| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.55174774_55174793delinsTC | CA180811 | EGFR | c.2078_2097delinsTC (p.Glu693_Ser699delinsVal) c.586_605delinsTC c.2237_2256delinsTC (p.Glu746_Ser752delinsVal) c.*28+1846_*28+1865delinsTC (n.*28+1846_*28+1865delinsTC) c.2102_2121delinsTC (p.Glu701_Ser707delinsVal) c.1436_1455delinsTC (p.Glu479_Ser485delinsVal) | ClinVar dbSNP COSMIC |
| 7 | g.55174774_55174793delinsTG | CA645561509 | EGFR | c.2078_2097delinsTG (p.Glu693_Ser699delinsVal) c.586_605delinsTG c.2237_2256delinsTG (p.Glu746_Ser752delinsVal) c.*28+1846_*28+1865delinsTG (n.*28+1846_*28+1865delinsTG) c.2102_2121delinsTG (p.Glu701_Ser707delinsVal) c.1436_1455delinsTG (p.Glu479_Ser485delinsVal) | dbSNP COSMIC |