ttype patient gene classification type chr pos ref_allele newbase context65 cons46 BRCA BR-MEX-191 TRIM36 SNP Missense_Mutation 5 114482834 G A 45 52 ESO ESO-155 TRIM36 SNP Missense_Mutation 5 114469670 A G 16 88 HNSC HN_62426 TRIM36 SNP Nonsense 5 114482807 G A 45 100 HNSC HN_62739 TRIM36 SNP Missense 5 114472817 G C 48 92 HNSC HN_63021 TRIM36 SNP Missense 5 114462228 T C 64 69 LUAD LUAD-CHTN-3090416 TRIM36 SNP Nonsense_Mutation 5 114482990 G A 37 68 MEL ME009 TRIM36 SNP Missense_Mutation 5 114469578 G A 33 60 MEL ME009 TRIM36 SNP Silent 5 114477045 G A 44 64 MEL ME044 TRIM36 SNP Missense_Mutation 5 114499263 G A 37 71 MEL MEL-JWCI-WGS-36 TRIM36 SNP Missense_Mutation 5 114499251 G A 43 74 MEL MEL-JWCI-WGS-7 TRIM36 SNP Missense_Mutation 5 114466425 C T 32 98 MEL MEL-JWCI-WGS-7 TRIM36 SNP Missense_Mutation 5 114472768 G A 33 67 MEL MEL-Ma-Mel-04 TRIM36 SNP Missense_Mutation 5 114466349 A G 2 90 MEL MEL-Ma-Mel-114 TRIM36 SNP Silent 5 114462536 C T 26 37 MEL MEL-Ma-Mel-19 TRIM36 SNP Missense_Mutation 5 114477062 A C 9 60 LUAD TCGA-05-4396 TRIM36 SNP Missense_Mutation 5 114499299 C G 22 74 LUAD TCGA-05-4417 TRIM36 SNP Missense_Mutation 5 114482933 T C 59 69 OV TCGA-09-1659 TRIM36 SNP Missense_Mutation 5 114482962 T A 62 79 OV TCGA-09-2049 TRIM36 SNP Missense_Mutation 5 114469806 C T 20 66 OV TCGA-13-0730 TRIM36 SNP Missense_Mutation 5 114482905 G A 47 83 LUSC TCGA-18-3409 TRIM36 SNP Missense_Mutation 5 114499374 G A 43 96 OV TCGA-29-2427 TRIM36 SNP Silent 5 114469588 T C 54 48 LUSC TCGA-34-5231 TRIM36 SNP Missense_Mutation 5 114462205 T C 51 46 LUAD TCGA-35-3615 TRIM36 SNP Missense_Mutation 5 114466398 A C 3 90 LUSC TCGA-39-5029 TRIM36 SNP Missense_Mutation 5 114469806 C A 20 66 LUAD TCGA-50-5072 TRIM36 SNP Silent 5 114482982 G A 45 64 LUAD TCGA-91-6836 TRIM36 SNP Silent 5 114466308 G T 39 61 CRC TCGA-AA-3710 TRIM36 SNP Missense_Mutation 5 114499257 G T 43 50 CRC TCGA-AA-3977 TRIM36 SNP Missense_Mutation 5 114499229 C T 31 80 CRC TCGA-AA-3984 TRIM36 SNP Missense_Mutation 5 114466469 C T 27 99 CRC TCGA-AG-3601 TRIM36 SNP Missense_Mutation 5 114462493 G C 44 97 UCEC TCGA-AP-A054 TRIM36 SNP Missense_Mutation 5 114482917 T C 58 77 UCEC TCGA-AX-A0J0 TRIM36 SNP Silent 5 114462356 T G 53 51 UCEC TCGA-AX-A0J0 TRIM36 SNP Nonsense_Mutation 5 114473237 G T 45 77 UCEC TCGA-AX-A0J0 TRIM36 SNP Missense_Mutation 5 114499237 T G 64 58 KIRC TCGA-B0-5109 TRIM36 SNP Missense_Mutation 5 114513529 C T 23 48 KIRC TCGA-B0-5115 TRIM36 SNP Nonsense_Mutation 5 114499350 T A 61 75 UCEC TCGA-B5-A11E TRIM36 SNP Missense_Mutation 5 114462325 G T 35 99 UCEC TCGA-B5-A11E TRIM36 SNP Nonsense_Mutation 5 114482894 C A 32 100 UCEC TCGA-B5-A11N TRIM36 SNP Nonsense_Mutation 5 114469587 C A 32 96 UCEC TCGA-BG-A0MQ TRIM36 SNP Missense_Mutation 5 114466317 G A 39 98 BLCA TCGA-BL-A13J TRIM36 SNP Missense_Mutation 5 114469698 C G 29 65 UCEC TCGA-BS-A0UV TRIM36 SNP Splice_site 5 114513447 C A 24 59 BLCA TCGA-BT-A20O TRIM36 SNP Missense_Mutation 5 114499268 C T 31 96 HNSC TCGA-CR-7370 TRIM36 SNP Missense_Mutation 5 114472790 A G 3 85 HNSC TCGA-CV-7414 TRIM36 SNP Missense_Mutation 5 114469606 G C 33 57 HNSC TCGA-CV-7423 TRIM36 SNP Missense_Mutation 5 114499269 G C 37 71 UCEC TCGA-D1-A103 TRIM36 SNP Nonsense_Mutation 5 114469702 C T 30 93 UCEC TCGA-D1-A103 TRIM36 SNP Missense_Mutation 5 114499229 C T 31 80 UCEC TCGA-D1-A167 TRIM36 SNP Missense_Mutation 5 114462461 T A 52 45 BLCA TCGA-DK-A1AD TRIM36 SNP Silent 5 114466549 A G 16 48 HNSC TCGA-DQ-7592 TRIM36 SNP Missense_Mutation 5 114462268 C T 22 99 BRCA TCGA-E9-A1R5 TRIM36 SNP Missense_Mutation 5 114482989 C T 31 98 BLCA TCGA-H4-A2HQ TRIM36 SNP Missense_Mutation 5 114473227 C G 29 55