| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.55155917G>T | CA10586342 | EGFR | c.818G>T (p.Cys273Phe) n.1167G>T c.977G>T (p.Cys326Phe) c.842G>T (p.Cys281Phe) c.176G>T (p.Cys59Phe) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |
| 7 | g.55155917G>A | CA367578104 | EGFR | c.818G>A (p.Cys273Tyr) n.1167G>A c.977G>A (p.Cys326Tyr) c.842G>A (p.Cys281Tyr) c.176G>A (p.Cys59Tyr) | dbSNP COSMIC COSMIC |