Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
15 | g.66435103T>G | CA16602881 | MAP2K1 | c.91T>G (p.Phe31Val) c.157T>G (p.Phe53Val) n.593T>G n.668T>G | ClinVar dbSNP COSMIC |
15 | g.66435103T>A | CA16602882 | MAP2K1 | c.91T>A (p.Phe31Ile) c.157T>A (p.Phe53Ile) n.593T>A n.668T>A | ClinVar dbSNP COSMIC |
15 | g.66435103T>C | CA16602452 | MAP2K1 | c.91T>C (p.Phe31Leu) c.157T>C (p.Phe53Leu) n.593T>C n.668T>C | ClinVar dbSNP COSMIC |