| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.55181317_55181319delinsTGGG | CA176010 | EGFR,EGFR-AS1 | c.2149_2151delinsTGGG (p.Asp717TrpfsTer?) c.657_659delinsTGGG c.2308_2310delinsTGGG (p.Asp770TrpfsTer?) c.*28+8389_*28+8391delinsTGGG (n.*28+8389_*28+8391delinsTGGG) c.2173_2175delinsTGGG (p.Asp725TrpfsTer?) n.1252_1254delinsCCCA c.1507_1509delinsTGGG (p.Asp503TrpfsTer?) | ClinVar dbSNP |
| 7 | g.55181319_55181320insGGCGAC | CA645561573 | EGFR,EGFR-AS1 | c.2151_2152insGGCGAC (p.Asp717_Asn718insGlyAsp) c.659_660insGGCGAC c.2310_2311insGGCGAC (p.Asp770_Asn771insGlyAsp) c.*28+8391_*28+8392insGGCGAC (n.*28+8391_*28+8392insGGCGAC) c.2175_2176insGGCGAC (p.Asp725_Asn726insGlyAsp) n.1254_1255insGCCGTC c.1509_1510insGGCGAC (p.Asp503_Asn504insGlyAsp) | dbSNP COSMIC |