| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.55181438G>C | CA367578984 | EGFR,EGFR-AS1 | c.2270G>C (p.Gly757Ala) c.778G>C c.2429G>C (p.Gly810Ala) c.*28+8510G>C (n.*28+8510G>C) c.2294G>C (p.Gly765Ala) n.1133C>G c.1628G>C (p.Gly543Ala) | dbSNP COSMIC |
| 7 | g.55181438G>A | CA16602727 | EGFR,EGFR-AS1 | c.2270G>A (p.Gly757Asp) c.778G>A c.2429G>A (p.Gly810Asp) c.*28+8510G>A (n.*28+8510G>A) c.2294G>A (p.Gly765Asp) n.1133C>T c.1628G>A (p.Gly543Asp) | ClinVar dbSNP COSMIC |
| 7 | g.55181438G>T | CA367578985 | EGFR,EGFR-AS1 | c.2270G>T (p.Gly757Val) c.778G>T c.2429G>T (p.Gly810Val) c.*28+8510G>T (n.*28+8510G>T) c.2294G>T (p.Gly765Val) n.1133C>A c.1628G>T (p.Gly543Val) | dbSNP |