Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.55174773G>A | CA16602724 | EGFR | c.2077G>A (p.Glu693Lys) c.585G>A c.2236G>A (p.Glu746Lys) c.*28+1845G>A (n.*28+1845G>A) c.2101G>A (p.Glu701Lys) c.1435G>A (p.Glu479Lys) | ClinVar dbSNP COSMIC |
7 | g.55174773G>C | CA180723 | EGFR | c.2077G>C (p.Glu693Gln) c.585G>C c.2236G>C (p.Glu746Gln) c.*28+1845G>C (n.*28+1845G>C) c.2101G>C (p.Glu701Gln) c.1435G>C (p.Glu479Gln) | ClinVar dbSNP |