Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
15 | g.66436837G>T | CA280038 | MAP2K1 | c.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 |
15 | g.66436837G>A | CA16602251 | MAP2K1 | c.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 |
15 | g.66436837G>C | CA392930767 | MAP2K1 | c.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 |