Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.55181327A>G | CA16602544 | EGFR,EGFR-AS1 | c.2159A>G (p.His720Arg) c.667A>G c.2318A>G (p.His773Arg) c.*28+8399A>G (n.*28+8399A>G) c.2183A>G (p.His728Arg) n.1244T>C c.1517A>G (p.His506Arg) | ClinVar dbSNP COSMIC |
7 | g.55181327A>T | CA367578706 | EGFR,EGFR-AS1 | c.2159A>T (p.His720Leu) c.667A>T c.2318A>T (p.His773Leu) c.*28+8399A>T (n.*28+8399A>T) c.2183A>T (p.His728Leu) n.1244T>A c.1517A>T (p.His506Leu) | dbSNP COSMIC |
7 | g.55181327A>C | CA367578708 | EGFR,EGFR-AS1 | c.2159A>C (p.His720Pro) c.667A>C c.2318A>C (p.His773Pro) c.*28+8399A>C (n.*28+8399A>C) c.2183A>C (p.His728Pro) n.1244T>G c.1517A>C (p.His506Pro) | dbSNP COSMIC |