| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.55091656A>G | CA12661679 | EGFR | n.279-50630A>G c.89-50630A>G (n.89-50630A>G) n.216-27400A>G c.89-64174A>G (n.89-64174A>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.55091656A>T | CA158905085 | EGFR | n.279-50630A>T c.89-50630A>T (n.89-50630A>T) n.216-27400A>T c.89-64174A>T (n.89-64174A>T) | dbSNP |