| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.55161562G>A | CA158441 | EGFR | c.1403G>A (p.Arg468Lys) c.1562G>A (p.Arg521Lys) c.1427G>A (p.Arg476Lys) c.761G>A (p.Arg254Lys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.55161562G>T | CA158918328 | EGFR | c.1403G>T (p.Arg468Met) c.1562G>T (p.Arg521Met) c.1427G>T (p.Arg476Met) c.761G>T (p.Arg254Met) | dbSNP |
| 7 | g.55161562G>C | CA158918331 | EGFR | c.1403G>C (p.Arg468Thr) c.1562G>C (p.Arg521Thr) c.1427G>C (p.Arg476Thr) c.761G>C (p.Arg254Thr) | dbSNP |