ttype patient gene classification type chr pos ref_allele newbase context65 cons46 LUAD LUAD-S01315 PRR11 SNP Missense_Mutation 17 57270952 G T 33 59 MEL MEL-Ma-Mel-37 PRR11 SNP Missense_Mutation 17 57272719 C T 30 59 LUAD TCGA-05-4397 PRR11 SNP Splice_site 17 57247240 A T 3 70 LUAD TCGA-05-4410 PRR11 SNP Missense_Mutation 17 57262850 G T 37 46 LUSC TCGA-22-5485 PRR11 SNP Missense_Mutation 17 57272786 G T 37 58 OV TCGA-23-1110 PRR11 DEL Frame_Shift_Del 17 57262467 TCCTGGAACTTCAATTT - 50 51 OV TCGA-24-2293 PRR11 SNP Missense_Mutation 17 57278973 G A 34 56 LUSC TCGA-43-2578 PRR11 SNP Missense_Mutation 17 57275130 G T 42 80 LUSC TCGA-46-3768 PRR11 SNP Missense_Mutation 17 57262807 G A 33 61 BRCA TCGA-A7-A0D9 PRR11 SNP Missense_Mutation 17 57262856 T C 56 63 BRCA TCGA-AO-A0J4 PRR11 SNP Missense_Mutation 17 57262479 A T 5 57 UCEC TCGA-AP-A059 PRR11 SNP Nonsense_Mutation 17 57247132 C T 19 51 UCEC TCGA-B5-A11E PRR11 SNP Silent 17 57262418 C T 31 46 HNSC TCGA-BB-4223 PRR11 SNP Missense_Mutation 17 57270903 G A 45 53 KIRC TCGA-BP-4976 PRR11 SNP Missense_Mutation 17 57262419 G C 39 52 HNSC TCGA-CN-5360 PRR11 SNP Silent 17 57270975 C A 21 50 BLCA TCGA-FD-A3B6 PRR11 SNP Silent 17 57275120 G A 45 48 HNSC TCGA-HL-7533 PRR11 SNP Silent 17 57270939 G C 45 45