ttype patient gene classification type chr pos ref_allele newbase context65 cons46 LUAD LUAD-B02216 GPKOW SNP Silent 23 48970872 C A 29 53 LUAD LUAD-B02594 GPKOW SNP Missense_Mutation 23 48979960 C A 26 55 MEL MEL-13447 GPKOW SNP Missense_Mutation 23 48974028 C T 30 83 MEL MEL-Ma-Mel-65 GPKOW SNP Missense_Mutation 23 48979019 G A 42 52 MEL MEL-Ma-Mel-86 GPKOW SNP Missense_Mutation 23 48978783 C T 23 46 MM MM-0579 GPKOW SNP Missense_Mutation 23 48970576 C T 29 61 GBM TCGA-06-0125 GPKOW SNP Missense_Mutation 23 48976107 G A 38 56 OV TCGA-13-1409 GPKOW SNP Missense_Mutation 23 48976067 G T 44 85 LUAD TCGA-17-Z060 GPKOW INS Frame_Shift_Ins 23 48979004 - T 6 64 LUAD TCGA-50-5931 GPKOW SNP Silent 23 48972658 G C 35 52 LUAD TCGA-50-6590 GPKOW SNP Missense_Mutation 23 48976099 C A 21 86 LUAD TCGA-50-6594 GPKOW SNP Missense_Mutation 23 48972137 C A 32 88 LUAD TCGA-55-1592 GPKOW SNP Missense_Mutation 23 48973405 C T 29 65 LUAD TCGA-55-1592 GPKOW SNP Silent 23 48973451 C T 29 51 OV TCGA-59-2348 GPKOW SNP Silent 23 48979003 C T 21 55 LUSC TCGA-60-2720 GPKOW SNP Missense_Mutation 23 48973958 T C 49 66 LUAD TCGA-75-5125 GPKOW DEL Frame_Shift_Del 23 48978780 C - 30 56 UCEC TCGA-AP-A051 GPKOW SNP Silent 23 48976108 C T 25 52 UCEC TCGA-AP-A059 GPKOW SNP Missense_Mutation 23 48972134 C T 17 75 UCEC TCGA-AP-A0LE GPKOW SNP Splice_site 23 48979897 C A 24 76 UCEC TCGA-AP-A0LM GPKOW SNP Missense_Mutation 23 48976071 G A 39 73 CRC TCGA-AY-4070 GPKOW SNP Missense_Mutation 23 48970807 C T 26 85 KIRC TCGA-B0-5713 GPKOW SNP Silent 23 48979947 A T 11 46 UCEC TCGA-B5-A11N GPKOW SNP Nonsense_Mutation 23 48970633 C A 32 75 UCEC TCGA-B5-A11N GPKOW SNP Missense_Mutation 23 48978770 T G 58 54 UCEC TCGA-B5-A11U GPKOW SNP Missense_Mutation 23 48973985 A G 2 77 HNSC TCGA-BA-4077 GPKOW SNP Missense_Mutation 23 48972603 C G 32 52 UCEC TCGA-BG-A0VW GPKOW SNP Missense_Mutation 23 48980024 C T 25 74 BRCA TCGA-BH-A0HU GPKOW SNP Missense_Mutation 23 48972279 T C 60 60 BLCA TCGA-BT-A2LB GPKOW SNP Missense_Mutation 23 48973498 C T 29 85 HNSC TCGA-CQ-5326 GPKOW SNP Silent 23 48979986 C G 30 55 HNSC TCGA-CR-7370 GPKOW DNP Silent 23 48979050 GG TT 39 63 UCEC TCGA-D1-A163 GPKOW SNP Silent 23 48976078 G A 46 60 UCEC TCGA-D1-A16D GPKOW SNP Missense_Mutation 23 48976074 C T 23 86 UCEC TCGA-D1-A17Q GPKOW SNP Missense_Mutation 23 48973404 T C 58 65 BRCA TCGA-D8-A141 GPKOW SNP Missense_Mutation 23 48978773 G T 46 53