Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.29220734G>T | CA16602591 | ALK | c.3617C>A (p.Ser1206Tyr) c.844C>A n.494C>A c.413C>A (p.Ser138Tyr) c.497C>A (p.Ser166Tyr) c.2486C>A (p.Ser829Tyr) c.770C>A (p.Ser257Tyr) | ClinVar dbSNP COSMIC |
2 | g.29220734G>C | CA346472998 | ALK | c.3617C>G (p.Ser1206Cys) c.844C>G n.494C>G c.413C>G (p.Ser138Cys) c.497C>G (p.Ser166Cys) c.2486C>G (p.Ser829Cys) c.770C>G (p.Ser257Cys) | dbSNP |
2 | g.29220734G>A | CA346472997 | ALK | c.3617C>T (p.Ser1206Phe) c.844C>T n.494C>T c.413C>T (p.Ser138Phe) c.497C>T (p.Ser166Phe) c.2486C>T (p.Ser829Phe) c.770C>T (p.Ser257Phe) | dbSNP |