ttype patient gene classification type chr pos ref_allele newbase context65 cons46 HNSC HN_63080 GTSF1 SNP Missense 12 54856471 C T 29 72 MED MD-144 GTSF1 SNP Missense_Mutation 12 54857054 C T 26 74 MEL ME009 GTSF1 SNP Silent 12 54858938 G A 44 65 MEL MEL-JWCI-WGS-43 GTSF1 SNP Missense_Mutation 12 54858877 G A 41 90 LUAD TCGA-38-4630 GTSF1 SNP Splice_site 12 54858851 C A 24 77 CRC TCGA-AA-3977 GTSF1 SNP Silent 12 54865021 A C 3 56 UCEC TCGA-AP-A051 GTSF1 SNP Missense_Mutation 12 54857035 G T 34 90 UCEC TCGA-B5-A11E GTSF1 SNP Missense_Mutation 12 54854250 G A 38 77 BRCA TCGA-BH-A1EW GTSF1 SNP Missense_Mutation 12 54857054 C T 26 74 UCEC TCGA-BK-A0C9 GTSF1 SNP Nonsense_Mutation 12 54854203 G A 38 65 KIRC TCGA-CZ-4865 GTSF1 SNP Silent 12 54856986 A G 6 64 HNSC TCGA-D6-6516 GTSF1 DNP Missense_Mutation 12 54857043 GG AA 35 62 BLCA TCGA-DK-A3IL GTSF1 SNP Missense_Mutation 12 54854248 T C 54 73