| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 15 | g.66435105T>G | CA16602880 | MAP2K1 | c.93T>G (p.Phe31Leu) c.159T>G (p.Phe53Leu) n.595T>G n.670T>G | ClinVar dbSNP COSMIC |
| 15 | g.66435105T>C | CA490855927 | MAP2K1 | c.93T>C (p.Phe31=) c.159T>C (p.Phe53=) n.595T>C n.670T>C | dbSNP |
| 15 | g.66435105T>A | CA392929197 | MAP2K1 | c.93T>A (p.Phe31Leu) c.159T>A (p.Phe53Leu) n.595T>A n.670T>A | dbSNP COSMIC |