| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.55174737G>A | CA16602539 | EGFR | c.2041G>A (p.Glu681Lys) c.549G>A c.2200G>A (p.Glu734Lys) c.*28+1809G>A (n.*28+1809G>A) c.2065G>A (p.Glu689Lys) c.1399G>A (p.Glu467Lys) | ClinVar dbSNP gnomAD v4 COSMIC |
| 7 | g.55174737G= | CA1708918288 | EGFR | c.2041G= (p.Glu681=) c.549G= c.2200G= (p.Glu734=) c.*28+1809G= (n.*28+1809G=) c.2065G= (p.Glu689=) c.1399G= (p.Glu467=) | dbSNP |