Chr Mutation (hg38) CAid Gene Transcript Linkouts
5g.56859751G>ACA359802386MAP3K1c.670G>A (p.Glu224Lys)
c.292G>A (p.Glu98Lys)
c.415G>A (p.Glu139Lys)
c.259G>A (p.Glu87Lys)
c.181G>A (p.Glu61Lys)
n.701G>A
5g.56859751G>CCA3272584MAP3K1c.670G>C (p.Glu224Gln)
c.292G>C (p.Glu98Gln)
c.415G>C (p.Glu139Gln)
c.259G>C (p.Glu87Gln)
c.181G>C (p.Glu61Gln)
n.701G>C
dbSNP ExAC gnomAD v2
5g.56859751G=CA1548129192MAP3K1c.670G= (p.Glu224=)
c.292G= (p.Glu98=)
c.415G= (p.Glu139=)
c.259G= (p.Glu87=)
c.181G= (p.Glu61=)
n.701G=
5g.56859751G>TCA359802387MAP3K1c.670G>T (p.Glu224Ter)
c.292G>T (p.Glu98Ter)
c.415G>T (p.Glu139Ter)
c.259G>T (p.Glu87Ter)
c.181G>T (p.Glu61Ter)
n.701G>T
5g.56859752A=CA1548129193MAP3K1c.671A= (p.Glu224=)
c.293A= (p.Glu98=)
c.416A= (p.Glu139=)
c.260A= (p.Glu87=)
c.182A= (p.Glu61=)
n.702A=
5g.56859752A>CCA359802388MAP3K1c.671A>C (p.Glu224Ala)
c.293A>C (p.Glu98Ala)
c.416A>C (p.Glu139Ala)
c.260A>C (p.Glu87Ala)
c.182A>C (p.Glu61Ala)
n.702A>C
5g.56859752A>GCA3272585MAP3K1c.671A>G (p.Glu224Gly)
c.293A>G (p.Glu98Gly)
c.416A>G (p.Glu139Gly)
c.260A>G (p.Glu87Gly)
c.182A>G (p.Glu61Gly)
n.702A>G
dbSNP ExAC gnomAD v2 gnomAD v4
5g.56859752A>TCA359802389MAP3K1c.671A>T (p.Glu224Val)
c.293A>T (p.Glu98Val)
c.416A>T (p.Glu139Val)
c.260A>T (p.Glu87Val)
c.182A>T (p.Glu61Val)
n.702A>T
5g.56859753A>CCA359802390MAP3K1c.672A>C (p.Glu224Asp)
c.294A>C (p.Glu98Asp)
c.417A>C (p.Glu139Asp)
c.261A>C (p.Glu87Asp)
c.183A>C (p.Glu61Asp)
n.703A>C
5g.56859753A>GCA444391634MAP3K1c.672A>G (p.Glu224=)
c.294A>G (p.Glu98=)
c.417A>G (p.Glu139=)
c.261A>G (p.Glu87=)
c.183A>G (p.Glu61=)
n.703A>G
5g.56859753A>TCA359802391MAP3K1c.672A>T (p.Glu224Asp)
c.294A>T (p.Glu98Asp)
c.417A>T (p.Glu139Asp)
c.261A>T (p.Glu87Asp)
c.183A>T (p.Glu61Asp)
n.703A>T
5g.56859754A=CA1548129194MAP3K1c.673A= (p.Met225=)
c.295A= (p.Met99=)
c.418A= (p.Met140=)
c.262A= (p.Met88=)
c.184A= (p.Met62=)
n.704A=
5g.56859754A>CCA359802392MAP3K1c.673A>C (p.Met225Leu)
c.295A>C (p.Met99Leu)
c.418A>C (p.Met140Leu)
c.262A>C (p.Met88Leu)
c.184A>C (p.Met62Leu)
n.704A>C
5g.56859754A>GCA359802394MAP3K1c.673A>G (p.Met225Val)
c.295A>G (p.Met99Val)
c.418A>G (p.Met140Val)
c.262A>G (p.Met88Val)
c.184A>G (p.Met62Val)
n.704A>G
dbSNP gnomAD v4
5g.56859754A>TCA359802393MAP3K1c.673A>T (p.Met225Leu)
c.295A>T (p.Met99Leu)
c.418A>T (p.Met140Leu)
c.262A>T (p.Met88Leu)
c.184A>T (p.Met62Leu)
n.704A>T
gnomAD v4
5g.56859755T>ACA359802395MAP3K1c.674T>A (p.Met225Lys)
c.296T>A (p.Met99Lys)
c.419T>A (p.Met140Lys)
c.263T>A (p.Met88Lys)
c.185T>A (p.Met62Lys)
n.705T>A
5g.56859755T>CCA3272586MAP3K1c.674T>C (p.Met225Thr)
c.296T>C (p.Met99Thr)
c.419T>C (p.Met140Thr)
c.263T>C (p.Met88Thr)
c.185T>C (p.Met62Thr)
n.705T>C
dbSNP ExAC gnomAD v2 gnomAD v4
5g.56859755T>GCA359802396MAP3K1c.674T>G (p.Met225Arg)
c.296T>G (p.Met99Arg)
c.419T>G (p.Met140Arg)
c.263T>G (p.Met88Arg)
c.185T>G (p.Met62Arg)
n.705T>G
5g.56859755T=CA1548129195MAP3K1c.674T= (p.Met225=)
c.296T= (p.Met99=)
c.419T= (p.Met140=)
c.263T= (p.Met88=)
c.185T= (p.Met62=)
n.705T=
5g.56859756G>ACA359802397MAP3K1c.675G>A (p.Met225Ile)
c.297G>A (p.Met99Ile)
c.420G>A (p.Met140Ile)
c.264G>A (p.Met88Ile)
c.186G>A (p.Met62Ile)
n.706G>A
COSMIC
5g.56859756G>CCA359802398MAP3K1c.675G>C (p.Met225Ile)
c.297G>C (p.Met99Ile)
c.420G>C (p.Met140Ile)
c.264G>C (p.Met88Ile)
c.186G>C (p.Met62Ile)
n.706G>C
5g.56859756G=CA1548129196MAP3K1c.675G= (p.Met225=)
c.297G= (p.Met99=)
c.420G= (p.Met140=)
c.264G= (p.Met88=)
c.186G= (p.Met62=)
n.706G=
5g.56859756G>TCA119520073MAP3K1c.675G>T (p.Met225Ile)
c.297G>T (p.Met99Ile)
c.420G>T (p.Met140Ile)
c.264G>T (p.Met88Ile)
c.186G>T (p.Met62Ile)
n.706G>T
dbSNP gnomAD v4
5g.56859757A>CCA359802399MAP3K1c.676A>C (p.Asn226His)
c.298A>C (p.Asn100His)
c.421A>C (p.Asn141His)
c.265A>C (p.Asn89His)
c.187A>C (p.Asn63His)
n.707A>C
5g.56859757A>GCA359802400MAP3K1c.676A>G (p.Asn226Asp)
c.298A>G (p.Asn100Asp)
c.421A>G (p.Asn141Asp)
c.265A>G (p.Asn89Asp)
c.187A>G (p.Asn63Asp)
n.707A>G
gnomAD v4
5g.56859757A>TCA359802401MAP3K1c.676A>T (p.Asn226Tyr)
c.298A>T (p.Asn100Tyr)
c.421A>T (p.Asn141Tyr)
c.265A>T (p.Asn89Tyr)
c.187A>T (p.Asn63Tyr)
n.707A>T
5g.56859758A>CCA359802402MAP3K1c.677A>C (p.Asn226Thr)
c.299A>C (p.Asn100Thr)
c.422A>C (p.Asn141Thr)
c.266A>C (p.Asn89Thr)
c.188A>C (p.Asn63Thr)
n.708A>C
5g.56859758A>GCA359802403MAP3K1c.677A>G (p.Asn226Ser)
c.299A>G (p.Asn100Ser)
c.422A>G (p.Asn141Ser)
c.266A>G (p.Asn89Ser)
c.188A>G (p.Asn63Ser)
n.708A>G
5g.56859758A>TCA359802404MAP3K1c.677A>T (p.Asn226Ile)
c.299A>T (p.Asn100Ile)
c.422A>T (p.Asn141Ile)
c.266A>T (p.Asn89Ile)
c.188A>T (p.Asn63Ile)
n.708A>T
5g.56859759T>ACA359802406MAP3K1c.678T>A (p.Asn226Lys)
c.300T>A (p.Asn100Lys)
c.423T>A (p.Asn141Lys)
c.267T>A (p.Asn89Lys)
c.189T>A (p.Asn63Lys)
n.709T>A
5g.56859759T>CCA444391636MAP3K1c.678T>C (p.Asn226=)
c.300T>C (p.Asn100=)
c.423T>C (p.Asn141=)
c.267T>C (p.Asn89=)
c.189T>C (p.Asn63=)
n.709T>C
5g.56859759T>GCA359802405MAP3K1c.678T>G (p.Asn226Lys)
c.300T>G (p.Asn100Lys)
c.423T>G (p.Asn141Lys)
c.267T>G (p.Asn89Lys)
c.189T>G (p.Asn63Lys)
n.709T>G
5g.56859760C>ACA359802407MAP3K1c.679C>A (p.His227Asn)
c.301C>A (p.His101Asn)
c.424C>A (p.His142Asn)
c.268C>A (p.His90Asn)
c.190C>A (p.His64Asn)
n.710C>A
5g.56859760C>GCA359802408MAP3K1c.679C>G (p.His227Asp)
c.301C>G (p.His101Asp)
c.424C>G (p.His142Asp)
c.268C>G (p.His90Asp)
c.190C>G (p.His64Asp)
n.710C>G
5g.56859760C>TCA359802409MAP3K1c.679C>T (p.His227Tyr)
c.301C>T (p.His101Tyr)
c.424C>T (p.His142Tyr)
c.268C>T (p.His90Tyr)
c.190C>T (p.His64Tyr)
n.710C>T
5g.56859761A>CCA359802410MAP3K1c.680A>C (p.His227Pro)
c.302A>C (p.His101Pro)
c.425A>C (p.His142Pro)
c.269A>C (p.His90Pro)
c.191A>C (p.His64Pro)
n.711A>C
5g.56859761A>GCA359802411MAP3K1c.680A>G (p.His227Arg)
c.302A>G (p.His101Arg)
c.425A>G (p.His142Arg)
c.269A>G (p.His90Arg)
c.191A>G (p.His64Arg)
n.711A>G
5g.56859761A>TCA359802412MAP3K1c.680A>T (p.His227Leu)
c.302A>T (p.His101Leu)
c.425A>T (p.His142Leu)
c.269A>T (p.His90Leu)
c.191A>T (p.His64Leu)
n.711A>T
5g.56859762C>ACA359802413MAP3K1c.681C>A (p.His227Gln)
c.303C>A (p.His101Gln)
c.426C>A (p.His142Gln)
c.270C>A (p.His90Gln)
c.192C>A (p.His64Gln)
n.712C>A
5g.56859762C=CA1548129197MAP3K1c.681C= (p.His227=)
c.303C= (p.His101=)
c.426C= (p.His142=)
c.270C= (p.His90=)
c.192C= (p.His64=)
n.712C=
5g.56859762C>GCA359802414MAP3K1c.681C>G (p.His227Gln)
c.303C>G (p.His101Gln)
c.426C>G (p.His142Gln)
c.270C>G (p.His90Gln)
c.192C>G (p.His64Gln)
n.712C>G
5g.56859762C>TCA3272587MAP3K1c.681C>T (p.His227=)
c.303C>T (p.His101=)
c.426C>T (p.His142=)
c.270C>T (p.His90=)
c.192C>T (p.His64=)
n.712C>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
5g.56859763T>ACA359802415MAP3K1c.682T>A (p.Leu228Ile)
c.304T>A (p.Leu102Ile)
c.427T>A (p.Leu143Ile)
c.271T>A (p.Leu91Ile)
c.193T>A (p.Leu65Ile)
n.713T>A
5g.56859763T>CCA444391640MAP3K1c.682T>C (p.Leu228=)
c.304T>C (p.Leu102=)
c.427T>C (p.Leu143=)
c.271T>C (p.Leu91=)
c.193T>C (p.Leu65=)
n.713T>C
5g.56859763T>GCA359802416MAP3K1c.682T>G (p.Leu228Val)
c.304T>G (p.Leu102Val)
c.427T>G (p.Leu143Val)
c.271T>G (p.Leu91Val)
c.193T>G (p.Leu65Val)
n.713T>G
5g.56859764T>ACA359802419MAP3K1c.683T>A (p.Leu228Ter)
c.305T>A (p.Leu102Ter)
c.428T>A (p.Leu143Ter)
c.272T>A (p.Leu91Ter)
c.194T>A (p.Leu65Ter)
n.714T>A
5g.56859764T>CCA359802418MAP3K1c.683T>C (p.Leu228Ser)
c.305T>C (p.Leu102Ser)
c.428T>C (p.Leu143Ser)
c.272T>C (p.Leu91Ser)
c.194T>C (p.Leu65Ser)
n.714T>C
5g.56859764T>GCA359802417MAP3K1c.683T>G (p.Leu228Ter)
c.305T>G (p.Leu102Ter)
c.428T>G (p.Leu143Ter)
c.272T>G (p.Leu91Ter)
c.194T>G (p.Leu65Ter)
n.714T>G
5g.56859765A>CCA359802420MAP3K1c.684A>C (p.Leu228Phe)
c.306A>C (p.Leu102Phe)
c.429A>C (p.Leu143Phe)
c.273A>C (p.Leu91Phe)
c.195A>C (p.Leu65Phe)
n.715A>C
5g.56859765A>GCA444391641MAP3K1c.684A>G (p.Leu228=)
c.306A>G (p.Leu102=)
c.429A>G (p.Leu143=)
c.273A>G (p.Leu91=)
c.195A>G (p.Leu65=)
n.715A>G

Number of alleles fetched