| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.55191821C>T | CA135933 | EGFR | c.2413C>T (p.Leu805=) c.899+22C>T c.2572C>T (p.Leu858=) c.*28+18893C>T (n.*28+18893C>T) c.2437C>T (p.Leu813=) c.1771C>T (p.Leu591=) | ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC |
| 7 | g.55191821C>A | CA135930 | EGFR | c.2413C>A (p.Leu805Met) c.899+22C>A c.2572C>A (p.Leu858Met) c.*28+18893C>A (n.*28+18893C>A) c.2437C>A (p.Leu813Met) c.1771C>A (p.Leu591Met) | ClinVar dbSNP COSMIC |