| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.55174014G>A | CA126722 | EGFR | c.1996G>A (p.Gly666Ser) c.504G>A c.2155G>A (p.Gly719Ser) c.*28+1086G>A (n.*28+1086G>A) c.2020G>A (p.Gly674Ser) c.1354G>A (p.Gly452Ser) | ClinVar dbSNP COSMIC |
| 7 | g.55174014G>C | CA135772 | EGFR | c.1996G>C (p.Gly666Arg) c.504G>C c.2155G>C (p.Gly719Arg) c.*28+1086G>C (n.*28+1086G>C) c.2020G>C (p.Gly674Arg) c.1354G>C (p.Gly452Arg) | ClinVar dbSNP |
| 7 | g.55174014G>T | CA126719 | EGFR | c.1996G>T (p.Gly666Cys) c.504G>T c.2155G>T (p.Gly719Cys) c.*28+1086G>T (n.*28+1086G>T) c.2020G>T (p.Gly674Cys) c.1354G>T (p.Gly452Cys) | ClinVar dbSNP COSMIC |
| 7 | g.55174014G= | CA1708917917 | EGFR | c.1996G= (p.Gly666=) c.504G= c.2155G= (p.Gly719=) c.*28+1086G= (n.*28+1086G=) c.2020G= (p.Gly674=) c.1354G= (p.Gly452=) | dbSNP |