| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.55143387G>C | CA367575787 | EGFR | c.164G>C (p.Arg55Thr) n.513G>C c.323G>C (p.Arg108Thr) c.89-12443G>C (n.89-12443G>C) | dbSNP |
| 7 | g.55143387G>A | CA16602662 | EGFR | c.164G>A (p.Arg55Lys) n.513G>A c.323G>A (p.Arg108Lys) c.89-12443G>A (n.89-12443G>A) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |