| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.55174725C>T | CA158932443 | EGFR | c.2029C>T (p.Leu677Phe) c.537C>T c.2188C>T (p.Leu730Phe) c.*28+1797C>T (n.*28+1797C>T) c.2053C>T (p.Leu685Phe) c.1387C>T (p.Leu463Phe) | dbSNP COSMIC |
| 7 | g.55174725C>G | CA151172 | EGFR | c.2029C>G (p.Leu677Val) c.537C>G c.2188C>G (p.Leu730Val) c.*28+1797C>G (n.*28+1797C>G) c.2053C>G (p.Leu685Val) c.1387C>G (p.Leu463Val) | ClinVar dbSNP |
| 7 | g.55174725C= | CA1708918281 | EGFR | c.2029C= (p.Leu677=) c.537C= c.2188C= (p.Leu730=) c.*28+1797C= (n.*28+1797C=) c.2053C= (p.Leu685=) c.1387C= (p.Leu463=) | dbSNP |