| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.55201223C>T | CA4266232 | EGFR | c.2823C>T (p.Asp941=) c.900-4124C>T n.726C>T n.651C>T c.2982C>T (p.Asp994=) c.*28+28295C>T (n.*28+28295C>T) c.2847C>T (p.Asp949=) c.2181C>T (p.Asp727=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.55201223C>G | CA367582409 | EGFR | c.2823C>G (p.Asp941Glu) c.900-4124C>G n.726C>G n.651C>G c.2982C>G (p.Asp994Glu) c.*28+28295C>G (n.*28+28295C>G) c.2847C>G (p.Asp949Glu) c.2181C>G (p.Asp727Glu) | dbSNP |