| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.55174735C>A | CA367583991 | EGFR | c.2039C>A (p.Pro680Gln) c.547C>A c.2198C>A (p.Pro733Gln) c.*28+1807C>A (n.*28+1807C>A) c.2063C>A (p.Pro688Gln) c.1397C>A (p.Pro466Gln) | dbSNP |
| 7 | g.55174735C>T | CA16602538 | EGFR | c.2039C>T (p.Pro680Leu) c.547C>T c.2198C>T (p.Pro733Leu) c.*28+1807C>T (n.*28+1807C>T) c.2063C>T (p.Pro688Leu) c.1397C>T (p.Pro466Leu) | ClinVar dbSNP COSMIC |
| 7 | g.55174735C>G | CA367583993 | EGFR | c.2039C>G (p.Pro680Arg) c.547C>G c.2198C>G (p.Pro733Arg) c.*28+1807C>G (n.*28+1807C>G) c.2063C>G (p.Pro688Arg) c.1397C>G (p.Pro466Arg) | dbSNP |