Chr Mutation (hg38) CAid Gene Transcript Linkouts
5g.56872885C>GCA444212696MAP3K1c.1566C>G (p.Thr522=)
c.1188C>G (p.Thr396=)
c.1311C>G (p.Thr437=)
c.1155C>G (p.Thr385=)
c.1077C>G (p.Thr359=)
n.1597C>G
dbSNP gnomAD v4
5g.56872885C>TCA3272801MAP3K1c.1566C>T (p.Thr522=)
c.1188C>T (p.Thr396=)
c.1311C>T (p.Thr437=)
c.1155C>T (p.Thr385=)
c.1077C>T (p.Thr359=)
n.1597C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4

Number of alleles fetched