| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.55181437G>C | CA367578983 | EGFR,EGFR-AS1 | c.2269G>C (p.Gly757Arg) c.777G>C c.2428G>C (p.Gly810Arg) c.*28+8509G>C (n.*28+8509G>C) c.2293G>C (p.Gly765Arg) n.1134C>G c.1627G>C (p.Gly543Arg) | dbSNP |
| 7 | g.55181437G>T | CA367578982 | EGFR,EGFR-AS1 | c.2269G>T (p.Gly757Cys) c.777G>T c.2428G>T (p.Gly810Cys) c.*28+8509G>T (n.*28+8509G>T) c.2293G>T (p.Gly765Cys) n.1134C>A c.1627G>T (p.Gly543Cys) | dbSNP |
| 7 | g.55181437G>A | CA16602726 | EGFR,EGFR-AS1 | c.2269G>A (p.Gly757Ser) c.777G>A c.2428G>A (p.Gly810Ser) c.*28+8509G>A (n.*28+8509G>A) c.2293G>A (p.Gly765Ser) n.1134C>T c.1627G>A (p.Gly543Ser) | ClinVar dbSNP COSMIC |