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 |