| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.55200396C>A | CA367582016 | EGFR | c.2770C>A (p.Arg924Ser) c.900-4951C>A n.673C>A c.2929C>A (p.Arg977Ser) c.*28+27468C>A (n.*28+27468C>A) c.2794C>A (p.Arg932Ser) n.259C>A c.2128C>A (p.Arg710Ser) | dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.55200396C>T | CA158937483 | EGFR | c.2770C>T (p.Arg924Cys) c.900-4951C>T n.673C>T c.2929C>T (p.Arg977Cys) c.*28+27468C>T (n.*28+27468C>T) c.2794C>T (p.Arg932Cys) n.259C>T c.2128C>T (p.Arg710Cys) | ClinVar dbSNP gnomAD v4 |
| 7 | g.55200396C>G | CA367582017 | EGFR | c.2770C>G (p.Arg924Gly) c.900-4951C>G n.673C>G c.2929C>G (p.Arg977Gly) c.*28+27468C>G (n.*28+27468C>G) c.2794C>G (p.Arg932Gly) n.259C>G c.2128C>G (p.Arg710Gly) | dbSNP |