ttype patient gene classification type chr pos ref_allele newbase context65 cons46 CLL CLL-JJ NOM1 SNP Silent 7 156759693 C T 20 51 ESO ESO-143 NOM1 SNP Silent 7 156742875 G A 43 45 LUAD LUAD-CHTN-3090346 NOM1 SNP Missense_Mutation 7 156755709 A G 2 50 LUAD LUAD-D02185 NOM1 SNP Missense_Mutation 7 156755715 G T 42 81 LUAD LUAD-F00170 NOM1 SNP Silent 7 156743172 C T 23 47 LUAD LUAD-S01315 NOM1 SNP Missense_Mutation 7 156742933 G T 38 58 LUAD LUAD-S01413 NOM1 SNP Missense_Mutation 7 156743119 G T 39 69 MEL MEL-Ma-Mel-15 NOM1 SNP Missense_Mutation 7 156762254 C T 19 64 MM MM-0425-FIX NOM1 SNP Missense 7 156746844 T A 55 89 MM MM-0629 NOM1 SNP Missense_Mutation 7 156752795 C T 29 82 LUAD TCGA-05-4250 NOM1 SNP Missense_Mutation 7 156742967 A G 2 83 LUAD TCGA-05-4396 NOM1 SNP Silent 7 156754916 C A 23 40 LUAD TCGA-05-4396 NOM1 SNP Missense_Mutation 7 156759745 C A 21 69 OV TCGA-13-1408 NOM1 SNP Splice_Site 7 156759098 T A 57 90 LUAD TCGA-17-Z057 NOM1 SNP Missense_Mutation 7 156746815 G T 47 69 LUAD TCGA-17-Z060 NOM1 SNP Missense_Mutation 7 156756633 A G 7 76 GBM TCGA-26-6173 NOM1 SNP Missense_Mutation 7 156743012 G A 44 90 LUSC TCGA-34-2600 NOM1 SNP Missense_Mutation 7 156746852 G A 42 56 LUSC TCGA-34-5231 NOM1 SNP Silent 7 156742848 G T 38 46 LUSC TCGA-56-5897 NOM1 SNP Nonsense_Mutation 7 156743221 G T 41 47 LUAD TCGA-73-4666 NOM1 SNP Silent 7 156752721 C A 23 43 UCEC TCGA-A5-A0G9 NOM1 SNP Missense_Mutation 7 156746891 G A 38 50 UCEC TCGA-A5-A0VP NOM1 SNP Silent 7 156762298 C T 19 50 CRC TCGA-A6-2672 NOM1 SNP Missense_Mutation 7 156759046 T C 56 91 CRC TCGA-A6-2672 NOM1 SNP Missense_Mutation 7 156759670 A G 7 91 CRC TCGA-AA-3552 NOM1 SNP Silent 7 156755710 C T 19 45 CRC TCGA-AA-3672 NOM1 SNP Silent 7 156761801 G A 47 46 CRC TCGA-AA-3842 NOM1 SNP Missense_Mutation 7 156752548 G A 39 82 CRC TCGA-AA-A02F NOM1 SNP Nonsense_Mutation 7 156743149 G T 41 77 AML TCGA-AB-2828 NOM1 SNP Silent 7 156758976 G A 35 67 AML TCGA-AB-2828 NOM1 SNP Missense_Mutation 7 156762340 A T 11 49 CRC TCGA-AF-2689 NOM1 SNP Missense_Mutation 7 156754863 A G 10 86 CRC TCGA-AG-A002 NOM1 SNP Missense_Mutation 7 156743316 G T 35 41 CRC TCGA-AG-A002 NOM1 SNP Missense_Mutation 7 156745276 A C 1 59 UCEC TCGA-AP-A051 NOM1 SNP Missense_Mutation 7 156746859 G A 34 97 UCEC TCGA-AP-A056 NOM1 SNP Missense_Mutation 7 156762286 C A 32 86 UCEC TCGA-AP-A0LM NOM1 SNP Missense_Mutation 7 156759760 A C 1 77 UCEC TCGA-AX-A064 NOM1 SNP Missense_Mutation 7 156759022 C A 24 58 UCEC TCGA-AX-A0J1 NOM1 SNP Missense_Mutation 7 156743249 C T 27 46 UCEC TCGA-B5-A11E NOM1 SNP Silent 7 156759714 G A 37 51 HNSC TCGA-BA-5149 NOM1 SNP Missense_Mutation 7 156755792 G T 48 75 UCEC TCGA-BS-A0U7 NOM1 SNP Silent 7 156743391 C T 24 47 UCEC TCGA-BS-A0UF NOM1 SNP Missense_Mutation 7 156743072 A G 10 83 UCEC TCGA-BS-A0UF NOM1 SNP Missense_Mutation 7 156759068 A C 1 77 UCEC TCGA-BS-A0UJ NOM1 SNP Missense_Mutation 7 156756639 T C 51 89 KIRC TCGA-CJ-5683 NOM1 SNP Missense_Mutation 7 156759742 G A 42 65 HNSC TCGA-CN-4723 NOM1 SNP Missense_Mutation 7 156746954 C T 32 63 HNSC TCGA-CR-7380 NOM1 SNP Silent 7 156762310 C T 17 51 KIRC TCGA-CW-6093 NOM1 SNP Silent 7 156752790 T G 56 36 KIRC TCGA-CZ-4863 NOM1 SNP Missense_Mutation 7 156761876 T G 60 54 KIRC TCGA-CZ-5988 NOM1 SNP Missense_Mutation 7 156752728 G T 33 95 BLCA TCGA-DK-A1AC NOM1 SNP Missense_Mutation 7 156743173 G A 37 71 BLCA TCGA-DK-A1AC NOM1 SNP Missense_Mutation 7 156754887 G A 45 93 BRCA TCGA-E2-A15R NOM1 SNP Missense_Mutation 7 156742517 G A 43 65 BLCA TCGA-G2-A2ES NOM1 SNP Missense_Mutation 7 156745289 A G 2 84