| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.55181370G>A | CA135896 | EGFR,EGFR-AS1 | c.2202G>A (p.Gln734=) c.710G>A c.2361G>A (p.Gln787=) c.*28+8442G>A (n.*28+8442G>A) c.2226G>A (p.Gln742=) n.1201C>T c.1560G>A (p.Gln520=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.55181370G>T | CA367578836 | EGFR,EGFR-AS1 | c.2202G>T (p.Gln734His) c.710G>T c.2361G>T (p.Gln787His) c.*28+8442G>T (n.*28+8442G>T) c.2226G>T (p.Gln742His) n.1201C>A c.1560G>T (p.Gln520His) | ClinVar dbSNP |
| 7 | g.55181370G>C | CA367578835 | EGFR,EGFR-AS1 | c.2202G>C (p.Gln734His) c.710G>C c.2361G>C (p.Gln787His) c.*28+8442G>C (n.*28+8442G>C) c.2226G>C (p.Gln742His) n.1201C>G c.1560G>C (p.Gln520His) | dbSNP |