| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.55160314A>C | CA367579689 | EGFR | c.1315A>C (p.Ser439Arg) c.1474A>C (p.Ser492Arg) c.1339A>C (p.Ser447Arg) c.673A>C (p.Ser225Arg) | dbSNP COSMIC |
| 7 | g.55160314A>T | CA367579688 | EGFR | c.1315A>T (p.Ser439Cys) c.1474A>T (p.Ser492Cys) c.1339A>T (p.Ser447Cys) c.673A>T (p.Ser225Cys) | dbSNP |
| 7 | g.55160314A>G | CA16602560 | EGFR | c.1315A>G (p.Ser439Gly) c.1474A>G (p.Ser492Gly) c.1339A>G (p.Ser447Gly) c.673A>G (p.Ser225Gly) | ClinVar dbSNP gnomAD v4 |