| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.55174730G>T | CA367583970 | EGFR | c.2034G>T (p.Trp678Cys) c.542G>T c.2193G>T (p.Trp731Cys) c.*28+1802G>T (n.*28+1802G>T) c.2058G>T (p.Trp686Cys) c.1392G>T (p.Trp464Cys) | dbSNP |
| 7 | g.55174730G>A | CA16602723 | EGFR | c.2034G>A (p.Trp678Ter) c.542G>A c.2193G>A (p.Trp731Ter) c.*28+1802G>A (n.*28+1802G>A) c.2058G>A (p.Trp686Ter) c.1392G>A (p.Trp464Ter) | ClinVar dbSNP COSMIC |
| 7 | g.55174730G>C | CA367583968 | EGFR | c.2034G>C (p.Trp678Cys) c.542G>C c.2193G>C (p.Trp731Cys) c.*28+1802G>C (n.*28+1802G>C) c.2058G>C (p.Trp686Cys) c.1392G>C (p.Trp464Cys) | dbSNP |