Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.55181321_55181323dup | CA135857 | EGFR,EGFR-AS1 | c.2153_2155dup (p.Asn718_Pro719insHis) c.661_663dup c.2312_2314dup (p.Asn771_Pro772insHis) c.*28+8393_*28+8395dup (n.*28+8393_*28+8395dup) c.2177_2179dup (p.Asn726_Pro727insHis) n.1248_1250dup c.1511_1513dup (p.Asn504_Pro505insHis) | ClinVar dbSNP COSMIC |
7 | g.55181323_55181324insACCACC | CA2714508310 | EGFR,EGFR-AS1 | c.2155_2156insACCACC (p.Asn718_Pro719insHisHis) c.663_664insACCACC c.2314_2315insACCACC (p.Asn771_Pro772insHisHis) c.*28+8395_*28+8396insACCACC (n.*28+8395_*28+8396insACCACC) c.2179_2180insACCACC (p.Asn726_Pro727insHisHis) n.1250_1251insGGTGGT c.1513_1514insACCACC (p.Asn504_Pro505insHisHis) | dbSNP |
7 | g.55181323_55181324insGGCACC | CA645561598 | EGFR,EGFR-AS1 | c.2155_2156insGGCACC (p.Asn718_Pro719insArgHis) c.663_664insGGCACC c.2314_2315insGGCACC (p.Asn771_Pro772insArgHis) c.*28+8395_*28+8396insGGCACC (n.*28+8395_*28+8396insGGCACC) c.2179_2180insGGCACC (p.Asn726_Pro727insArgHis) n.1250_1251insGCCGGT c.1513_1514insGGCACC (p.Asn504_Pro505insArgHis) | dbSNP COSMIC |