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18 lines (18 loc) · 1.62 KB
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NCBI_Build Hugo_Symbol Variant_Classification Tumor_Sample_Barcode HGVSp_Short HGVSp HGVSg Chromosome Start_Position End_Position Reference_Allele Tumor_Seq_Allele1 Tumor_Seq_Allele2
GRCh37 CUL1 Missense_Mutation TCGA-A6-2672-01A-01W-0833-10 p.Y466S Tyr466Ser
GRCh37 AKT3 Nonsense_Mutation TCGA-05-4417-01 p.E182* Glu182*
GRCh37 PIK3CA Missense_Mutation TCGA-02-0033-01 p.E542K Glu542Lys 3:g.178936082G>A 3 178936082 178936082 G A A
GRCh37 FGFR3 Missense_Mutation TCGA-05-4417-01 p.V271M Val271Met
GRCh37 EGFR Missense_Mutation TCGA-06-0155-01 p.H304Y His304Tyr 7:g.55223543C>T 7 55223543 55223543 C T T
GRCh37 PTEN Missense_Mutation TCGA-06-0155-01 p.C136R Cys136Arg 10:g.89692922T>C 10 89692922 89692922 T C C
GRCh37 FGFR2 Missense_Mutation TCGA-02-0033-01 p.Q212K Gln121Lys
GRCh37 ATM Missense_Mutation TCGA-05-4417-01 p.L2890R Leu2890Arg
GRCh37 KRAS Missense_Mutation TCGA-05-4417-01 p.G12C Gly12Cys 12:g.25398285C>A 12 25398285 25398285 C A A
GRCh37 KRAS Missense_Mutation TCGA-05-4417-01 p.G12C Gly12Cys 12:g.25398285_25398286delinsAG 12 25398285 25398286 CA AG AG
GRCh37 RB1 Nonsense_Mutation TCGA-02-0033-01 p.Q702* Gln702*
GRCh37 TP53 Missense_Mutation TCGA-02-0033-01 p.R248Q Arg248Gln 17:g.7577538C>T 17 7577538 7577538 C T T
GRCh37 NF1 Splice_Site TCGA-02-0033-01 p.X1445_splice X1445_splice 17:g.29586049G>A 17 29586049 29586049 G A A
GRCh37 STK11 Missense_Mutation TCGA-05-4417-01 p.H168R His168Arg
GRCh37 TERT 5'Flank TCGA-05-4417-01 5:g.1295228G>A 5 1295228 1295228 G A A
GRCh37 MYD88 Missense_Mutation TCGA-05-4417-01 M232T
GRCh37 EGFR Missense_Mutation TCGA-05-4417-01 T790M