| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.55174775_55174785delinsTC | CA645561522 | EGFR | c.2079_2089delinsTC (p.Glu693_Ala697delinsAspPro) c.587_597delinsTC c.2238_2248delinsTC (p.Glu746_Ala750delinsAspPro) c.*28+1847_*28+1857delinsTC (n.*28+1847_*28+1857delinsTC) c.2103_2113delinsTC (p.Glu701_Ala705delinsAspPro) c.1437_1447delinsTC (p.Glu479_Ala483delinsAspPro) | dbSNP COSMIC |
| 7 | g.55174775_55174785delinsGC | CA181028 | EGFR | c.2079_2089delinsGC (p.Leu694_Ala697delinsPro) c.587_597delinsGC c.2238_2248delinsGC (p.Leu747_Ala750delinsPro) c.*28+1847_*28+1857delinsGC (n.*28+1847_*28+1857delinsGC) c.2103_2113delinsGC (p.Leu702_Ala705delinsPro) c.1437_1447delinsGC (p.Leu480_Ala483delinsPro) | ClinVar dbSNP COSMIC |