| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.55174740G>A | CA16602540 | EGFR | c.2044G>A (p.Gly682Ser) c.552G>A c.2203G>A (p.Gly735Ser) c.*28+1812G>A (n.*28+1812G>A) c.2068G>A (p.Gly690Ser) c.1402G>A (p.Gly468Ser) | ClinVar dbSNP COSMIC |
| 7 | g.55174740G= | CA1708918289 | EGFR | c.2044G= (p.Gly682=) c.552G= c.2203G= (p.Gly735=) c.*28+1812G= (n.*28+1812G=) c.2068G= (p.Gly690=) c.1402G= (p.Gly468=) | dbSNP |
| 7 | g.55174740G>T | CA367584013 | EGFR | c.2044G>T (p.Gly682Cys) c.552G>T c.2203G>T (p.Gly735Cys) c.*28+1812G>T (n.*28+1812G>T) c.2068G>T (p.Gly690Cys) c.1402G>T (p.Gly468Cys) | dbSNP |