ttype patient gene classification type chr pos ref_allele newbase context65 cons46 BRCA BR-MEX-105 CHRD SNP Silent 3 184100495 C T 29 52 DLBCL DLBCL-Ls2089 CHRD SNP Silent 3 184103855 C T 24 72 ESO ESO-0459 CHRD SNP Silent 3 184104453 C T 21 56 ESO ESO-049 CHRD SNP Missense_Mutation 3 184102397 G A 40 78 HNSC HN_62426 CHRD SNP Synonymous 3 184099309 G C 37 40 HNSC HN_62505 CHRD SNP Splice_Site_SNP 3 184099413 G A 44 84 MEL ME043 CHRD SNP Splice_site 3 184100562 G A 43 66 MEL MEL-13561 CHRD SNP Missense_Mutation 3 184106480 C T 22 88 MEL MEL-JWCI-WGS-1 CHRD SNP Missense_Mutation 3 184106498 G A 41 86 MEL MEL-Ma-Mel-05 CHRD SNP Missense_Mutation 3 184106506 A T 11 80 MEL MEL-Ma-Mel-105 CHRD SNP Missense_Mutation 3 184100267 C T 22 56 NB NB-0058 CHRD SNP Silent 3 184100435 C T 21 65 LUAD TCGA-05-4250 CHRD SNP Silent 3 184104849 T C 51 46 LUAD TCGA-05-4396 CHRD SNP Missense_Mutation 3 184100193 G T 39 76 LUAD TCGA-05-4396 CHRD DNP Missense_Mutation 3 184106428 CG AT 23 58 LUAD TCGA-05-4410 CHRD SNP Missense_Mutation 3 184102866 G T 43 89 OV TCGA-13-1504 CHRD SNP Silent 3 184104504 G A 38 31 LUAD TCGA-17-Z043 CHRD SNP Missense_Mutation 3 184105183 G A 39 67 LUAD TCGA-17-Z055 CHRD SNP Silent 3 184098565 G T 46 53 LUSC TCGA-18-3409 CHRD SNP Missense_Mutation 3 184106703 G A 39 74 OV TCGA-24-1431 CHRD SNP Missense_Mutation 3 184102421 G A 39 90 GBM TCGA-32-4213 CHRD SNP Missense_Mutation 3 184099068 A G 5 85 LUSC TCGA-34-5927 CHRD SNP Missense_Mutation 3 184100484 C A 24 56 LUSC TCGA-39-5024 CHRD SNP Splice_Site 3 184104631 A G 7 79 LUSC TCGA-46-6026 CHRD SNP Missense_Mutation 3 184100816 G T 46 75 LUAD TCGA-49-4487 CHRD SNP Missense_Mutation 3 184106762 C A 23 63 LUAD TCGA-50-5051 CHRD SNP Missense_Mutation 3 184106429 G T 39 88 LUAD TCGA-50-5930 CHRD SNP Silent 3 184104519 G T 38 49 LUSC TCGA-60-2722 CHRD SNP Missense_Mutation 3 184105818 C T 30 87 LUAD TCGA-64-1676 CHRD SNP Splice_Site 3 184104632 G T 33 85 LUSC TCGA-66-2768 CHRD SNP Missense_Mutation 3 184100882 G T 42 54 LUAD TCGA-67-3771 CHRD SNP Missense_Mutation 3 184102332 G C 44 78 LUAD TCGA-71-6725 CHRD SNP Missense_Mutation 3 184103862 C T 23 65 LUAD TCGA-91-6829 CHRD SNP Silent 3 184105191 C A 27 67 BRCA TCGA-A2-A0CT CHRD SNP Silent 3 184104513 C T 19 49 UCEC TCGA-A5-A0VP CHRD SNP Silent 3 184105199 G A 39 48 UCEC TCGA-A5-A0VP CHRD SNP Missense_Mutation 3 184105204 C T 19 89 BRCA TCGA-A8-A07Z CHRD SNP Missense_Mutation 3 184102997 C T 27 62 CRC TCGA-AA-3833 CHRD SNP Missense_Mutation 3 184105733 G T 35 62 CRC TCGA-AA-3947 CHRD SNP Missense_Mutation 3 184102931 G T 47 60 CRC TCGA-AA-A010 CHRD SNP Missense_Mutation 3 184102959 C T 26 74 CRC TCGA-AA-A010 CHRD SNP Nonsense_Mutation 3 184106750 C T 31 53 CRC TCGA-AA-A02Y CHRD SNP Missense_Mutation 3 184102983 C T 19 48 CRC TCGA-AG-A014 CHRD SNP Missense_Mutation 3 184101188 T A 51 49 UCEC TCGA-AP-A051 CHRD SNP Silent 3 184107204 C A 28 64 UCEC TCGA-AP-A059 CHRD SNP Missense_Mutation 3 184102473 G A 38 67 UCEC TCGA-AP-A0LM CHRD SNP Missense_Mutation 3 184099783 C A 24 82 UCEC TCGA-AP-A0LM CHRD SNP Missense_Mutation 3 184100253 T C 59 73 UCEC TCGA-AP-A0LM CHRD SNP Splice_site 3 184102807 G A 38 53 UCEC TCGA-AP-A0LM CHRD SNP Silent 3 184107198 C T 23 3 UCEC TCGA-AX-A05Z CHRD SNP Missense_Mutation 3 184106720 C T 26 49 UCEC TCGA-AX-A0J0 CHRD SNP Nonsense_Mutation 3 184105731 G T 33 88 KIRC TCGA-B0-4710 CHRD SNP Missense_Mutation 3 184100196 C T 25 68 UCEC TCGA-B5-A0JY CHRD SNP Missense_Mutation 3 184100704 T A 56 82 UCEC TCGA-B5-A11E CHRD SNP Silent 3 184101195 C T 24 64 UCEC TCGA-B5-A11E CHRD SNP Missense_Mutation 3 184104881 G A 39 58 BRCA TCGA-B6-A0WZ CHRD SNP Missense_Mutation 3 184100846 G A 41 87 HNSC TCGA-BA-4076 CHRD SNP Missense_Mutation 3 184099067 C G 25 92 HNSC TCGA-BA-5151 CHRD SNP Splice_Site 3 184101432 T C 59 62 HNSC TCGA-BA-6871 CHRD SNP Missense_Mutation 3 184102418 G T 33 91 BRCA TCGA-BH-A18K CHRD SNP Missense_Mutation 3 184104637 G A 37 85 KIRC TCGA-BP-4962 CHRD SNP Missense_Mutation 3 184103856 T G 55 81 KIRC TCGA-BP-4988 CHRD SNP Silent 3 184102984 G T 38 51 BLCA TCGA-BT-A2LB CHRD SNP Missense_Mutation 3 184099561 C T 31 55 HNSC TCGA-CN-6013 CHRD SNP Silent 3 184104641 G A 39 34 HNSC TCGA-CQ-5327 CHRD SNP Silent 3 184100495 C T 29 52 HNSC TCGA-CV-7104 CHRD SNP Missense_Mutation 3 184104380 C T 27 42 HNSC TCGA-CV-7406 CHRD SNP Missense_Mutation 3 184104374 C G 32 62 UCEC TCGA-D1-A103 CHRD SNP Missense_Mutation 3 184100202 C A 24 77 UCEC TCGA-D1-A103 CHRD SNP Missense_Mutation 3 184100517 C T 25 93 UCEC TCGA-D1-A103 CHRD SNP Missense_Mutation 3 184105191 C T 27 67 UCEC TCGA-D1-A177 CHRD SNP Missense_Mutation 3 184098488 T G 56 79 HNSC TCGA-DQ-7595 CHRD SNP Missense_Mutation 3 184105203 A G 14 82 BLCA TCGA-GV-A3JX CHRD SNP Missense_Mutation 3 184104518 C T 23 55 BLCA TCGA-GV-A3JZ CHRD SNP Nonsense_Mutation 3 184099750 C G 29 66