ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-0029 GSPT1 SNP Missense_Mutation 16 11969732 G A 39 94 LUAD LUAD-RT-S01777 GSPT1 SNP Missense_Mutation 16 11976922 C G 30 93 MED MD-326 GSPT1 SNP Missense_Mutation 16 11980402 G T 48 52 MEL MEL-JWCI-14 GSPT1 SNP Splice_site 16 11969784 G A 35 79 OV TCGA-13-0884 GSPT1 SNP Silent 16 11990467 C A 27 27 LUSC TCGA-18-3421 GSPT1 SNP Silent 16 11979113 T C 51 51 OV TCGA-31-1959 GSPT1 SNP Missense_Mutation 16 11980775 C T 24 95 LUAD TCGA-35-3621 GSPT1 SNP Missense_Mutation 16 11980689 G C 35 68 LUAD TCGA-44-2661 GSPT1 SNP Missense_Mutation 16 11969965 C A 17 93 KIRC TCGA-A3-3365 GSPT1 DEL Frame_Shift_Del 16 11984971 T - 56 66 BRCA TCGA-A8-A09I GSPT1 SNP Missense_Mutation 16 11980419 A G 3 84 AML TCGA-AB-2808 GSPT1 SNP Missense_Mutation 16 11981513 G A 46 94 UCEC TCGA-AP-A0LM GSPT1 SNP Missense_Mutation 16 11980636 C A 32 53 UCEC TCGA-B5-A0JY GSPT1 SNP Silent 16 11980450 C T 32 63 UCEC TCGA-B5-A11N GSPT1 SNP Missense_Mutation 16 11979060 A G 7 73 UCEC TCGA-B5-A11R GSPT1 SNP Missense_Mutation 16 11990589 C T 32 94 BRCA TCGA-B6-A0RL GSPT1 SNP Missense_Mutation 16 11984967 G A 40 95 BRCA TCGA-B6-A0WV GSPT1 INS Splice_Site 16 11988808 - A 61 65 BRCA TCGA-BH-A0DZ GSPT1 SNP Missense_Mutation 16 11971338 C G 32 93 BRCA TCGA-BH-A0WA GSPT1 SNP Silent 16 12009404 C T 22 44 BRCA TCGA-C8-A12X GSPT1 SNP Missense_Mutation 16 11976892 G A 34 93 KIRC TCGA-CJ-4920 GSPT1 SNP Missense_Mutation 16 11971401 C T 17 94 UCEC TCGA-D1-A16Y GSPT1 SNP Silent 16 11981523 G A 39 35 BLCA TCGA-G2-A2EO GSPT1 SNP Missense_Mutation 16 11980398 G A 45 77