| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 2 | g.29222347A>C | CA346462883 | ALK | c.3512T>G (p.Ile1171Ser) c.739T>G n.389T>G c.308T>G (p.Ile103Ser) c.392T>G (p.Ile131Ser) c.206T>G (p.Ile69Ser) c.2381T>G (p.Ile794Ser) c.665T>G (p.Ile222Ser) | dbSNP COSMIC |
| 2 | g.29222347A>T | CA16602371 | ALK | c.3512T>A (p.Ile1171Asn) c.739T>A n.389T>A c.308T>A (p.Ile103Asn) c.392T>A (p.Ile131Asn) c.206T>A (p.Ile69Asn) c.2381T>A (p.Ile794Asn) c.665T>A (p.Ile222Asn) | ClinVar dbSNP COSMIC |
| 2 | g.29222347A>G | CA346462880 | ALK | c.3512T>C (p.Ile1171Thr) c.739T>C n.389T>C c.308T>C (p.Ile103Thr) c.392T>C (p.Ile131Thr) c.206T>C (p.Ile69Thr) c.2381T>C (p.Ile794Thr) c.665T>C (p.Ile222Thr) | ClinVar dbSNP COSMIC |