| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.55191822T>A | CA16602729 | EGFR | c.2414T>A (p.Leu805Gln) c.899+23T>A c.2573T>A (p.Leu858Gln) c.*28+18894T>A (n.*28+18894T>A) c.2438T>A (p.Leu813Gln) c.1772T>A (p.Leu591Gln) | ClinVar dbSNP COSMIC |
| 7 | g.55191822T>G | CA126713 | EGFR | c.2414T>G (p.Leu805Arg) c.899+23T>G c.2573T>G (p.Leu858Arg) c.*28+18894T>G (n.*28+18894T>G) c.2438T>G (p.Leu813Arg) c.1772T>G (p.Leu591Arg) | ClinVar dbSNP COSMIC |
| 7 | g.55191822T= | CA1708922630 | EGFR | c.2414T= (p.Leu805=) c.899+23T= c.2573T= (p.Leu858=) c.*28+18894T= (n.*28+18894T=) c.2438T= (p.Leu813=) c.1772T= (p.Leu591=) | dbSNP |