Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.55181402T>C | CA367578906 | EGFR,EGFR-AS1 | c.2234T>C (p.Leu745Pro) c.742T>C c.2393T>C (p.Leu798Pro) c.*28+8474T>C (n.*28+8474T>C) c.2258T>C (p.Leu753Pro) n.1169A>G c.1592T>C (p.Leu531Pro) | dbSNP |
7 | g.55181402T>A | CA151175 | EGFR,EGFR-AS1 | c.2234T>A (p.Leu745His) c.742T>A c.2393T>A (p.Leu798His) c.*28+8474T>A (n.*28+8474T>A) c.2258T>A (p.Leu753His) n.1169A>T c.1592T>A (p.Leu531His) | ClinVar dbSNP COSMIC |