| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 2 | g.29209816C>G | CA16602590 | ALK | c.3806G>C (p.Gly1269Ala) c.1033G>C n.683G>C c.602G>C (p.Gly201Ala) c.686G>C (p.Gly229Ala) c.2675G>C (p.Gly892Ala) c.959G>C (p.Gly320Ala) | ClinVar dbSNP COSMIC |
| 2 | g.29209816C>A | CA346469632 | ALK | c.3806G>T (p.Gly1269Val) c.1033G>T n.683G>T c.602G>T (p.Gly201Val) c.686G>T (p.Gly229Val) c.2675G>T (p.Gly892Val) c.959G>T (p.Gly320Val) | dbSNP |
| 2 | g.29209816C>T | CA346469633 | ALK | c.3806G>A (p.Gly1269Glu) c.1033G>A n.683G>A c.602G>A (p.Gly201Glu) c.686G>A (p.Gly229Glu) c.2675G>A (p.Gly892Glu) c.959G>A (p.Gly320Glu) | ClinVar dbSNP COSMIC |