| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.55173927G>T | CA367583384 | EGFR | c.1909G>T (p.Glu637Ter) c.417G>T c.2068G>T (p.Glu690Ter) c.*28+999G>T (n.*28+999G>T) c.1933G>T (p.Glu645Ter) c.1267G>T (p.Glu423Ter) | dbSNP |
| 7 | g.55173927G>C | CA367583382 | EGFR | c.1909G>C (p.Glu637Gln) c.417G>C c.2068G>C (p.Glu690Gln) c.*28+999G>C (n.*28+999G>C) c.1933G>C (p.Glu645Gln) c.1267G>C (p.Glu423Gln) | dbSNP |
| 7 | g.55173927G>A | CA16602609 | EGFR | c.1909G>A (p.Glu637Lys) c.417G>A c.2068G>A (p.Glu690Lys) c.*28+999G>A (n.*28+999G>A) c.1933G>A (p.Glu645Lys) c.1267G>A (p.Glu423Lys) | ClinVar dbSNP |