| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.55191831T>G | CA135940 | EGFR | c.2423T>G (p.Leu808Arg) c.899+32T>G c.2582T>G (p.Leu861Arg) c.*28+18903T>G (n.*28+18903T>G) c.2447T>G (p.Leu816Arg) c.1781T>G (p.Leu594Arg) | ClinVar dbSNP COSMIC |
| 7 | g.55191831T>C | CA16602602 | EGFR | c.2423T>C (p.Leu808Pro) c.899+32T>C c.2582T>C (p.Leu861Pro) c.*28+18903T>C (n.*28+18903T>C) c.2447T>C (p.Leu816Pro) c.1781T>C (p.Leu594Pro) | ClinVar dbSNP |
| 7 | g.55191831T>A | CA176021 | EGFR | c.2423T>A (p.Leu808Gln) c.899+32T>A c.2582T>A (p.Leu861Gln) c.*28+18903T>A (n.*28+18903T>A) c.2447T>A (p.Leu816Gln) c.1781T>A (p.Leu594Gln) | ClinVar dbSNP COSMIC |
| 7 | g.55191831T= | CA1708922660 | EGFR | c.2423T= (p.Leu808=) c.899+32T= c.2582T= (p.Leu861=) c.*28+18903T= (n.*28+18903T=) c.2447T= (p.Leu816=) c.1781T= (p.Leu594=) | dbSNP |