Chr Mutation (hg38) CAid Gene Transcript Linkouts
5g.56881733A=CA1548139276MAP3K1c.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=
5g.56881733A>CCA359786002MAP3K1c.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
5g.56881733A>GCA359786003MAP3K1c.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
5g.56881733A>TCA359786004MAP3K1c.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
5g.56881734G>ACA3273012MAP3K1c.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
5g.56881734G>CCA3273013MAP3K1c.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
5g.56881734G=CA1548139277MAP3K1c.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=
5g.56881734G>TCA359786005MAP3K1c.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
5g.56881735T>ACA359786006MAP3K1c.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
5g.56881735T>CCA444399143MAP3K1c.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
5g.56881735T>GCA359786007MAP3K1c.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
5g.56881736T>ACA359786008MAP3K1c.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
5g.56881736T>CCA359786009MAP3K1c.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
5g.56881736T>GCA359786010MAP3K1c.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
5g.56881737C>ACA359786013MAP3K1c.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
5g.56881737C=CA1548139278MAP3K1c.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=
5g.56881737C>GCA359786012MAP3K1c.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
5g.56881737C>TCA359786011MAP3K1c.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
5g.56881738delCA645557008MAP3K1c.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
5g.56881738C>ACA444399144MAP3K1c.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
5g.56881738C=CA1548139279MAP3K1c.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=
5g.56881738C>GCA444399145MAP3K1c.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
5g.56881738C>TCA444399146MAP3K1c.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
5g.56881739A>CCA359786014MAP3K1c.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
5g.56881739A>GCA359786015MAP3K1c.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
5g.56881739A>TCA359786016MAP3K1c.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
5g.56881740C>ACA359786017MAP3K1c.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
5g.56881740C>GCA359786018MAP3K1c.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
5g.56881740C>TCA359786019MAP3K1c.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
5g.56881741T>ACA444399147MAP3K1c.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
5g.56881741T>CCA444399148MAP3K1c.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
5g.56881741T>GCA444399149MAP3K1c.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
5g.56881742C>ACA359786020MAP3K1c.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
5g.56881742C=CA1548139280MAP3K1c.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=
5g.56881742C>GCA359786021MAP3K1c.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
5g.56881742C>TCA359786022MAP3K1c.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
5g.56881743A>CCA359786023MAP3K1c.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
5g.56881743A>GCA359786024MAP3K1c.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
5g.56881743A>TCA359786025MAP3K1c.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
5g.56881744C>ACA359786027MAP3K1c.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
5g.56881744C=CA1548139281MAP3K1c.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=
5g.56881744C>GCA359786026MAP3K1c.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
5g.56881744C>TCA119079090MAP3K1c.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
5g.56881745T>ACA359786028MAP3K1c.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
5g.56881745T>CCA359786030MAP3K1c.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
5g.56881745T>GCA359786029MAP3K1c.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
5g.56881746T>ACA359786031MAP3K1c.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
5g.56881746T>CCA359786032MAP3K1c.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
5g.56881746T>GCA359786033MAP3K1c.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
5g.56881747C>ACA359786034MAP3K1c.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
5g.56881747C=CA1548139282MAP3K1c.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=
5g.56881747C>GCA119079093MAP3K1c.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
5g.56881747C>TCA444399150MAP3K1c.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
5g.56881748A=CA1548139283MAP3K1c.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=
5g.56881748A>CCA359786035MAP3K1c.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
5g.56881748A>GCA3273014MAP3K1c.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
5g.56881748A>TCA359786036MAP3K1c.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
5g.56881749C>ACA359786037MAP3K1c.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
5g.56881749C=CA1548139284MAP3K1c.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=
5g.56881749C>GCA359786038MAP3K1c.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
5g.56881749C>TCA359786039MAP3K1c.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
5g.56881750C>ACA444399151MAP3K1c.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
5g.56881750C=CA1548139285MAP3K1c.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=
5g.56881750C>GCA444399152MAP3K1c.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
5g.56881750C>TCA3273015MAP3K1c.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
5g.56881751A=CA1548139286MAP3K1c.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=
5g.56881751A>CCA444399153MAP3K1c.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
5g.56881751A>GCA359786040MAP3K1c.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
5g.56881751A>TCA359786041MAP3K1c.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
5g.56881752G>ACA359786042MAP3K1c.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
5g.56881752G>CCA359786043MAP3K1c.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
5g.56881752G=CA1548139287MAP3K1c.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=
5g.56881752G>TCA359786044MAP3K1c.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
5g.56881753G>ACA444399154MAP3K1c.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
5g.56881753G>CCA359786045MAP3K1c.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
5g.56881753G>TCA359786046MAP3K1c.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
5g.56881754A>CCA359786047MAP3K1c.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
5g.56881754A>GCA359786048MAP3K1c.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
5g.56881754A>TCA359786049MAP3K1c.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
5g.56881755T>ACA359786050MAP3K1c.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
5g.56881755T>CCA3273016MAP3K1c.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
5g.56881755T>GCA359786051MAP3K1c.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
5g.56881755T=CA1548139288MAP3K1c.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=
5g.56881756G>ACA359786053MAP3K1c.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
5g.56881756G>CCA359786054MAP3K1c.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
5g.56881756G>TCA359786052MAP3K1c.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
5g.56881758_56881762dupCA2708984055MAP3K1c.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
5g.56881757C>ACA3273018MAP3K1c.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
5g.56881757C=CA1548139289MAP3K1c.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=
5g.56881757C>GCA359786055MAP3K1c.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
5g.56881757C>TCA3273017MAP3K1c.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
5g.56881758G>ACA3273019MAP3K1c.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
5g.56881758G>CCA359786056MAP3K1c.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
5g.56881758G=CA1548139290MAP3K1c.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=
5g.56881758G>TCA359786057MAP3K1c.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
5g.56881759T>ACA444399155MAP3K1c.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
5g.56881759T>CCA444399156MAP3K1c.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
5g.56881759T>GCA444399157MAP3K1c.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
5g.56881760C>ACA359786058MAP3K1c.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
5g.56881760C=CA1548139291MAP3K1c.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=
5g.56881760C>GCA359786059MAP3K1c.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
5g.56881760C>TCA3273020MAP3K1c.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
5g.56881761G>ACA359786060MAP3K1c.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
5g.56881761G>CCA359786061MAP3K1c.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
5g.56881761G=CA1548139292MAP3K1c.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=
5g.56881761G>TCA359786062MAP3K1c.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
5g.56881762C>ACA444399158MAP3K1c.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
5g.56881762C>GCA444399159MAP3K1c.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
5g.56881762C>TCA444399160MAP3K1c.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
5g.56881763C>ACA359786063MAP3K1c.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
5g.56881763C=CA1548139293MAP3K1c.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=
5g.56881763C>GCA359786064MAP3K1c.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
5g.56881763C>TCA3273021MAP3K1c.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
5g.56881764G>ACA119079184MAP3K1c.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
5g.56881764G>CCA359786065MAP3K1c.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
5g.56881764G=CA1548139294MAP3K1c.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=
5g.56881764G>TCA359786066MAP3K1c.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
5g.56881765T>ACA444399161MAP3K1c.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
5g.56881765T>CCA444399162MAP3K1c.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
5g.56881765T>GCA444399163MAP3K1c.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
5g.56881766T>ACA359786067MAP3K1c.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
5g.56881766T>CCA444399164MAP3K1c.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
5g.56881766T>GCA359786068MAP3K1c.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
5g.56881767T>ACA359786071MAP3K1c.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
5g.56881767T>CCA359786069MAP3K1c.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
5g.56881767T>GCA359786070MAP3K1c.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
5g.56881768G>ACA444399165MAP3K1c.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
5g.56881768G>CCA359786072MAP3K1c.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
5g.56881768G>TCA359786073MAP3K1c.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
5g.56881769A>CCA359786074MAP3K1c.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
5g.56881769A>GCA359786075MAP3K1c.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
5g.56881769A>TCA359786076MAP3K1c.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
5g.56881770T>ACA359786079MAP3K1c.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
5g.56881770T>CCA359786078MAP3K1c.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
5g.56881770T>GCA359786077MAP3K1c.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
5g.56881771G>ACA3273022MAP3K1c.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
5g.56881771G>CCA359786081MAP3K1c.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
5g.56881771G=CA1548139295MAP3K1c.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=
5g.56881771G>TCA359786080MAP3K1c.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
5g.56881772delCA444399166MAP3K1c.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
5g.56881772G>ACA359786082MAP3K1c.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
5g.56881772G>CCA359786084MAP3K1c.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
5g.56881772G>TCA359786083MAP3K1c.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
5g.56881773C>ACA359786085MAP3K1c.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
5g.56881773C=CA1548139296MAP3K1c.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=
5g.56881773C>GCA359786086MAP3K1c.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
5g.56881773C>TCA359786087MAP3K1c.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
5g.56881774T>ACA444399167MAP3K1c.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
5g.56881774T>CCA444399168MAP3K1c.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
5g.56881774T>GCA444399169MAP3K1c.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
5g.56881775A=CA1548139297MAP3K1c.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=
5g.56881775A>CCA359786088MAP3K1c.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
5g.56881775A>GCA359786089MAP3K1c.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
5g.56881775A>TCA359786090MAP3K1c.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
5g.56881776T>ACA359786091MAP3K1c.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
5g.56881776T>CCA359786092MAP3K1c.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
5g.56881776T>GCA359786093MAP3K1c.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
5g.56881777T>ACA444399171MAP3K1c.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
5g.56881777T>CCA444399172MAP3K1c.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
5g.56881777T>GCA359786094MAP3K1c.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
5g.56881777T=CA1548139298MAP3K1c.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=
5g.56881778G>ACA359786097MAP3K1c.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
5g.56881778G>CCA359786096MAP3K1c.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
5g.56881778G>TCA359786095MAP3K1c.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
5g.56881779C>ACA359786098MAP3K1c.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
5g.56881779C=CA1548139299MAP3K1c.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=
5g.56881779C>GCA359786099MAP3K1c.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
5g.56881779C>TCA359786100MAP3K1c.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
5g.56881780A>CCA444399175MAP3K1c.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
5g.56881780A>GCA444399176MAP3K1c.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
5g.56881780A>TCA444399177MAP3K1c.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
5g.56881781G>ACA359786101MAP3K1c.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
5g.56881781G>CCA359786102MAP3K1c.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
5g.56881781G>TCA359786103MAP3K1c.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
5g.56881782A>CCA359786104MAP3K1c.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
5g.56881782A>GCA359786105MAP3K1c.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
5g.56881782A>TCA359786106MAP3K1c.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
5g.56881783T>ACA119079191MAP3K1c.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
5g.56881783T>CCA444399179MAP3K1c.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
5g.56881783T>GCA359786107MAP3K1c.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
5g.56881783T=CA1548139300MAP3K1c.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=
5g.56881784G>ACA359786110MAP3K1c.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
5g.56881784G>CCA359786109MAP3K1c.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
5g.56881784G>TCA359786108MAP3K1c.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
5g.56881785A>CCA359786111MAP3K1c.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
5g.56881785A>GCA359786112MAP3K1c.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
5g.56881785A>TCA359786113MAP3K1c.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
5g.56881786G>ACA3273023MAP3K1c.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
5g.56881786G>CCA359786114MAP3K1c.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
5g.56881786G=CA1548139301MAP3K1c.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=
5g.56881786G>TCA359786115MAP3K1c.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
5g.56881787G>ACA359786116MAP3K1c.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
5g.56881787G>CCA359786117MAP3K1c.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
5g.56881787G=CA1548139302MAP3K1c.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=
5g.56881787G>TCA3273024MAP3K1c.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
5g.56881788T>ACA359786118MAP3K1c.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
5g.56881788T>CCA3273025MAP3K1c.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
5g.56881788T>GCA359786119MAP3K1c.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
5g.56881788T=CA1548139303MAP3K1c.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=
5g.56881789G>ACA444399185MAP3K1c.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
5g.56881789G>CCA444399186MAP3K1c.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
5g.56881789G=CA1548139304MAP3K1c.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=
5g.56881789G>TCA444399188MAP3K1c.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
5g.56881790G>ACA359786122MAP3K1c.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
5g.56881790G>CCA359786120MAP3K1c.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
5g.56881790G>TCA359786121MAP3K1c.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
5g.56881791A=CA1548139305MAP3K1c.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=
5g.56881791A>CCA359786123MAP3K1c.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
5g.56881791A>GCA359786124MAP3K1c.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
5g.56881791A>TCA359786125MAP3K1c.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
5g.56881792A=CA1548139306MAP3K1c.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=
5g.56881792A>CCA359786126MAP3K1c.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
5g.56881792A>GCA444399194MAP3K1c.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
5g.56881792A>TCA359786127MAP3K1c.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
5g.56881793A>CCA359786128MAP3K1c.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
5g.56881793A>GCA359786129MAP3K1c.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
5g.56881793A>TCA359786130MAP3K1c.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
5g.56881794T>ACA359786131MAP3K1c.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
5g.56881794T>CCA359786132MAP3K1c.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
5g.56881794T>GCA359786133MAP3K1c.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
5g.56881795T>ACA444399198MAP3K1c.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
5g.56881795T>CCA444399199MAP3K1c.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
5g.56881795T>GCA359786134MAP3K1c.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
5g.56881796G>ACA359786136MAP3K1c.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
5g.56881796G>CCA359786137MAP3K1c.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
5g.56881796G>TCA359786135MAP3K1c.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
5g.56881797C>ACA359786139MAP3K1c.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
5g.56881797C=CA1548139307MAP3K1c.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=
5g.56881797C>GCA3273026MAP3K1c.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
5g.56881797C>TCA359786138MAP3K1c.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
5g.56881798C>ACA444399202MAP3K1c.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
5g.56881798C=CA1548139308MAP3K1c.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=
5g.56881798C>GCA444399203MAP3K1c.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
5g.56881798C>TCA3273027MAP3K1c.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
5g.56881799G>ACA3273028MAP3K1c.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
5g.56881799G>CCA359786140MAP3K1c.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
5g.56881799G=CA1548139309MAP3K1c.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=
5g.56881799G>TCA359786141MAP3K1c.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
5g.56881800A=CA1548139310MAP3K1c.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=
5g.56881800A>CCA359786142MAP3K1c.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
5g.56881800A>GCA359786143MAP3K1c.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
5g.56881800A>TCA359786144MAP3K1c.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
5g.56881801A>CCA359786145MAP3K1c.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
5g.56881801A>GCA444399205MAP3K1c.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
5g.56881801A>TCA359786146MAP3K1c.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
5g.56881802G>ACA359786149MAP3K1c.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
5g.56881802G>CCA359786148MAP3K1c.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
5g.56881802G>TCA359786147MAP3K1c.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
5g.56881803C>ACA359786150MAP3K1c.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
5g.56881803C>GCA359786151MAP3K1c.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
5g.56881803C>TCA359786152MAP3K1c.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
5g.56881804C>ACA444399209MAP3K1c.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
5g.56881804C=CA1548139311MAP3K1c.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=
5g.56881804C>GCA119079229MAP3K1c.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
5g.56881804C>TCA444399211MAP3K1c.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
5g.56881805A=CA1548139312MAP3K1c.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=
5g.56881805A>CCA359786153MAP3K1c.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
5g.56881805A>GCA3273029MAP3K1c.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
5g.56881805A>TCA359786154MAP3K1c.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
5g.56881806T>ACA359786155MAP3K1c.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
5g.56881806T>CCA359786156MAP3K1c.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
5g.56881806T>GCA359786157MAP3K1c.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
5g.56881807C>ACA444399216MAP3K1c.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
5g.56881807C=CA1548139313MAP3K1c.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=
5g.56881807C>GCA359786158MAP3K1c.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
5g.56881807C>TCA444399215MAP3K1c.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
5g.56881808C>ACA359786159MAP3K1c.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
5g.56881808C=CA1548139314MAP3K1c.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=
5g.56881808C>GCA359786160MAP3K1c.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
5g.56881808C>TCA3273030MAP3K1c.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
5g.56881809A=CA1548139315MAP3K1c.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=
5g.56881809A>CCA359786162MAP3K1c.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
5g.56881809A>GCA359786163MAP3K1c.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
5g.56881809A>TCA359786161MAP3K1c.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
5g.56881810G>ACA444399221MAP3K1c.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
5g.56881810G>CCA359786164MAP3K1c.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
5g.56881810G>TCA359786165MAP3K1c.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
5g.56881810_56881811insCTGAGTGTTTCCAGTTCCACTCACTTCACCAGGATGCGTCGCCGTCA2673909975MAP3K1c.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
5g.56881811T>ACA359786166MAP3K1c.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
5g.56881811T>CCA444399222MAP3K1c.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
5g.56881811T>GCA359786167MAP3K1c.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
5g.56881811T=CA1548139316MAP3K1c.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=
5g.56881812T>ACA359786168MAP3K1c.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
5g.56881812T>CCA359786169MAP3K1c.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
5g.56881812T>GCA359786170MAP3K1c.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
5g.56881813G>ACA444399224MAP3K1c.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
5g.56881813G>CCA359786171MAP3K1c.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
5g.56881813G=CA1548139317MAP3K1c.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=
5g.56881813G>TCA359786172MAP3K1c.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
5g.56881814G>ACA119079250MAP3K1c.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
5g.56881814G>CCA359786173MAP3K1c.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
5g.56881814G=CA1548139318MAP3K1c.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=
5g.56881814G>TCA359786174MAP3K1c.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
5g.56881815G>ACA359786175MAP3K1c.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
5g.56881815G>CCA359786176MAP3K1c.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
5g.56881815G=CA1548139319MAP3K1c.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=
5g.56881815G>TCA3273031MAP3K1c.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
5g.56881816C>ACA444399227MAP3K1c.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
5g.56881816C=CA1548139320MAP3K1c.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=
5g.56881816C>GCA444399230MAP3K1c.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
5g.56881816C>TCA444399231MAP3K1c.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
5g.56881817G>ACA3273032MAP3K1c.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
5g.56881817G>CCA359786177MAP3K1c.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
5g.56881817G=CA1548139321MAP3K1c.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=
5g.56881817G>TCA359786178MAP3K1c.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
5g.56881818T>ACA359786179MAP3K1c.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
5g.56881818T>CCA359786180MAP3K1c.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
5g.56881818T>GCA359786181MAP3K1c.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
5g.56881819A>CCA444399235MAP3K1c.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
5g.56881819A>GCA444399236MAP3K1c.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
5g.56881819A>TCA444399237MAP3K1c.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
5g.56881820G>ACA359786184MAP3K1c.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
5g.56881820G>CCA359786182MAP3K1c.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
5g.56881820G=CA1548139322MAP3K1c.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=
5g.56881820G>TCA359786183MAP3K1c.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
5g.56881821A>CCA359786185MAP3K1c.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
5g.56881821A>GCA359786186MAP3K1c.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
5g.56881821A>TCA359786187MAP3K1c.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
5g.56881822A>CCA359786188MAP3K1c.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
5g.56881822A>GCA444399240MAP3K1c.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
5g.56881822A>TCA359786189MAP3K1c.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
5g.56881823G>ACA359786192MAP3K1c.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
5g.56881823G>CCA359786191MAP3K1c.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
5g.56881823G>TCA359786190MAP3K1c.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
5g.56881823_56881839delinsGACACTTTGGATGGTCACA1548139323MAP3K1c.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
5g.56881824A>CCA359786193MAP3K1c.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
5g.56881824A>GCA359786195MAP3K1c.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
5g.56881824A>TCA359786194MAP3K1c.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
5g.56881827_56881842delCA913189871MAP3K1c.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
5g.56881825C>ACA359786196MAP3K1c.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
5g.56881825C>GCA359786197MAP3K1c.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
5g.56881825C>TCA444399245MAP3K1c.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
5g.56881826A=CA1548139324MAP3K1c.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=
5g.56881826A>CCA359786198MAP3K1c.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
5g.56881826A>GCA359786200MAP3K1c.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
5g.56881826A>TCA359786199MAP3K1c.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
5g.56881827C>ACA359786201MAP3K1c.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
5g.56881827C>GCA359786202MAP3K1c.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
5g.56881827C>TCA359786203MAP3K1c.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
5g.56881828T>ACA444399251MAP3K1c.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
5g.56881828T>CCA444399252MAP3K1c.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
5g.56881828T>GCA444399250MAP3K1c.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
5g.56881828T=CA1548139325MAP3K1c.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=
5g.56881830delCA645557009MAP3K1c.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
5g.56881829T>ACA359786204MAP3K1c.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
5g.56881829T>CCA444399253MAP3K1c.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
5g.56881829T>GCA359786205MAP3K1c.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
5g.56881830T>ACA359786206MAP3K1c.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
5g.56881830T>CCA3273033MAP3K1c.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
5g.56881830T>GCA359786207MAP3K1c.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
5g.56881830T=CA1548139326MAP3K1c.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=
5g.56881831G>ACA444399257MAP3K1c.2631G>A (p.Leu877=)
c.2253G>A (p.Leu751=)
c.2376G>A (p.Leu792=)
c.2352G>A (p.Leu784=)
c.2220G>A (p.Leu740=)
c.2142G>A (p.Leu714=)
n.2662G>A
5g.56881831G>CCA359786208MAP3K1c.2631G>C (p.Leu877Phe)
c.2253G>C (p.Leu751Phe)
c.2376G>C (p.Leu792Phe)
c.2352G>C (p.Leu784Phe)
c.2220G>C (p.Leu740Phe)
c.2142G>C (p.Leu714Phe)
n.2662G>C
5g.56881831G>TCA359786209MAP3K1c.2631G>T (p.Leu877Phe)
c.2253G>T (p.Leu751Phe)
c.2376G>T (p.Leu792Phe)
c.2352G>T (p.Leu784Phe)
c.2220G>T (p.Leu740Phe)
c.2142G>T (p.Leu714Phe)
n.2662G>T
5g.56881832G>ACA359786212MAP3K1c.2632G>A (p.Asp878Asn)
c.2254G>A (p.Asp752Asn)
c.2377G>A (p.Asp793Asn)
c.2353G>A (p.Asp785Asn)
c.2221G>A (p.Asp741Asn)
c.2143G>A (p.Asp715Asn)
n.2663G>A
5g.56881832G>CCA359786211MAP3K1c.2632G>C (p.Asp878His)
c.2254G>C (p.Asp752His)
c.2377G>C (p.Asp793His)
c.2353G>C (p.Asp785His)
c.2221G>C (p.Asp741His)
c.2143G>C (p.Asp715His)
n.2663G>C
dbSNP
5g.56881832G>TCA359786210MAP3K1c.2632G>T (p.Asp878Tyr)
c.2254G>T (p.Asp752Tyr)
c.2377G>T (p.Asp793Tyr)
c.2353G>T (p.Asp785Tyr)
c.2221G>T (p.Asp741Tyr)
c.2143G>T (p.Asp715Tyr)
n.2663G>T
5g.56881833A=CA1548139327MAP3K1c.2633A= (p.Asp878=)
c.2255A= (p.Asp752=)
c.2378A= (p.Asp793=)
c.2354A= (p.Asp785=)
c.2222A= (p.Asp741=)
c.2144A= (p.Asp715=)
n.2664A=
5g.56881833A>CCA359786213MAP3K1c.2633A>C (p.Asp878Ala)
c.2255A>C (p.Asp752Ala)
c.2378A>C (p.Asp793Ala)
c.2354A>C (p.Asp785Ala)
c.2222A>C (p.Asp741Ala)
c.2144A>C (p.Asp715Ala)
n.2664A>C
5g.56881833A>GCA3273034MAP3K1c.2633A>G (p.Asp878Gly)
c.2255A>G (p.Asp752Gly)
c.2378A>G (p.Asp793Gly)
c.2354A>G (p.Asp785Gly)
c.2222A>G (p.Asp741Gly)
c.2144A>G (p.Asp715Gly)
n.2664A>G
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
5g.56881833A>TCA359786214MAP3K1c.2633A>T (p.Asp878Val)
c.2255A>T (p.Asp752Val)
c.2378A>T (p.Asp793Val)
c.2354A>T (p.Asp785Val)
c.2222A>T (p.Asp741Val)
c.2144A>T (p.Asp715Val)
n.2664A>T

Number of alleles fetched