| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.55163737C>T | CA16602665 | EGFR | c.1477C>T (p.Pro493Ser) c.1636C>T (p.Pro546Ser) c.1501C>T (p.Pro501Ser) c.835C>T (p.Pro279Ser) | ClinVar dbSNP COSMIC |
| 7 | g.55163737C>G | CA367580406 | EGFR | c.1477C>G (p.Pro493Ala) c.1636C>G (p.Pro546Ala) c.1501C>G (p.Pro501Ala) c.835C>G (p.Pro279Ala) | ClinVar dbSNP |
| 7 | g.55163737C>A | CA367580405 | EGFR | c.1477C>A (p.Pro493Thr) c.1636C>A (p.Pro546Thr) c.1501C>A (p.Pro501Thr) c.835C>A (p.Pro279Thr) | dbSNP |