| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.55143386A>T | CA367575786 | EGFR | c.163A>T (p.Arg55Ter) n.512A>T c.322A>T (p.Arg108Ter) c.89-12444A>T (n.89-12444A>T) | dbSNP |
| 7 | g.55143386A>G | CA16602838 | EGFR | c.163A>G (p.Arg55Gly) n.512A>G c.322A>G (p.Arg108Gly) c.89-12444A>G (n.89-12444A>G) | ClinVar dbSNP COSMIC COSMIC |