| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.55174792C>G | CA367584186 | EGFR | c.2096C>G (p.Ser699Cys) c.604C>G c.2255C>G (p.Ser752Cys) c.*28+1864C>G (n.*28+1864C>G) c.2120C>G (p.Ser707Cys) c.1454C>G (p.Ser485Cys) | dbSNP |
| 7 | g.55174792C>T | CA367584187 | EGFR | c.2096C>T (p.Ser699Phe) c.604C>T c.2255C>T (p.Ser752Phe) c.*28+1864C>T (n.*28+1864C>T) c.2120C>T (p.Ser707Phe) c.1454C>T (p.Ser485Phe) | dbSNP COSMIC |
| 7 | g.55174792C>A | CA16602725 | EGFR | c.2096C>A (p.Ser699Tyr) c.604C>A c.2255C>A (p.Ser752Tyr) c.*28+1864C>A (n.*28+1864C>A) c.2120C>A (p.Ser707Tyr) c.1454C>A (p.Ser485Tyr) | ClinVar dbSNP COSMIC |