| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.55165350G>C | CA16602837 | EGFR | c.1634G>C (p.Gly545Ala) c.142G>C c.1793G>C (p.Gly598Ala) c.1658G>C (p.Gly553Ala) c.992G>C (p.Gly331Ala) | ClinVar dbSNP COSMIC COSMIC |
| 7 | g.55165350G>A | CA367580850 | EGFR | c.1634G>A (p.Gly545Glu) c.142G>A c.1793G>A (p.Gly598Glu) c.1658G>A (p.Gly553Glu) c.992G>A (p.Gly331Glu) | dbSNP |
| 7 | g.55165350G>T | CA4265696 | EGFR | c.1634G>T (p.Gly545Val) c.142G>T c.1793G>T (p.Gly598Val) c.1658G>T (p.Gly553Val) c.992G>T (p.Gly331Val) | ClinVar dbSNP ExAC gnomAD v2 COSMIC COSMIC COSMIC |