| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.55154129C>G | CA367577849 | EGFR | c.707C>G (p.Ala236Gly) n.1056C>G c.866C>G (p.Ala289Gly) c.731C>G (p.Ala244Gly) c.89-1701C>G (n.89-1701C>G) | dbSNP |
| 7 | g.55154129C>A | CA16602834 | EGFR | c.707C>A (p.Ala236Asp) n.1056C>A c.866C>A (p.Ala289Asp) c.731C>A (p.Ala244Asp) c.89-1701C>A (n.89-1701C>A) | ClinVar dbSNP COSMIC COSMIC |
| 7 | g.55154129C>T | CA16602664 | EGFR | c.707C>T (p.Ala236Val) n.1056C>T c.866C>T (p.Ala289Val) c.731C>T (p.Ala244Val) c.89-1701C>T (n.89-1701C>T) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |