Chr Mutation (hg38) CAid Gene Transcript Linkouts
15g.66436837G>TCA280038MAP2K1c.317G>T (p.Gly106Val)
c.383G>T (p.Gly128Val)
c.291+1600G>T (n.291+1600G>T)
n.819G>T
n.894G>T
ClinVar dbSNP COSMIC
15g.66436837G>ACA16602251MAP2K1c.317G>A (p.Gly106Asp)
c.383G>A (p.Gly128Asp)
c.291+1600G>A (n.291+1600G>A)
n.819G>A
n.894G>A
ClinVar dbSNP COSMIC
15g.66436837G>CCA392930767MAP2K1c.317G>C (p.Gly106Ala)
c.383G>C (p.Gly128Ala)
c.291+1600G>C (n.291+1600G>C)
n.819G>C
n.894G>C
ClinVar dbSNP

Number of alleles fetched