ttype patient gene classification type chr pos ref_allele newbase context65 cons46 BRCA BR-0026 ING1 SNP Silent 13 111366526 C T 30 55 CLL CLL_138 ING1 SNP Silent 13 111367919 G A 41 71 ESO ESO-0071 ING1 SNP Missense_Mutation 13 111372206 G A 46 100 ESO ESO-117 ING1 SNP Missense_Mutation 13 111367915 C T 31 46 LUAD LUAD-AEIUF ING1 SNP Missense_Mutation 13 111367831 G T 37 31 LUAD LUAD-S01468 ING1 SNP Missense_Mutation 13 111371668 G T 38 69 MEL ME009 ING1 SNP Splice_site 13 111366632 G A 35 87 LUAD TCGA-05-4410 ING1 SNP Missense_Mutation 13 111371668 G T 38 69 GBM TCGA-06-5858 ING1 SNP Missense_Mutation 13 111371669 C T 27 99 OV TCGA-24-1424 ING1 SNP Missense_Mutation 13 111372144 G T 44 100 LUSC TCGA-37-4135 ING1 SNP Missense_Mutation 13 111368196 G T 39 57 LUAD TCGA-50-6590 ING1 DNP Missense_Mutation 13 111367917 GG TT 43 41 LUAD TCGA-55-1595 ING1 SNP Missense_Mutation 13 111368110 G T 37 55 UCEC TCGA-A5-A0VP ING1 SNP Missense_Mutation 13 111371713 G A 40 99 CRC TCGA-A6-2672 ING1 SNP Missense_Mutation 13 111371923 G A 38 71 CRC TCGA-AA-3949 ING1 SNP Missense_Mutation 13 111372142 T C 59 92 CRC TCGA-AA-A010 ING1 SNP Missense_Mutation 13 111371944 G A 37 100 CRC TCGA-AA-A01F ING1 SNP Missense_Mutation 13 111372139 G A 37 100 CRC TCGA-AA-A03F ING1 SNP Nonsense_Mutation 13 111372025 C T 27 46 CRC TCGA-AF-3913 ING1 SNP Nonsense_Mutation 13 111372025 C T 27 46 UCEC TCGA-AP-A056 ING1 SNP Missense_Mutation 13 111371744 G A 38 100 UCEC TCGA-AP-A059 ING1 SNP Silent 13 111371784 G A 38 25 UCEC TCGA-AP-A059 ING1 SNP Nonsense_Mutation 13 111372144 G A 44 100 UCEC TCGA-AP-A0LM ING1 SNP Nonsense_Mutation 13 111372025 C T 27 46 BRCA TCGA-AR-A1AH ING1 SNP Missense_Mutation 13 111371953 G T 38 54 UCEC TCGA-B5-A0JY ING1 SNP Nonsense_Mutation 13 111372064 G T 37 85 UCEC TCGA-B5-A0JZ ING1 SNP Silent 13 111372117 C T 27 40 UCEC TCGA-B5-A11E ING1 SNP Missense_Mutation 13 111371953 G A 38 54 UCEC TCGA-B5-A11W ING1 SNP Nonsense_Mutation 13 111372025 C T 27 46 UCEC TCGA-BG-A0M9 ING1 SNP Nonsense_Mutation 13 111372127 G T 37 100 UCEC TCGA-BS-A0TC ING1 SNP Missense_Mutation 13 111372064 G A 37 85 HNSC TCGA-CN-6989 ING1 SNP Silent 13 111371619 C T 27 28 HNSC TCGA-CQ-5331 ING1 SNP Missense_Mutation 13 111372242 T G 55 92 UCEC TCGA-D1-A168 ING1 SNP Nonsense_Mutation 13 111372025 C T 27 46 UCEC TCGA-D1-A17C ING1 SNP Missense_Mutation 13 111372118 G T 37 100 UCEC TCGA-D1-A17D ING1 SNP Splice_site 13 111365324 G T 43 51 UCEC TCGA-D1-A17Q ING1 SNP Missense_Mutation 13 111371951 G A 42 71 BRCA TCGA-D8-A1JN ING1 SNP Silent 13 111371874 C T 21 35