| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 15 | g.66435104T>C | CA279966 | MAP2K1 | c.92T>C (p.Phe31Ser) c.158T>C (p.Phe53Ser) n.594T>C n.669T>C | ClinVar dbSNP |
| 15 | g.66435104T>A | CA392929195 | MAP2K1 | c.92T>A (p.Phe31Tyr) c.158T>A (p.Phe53Tyr) n.594T>A n.669T>A | dbSNP COSMIC |
| 15 | g.66435104T>G | CA392929193 | MAP2K1 | c.92T>G (p.Phe31Cys) c.158T>G (p.Phe53Cys) n.594T>G n.669T>G | dbSNP COSMIC |