| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 2 | g.29214054C>T | CA16602369 | ALK | c.3673G>A (p.Asp1225Asn) c.900G>A n.550G>A c.469G>A (p.Asp157Asn) c.553G>A (p.Asp185Asn) c.2542G>A (p.Asp848Asn) c.826G>A (p.Asp276Asn) | ClinVar dbSNP COSMIC |
| 2 | g.29214054C>A | CA346471557 | ALK | c.3673G>T (p.Asp1225Tyr) c.900G>T n.550G>T c.469G>T (p.Asp157Tyr) c.553G>T (p.Asp185Tyr) c.2542G>T (p.Asp848Tyr) c.826G>T (p.Asp276Tyr) | dbSNP |
| 2 | g.29214054C>G | CA346471558 | ALK | c.3673G>C (p.Asp1225His) c.900G>C n.550G>C c.469G>C (p.Asp157His) c.553G>C (p.Asp185His) c.2542G>C (p.Asp848His) c.826G>C (p.Asp276His) | dbSNP |