ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-171 CNN2 SNP Missense_Mutation 19 1031110 G T 38 70 MEL MEL-JWCI-WGS-19 CNN2 SNP Missense_Mutation 19 1036538 G A 43 87 MEL MEL-Ma-Mel-65 CNN2 SNP Silent 19 1032578 C T 29 66 GBM TCGA-14-1034 CNN2 SNP Silent 19 1032680 C T 31 23 LUAD TCGA-49-4490 CNN2 SNP Silent 19 1031150 C A 23 30 LUSC TCGA-66-2785 CNN2 SNP Silent 19 1036486 C G 21 53 CRC TCGA-AA-3848 CNN2 SNP Missense_Mutation 19 1036169 T C 58 82 CRC TCGA-AG-A002 CNN2 SNP Silent 19 1036489 G T 33 56 CRC TCGA-AG-A02N CNN2 SNP Silent 19 1036152 C T 27 33 UCEC TCGA-B5-A11E CNN2 SNP Silent 19 1031120 C T 31 45 BRCA TCGA-BH-A0AU CNN2 SNP Missense_Mutation 19 1032430 C G 29 56 UCEC TCGA-BS-A0UJ CNN2 SNP Missense_Mutation 19 1032576 T C 56 80 BLCA TCGA-BT-A3PK CNN2 SNP Missense_Mutation 19 1032581 C G 29 72 HNSC TCGA-CR-6472 CNN2 SNP Missense_Mutation 19 1032417 C G 30 89 KIRC TCGA-CZ-4854 CNN2 SNP Missense_Mutation 19 1036169 T A 58 82 BLCA TCGA-GV-A3JZ CNN2 SNP Missense_Mutation 19 1037770 G C 33 75