>C (p.Leu771Ser) c.2288T>C (p.Leu763Ser) c.2156T>C (p.Leu719Ser) c.2078T>C (p.Leu693Ser) n.2598T>C | |
5 | g.56881767T>G | CA359786070 | MAP3K1 | c.2567T>G (p.Leu856Trp) c.2189T>G (p.Leu730Trp) c.2312T>G (p.Leu771Trp) c.2288T>G (p.Leu763Trp) c.2156T>G (p.Leu719Trp) c.2078T>G (p.Leu693Trp) n.2598T>G | gnomAD v4 |
5 | g.56881768G>A | CA444399165 | MAP3K1 | c.2568G>A (p.Leu856=) c.2190G>A (p.Leu730=) c.2313G>A (p.Leu771=) c.2289G>A (p.Leu763=) c.2157G>A (p.Leu719=) c.2079G>A (p.Leu693=) n.2599G>A | |
5 | g.56881768G>C | CA359786072 | MAP3K1 | c.2568G>C (p.Leu856Phe) c.2190G>C (p.Leu730Phe) c.2313G>C (p.Leu771Phe) c.2289G>C (p.Leu763Phe) c.2157G>C (p.Leu719Phe) c.2079G>C (p.Leu693Phe) n.2599G>C | |
5 | g.56881768G>T | CA359786073 | MAP3K1 | c.2568G>T (p.Leu856Phe) c.2190G>T (p.Leu730Phe) c.2313G>T (p.Leu771Phe) c.2289G>T (p.Leu763Phe) c.2157G>T (p.Leu719Phe) c.2079G>T (p.Leu693Phe) n.2599G>T | |
5 | g.56881769A>C | CA359786074 | MAP3K1 | c.2569A>C (p.Met857Leu) c.2191A>C (p.Met731Leu) c.2314A>C (p.Met772Leu) c.2290A>C (p.Met764Leu) c.2158A>C (p.Met720Leu) c.2080A>C (p.Met694Leu) n.2600A>C | |
5 | g.56881769A>G | CA359786075 | MAP3K1 | c.2569A>G (p.Met857Val) c.2191A>G (p.Met731Val) c.2314A>G (p.Met772Val) c.2290A>G (p.Met764Val) c.2158A>G (p.Met720Val) c.2080A>G (p.Met694Val) n.2600A>G | |
5 | g.56881769A>T | CA359786076 | MAP3K1 | c.2569A>T (p.Met857Leu) c.2191A>T (p.Met731Leu) c.2314A>T (p.Met772Leu) c.2290A>T (p.Met764Leu) c.2158A>T (p.Met720Leu) c.2080A>T (p.Met694Leu) n.2600A>T | |
5 | g.56881770T>A | CA359786079 | MAP3K1 | c.2570T>A (p.Met857Lys) c.2192T>A (p.Met731Lys) c.2315T>A (p.Met772Lys) c.2291T>A (p.Met764Lys) c.2159T>A (p.Met720Lys) c.2081T>A (p.Met694Lys) n.2601T>A | |
5 | g.56881770T>C | CA359786078 | MAP3K1 | c.2570T>C (p.Met857Thr) c.2192T>C (p.Met731Thr) c.2315T>C (p.Met772Thr) c.2291T>C (p.Met764Thr) c.2159T>C (p.Met720Thr) c.2081T>C (p.Met694Thr) n.2601T>C | gnomAD v4 |
5 | g.56881770T>G | CA359786077 | MAP3K1 | c.2570T>G (p.Met857Arg) c.2192T>G (p.Met731Arg) c.2315T>G (p.Met772Arg) c.2291T>G (p.Met764Arg) c.2159T>G (p.Met720Arg) c.2081T>G (p.Met694Arg) n.2601T>G | |
5 | g.56881771G>A | CA3273022 | MAP3K1 | c.2571G>A (p.Met857Ile) c.2193G>A (p.Met731Ile) c.2316G>A (p.Met772Ile) c.2292G>A (p.Met764Ile) c.2160G>A (p.Met720Ile) c.2082G>A (p.Met694Ile) n.2602G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.56881771G>C | CA359786081 | MAP3K1 | c.2571G>C (p.Met857Ile) c.2193G>C (p.Met731Ile) c.2316G>C (p.Met772Ile) c.2292G>C (p.Met764Ile) c.2160G>C (p.Met720Ile) c.2082G>C (p.Met694Ile) n.2602G>C | |
5 | g.56881771G= | CA1548139295 | MAP3K1 | c.2571G= (p.Met857=) c.2193G= (p.Met731=) c.2316G= (p.Met772=) c.2292G= (p.Met764=) c.2160G= (p.Met720=) c.2082G= (p.Met694=) n.2602G= | |
5 | g.56881771G>T | CA359786080 | MAP3K1 | c.2571G>T (p.Met857Ile) c.2193G>T (p.Met731Ile) c.2316G>T (p.Met772Ile) c.2292G>T (p.Met764Ile) c.2160G>T (p.Met720Ile) c.2082G>T (p.Met694Ile) n.2602G>T | |
5 | g.56881772del | CA444399166 | MAP3K1 | c.2572del (p.Ala858LeufsTer16) c.2194del (p.Ala732LeufsTer16) c.2317del (p.Ala773LeufsTer16) c.2293del (p.Ala765LeufsTer16) c.2161del (p.Ala721LeufsTer16) c.2083del (p.Ala695LeufsTer16) n.2603del | COSMIC |
5 | g.56881772G>A | CA359786082 | MAP3K1 | c.2572G>A (p.Ala858Thr) c.2194G>A (p.Ala732Thr) c.2317G>A (p.Ala773Thr) c.2293G>A (p.Ala765Thr) c.2161G>A (p.Ala721Thr) c.2083G>A (p.Ala695Thr) n.2603G>A | dbSNP gnomAD v4 |
5 | g.56881772G>C | CA359786084 | MAP3K1 | c.2572G>C (p.Ala858Pro) c.2194G>C (p.Ala732Pro) c.2317G>C (p.Ala773Pro) c.2293G>C (p.Ala765Pro) c.2161G>C (p.Ala721Pro) c.2083G>C (p.Ala695Pro) n.2603G>C | dbSNP |
5 | g.56881772G>T | CA359786083 | MAP3K1 | c.2572G>T (p.Ala858Ser) c.2194G>T (p.Ala732Ser) c.2317G>T (p.Ala773Ser) c.2293G>T (p.Ala765Ser) c.2161G>T (p.Ala721Ser) c.2083G>T (p.Ala695Ser) n.2603G>T | |
5 | g.56881773C>A | CA359786085 | MAP3K1 | c.2573C>A (p.Ala858Asp) c.2195C>A (p.Ala732Asp) c.2318C>A (p.Ala773Asp) c.2294C>A (p.Ala765Asp) c.2162C>A (p.Ala721Asp) c.2084C>A (p.Ala695Asp) n.2604C>A | |
5 | g.56881773C= | CA1548139296 | MAP3K1 | c.2573C= (p.Ala858=) c.2195C= (p.Ala732=) c.2318C= (p.Ala773=) c.2294C= (p.Ala765=) c.2162C= (p.Ala721=) c.2084C= (p.Ala695=) n.2604C= | |
5 | g.56881773C>G | CA359786086 | MAP3K1 | c.2573C>G (p.Ala858Gly) c.2195C>G (p.Ala732Gly) c.2318C>G (p.Ala773Gly) c.2294C>G (p.Ala765Gly) c.2162C>G (p.Ala721Gly) c.2084C>G (p.Ala695Gly) n.2604C>G | dbSNP |
5 | g.56881773C>T | CA359786087 | MAP3K1 | c.2573C>T (p.Ala858Val) c.2195C>T (p.Ala732Val) c.2318C>T (p.Ala773Val) c.2294C>T (p.Ala765Val) c.2162C>T (p.Ala721Val) c.2084C>T (p.Ala695Val) n.2604C>T | dbSNP |
5 | g.56881774T>A | CA444399167 | MAP3K1 | c.2574T>A (p.Ala858=) c.2196T>A (p.Ala732=) c.2319T>A (p.Ala773=) c.2295T>A (p.Ala765=) c.2163T>A (p.Ala721=) c.2085T>A (p.Ala695=) n.2605T>A | |
5 | g.56881774T>C | CA444399168 | MAP3K1 | c.2574T>C (p.Ala858=) c.2196T>C (p.Ala732=) c.2319T>C (p.Ala773=) c.2295T>C (p.Ala765=) c.2163T>C (p.Ala721=) c.2085T>C (p.Ala695=) n.2605T>C | |
5 | g.56881774T>G | CA444399169 | MAP3K1 | c.2574T>G (p.Ala858=) c.2196T>G (p.Ala732=) c.2319T>G (p.Ala773=) c.2295T>G (p.Ala765=) c.2163T>G (p.Ala721=) c.2085T>G (p.Ala695=) n.2605T>G | |
5 | g.56881775A= | CA1548139297 | MAP3K1 | c.2575A= (p.Ile859=) c.2197A= (p.Ile733=) c.2320A= (p.Ile774=) c.2296A= (p.Ile766=) c.2164A= (p.Ile722=) c.2086A= (p.Ile696=) n.2606A= | |
5 | g.56881775A>C | CA359786088 | MAP3K1 | c.2575A>C (p.Ile859Leu) c.2197A>C (p.Ile733Leu) c.2320A>C (p.Ile774Leu) c.2296A>C (p.Ile766Leu) c.2164A>C (p.Ile722Leu) c.2086A>C (p.Ile696Leu) n.2606A>C | |
5 | g.56881775A>G | CA359786089 | MAP3K1 | c.2575A>G (p.Ile859Val) c.2197A>G (p.Ile733Val) c.2320A>G (p.Ile774Val) c.2296A>G (p.Ile766Val) c.2164A>G (p.Ile722Val) c.2086A>G (p.Ile696Val) n.2606A>G | dbSNP gnomAD v3 gnomAD v4 |
5 | g.56881775A>T | CA359786090 | MAP3K1 | c.2575A>T (p.Ile859Phe) c.2197A>T (p.Ile733Phe) c.2320A>T (p.Ile774Phe) c.2296A>T (p.Ile766Phe) c.2164A>T (p.Ile722Phe) c.2086A>T (p.Ile696Phe) n.2606A>T | |
5 | g.56881776T>A | CA359786091 | MAP3K1 | c.2576T>A (p.Ile859Asn) c.2198T>A (p.Ile733Asn) c.2321T>A (p.Ile774Asn) c.2297T>A (p.Ile766Asn) c.2165T>A (p.Ile722Asn) c.2087T>A (p.Ile696Asn) n.2607T>A | |
5 | g.56881776T>C | CA359786092 | MAP3K1 | c.2576T>C (p.Ile859Thr) c.2198T>C (p.Ile733Thr) c.2321T>C (p.Ile774Thr) c.2297T>C (p.Ile766Thr) c.2165T>C (p.Ile722Thr) c.2087T>C (p.Ile696Thr) n.2607T>C | gnomAD v4 |
5 | g.56881776T>G | CA359786093 | MAP3K1 | c.2576T>G (p.Ile859Ser) c.2198T>G (p.Ile733Ser) c.2321T>G (p.Ile774Ser) c.2297T>G (p.Ile766Ser) c.2165T>G (p.Ile722Ser) c.2087T>G (p.Ile696Ser) n.2607T>G | |
5 | g.56881777T>A | CA444399171 | MAP3K1 | c.2577T>A (p.Ile859=) c.2199T>A (p.Ile733=) c.2322T>A (p.Ile774=) c.2298T>A (p.Ile766=) c.2166T>A (p.Ile722=) c.2088T>A (p.Ile696=) n.2608T>A | |
5 | g.56881777T>C | CA444399172 | MAP3K1 | c.2577T>C (p.Ile859=) c.2199T>C (p.Ile733=) c.2322T>C (p.Ile774=) c.2298T>C (p.Ile766=) c.2166T>C (p.Ile722=) c.2088T>C (p.Ile696=) n.2608T>C | dbSNP gnomAD v2 gnomAD v4 |
5 | g.56881777T>G | CA359786094 | MAP3K1 | c.2577T>G (p.Ile859Met) c.2199T>G (p.Ile733Met) c.2322T>G (p.Ile774Met) c.2298T>G (p.Ile766Met) c.2166T>G (p.Ile722Met) c.2088T>G (p.Ile696Met) n.2608T>G | |
5 | g.56881777T= | CA1548139298 | MAP3K1 | c.2577T= (p.Ile859=) c.2199T= (p.Ile733=) c.2322T= (p.Ile774=) c.2298T= (p.Ile766=) c.2166T= (p.Ile722=) c.2088T= (p.Ile696=) n.2608T= | |
5 | g.56881778G>A | CA359786097 | MAP3K1 | c.2578G>A (p.Ala860Thr) c.2200G>A (p.Ala734Thr) c.2323G>A (p.Ala775Thr) c.2299G>A (p.Ala767Thr) c.2167G>A (p.Ala723Thr) c.2089G>A (p.Ala697Thr) n.2609G>A | |
5 | g.56881778G>C | CA359786096 | MAP3K1 | c.2578G>C (p.Ala860Pro) c.2200G>C (p.Ala734Pro) c.2323G>C (p.Ala775Pro) c.2299G>C (p.Ala767Pro) c.2167G>C (p.Ala723Pro) c.2089G>C (p.Ala697Pro) n.2609G>C | |
5 | g.56881778G>T | CA359786095 | MAP3K1 | c.2578G>T (p.Ala860Ser) c.2200G>T (p.Ala734Ser) c.2323G>T (p.Ala775Ser) c.2299G>T (p.Ala767Ser) c.2167G>T (p.Ala723Ser) c.2089G>T (p.Ala697Ser) n.2609G>T | |
5 | g.56881779C>A | CA359786098 | MAP3K1 | c.2579C>A (p.Ala860Glu) c.2201C>A (p.Ala734Glu) c.2324C>A (p.Ala775Glu) c.2300C>A (p.Ala767Glu) c.2168C>A (p.Ala723Glu) c.2090C>A (p.Ala697Glu) n.2610C>A | dbSNP |
5 | g.56881779C= | CA1548139299 | MAP3K1 | c.2579C= (p.Ala860=) c.2201C= (p.Ala734=) c.2324C= (p.Ala775=) c.2300C= (p.Ala767=) c.2168C= (p.Ala723=) c.2090C= (p.Ala697=) n.2610C= | |
5 | g.56881779C>G | CA359786099 | MAP3K1 | c.2579C>G (p.Ala860Gly) c.2201C>G (p.Ala734Gly) c.2324C>G (p.Ala775Gly) c.2300C>G (p.Ala767Gly) c.2168C>G (p.Ala723Gly) c.2090C>G (p.Ala697Gly) n.2610C>G | |
5 | g.56881779C>T | CA359786100 | MAP3K1 | c.2579C>T (p.Ala860Val) c.2201C>T (p.Ala734Val) c.2324C>T (p.Ala775Val) c.2300C>T (p.Ala767Val) c.2168C>T (p.Ala723Val) c.2090C>T (p.Ala697Val) n.2610C>T | dbSNP gnomAD v4 |
5 | g.56881780A>C | CA444399175 | MAP3K1 | c.2580A>C (p.Ala860=) c.2202A>C (p.Ala734=) c.2325A>C (p.Ala775=) c.2301A>C (p.Ala767=) c.2169A>C (p.Ala723=) c.2091A>C (p.Ala697=) n.2611A>C | |
5 | g.56881780A>G | CA444399176 | MAP3K1 | c.2580A>G (p.Ala860=) c.2202A>G (p.Ala734=) c.2325A>G (p.Ala775=) c.2301A>G (p.Ala767=) c.2169A>G (p.Ala723=) c.2091A>G (p.Ala697=) n.2611A>G | |
5 | g.56881780A>T | CA444399177 | MAP3K1 | c.2580A>T (p.Ala860=) c.2202A>T (p.Ala734=) c.2325A>T (p.Ala775=) c.2301A>T (p.Ala767=) c.2169A>T (p.Ala723=) c.2091A>T (p.Ala697=) n.2611A>T | |
5 | g.56881781G>A | CA359786101 | MAP3K1 | c.2581G>A (p.Asp861Asn) c.2203G>A (p.Asp735Asn) c.2326G>A (p.Asp776Asn) c.2302G>A (p.Asp768Asn) c.2170G>A (p.Asp724Asn) c.2092G>A (p.Asp698Asn) n.2612G>A | |
5 | g.56881781G>C | CA359786102 | MAP3K1 | c.2581G>C (p.Asp861His) c.2203G>C (p.Asp735His) c.2326G>C (p.Asp776His) c.2302G>C (p.Asp768His) c.2170G>C (p.Asp724His) c.2092G>C (p.Asp698His) n.2612G>C | |
5 | g.56881781G>T | CA359786103 | MAP3K1 | c.2581G>T (p.Asp861Tyr) c.2203G>T (p.Asp735Tyr) c.2326G>T (p.Asp776Tyr) c.2302G>T (p.Asp768Tyr) c.2170G>T (p.Asp724Tyr) c.2092G>T (p.Asp698Tyr) n.2612G>T | |
5 | g.56881782A>C | CA359786104 | MAP3K1 | c.2582A>C (p.Asp861Ala) c.2204A>C (p.Asp735Ala) c.2327A>C (p.Asp776Ala) c.2303A>C (p.Asp768Ala) c.2171A>C (p.Asp724Ala) c.2093A>C (p.Asp698Ala) n.2613A>C | |
5 | g.56881782A>G | CA359786105 | MAP3K1 | c.2582A>G (p.Asp861Gly) c.2204A>G (p.Asp735Gly) c.2327A>G (p.Asp776Gly) c.2303A>G (p.Asp768Gly) c.2171A>G (p.Asp724Gly) c.2093A>G (p.Asp698Gly) n.2613A>G | |
5 | g.56881782A>T | CA359786106 | MAP3K1 | c.2582A>T (p.Asp861Val) c.2204A>T (p.Asp735Val) c.2327A>T (p.Asp776Val) c.2303A>T (p.Asp768Val) c.2171A>T (p.Asp724Val) c.2093A>T (p.Asp698Val) n.2613A>T | |
5 | g.56881783T>A | CA119079191 | MAP3K1 | c.2583T>A (p.Asp861Glu) c.2205T>A (p.Asp735Glu) c.2328T>A (p.Asp776Glu) c.2304T>A (p.Asp768Glu) c.2172T>A (p.Asp724Glu) c.2094T>A (p.Asp698Glu) n.2614T>A | dbSNP gnomAD v3 gnomAD v4 |
5 | g.56881783T>C | CA444399179 | MAP3K1 | c.2583T>C (p.Asp861=) c.2205T>C (p.Asp735=) c.2328T>C (p.Asp776=) c.2304T>C (p.Asp768=) c.2172T>C (p.Asp724=) c.2094T>C (p.Asp698=) n.2614T>C | dbSNP gnomAD v3 gnomAD v4 |
5 | g.56881783T>G | CA359786107 | MAP3K1 | c.2583T>G (p.Asp861Glu) c.2205T>G (p.Asp735Glu) c.2328T>G (p.Asp776Glu) c.2304T>G (p.Asp768Glu) c.2172T>G (p.Asp724Glu) c.2094T>G (p.Asp698Glu) n.2614T>G | |
5 | g.56881783T= | CA1548139300 | MAP3K1 | c.2583T= (p.Asp861=) c.2205T= (p.Asp735=) c.2328T= (p.Asp776=) c.2304T= (p.Asp768=) c.2172T= (p.Asp724=) c.2094T= (p.Asp698=) n.2614T= | |
5 | g.56881784G>A | CA359786110 | MAP3K1 | c.2584G>A (p.Glu862Lys) c.2206G>A (p.Glu736Lys) c.2329G>A (p.Glu777Lys) c.2305G>A (p.Glu769Lys) c.2173G>A (p.Glu725Lys) c.2095G>A (p.Glu699Lys) n.2615G>A | |
5 | g.56881784G>C | CA359786109 | MAP3K1 | c.2584G>C (p.Glu862Gln) c.2206G>C (p.Glu736Gln) c.2329G>C (p.Glu777Gln) c.2305G>C (p.Glu769Gln) c.2173G>C (p.Glu725Gln) c.2095G>C (p.Glu699Gln) n.2615G>C | |
5 | g.56881784G>T | CA359786108 | MAP3K1 | c.2584G>T (p.Glu862Ter) c.2206G>T (p.Glu736Ter) c.2329G>T (p.Glu777Ter) c.2305G>T (p.Glu769Ter) c.2173G>T (p.Glu725Ter) c.2095G>T (p.Glu699Ter) n.2615G>T | gnomAD v4 |
5 | g.56881785A>C | CA359786111 | MAP3K1 | c.2585A>C (p.Glu862Ala) c.2207A>C (p.Glu736Ala) c.2330A>C (p.Glu777Ala) c.2306A>C (p.Glu769Ala) c.2174A>C (p.Glu725Ala) c.2096A>C (p.Glu699Ala) n.2616A>C | |
5 | g.56881785A>G | CA359786112 | MAP3K1 | c.2585A>G (p.Glu862Gly) c.2207A>G (p.Glu736Gly) c.2330A>G (p.Glu777Gly) c.2306A>G (p.Glu769Gly) c.2174A>G (p.Glu725Gly) c.2096A>G (p.Glu699Gly) n.2616A>G | |
5 | g.56881785A>T | CA359786113 | MAP3K1 | c.2585A>T (p.Glu862Val) c.2207A>T (p.Glu736Val) c.2330A>T (p.Glu777Val) c.2306A>T (p.Glu769Val) c.2174A>T (p.Glu725Val) c.2096A>T (p.Glu699Val) n.2616A>T | |
5 | g.56881786G>A | CA3273023 | MAP3K1 | c.2586G>A (p.Glu862=) c.2208G>A (p.Glu736=) c.2331G>A (p.Glu777=) c.2307G>A (p.Glu769=) c.2175G>A (p.Glu725=) c.2097G>A (p.Glu699=) n.2617G>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
5 | g.56881786G>C | CA359786114 | MAP3K1 | c.2586G>C (p.Glu862Asp) c.2208G>C (p.Glu736Asp) c.2331G>C (p.Glu777Asp) c.2307G>C (p.Glu769Asp) c.2175G>C (p.Glu725Asp) c.2097G>C (p.Glu699Asp) n.2617G>C | |
5 | g.56881786G= | CA1548139301 | MAP3K1 | c.2586G= (p.Glu862=) c.2208G= (p.Glu736=) c.2331G= (p.Glu777=) c.2307G= (p.Glu769=) c.2175G= (p.Glu725=) c.2097G= (p.Glu699=) n.2617G= | |
5 | g.56881786G>T | CA359786115 | MAP3K1 | c.2586G>T (p.Glu862Asp) c.2208G>T (p.Glu736Asp) c.2331G>T (p.Glu777Asp) c.2307G>T (p.Glu769Asp) c.2175G>T (p.Glu725Asp) c.2097G>T (p.Glu699Asp) n.2617G>T | |
5 | g.56881787G>A | CA359786116 | MAP3K1 | c.2587G>A (p.Val863Met) c.2209G>A (p.Val737Met) c.2332G>A (p.Val778Met) c.2308G>A (p.Val770Met) c.2176G>A (p.Val726Met) c.2098G>A (p.Val700Met) n.2618G>A | dbSNP |
5 | g.56881787G>C | CA359786117 | MAP3K1 | c.2587G>C (p.Val863Leu) c.2209G>C (p.Val737Leu) c.2332G>C (p.Val778Leu) c.2308G>C (p.Val770Leu) c.2176G>C (p.Val726Leu) c.2098G>C (p.Val700Leu) n.2618G>C | |
5 | g.56881787G= | CA1548139302 | MAP3K1 | c.2587G= (p.Val863=) c.2209G= (p.Val737=) c.2332G= (p.Val778=) c.2308G= (p.Val770=) c.2176G= (p.Val726=) c.2098G= (p.Val700=) n.2618G= | |
5 | g.56881787G>T | CA3273024 | MAP3K1 | c.2587G>T (p.Val863Leu) c.2209G>T (p.Val737Leu) c.2332G>T (p.Val778Leu) c.2308G>T (p.Val770Leu) c.2176G>T (p.Val726Leu) c.2098G>T (p.Val700Leu) n.2618G>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.56881788T>A | CA359786118 | MAP3K1 | c.2588T>A (p.Val863Glu) c.2210T>A (p.Val737Glu) c.2333T>A (p.Val778Glu) c.2309T>A (p.Val770Glu) c.2177T>A (p.Val726Glu) c.2099T>A (p.Val700Glu) n.2619T>A | |
5 | g.56881788T>C | CA3273025 | MAP3K1 | c.2588T>C (p.Val863Ala) c.2210T>C (p.Val737Ala) c.2333T>C (p.Val778Ala) c.2309T>C (p.Val770Ala) c.2177T>C (p.Val726Ala) c.2099T>C (p.Val700Ala) n.2619T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.56881788T>G | CA359786119 | MAP3K1 | c.2588T>G (p.Val863Gly) c.2210T>G (p.Val737Gly) c.2333T>G (p.Val778Gly) c.2309T>G (p.Val770Gly) c.2177T>G (p.Val726Gly) c.2099T>G (p.Val700Gly) n.2619T>G | |
5 | g.56881788T= | CA1548139303 | MAP3K1 | c.2588T= (p.Val863=) c.2210T= (p.Val737=) c.2333T= (p.Val778=) c.2309T= (p.Val770=) c.2177T= (p.Val726=) c.2099T= (p.Val700=) n.2619T= | |
5 | g.56881789G>A | CA444399185 | MAP3K1 | c.2589G>A (p.Val863=) c.2211G>A (p.Val737=) c.2334G>A (p.Val778=) c.2310G>A (p.Val770=) c.2178G>A (p.Val726=) c.2100G>A (p.Val700=) n.2620G>A | dbSNP |
5 | g.56881789G>C | CA444399186 | MAP3K1 | c.2589G>C (p.Val863=) c.2211G>C (p.Val737=) c.2334G>C (p.Val778=) c.2310G>C (p.Val770=) c.2178G>C (p.Val726=) c.2100G>C (p.Val700=) n.2620G>C | |
5 | g.56881789G= | CA1548139304 | MAP3K1 | c.2589G= (p.Val863=) c.2211G= (p.Val737=) c.2334G= (p.Val778=) c.2310G= (p.Val770=) c.2178G= (p.Val726=) c.2100G= (p.Val700=) n.2620G= | |
5 | g.56881789G>T | CA444399188 | MAP3K1 | c.2589G>T (p.Val863=) c.2211G>T (p.Val737=) c.2334G>T (p.Val778=) c.2310G>T (p.Val770=) c.2178G>T (p.Val726=) c.2100G>T (p.Val700=) n.2620G>T | |
5 | g.56881790G>A | CA359786122 | MAP3K1 | c.2590G>A (p.Glu864Lys) c.2212G>A (p.Glu738Lys) c.2335G>A (p.Glu779Lys) c.2311G>A (p.Glu771Lys) c.2179G>A (p.Glu727Lys) c.2101G>A (p.Glu701Lys) n.2621G>A | gnomAD v4 |
5 | g.56881790G>C | CA359786120 | MAP3K1 | c.2590G>C (p.Glu864Gln) c.2212G>C (p.Glu738Gln) c.2335G>C (p.Glu779Gln) c.2311G>C (p.Glu771Gln) c.2179G>C (p.Glu727Gln) c.2101G>C (p.Glu701Gln) n.2621G>C | |
5 | g.56881790G>T | CA359786121 | MAP3K1 | c.2590G>T (p.Glu864Ter) c.2212G>T (p.Glu738Ter) c.2335G>T (p.Glu779Ter) c.2311G>T (p.Glu771Ter) c.2179G>T (p.Glu727Ter) c.2101G>T (p.Glu701Ter) n.2621G>T | |
5 | g.56881791A= | CA1548139305 | MAP3K1 | c.2591A= (p.Glu864=) c.2213A= (p.Glu738=) c.2336A= (p.Glu779=) c.2312A= (p.Glu771=) c.2180A= (p.Glu727=) c.2102A= (p.Glu701=) n.2622A= | |
5 | g.56881791A>C | CA359786123 | MAP3K1 | c.2591A>C (p.Glu864Ala) c.2213A>C (p.Glu738Ala) c.2336A>C (p.Glu779Ala) c.2312A>C (p.Glu771Ala) c.2180A>C (p.Glu727Ala) c.2102A>C (p.Glu701Ala) n.2622A>C | dbSNP gnomAD v2 gnomAD v4 |
5 | g.56881791A>G | CA359786124 | MAP3K1 | c.2591A>G (p.Glu864Gly) c.2213A>G (p.Glu738Gly) c.2336A>G (p.Glu779Gly) c.2312A>G (p.Glu771Gly) c.2180A>G (p.Glu727Gly) c.2102A>G (p.Glu701Gly) n.2622A>G | dbSNP |
5 | g.56881791A>T | CA359786125 | MAP3K1 | c.2591A>T (p.Glu864Val) c.2213A>T (p.Glu738Val) c.2336A>T (p.Glu779Val) c.2312A>T (p.Glu771Val) c.2180A>T (p.Glu727Val) c.2102A>T (p.Glu701Val) n.2622A>T | |
5 | g.56881792A= | CA1548139306 | MAP3K1 | c.2592A= (p.Glu864=) c.2214A= (p.Glu738=) c.2337A= (p.Glu779=) c.2313A= (p.Glu771=) c.2181A= (p.Glu727=) c.2103A= (p.Glu701=) n.2623A= | |
5 | g.56881792A>C | CA359786126 | MAP3K1 | c.2592A>C (p.Glu864Asp) c.2214A>C (p.Glu738Asp) c.2337A>C (p.Glu779Asp) c.2313A>C (p.Glu771Asp) c.2181A>C (p.Glu727Asp) c.2103A>C (p.Glu701Asp) n.2623A>C | dbSNP gnomAD v2 gnomAD v4 COSMIC |
5 | g.56881792A>G | CA444399194 | MAP3K1 | c.2592A>G (p.Glu864=) c.2214A>G (p.Glu738=) c.2337A>G (p.Glu779=) c.2313A>G (p.Glu771=) c.2181A>G (p.Glu727=) c.2103A>G (p.Glu701=) n.2623A>G | dbSNP gnomAD v3 gnomAD v4 |
5 | g.56881792A>T | CA359786127 | MAP3K1 | c.2592A>T (p.Glu864Asp) c.2214A>T (p.Glu738Asp) c.2337A>T (p.Glu779Asp) c.2313A>T (p.Glu771Asp) c.2181A>T (p.Glu727Asp) c.2103A>T (p.Glu701Asp) n.2623A>T | |
5 | g.56881793A>C | CA359786128 | MAP3K1 | c.2593A>C (p.Ile865Leu) c.2215A>C (p.Ile739Leu) c.2338A>C (p.Ile780Leu) c.2314A>C (p.Ile772Leu) c.2182A>C (p.Ile728Leu) c.2104A>C (p.Ile702Leu) n.2624A>C | gnomAD v4 |
5 | g.56881793A>G | CA359786129 | MAP3K1 | c.2593A>G (p.Ile865Val) c.2215A>G (p.Ile739Val) c.2338A>G (p.Ile780Val) c.2314A>G (p.Ile772Val) c.2182A>G (p.Ile728Val) c.2104A>G (p.Ile702Val) n.2624A>G | |
5 | g.56881793A>T | CA359786130 | MAP3K1 | c.2593A>T (p.Ile865Phe) c.2215A>T (p.Ile739Phe) c.2338A>T (p.Ile780Phe) c.2314A>T (p.Ile772Phe) c.2182A>T (p.Ile728Phe) c.2104A>T (p.Ile702Phe) n.2624A>T | |
5 | g.56881794T>A | CA359786131 | MAP3K1 | c.2594T>A (p.Ile865Asn) c.2216T>A (p.Ile739Asn) c.2339T>A (p.Ile780Asn) c.2315T>A (p.Ile772Asn) c.2183T>A (p.Ile728Asn) c.2105T>A (p.Ile702Asn) n.2625T>A | |
5 | g.56881794T>C | CA359786132 | MAP3K1 | c.2594T>C (p.Ile865Thr) c.2216T>C (p.Ile739Thr) c.2339T>C (p.Ile780Thr) c.2315T>C (p.Ile772Thr) c.2183T>C (p.Ile728Thr) c.2105T>C (p.Ile702Thr) n.2625T>C | |
5 | g.56881794T>G | CA359786133 | MAP3K1 | c.2594T>G (p.Ile865Ser) c.2216T>G (p.Ile739Ser) c.2339T>G (p.Ile780Ser) c.2315T>G (p.Ile772Ser) c.2183T>G (p.Ile728Ser) c.2105T>G (p.Ile702Ser) n.2625T>G | |
5 | g.56881795T>A | CA444399198 | MAP3K1 | c.2595T>A (p.Ile865=) c.2217T>A (p.Ile739=) c.2340T>A (p.Ile780=) c.2316T>A (p.Ile772=) c.2184T>A (p.Ile728=) c.2106T>A (p.Ile702=) n.2626T>A | |
5 | g.56881795T>C | CA444399199 | MAP3K1 | c.2595T>C (p.Ile865=) c.2217T>C (p.Ile739=) c.2340T>C (p.Ile780=) c.2316T>C (p.Ile772=) c.2184T>C (p.Ile728=) c.2106T>C (p.Ile702=) n.2626T>C | gnomAD v4 |
5 | g.56881795T>G | CA359786134 | MAP3K1 | c.2595T>G (p.Ile865Met) c.2217T>G (p.Ile739Met) c.2340T>G (p.Ile780Met) c.2316T>G (p.Ile772Met) c.2184T>G (p.Ile728Met) c.2106T>G (p.Ile702Met) n.2626T>G | |
5 | g.56881796G>A | CA359786136 | MAP3K1 | c.2596G>A (p.Ala866Thr) c.2218G>A (p.Ala740Thr) c.2341G>A (p.Ala781Thr) c.2317G>A (p.Ala773Thr) c.2185G>A (p.Ala729Thr) c.2107G>A (p.Ala703Thr) n.2627G>A | dbSNP |
5 | g.56881796G>C | CA359786137 | MAP3K1 | c.2596G>C (p.Ala866Pro) c.2218G>C (p.Ala740Pro) c.2341G>C (p.Ala781Pro) c.2317G>C (p.Ala773Pro) c.2185G>C (p.Ala729Pro) c.2107G>C (p.Ala703Pro) n.2627G>C | |
5 | g.56881796G>T | CA359786135 | MAP3K1 | c.2596G>T (p.Ala866Ser) c.2218G>T (p.Ala740Ser) c.2341G>T (p.Ala781Ser) c.2317G>T (p.Ala773Ser) c.2185G>T (p.Ala729Ser) c.2107G>T (p.Ala703Ser) n.2627G>T | |
5 | g.56881797C>A | CA359786139 | MAP3K1 | c.2597C>A (p.Ala866Asp) c.2219C>A (p.Ala740Asp) c.2342C>A (p.Ala781Asp) c.2318C>A (p.Ala773Asp) c.2186C>A (p.Ala729Asp) c.2108C>A (p.Ala703Asp) n.2628C>A | dbSNP |
5 | g.56881797C= | CA1548139307 | MAP3K1 | c.2597C= (p.Ala866=) c.2219C= (p.Ala740=) c.2342C= (p.Ala781=) c.2318C= (p.Ala773=) c.2186C= (p.Ala729=) c.2108C= (p.Ala703=) n.2628C= | |
5 | g.56881797C>G | CA3273026 | MAP3K1 | c.2597C>G (p.Ala866Gly) c.2219C>G (p.Ala740Gly) c.2342C>G (p.Ala781Gly) c.2318C>G (p.Ala773Gly) c.2186C>G (p.Ala729Gly) c.2108C>G (p.Ala703Gly) n.2628C>G | dbSNP ExAC gnomAD v2 |
5 | g.56881797C>T | CA359786138 | MAP3K1 | c.2597C>T (p.Ala866Val) c.2219C>T (p.Ala740Val) c.2342C>T (p.Ala781Val) c.2318C>T (p.Ala773Val) c.2186C>T (p.Ala729Val) c.2108C>T (p.Ala703Val) n.2628C>T | dbSNP |
5 | g.56881798C>A | CA444399202 | MAP3K1 | c.2598C>A (p.Ala866=) c.2220C>A (p.Ala740=) c.2343C>A (p.Ala781=) c.2319C>A (p.Ala773=) c.2187C>A (p.Ala729=) c.2109C>A (p.Ala703=) n.2629C>A | dbSNP |
5 | g.56881798C= | CA1548139308 | MAP3K1 | c.2598C= (p.Ala866=) c.2220C= (p.Ala740=) c.2343C= (p.Ala781=) c.2319C= (p.Ala773=) c.2187C= (p.Ala729=) c.2109C= (p.Ala703=) n.2629C= | |
5 | g.56881798C>G | CA444399203 | MAP3K1 | c.2598C>G (p.Ala866=) c.2220C>G (p.Ala740=) c.2343C>G (p.Ala781=) c.2319C>G (p.Ala773=) c.2187C>G (p.Ala729=) c.2109C>G (p.Ala703=) n.2629C>G | gnomAD v4 |
5 | g.56881798C>T | CA3273027 | MAP3K1 | c.2598C>T (p.Ala866=) c.2220C>T (p.Ala740=) c.2343C>T (p.Ala781=) c.2319C>T (p.Ala773=) c.2187C>T (p.Ala729=) c.2109C>T (p.Ala703=) n.2629C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.56881799G>A | CA3273028 | MAP3K1 | c.2599G>A (p.Glu867Lys) c.2221G>A (p.Glu741Lys) c.2344G>A (p.Glu782Lys) c.2320G>A (p.Glu774Lys) c.2188G>A (p.Glu730Lys) c.2110G>A (p.Glu704Lys) n.2630G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.56881799G>C | CA359786140 | MAP3K1 | c.2599G>C (p.Glu867Gln) c.2221G>C (p.Glu741Gln) c.2344G>C (p.Glu782Gln) c.2320G>C (p.Glu774Gln) c.2188G>C (p.Glu730Gln) c.2110G>C (p.Glu704Gln) n.2630G>C | |
5 | g.56881799G= | CA1548139309 | MAP3K1 | c.2599G= (p.Glu867=) c.2221G= (p.Glu741=) c.2344G= (p.Glu782=) c.2320G= (p.Glu774=) c.2188G= (p.Glu730=) c.2110G= (p.Glu704=) n.2630G= | |
5 | g.56881799G>T | CA359786141 | MAP3K1 | c.2599G>T (p.Glu867Ter) c.2221G>T (p.Glu741Ter) c.2344G>T (p.Glu782Ter) c.2320G>T (p.Glu774Ter) c.2188G>T (p.Glu730Ter) c.2110G>T (p.Glu704Ter) n.2630G>T | |
5 | g.56881800A= | CA1548139310 | MAP3K1 | c.2600A= (p.Glu867=) c.2222A= (p.Glu741=) c.2345A= (p.Glu782=) c.2321A= (p.Glu774=) c.2189A= (p.Glu730=) c.2111A= (p.Glu704=) n.2631A= | |
5 | g.56881800A>C | CA359786142 | MAP3K1 | c.2600A>C (p.Glu867Ala) c.2222A>C (p.Glu741Ala) c.2345A>C (p.Glu782Ala) c.2321A>C (p.Glu774Ala) c.2189A>C (p.Glu730Ala) c.2111A>C (p.Glu704Ala) n.2631A>C | dbSNP gnomAD v3 gnomAD v4 |
5 | g.56881800A>G | CA359786143 | MAP3K1 | c.2600A>G (p.Glu867Gly) c.2222A>G (p.Glu741Gly) c.2345A>G (p.Glu782Gly) c.2321A>G (p.Glu774Gly) c.2189A>G (p.Glu730Gly) c.2111A>G (p.Glu704Gly) n.2631A>G | |
5 | g.56881800A>T | CA359786144 | MAP3K1 | c.2600A>T (p.Glu867Val) c.2222A>T (p.Glu741Val) c.2345A>T (p.Glu782Val) c.2321A>T (p.Glu774Val) c.2189A>T (p.Glu730Val) c.2111A>T (p.Glu704Val) n.2631A>T | |
5 | g.56881801A>C | CA359786145 | MAP3K1 | c.2601A>C (p.Glu867Asp) c.2223A>C (p.Glu741Asp) c.2346A>C (p.Glu782Asp) c.2322A>C (p.Glu774Asp) c.2190A>C (p.Glu730Asp) c.2112A>C (p.Glu704Asp) n.2632A>C | |
5 | g.56881801A>G | CA444399205 | MAP3K1 | c.2601A>G (p.Glu867=) c.2223A>G (p.Glu741=) c.2346A>G (p.Glu782=) c.2322A>G (p.Glu774=) c.2190A>G (p.Glu730=) c.2112A>G (p.Glu704=) n.2632A>G | |
5 | g.56881801A>T | CA359786146 | MAP3K1 | c.2601A>T (p.Glu867Asp) c.2223A>T (p.Glu741Asp) c.2346A>T (p.Glu782Asp) c.2322A>T (p.Glu774Asp) c.2190A>T (p.Glu730Asp) c.2112A>T (p.Glu704Asp) n.2632A>T | |
5 | g.56881802G>A | CA359786149 | MAP3K1 | c.2602G>A (p.Ala868Thr) c.2224G>A (p.Ala742Thr) c.2347G>A (p.Ala783Thr) c.2323G>A (p.Ala775Thr) c.2191G>A (p.Ala731Thr) c.2113G>A (p.Ala705Thr) n.2633G>A | dbSNP |
5 | g.56881802G>C | CA359786148 | MAP3K1 | c.2602G>C (p.Ala868Pro) c.2224G>C (p.Ala742Pro) c.2347G>C (p.Ala783Pro) c.2323G>C (p.Ala775Pro) c.2191G>C (p.Ala731Pro) c.2113G>C (p.Ala705Pro) n.2633G>C | |
5 | g.56881802G>T | CA359786147 | MAP3K1 | c.2602G>T (p.Ala868Ser) c.2224G>T (p.Ala742Ser) c.2347G>T (p.Ala783Ser) c.2323G>T (p.Ala775Ser) c.2191G>T (p.Ala731Ser) c.2113G>T (p.Ala705Ser) n.2633G>T | |
5 | g.56881803C>A | CA359786150 | MAP3K1 | c.2603C>A (p.Ala868Asp) c.2225C>A (p.Ala742Asp) c.2348C>A (p.Ala783Asp) c.2324C>A (p.Ala775Asp) c.2192C>A (p.Ala731Asp) c.2114C>A (p.Ala705Asp) n.2634C>A | |
5 | g.56881803C>G | CA359786151 | MAP3K1 | c.2603C>G (p.Ala868Gly) c.2225C>G (p.Ala742Gly) c.2348C>G (p.Ala783Gly) c.2324C>G (p.Ala775Gly) c.2192C>G (p.Ala731Gly) c.2114C>G (p.Ala705Gly) n.2634C>G | gnomAD v4 |
5 | g.56881803C>T | CA359786152 | MAP3K1 | c.2603C>T (p.Ala868Val) c.2225C>T (p.Ala742Val) c.2348C>T (p.Ala783Val) c.2324C>T (p.Ala775Val) c.2192C>T (p.Ala731Val) c.2114C>T (p.Ala705Val) n.2634C>T | dbSNP |
5 | g.56881804C>A | CA444399209 | MAP3K1 | c.2604C>A (p.Ala868=) c.2226C>A (p.Ala742=) c.2349C>A (p.Ala783=) c.2325C>A (p.Ala775=) c.2193C>A (p.Ala731=) c.2115C>A (p.Ala705=) n.2635C>A | |
5 | g.56881804C= | CA1548139311 | MAP3K1 | c.2604C= (p.Ala868=) c.2226C= (p.Ala742=) c.2349C= (p.Ala783=) c.2325C= (p.Ala775=) c.2193C= (p.Ala731=) c.2115C= (p.Ala705=) n.2635C= | |
5 | g.56881804C>G | CA119079229 | MAP3K1 | c.2604C>G (p.Ala868=) c.2226C>G (p.Ala742=) c.2349C>G (p.Ala783=) c.2325C>G (p.Ala775=) c.2193C>G (p.Ala731=) c.2115C>G (p.Ala705=) n.2635C>G | dbSNP |
5 | g.56881804C>T | CA444399211 | MAP3K1 | c.2604C>T (p.Ala868=) c.2226C>T (p.Ala742=) c.2349C>T (p.Ala783=) c.2325C>T (p.Ala775=) c.2193C>T (p.Ala731=) c.2115C>T (p.Ala705=) n.2635C>T | gnomAD v4 |
5 | g.56881805A= | CA1548139312 | MAP3K1 | c.2605A= (p.Ile869=) c.2227A= (p.Ile743=) c.2350A= (p.Ile784=) c.2326A= (p.Ile776=) c.2194A= (p.Ile732=) c.2116A= (p.Ile706=) n.2636A= | |
5 | g.56881805A>C | CA359786153 | MAP3K1 | c.2605A>C (p.Ile869Leu) c.2227A>C (p.Ile743Leu) c.2350A>C (p.Ile784Leu) c.2326A>C (p.Ile776Leu) c.2194A>C (p.Ile732Leu) c.2116A>C (p.Ile706Leu) n.2636A>C | |
5 | g.56881805A>G | CA3273029 | MAP3K1 | c.2605A>G (p.Ile869Val) c.2227A>G (p.Ile743Val) c.2350A>G (p.Ile784Val) c.2326A>G (p.Ile776Val) c.2194A>G (p.Ile732Val) c.2116A>G (p.Ile706Val) n.2636A>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.56881805A>T | CA359786154 | MAP3K1 | c.2605A>T (p.Ile869Phe) c.2227A>T (p.Ile743Phe) c.2350A>T (p.Ile784Phe) c.2326A>T (p.Ile776Phe) c.2194A>T (p.Ile732Phe) c.2116A>T (p.Ile706Phe) n.2636A>T | |
5 | g.56881806T>A | CA359786155 | MAP3K1 | c.2606T>A (p.Ile869Asn) c.2228T>A (p.Ile743Asn) c.2351T>A (p.Ile784Asn) c.2327T>A (p.Ile776Asn) c.2195T>A (p.Ile732Asn) c.2117T>A (p.Ile706Asn) n.2637T>A | gnomAD v4 |
5 | g.56881806T>C | CA359786156 | MAP3K1 | c.2606T>C (p.Ile869Thr) c.2228T>C (p.Ile743Thr) c.2351T>C (p.Ile784Thr) c.2327T>C (p.Ile776Thr) c.2195T>C (p.Ile732Thr) c.2117T>C (p.Ile706Thr) n.2637T>C | |
5 | g.56881806T>G | CA359786157 | MAP3K1 | c.2606T>G (p.Ile869Ser) c.2228T>G (p.Ile743Ser) c.2351T>G (p.Ile784Ser) c.2327T>G (p.Ile776Ser) c.2195T>G (p.Ile732Ser) c.2117T>G (p.Ile706Ser) n.2637T>G | |
5 | g.56881807C>A | CA444399216 | MAP3K1 | c.2607C>A (p.Ile869=) c.2229C>A (p.Ile743=) c.2352C>A (p.Ile784=) c.2328C>A (p.Ile776=) c.2196C>A (p.Ile732=) c.2118C>A (p.Ile706=) n.2638C>A | |
5 | g.56881807C= | CA1548139313 | MAP3K1 | c.2607C= (p.Ile869=) c.2229C= (p.Ile743=) c.2352C= (p.Ile784=) c.2328C= (p.Ile776=) c.2196C= (p.Ile732=) c.2118C= (p.Ile706=) n.2638C= | |
5 | g.56881807C>G | CA359786158 | MAP3K1 | c.2607C>G (p.Ile869Met) c.2229C>G (p.Ile743Met) c.2352C>G (p.Ile784Met) c.2328C>G (p.Ile776Met) c.2196C>G (p.Ile732Met) c.2118C>G (p.Ile706Met) n.2638C>G | dbSNP gnomAD v2 gnomAD v4 |
5 | g.56881807C>T | CA444399215 | MAP3K1 | c.2607C>T (p.Ile869=) c.2229C>T (p.Ile743=) c.2352C>T (p.Ile784=) c.2328C>T (p.Ile776=) c.2196C>T (p.Ile732=) c.2118C>T (p.Ile706=) n.2638C>T | |
5 | g.56881808C>A | CA359786159 | MAP3K1 | c.2608C>A (p.Gln870Lys) c.2230C>A (p.Gln744Lys) c.2353C>A (p.Gln785Lys) c.2329C>A (p.Gln777Lys) c.2197C>A (p.Gln733Lys) c.2119C>A (p.Gln707Lys) n.2639C>A | |
5 | g.56881808C= | CA1548139314 | MAP3K1 | c.2608C= (p.Gln870=) c.2230C= (p.Gln744=) c.2353C= (p.Gln785=) c.2329C= (p.Gln777=) c.2197C= (p.Gln733=) c.2119C= (p.Gln707=) n.2639C= | |
5 | g.56881808C>G | CA359786160 | MAP3K1 | c.2608C>G (p.Gln870Glu) c.2230C>G (p.Gln744Glu) c.2353C>G (p.Gln785Glu) c.2329C>G (p.Gln777Glu) c.2197C>G (p.Gln733Glu) c.2119C>G (p.Gln707Glu) n.2639C>G | |
5 | g.56881808C>T | CA3273030 | MAP3K1 | c.2608C>T (p.Gln870Ter) c.2230C>T (p.Gln744Ter) c.2353C>T (p.Gln785Ter) c.2329C>T (p.Gln777Ter) c.2197C>T (p.Gln733Ter) c.2119C>T (p.Gln707Ter) n.2639C>T | dbSNP ExAC gnomAD v2 |
5 | g.56881809A= | CA1548139315 | MAP3K1 | c.2609A= (p.Gln870=) c.2231A= (p.Gln744=) c.2354A= (p.Gln785=) c.2330A= (p.Gln777=) c.2198A= (p.Gln733=) c.2120A= (p.Gln707=) n.2640A= | |
5 | g.56881809A>C | CA359786162 | MAP3K1 | c.2609A>C (p.Gln870Pro) c.2231A>C (p.Gln744Pro) c.2354A>C (p.Gln785Pro) c.2330A>C (p.Gln777Pro) c.2198A>C (p.Gln733Pro) c.2120A>C (p.Gln707Pro) n.2640A>C | |
5 | g.56881809A>G | CA359786163 | MAP3K1 | c.2609A>G (p.Gln870Arg) c.2231A>G (p.Gln744Arg) c.2354A>G (p.Gln785Arg) c.2330A>G (p.Gln777Arg) c.2198A>G (p.Gln733Arg) c.2120A>G (p.Gln707Arg) n.2640A>G | |
5 | g.56881809A>T | CA359786161 | MAP3K1 | c.2609A>T (p.Gln870Leu) c.2231A>T (p.Gln744Leu) c.2354A>T (p.Gln785Leu) c.2330A>T (p.Gln777Leu) c.2198A>T (p.Gln733Leu) c.2120A>T (p.Gln707Leu) n.2640A>T | dbSNP |
5 | g.56881810G>A | CA444399221 | MAP3K1 | c.2610G>A (p.Gln870=) c.2232G>A (p.Gln744=) c.2355G>A (p.Gln785=) c.2331G>A (p.Gln777=) c.2199G>A (p.Gln733=) c.2121G>A (p.Gln707=) n.2641G>A | dbSNP |
5 | g.56881810G>C | CA359786164 | MAP3K1 | c.2610G>C (p.Gln870His) c.2232G>C (p.Gln744His) c.2355G>C (p.Gln785His) c.2331G>C (p.Gln777His) c.2199G>C (p.Gln733His) c.2121G>C (p.Gln707His) n.2641G>C | |
5 | g.56881810G>T | CA359786165 | MAP3K1 | c.2610G>T (p.Gln870His) c.2232G>T (p.Gln744His) c.2355G>T (p.Gln785His) c.2331G>T (p.Gln777His) c.2199G>T (p.Gln733His) c.2121G>T (p.Gln707His) n.2641G>T | gnomAD v4 |
5 | g.56881810_56881811insCTGAGTGTTTCCAGTTCCACTCACTTCACCAGGATGCGTCGCCGT | CA2673909975 | MAP3K1 | c.2610_2611insCTGAGTGTTTCCAGTTCCACTCACTTCACCAGGATGCGTCGCCGT (p.Gln870_Leu871insLeuSerValSerSerSerThrHisPheThrArgMetArgArgArg) c.2232_2233insCTGAGTGTTTCCAGTTCCACTCACTTCACCAGGATGCGTCGCCGT (p.Gln744_Leu745insLeuSerValSerSerSerThrHisPheThrArgMetArgArgArg) c.2355_2356insCTGAGTGTTTCCAGTTCCACTCACTTCACCAGGATGCGTCGCCGT (p.Gln785_Leu786insLeuSerValSerSerSerThrHisPheThrArgMetArgArgArg) c.2331_2332insCTGAGTGTTTCCAGTTCCACTCACTTCACCAGGATGCGTCGCCGT (p.Gln777_Leu778insLeuSerValSerSerSerThrHisPheThrArgMetArgArgArg) c.2199_2200insCTGAGTGTTTCCAGTTCCACTCACTTCACCAGGATGCGTCGCCGT (p.Gln733_Leu734insLeuSerValSerSerSerThrHisPheThrArgMetArgArgArg) c.2121_2122insCTGAGTGTTTCCAGTTCCACTCACTTCACCAGGATGCGTCGCCGT (p.Gln707_Leu708insLeuSerValSerSerSerThrHisPheThrArgMetArgArgArg) n.2641_2642insCTGAGTGTTTCCAGTTCCACTCACTTCACCAGGATGCGTCGCCGT | gnomAD v4 |
5 | g.56881811T>A | CA359786166 | MAP3K1 | c.2611T>A (p.Leu871Met) c.2233T>A (p.Leu745Met) c.2356T>A (p.Leu786Met) c.2332T>A (p.Leu778Met) c.2200T>A (p.Leu734Met) c.2122T>A (p.Leu708Met) n.2642T>A | dbSNP gnomAD v4 |
5 | g.56881811T>C | CA444399222 | MAP3K1 | c.2611T>C (p.Leu871=) c.2233T>C (p.Leu745=) c.2356T>C (p.Leu786=) c.2332T>C (p.Leu778=) c.2200T>C (p.Leu734=) c.2122T>C (p.Leu708=) n.2642T>C | dbSNP |
5 | g.56881811T>G | CA359786167 | MAP3K1 | c.2611T>G (p.Leu871Val) c.2233T>G (p.Leu745Val) c.2356T>G (p.Leu786Val) c.2332T>G (p.Leu778Val) c.2200T>G (p.Leu734Val) c.2122T>G (p.Leu708Val) n.2642T>G | |
5 | g.56881811T= | CA1548139316 | MAP3K1 | c.2611T= (p.Leu871=) c.2233T= (p.Leu745=) c.2356T= (p.Leu786=) c.2332T= (p.Leu778=) c.2200T= (p.Leu734=) c.2122T= (p.Leu708=) n.2642T= | |
5 | g.56881812T>A | CA359786168 | MAP3K1 | c.2612T>A (p.Leu871Ter) c.2234T>A (p.Leu745Ter) c.2357T>A (p.Leu786Ter) c.2333T>A (p.Leu778Ter) c.2201T>A (p.Leu734Ter) c.2123T>A (p.Leu708Ter) n.2643T>A | |
5 | g.56881812T>C | CA359786169 | MAP3K1 | c.2612T>C (p.Leu871Ser) c.2234T>C (p.Leu745Ser) c.2357T>C (p.Leu786Ser) c.2333T>C (p.Leu778Ser) c.2201T>C (p.Leu734Ser) c.2123T>C (p.Leu708Ser) n.2643T>C | |
5 | g.56881812T>G | CA359786170 | MAP3K1 | c.2612T>G (p.Leu871Trp) c.2234T>G (p.Leu745Trp) c.2357T>G (p.Leu786Trp) c.2333T>G (p.Leu778Trp) c.2201T>G (p.Leu734Trp) c.2123T>G (p.Leu708Trp) n.2643T>G | |
5 | g.56881813G>A | CA444399224 | MAP3K1 | c.2613G>A (p.Leu871=) c.2235G>A (p.Leu745=) c.2358G>A (p.Leu786=) c.2334G>A (p.Leu778=) c.2202G>A (p.Leu734=) c.2124G>A (p.Leu708=) n.2644G>A | dbSNP |
5 | g.56881813G>C | CA359786171 | MAP3K1 | c.2613G>C (p.Leu871Phe) c.2235G>C (p.Leu745Phe) c.2358G>C (p.Leu786Phe) c.2334G>C (p.Leu778Phe) c.2202G>C (p.Leu734Phe) c.2124G>C (p.Leu708Phe) n.2644G>C | |
5 | g.56881813G= | CA1548139317 | MAP3K1 | c.2613G= (p.Leu871=) c.2235G= (p.Leu745=) c.2358G= (p.Leu786=) c.2334G= (p.Leu778=) c.2202G= (p.Leu734=) c.2124G= (p.Leu708=) n.2644G= | |
5 | g.56881813G>T | CA359786172 | MAP3K1 | c.2613G>T (p.Leu871Phe) c.2235G>T (p.Leu745Phe) c.2358G>T (p.Leu786Phe) c.2334G>T (p.Leu778Phe) c.2202G>T (p.Leu734Phe) c.2124G>T (p.Leu708Phe) n.2644G>T | |
5 | g.56881814G>A | CA119079250 | MAP3K1 | c.2614G>A (p.Gly872Ser) c.2236G>A (p.Gly746Ser) c.2359G>A (p.Gly787Ser) c.2335G>A (p.Gly779Ser) c.2203G>A (p.Gly735Ser) c.2125G>A (p.Gly709Ser) n.2645G>A | dbSNP |
5 | g.56881814G>C | CA359786173 | MAP3K1 | c.2614G>C (p.Gly872Arg) c.2236G>C (p.Gly746Arg) c.2359G>C (p.Gly787Arg) c.2335G>C (p.Gly779Arg) c.2203G>C (p.Gly735Arg) c.2125G>C (p.Gly709Arg) n.2645G>C | gnomAD v4 |
5 | g.56881814G= | CA1548139318 | MAP3K1 | c.2614G= (p.Gly872=) c.2236G= (p.Gly746=) c.2359G= (p.Gly787=) c.2335G= (p.Gly779=) c.2203G= (p.Gly735=) c.2125G= (p.Gly709=) n.2645G= | |
5 | g.56881814G>T | CA359786174 | MAP3K1 | c.2614G>T (p.Gly872Cys) c.2236G>T (p.Gly746Cys) c.2359G>T (p.Gly787Cys) c.2335G>T (p.Gly779Cys) c.2203G>T (p.Gly735Cys) c.2125G>T (p.Gly709Cys) n.2645G>T | |
5 | g.56881815G>A | CA359786175 | MAP3K1 | c.2615G>A (p.Gly872Asp) c.2237G>A (p.Gly746Asp) c.2360G>A (p.Gly787Asp) c.2336G>A (p.Gly779Asp) c.2204G>A (p.Gly735Asp) c.2126G>A (p.Gly709Asp) n.2646G>A | |
5 | g.56881815G>C | CA359786176 | MAP3K1 | c.2615G>C (p.Gly872Ala) c.2237G>C (p.Gly746Ala) c.2360G>C (p.Gly787Ala) c.2336G>C (p.Gly779Ala) c.2204G>C (p.Gly735Ala) c.2126G>C (p.Gly709Ala) n.2646G>C | |
5 | g.56881815G= | CA1548139319 | MAP3K1 | c.2615G= (p.Gly872=) c.2237G= (p.Gly746=) c.2360G= (p.Gly787=) c.2336G= (p.Gly779=) c.2204G= (p.Gly735=) c.2126G= (p.Gly709=) n.2646G= | |
5 | g.56881815G>T | CA3273031 | MAP3K1 | c.2615G>T (p.Gly872Val) c.2237G>T (p.Gly746Val) c.2360G>T (p.Gly787Val) c.2336G>T (p.Gly779Val) c.2204G>T (p.Gly735Val) c.2126G>T (p.Gly709Val) n.2646G>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.56881816C>A | CA444399227 | MAP3K1 | c.2616C>A (p.Gly872=) c.2238C>A (p.Gly746=) c.2361C>A (p.Gly787=) c.2337C>A (p.Gly779=) c.2205C>A (p.Gly735=) c.2127C>A (p.Gly709=) n.2647C>A | dbSNP |
5 | g.56881816C= | CA1548139320 | MAP3K1 | c.2616C= (p.Gly872=) c.2238C= (p.Gly746=) c.2361C= (p.Gly787=) c.2337C= (p.Gly779=) c.2205C= (p.Gly735=) c.2127C= (p.Gly709=) n.2647C= | |
5 | g.56881816C>G | CA444399230 | MAP3K1 | c.2616C>G (p.Gly872=) c.2238C>G (p.Gly746=) c.2361C>G (p.Gly787=) c.2337C>G (p.Gly779=) c.2205C>G (p.Gly735=) c.2127C>G (p.Gly709=) n.2647C>G | |
5 | g.56881816C>T | CA444399231 | MAP3K1 | c.2616C>T (p.Gly872=) c.2238C>T (p.Gly746=) c.2361C>T (p.Gly787=) c.2337C>T (p.Gly779=) c.2205C>T (p.Gly735=) c.2127C>T (p.Gly709=) n.2647C>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.56881817G>A | CA3273032 | MAP3K1 | c.2617G>A (p.Val873Ile) c.2239G>A (p.Val747Ile) c.2362G>A (p.Val788Ile) c.2338G>A (p.Val780Ile) c.2206G>A (p.Val736Ile) c.2128G>A (p.Val710Ile) n.2648G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.56881817G>C | CA359786177 | MAP3K1 | c.2617G>C (p.Val873Leu) c.2239G>C (p.Val747Leu) c.2362G>C (p.Val788Leu) c.2338G>C (p.Val780Leu) c.2206G>C (p.Val736Leu) c.2128G>C (p.Val710Leu) n.2648G>C | dbSNP |
5 | g.56881817G= | CA1548139321 | MAP3K1 | c.2617G= (p.Val873=) c.2239G= (p.Val747=) c.2362G= (p.Val788=) c.2338G= (p.Val780=) c.2206G= (p.Val736=) c.2128G= (p.Val710=) n.2648G= | |
5 | g.56881817G>T | CA359786178 | MAP3K1 | c.2617G>T (p.Val873Leu) c.2239G>T (p.Val747Leu) c.2362G>T (p.Val788Leu) c.2338G>T (p.Val780Leu) c.2206G>T (p.Val736Leu) c.2128G>T (p.Val710Leu) n.2648G>T | dbSNP gnomAD v2 gnomAD v4 |
5 | g.56881818T>A | CA359786179 | MAP3K1 | c.2618T>A (p.Val873Glu) c.2240T>A (p.Val747Glu) c.2363T>A (p.Val788Glu) c.2339T>A (p.Val780Glu) c.2207T>A (p.Val736Glu) c.2129T>A (p.Val710Glu) n.2649T>A | |
5 | g.56881818T>C | CA359786180 | MAP3K1 | c.2618T>C (p.Val873Ala) c.2240T>C (p.Val747Ala) c.2363T>C (p.Val788Ala) c.2339T>C (p.Val780Ala) c.2207T>C (p.Val736Ala) c.2129T>C (p.Val710Ala) n.2649T>C | |
5 | g.56881818T>G | CA359786181 | MAP3K1 | c.2618T>G (p.Val873Gly) c.2240T>G (p.Val747Gly) c.2363T>G (p.Val788Gly) c.2339T>G (p.Val780Gly) c.2207T>G (p.Val736Gly) c.2129T>G (p.Val710Gly) n.2649T>G | |
5 | g.56881819A>C | CA444399235 | MAP3K1 | c.2619A>C (p.Val873=) c.2241A>C (p.Val747=) c.2364A>C (p.Val788=) c.2340A>C (p.Val780=) c.2208A>C (p.Val736=) c.2130A>C (p.Val710=) n.2650A>C | |
5 | g.56881819A>G | CA444399236 | MAP3K1 | c.2619A>G (p.Val873=) c.2241A>G (p.Val747=) c.2364A>G (p.Val788=) c.2340A>G (p.Val780=) c.2208A>G (p.Val736=) c.2130A>G (p.Val710=) n.2650A>G | gnomAD v4 |
5 | g.56881819A>T | CA444399237 | MAP3K1 | c.2619A>T (p.Val873=) c.2241A>T (p.Val747=) c.2364A>T (p.Val788=) c.2340A>T (p.Val780=) c.2208A>T (p.Val736=) c.2130A>T (p.Val710=) n.2650A>T | |
5 | g.56881820G>A | CA359786184 | MAP3K1 | c.2620G>A (p.Glu874Lys) c.2242G>A (p.Glu748Lys) c.2365G>A (p.Glu789Lys) c.2341G>A (p.Glu781Lys) c.2209G>A (p.Glu737Lys) c.2131G>A (p.Glu711Lys) n.2651G>A | |
5 | g.56881820G>C | CA359786182 | MAP3K1 | c.2620G>C (p.Glu874Gln) c.2242G>C (p.Glu748Gln) c.2365G>C (p.Glu789Gln) c.2341G>C (p.Glu781Gln) c.2209G>C (p.Glu737Gln) c.2131G>C (p.Glu711Gln) n.2651G>C | dbSNP |
5 | g.56881820G= | CA1548139322 | MAP3K1 | c.2620G= (p.Glu874=) c.2242G= (p.Glu748=) c.2365G= (p.Glu789=) c.2341G= (p.Glu781=) c.2209G= (p.Glu737=) c.2131G= (p.Glu711=) n.2651G= | |
5 | g.56881820G>T | CA359786183 | MAP3K1 | c.2620G>T (p.Glu874Ter) c.2242G>T (p.Glu748Ter) c.2365G>T (p.Glu789Ter) c.2341G>T (p.Glu781Ter) c.2209G>T (p.Glu737Ter) c.2131G>T (p.Glu711Ter) n.2651G>T | |
5 | g.56881821A>C | CA359786185 | MAP3K1 | c.2621A>C (p.Glu874Ala) c.2243A>C (p.Glu748Ala) c.2366A>C (p.Glu789Ala) c.2342A>C (p.Glu781Ala) c.2210A>C (p.Glu737Ala) c.2132A>C (p.Glu711Ala) n.2652A>C | |
5 | g.56881821A>G | CA359786186 | MAP3K1 | c.2621A>G (p.Glu874Gly) c.2243A>G (p.Glu748Gly) c.2366A>G (p.Glu789Gly) c.2342A>G (p.Glu781Gly) c.2210A>G (p.Glu737Gly) c.2132A>G (p.Glu711Gly) n.2652A>G | |
5 | g.56881821A>T | CA359786187 | MAP3K1 | c.2621A>T (p.Glu874Val) c.2243A>T (p.Glu748Val) c.2366A>T (p.Glu789Val) c.2342A>T (p.Glu781Val) c.2210A>T (p.Glu737Val) c.2132A>T (p.Glu711Val) n.2652A>T | |
5 | g.56881822A>C | CA359786188 | MAP3K1 | c.2622A>C (p.Glu874Asp) c.2244A>C (p.Glu748Asp) c.2367A>C (p.Glu789Asp) c.2343A>C (p.Glu781Asp) c.2211A>C (p.Glu737Asp) c.2133A>C (p.Glu711Asp) n.2653A>C | |
5 | g.56881822A>G | CA444399240 | MAP3K1 | c.2622A>G (p.Glu874=) c.2244A>G (p.Glu748=) c.2367A>G (p.Glu789=) c.2343A>G (p.Glu781=) c.2211A>G (p.Glu737=) c.2133A>G (p.Glu711=) n.2653A>G | |
5 | g.56881822A>T | CA359786189 | MAP3K1 | c.2622A>T (p.Glu874Asp) c.2244A>T (p.Glu748Asp) c.2367A>T (p.Glu789Asp) c.2343A>T (p.Glu781Asp) c.2211A>T (p.Glu737Asp) c.2133A>T (p.Glu711Asp) n.2653A>T | |
5 | g.56881823G>A | CA359786192 | MAP3K1 | c.2623G>A (p.Asp875Asn) c.2245G>A (p.Asp749Asn) c.2368G>A (p.Asp790Asn) c.2344G>A (p.Asp782Asn) c.2212G>A (p.Asp738Asn) c.2134G>A (p.Asp712Asn) n.2654G>A | |
5 | g.56881823G>C | CA359786191 | MAP3K1 | c.2623G>C (p.Asp875His) c.2245G>C (p.Asp749His) c.2368G>C (p.Asp790His) c.2344G>C (p.Asp782His) c.2212G>C (p.Asp738His) c.2134G>C (p.Asp712His) n.2654G>C | |
5 | g.56881823G>T | CA359786190 | MAP3K1 | c.2623G>T (p.Asp875Tyr) c.2245G>T (p.Asp749Tyr) c.2368G>T (p.Asp790Tyr) c.2344G>T (p.Asp782Tyr) c.2212G>T (p.Asp738Tyr) c.2134G>T (p.Asp712Tyr) n.2654G>T | |
5 | g.56881823_56881839delinsGACACTTTGGATGGTCA | CA1548139323 | MAP3K1 | c.2623_2639delinsGACACTTTGGATGGTCA (p.Asp875=) c.2245_2261delinsGACACTTTGGATGGTCA (p.Asp749=) c.2368_2384delinsGACACTTTGGATGGTCA (p.Asp790=) c.2344_2360delinsGACACTTTGGATGGTCA (p.Asp782=) c.2212_2228delinsGACACTTTGGATGGTCA (p.Asp738=) c.2134_2150delinsGACACTTTGGATGGTCA (p.Asp712=) n.2654_2670delinsGACACTTTGGATGGTCA | |
5 | g.56881824A>C | CA359786193 | MAP3K1 | c.2624A>C (p.Asp875Ala) c.2246A>C (p.Asp749Ala) c.2369A>C (p.Asp790Ala) c.2345A>C (p.Asp782Ala) c.2213A>C (p.Asp738Ala) c.2135A>C (p.Asp712Ala) n.2655A>C | |
5 | g.56881824A>G | CA359786195 | MAP3K1 | c.2624A>G (p.Asp875Gly) c.2246A>G (p.Asp749Gly) c.2369A>G (p.Asp790Gly) c.2345A>G (p.Asp782Gly) c.2213A>G (p.Asp738Gly) c.2135A>G (p.Asp712Gly) n.2655A>G | dbSNP |
5 | g.56881824A>T | CA359786194 | MAP3K1 | c.2624A>T (p.Asp875Val) c.2246A>T (p.Asp749Val) c.2369A>T (p.Asp790Val) c.2345A>T (p.Asp782Val) c.2213A>T (p.Asp738Val) c.2135A>T (p.Asp712Val) n.2655A>T | |
5 | g.56881827_56881842del | CA913189871 | MAP3K1 | c.2627_2642del (p.Thr876ArgfsTer28) c.2249_2264del (p.Thr750ArgfsTer28) c.2372_2387del (p.Thr791ArgfsTer28) c.2348_2363del (p.Thr783ArgfsTer28) c.2216_2231del (p.Thr739ArgfsTer28) c.2138_2153del (p.Thr713ArgfsTer28) n.2658_2673del | ClinVar dbSNP |
5 | g.56881825C>A | CA359786196 | MAP3K1 | c.2625C>A (p.Asp875Glu) c.2247C>A (p.Asp749Glu) c.2370C>A (p.Asp790Glu) c.2346C>A (p.Asp782Glu) c.2214C>A (p.Asp738Glu) c.2136C>A (p.Asp712Glu) n.2656C>A | |
5 | g.56881825C>G | CA359786197 | MAP3K1 | c.2625C>G (p.Asp875Glu) c.2247C>G (p.Asp749Glu) c.2370C>G (p.Asp790Glu) c.2346C>G (p.Asp782Glu) c.2214C>G (p.Asp738Glu) c.2136C>G (p.Asp712Glu) n.2656C>G | |
5 | g.56881825C>T | CA444399245 | MAP3K1 | c.2625C>T (p.Asp875=) c.2247C>T (p.Asp749=) c.2370C>T (p.Asp790=) c.2346C>T (p.Asp782=) c.2214C>T (p.Asp738=) c.2136C>T (p.Asp712=) n.2656C>T | dbSNP |
5 | g.56881826A= | CA1548139324 | MAP3K1 | c.2626A= (p.Thr876=) c.2248A= (p.Thr750=) c.2371A= (p.Thr791=) c.2347A= (p.Thr783=) c.2215A= (p.Thr739=) c.2137A= (p.Thr713=) n.2657A= | |
5 | g.56881826A>C | CA359786198 | MAP3K1 | c.2626A>C (p.Thr876Pro) c.2248A>C (p.Thr750Pro) c.2371A>C (p.Thr791Pro) c.2347A>C (p.Thr783Pro) c.2215A>C (p.Thr739Pro) c.2137A>C (p.Thr713Pro) n.2657A>C | |
5 | g.56881826A>G | CA359786200 | MAP3K1 | c.2626A>G (p.Thr876Ala) c.2248A>G (p.Thr750Ala) c.2371A>G (p.Thr791Ala) c.2347A>G (p.Thr783Ala) c.2215A>G (p.Thr739Ala) c.2137A>G (p.Thr713Ala) n.2657A>G | dbSNP gnomAD v4 |
5 | g.56881826A>T | CA359786199 | MAP3K1 | c.2626A>T (p.Thr876Ser) c.2248A>T (p.Thr750Ser) c.2371A>T (p.Thr791Ser) c.2347A>T (p.Thr783Ser) c.2215A>T (p.Thr739Ser) c.2137A>T (p.Thr713Ser) n.2657A>T | dbSNP gnomAD v3 gnomAD v4 |
5 | g.56881827C>A | CA359786201 | MAP3K1 | c.2627C>A (p.Thr876Asn) c.2249C>A (p.Thr750Asn) c.2372C>A (p.Thr791Asn) c.2348C>A (p.Thr783Asn) c.2216C>A (p.Thr739Asn) c.2138C>A (p.Thr713Asn) n.2658C>A | |
5 | g.56881827C>G | CA359786202 | MAP3K1 | c.2627C>G (p.Thr876Ser) c.2249C>G (p.Thr750Ser) c.2372C>G (p.Thr791Ser) c.2348C>G (p.Thr783Ser) c.2216C>G (p.Thr739Ser) c.2138C>G (p.Thr713Ser) n.2658C>G | |
5 | g.56881827C>T | CA359786203 | MAP3K1 | c.2627C>T (p.Thr876Ile) c.2249C>T (p.Thr750Ile) c.2372C>T (p.Thr791Ile) c.2348C>T (p.Thr783Ile) c.2216C>T (p.Thr739Ile) c.2138C>T (p.Thr713Ile) n.2658C>T | |
5 | g.56881828T>A | CA444399251 | MAP3K1 | c.2628T>A (p.Thr876=) c.2250T>A (p.Thr750=) c.2373T>A (p.Thr791=) c.2349T>A (p.Thr783=) c.2217T>A (p.Thr739=) c.2139T>A (p.Thr713=) n.2659T>A | |
5 | g.56881828T>C | CA444399252 | MAP3K1 | c.2628T>C (p.Thr876=) c.2250T>C (p.Thr750=) c.2373T>C (p.Thr791=) c.2349T>C (p.Thr783=) c.2217T>C (p.Thr739=) c.2139T>C (p.Thr713=) n.2659T>C | dbSNP gnomAD v2 gnomAD v4 |
5 | g.56881828T>G | CA444399250 | MAP3K1 | c.2628T>G (p.Thr876=) c.2250T>G (p.Thr750=) c.2373T>G (p.Thr791=) c.2349T>G (p.Thr783=) c.2217T>G (p.Thr739=) c.2139T>G (p.Thr713=) n.2659T>G | |
5 | g.56881828T= | CA1548139325 | MAP3K1 | c.2628T= (p.Thr876=) c.2250T= (p.Thr750=) c.2373T= (p.Thr791=) c.2349T= (p.Thr783=) c.2217T= (p.Thr739=) c.2139T= (p.Thr713=) n.2659T= | |
5 | g.56881830del | CA645557009 | MAP3K1 | c.2630del (p.Leu877TrpfsTer?) c.2252del (p.Leu751TrpfsTer?) c.2375del (p.Leu792TrpfsTer?) c.2351del (p.Leu784TrpfsTer?) c.2219del (p.Leu740TrpfsTer?) c.2141del (p.Leu714TrpfsTer?) n.2661del | COSMIC |
5 | g.56881829T>A | CA359786204 | MAP3K1 | c.2629T>A (p.Leu877Met) c.2251T>A (p.Leu751Met) c.2374T>A (p.Leu792Met) c.2350T>A (p.Leu784Met) c.2218T>A (p.Leu740Met) c.2140T>A (p.Leu714Met) n.2660T>A | |
5 | g.56881829T>C | CA444399253 | MAP3K1 | c.2629T>C (p.Leu877=) c.2251T>C (p.Leu751=) c.2374T>C (p.Leu792=) c.2350T>C (p.Leu784=) c.2218T>C (p.Leu740=) c.2140T>C (p.Leu714=) n.2660T>C | |
5 | g.56881829T>G | CA359786205 | MAP3K1 | c.2629T>G (p.Leu877Val) c.2251T>G (p.Leu751Val) c.2374T>G (p.Leu792Val) c.2350T>G (p.Leu784Val) c.2218T>G (p.Leu740Val) c.2140T>G (p.Leu714Val) n.2660T>G | gnomAD v4 |
5 | g.56881830T>A | CA359786206 | MAP3K1 | c.2630T>A (p.Leu877Ter) c.2252T>A (p.Leu751Ter) c.2375T>A (p.Leu792Ter) c.2351T>A (p.Leu784Ter) c.2219T>A (p.Leu740Ter) c.2141T>A (p.Leu714Ter) n.2661T>A | |
5 | g.56881830T>C | CA3273033 | MAP3K1 | c.2630T>C (p.Leu877Ser) c.2252T>C (p.Leu751Ser) c.2375T>C (p.Leu792Ser) c.2351T>C (p.Leu784Ser) c.2219T>C (p.Leu740Ser) c.2141T>C (p.Leu714Ser) n.2661T>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
5 | g.56881830T>G | CA359786207 | MAP3K1 | c.2630T>G (p.Leu877Trp) c.2252T>G (p.Leu751Trp) c.2375T>G (p.Leu792Trp) c.2351T>G (p.Leu784Trp) c.2219T>G (p.Leu740Trp) c.2141T>G (p.Leu714Trp) n.2661T>G | |
5 | g.56881830T= | CA1548139326 | MAP3K1 | c.2630T= (p.Leu877=) c.2252T= (p.Leu751=) c.2375T= (p.Leu792=) c.2351T= (p.Leu784=) c.2219T= (p.Leu740=) c.2141T= (p.Leu714=) n.2661T= |