ttype patient gene classification type chr pos ref_allele newbase context65 cons46 LUAD LUAD-S01315 ING4 SNP Splice_Site 12 6761586 T A 55 86 MEL MEL-Ma-Mel-67 ING4 SNP Missense_Mutation 12 6761879 G A 37 94 MM MM-0505 ING4 SNP Silent 12 6762468 G T 41 60 OV TCGA-13-0891 ING4 SNP Missense_Mutation 12 6762177 G A 39 80 LUAD TCGA-17-Z045 ING4 SNP Missense_Mutation 12 6761907 C A 25 66 LUSC TCGA-39-5031 ING4 SNP Missense_Mutation 12 6761577 C G 29 93 LUSC TCGA-66-2768 ING4 SNP Missense_Mutation 12 6760378 C G 32 93 LUAD TCGA-73-4668 ING4 SNP Missense_Mutation 12 6760378 C G 32 93 BRCA TCGA-A8-A092 ING4 SNP Missense_Mutation 12 6762144 C T 29 94 CRC TCGA-AA-3864 ING4 SNP Missense_Mutation 12 6761865 G T 43 77 CRC TCGA-AA-A00K ING4 SNP Missense_Mutation 12 6762117 T A 55 67 UCEC TCGA-AP-A051 ING4 SNP Missense_Mutation 12 6762186 C A 32 82 UCEC TCGA-B5-A11E ING4 SNP Missense_Mutation 12 6761831 C T 27 73 UCEC TCGA-B5-A11J ING4 SNP Missense_Mutation 12 6762421 T C 55 88 KIRC TCGA-BP-4763 ING4 SNP Missense_Mutation 12 6762198 G A 38 54