| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.55174015G>C | CA135775 | EGFR | c.1997G>C (p.Gly666Ala) c.505G>C c.2156G>C (p.Gly719Ala) c.*28+1087G>C (n.*28+1087G>C) c.2021G>C (p.Gly674Ala) c.1355G>C (p.Gly452Ala) | ClinVar dbSNP COSMIC |
| 7 | g.55174015G>A | CA16602537 | EGFR | c.1997G>A (p.Gly666Asp) c.505G>A c.2156G>A (p.Gly719Asp) c.*28+1087G>A (n.*28+1087G>A) c.2021G>A (p.Gly674Asp) c.1355G>A (p.Gly452Asp) | ClinVar dbSNP COSMIC |
| 7 | g.55174015G= | CA1708917918 | EGFR | c.1997G= (p.Gly666=) c.505G= c.2156G= (p.Gly719=) c.*28+1087G= (n.*28+1087G=) c.2021G= (p.Gly674=) c.1355G= (p.Gly452=) | dbSNP |