| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.55181364C>A | CA455165150 | EGFR,EGFR-AS1 | c.2196C>A (p.Thr732=) c.704C>A c.2355C>A (p.Thr785=) c.*28+8436C>A (n.*28+8436C>A) c.2220C>A (p.Thr740=) n.1207G>T c.1554C>A (p.Thr518=) | dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.55181364C>T | CA135893 | EGFR,EGFR-AS1 | c.2196C>T (p.Thr732=) c.704C>T c.2355C>T (p.Thr785=) c.*28+8436C>T (n.*28+8436C>T) c.2220C>T (p.Thr740=) n.1207G>A c.1554C>T (p.Thr518=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.55181364C>G | CA455165151 | EGFR,EGFR-AS1 | c.2196C>G (p.Thr732=) c.704C>G c.2355C>G (p.Thr785=) c.*28+8436C>G (n.*28+8436C>G) c.2220C>G (p.Thr740=) n.1207G>C c.1554C>G (p.Thr518=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |