| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.55174794C>G | CA367584189 | EGFR | c.2098C>G (p.Pro700Ala) c.606C>G c.2257C>G (p.Pro753Ala) c.*28+1866C>G (n.*28+1866C>G) c.2122C>G (p.Pro708Ala) c.1456C>G (p.Pro486Ala) | dbSNP |
| 7 | g.55174794C>A | CA367584188 | EGFR | c.2098C>A (p.Pro700Thr) c.606C>A c.2257C>A (p.Pro753Thr) c.*28+1866C>A (n.*28+1866C>A) c.2122C>A (p.Pro708Thr) c.1456C>A (p.Pro486Thr) | dbSNP |
| 7 | g.55174794C>T | CA4266020 | EGFR | c.2098C>T (p.Pro700Ser) c.606C>T c.2257C>T (p.Pro753Ser) c.*28+1866C>T (n.*28+1866C>T) c.2122C>T (p.Pro708Ser) c.1456C>T (p.Pro486Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |