| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 2 | g.29214009A>T | CA346471266 | ALK | c.3718T>A (p.Leu1240Met) c.945T>A n.595T>A c.514T>A (p.Leu172Met) c.598T>A (p.Leu200Met) c.2587T>A (p.Leu863Met) c.871T>A (p.Leu291Met) | dbSNP |
| 2 | g.29214009A>C | CA279618 | ALK | c.3718T>G (p.Leu1240Val) c.945T>G n.595T>G c.514T>G (p.Leu172Val) c.598T>G (p.Leu200Val) c.2587T>G (p.Leu863Val) c.871T>G (p.Leu291Val) | ClinVar dbSNP COSMIC |