ttype patient gene classification type chr pos ref_allele newbase context65 cons46 BRCA BR-MEX-082 OR13C2 SNP Splice_site 9 107367908 T C 52 55 DLBCL DLBCL-Ls2590 OR13C2 SNP Missense_Mutation 9 107367527 T G 63 54 ESO ESO-0071 OR13C2 SNP Missense_Mutation 9 107367311 G A 34 53 ESO ESO-1145 OR13C2 SNP Missense_Mutation 9 107367322 T C 54 49 ESO ESO-161 OR13C2 SNP Missense_Mutation 9 107367502 A G 8 82 LUAD LUAD-S01331 OR13C2 SNP Missense_Mutation 9 107367499 C A 20 50 MEL ME009 OR13C2 SNP Missense_Mutation 9 107367545 G T 39 50 MEL ME012 OR13C2 SNP Missense_Mutation 9 107367899 C T 30 47 MEL MEL-JWCI-14 OR13C2 SNP Missense_Mutation 9 107367196 G A 41 53 MEL MEL-JWCI-WGS-1 OR13C2 SNP Missense_Mutation 9 107367184 G A 45 56 MEL MEL-JWCI-WGS-34 OR13C2 SNP Silent 9 107366964 G A 33 37 MEL MEL-JWCI-WGS-34 OR13C2 SNP Nonsense_Mutation 9 107367641 T A 64 53 MEL MEL-JWCI-WGS-38 OR13C2 SNP Silent 9 107367120 C T 20 42 MEL MEL-JWCI-WGS-7 OR13C2 SNP Missense_Mutation 9 107367196 G A 41 53 MEL MEL-Ma-Mel-102 OR13C2 SNP Missense_Mutation 9 107367100 G A 37 54 MEL MEL-Ma-Mel-114 OR13C2 SNP Missense_Mutation 9 107367878 C T 30 58 MEL MEL-Ma-Mel-36 OR13C2 SNP Missense_Mutation 9 107367354 C T 29 51 MEL MEL-Ma-Mel-65 OR13C2 SNP Missense_Mutation 9 107367259 G A 33 68 MEL MEL-Ma-Mel-67 OR13C2 SNP Nonsense_Mutation 9 107367900 C T 22 48 LUAD TCGA-05-4249 OR13C2 SNP Missense_Mutation 9 107367202 T A 64 79 LUAD TCGA-05-4382 OR13C2 SNP Missense_Mutation 9 107367473 C T 28 50 LUAD TCGA-05-4396 OR13C2 SNP Silent 9 107367099 C A 23 50 LUAD TCGA-17-Z031 OR13C2 SNP Missense_Mutation 9 107367580 G T 48 57 LUAD TCGA-35-4123 OR13C2 SNP Missense_Mutation 9 107367587 C T 22 61 LUAD TCGA-44-2656 OR13C2 SNP Missense_Mutation 9 107367610 T A 55 82 LUAD TCGA-44-2656 OR13C2 SNP Missense_Mutation 9 107367620 A T 7 69 LUSC TCGA-63-5128 OR13C2 SNP Missense_Mutation 9 107367215 C T 31 59 LUAD TCGA-64-5781 OR13C2 SNP Silent 9 107367420 C A 21 42 LUSC TCGA-66-2782 OR13C2 SNP Missense_Mutation 9 107367467 A T 10 60 BRCA TCGA-A8-A085 OR13C2 SNP Missense_Mutation 9 107367295 A C 5 69 CRC TCGA-AA-A010 OR13C2 SNP Missense_Mutation 9 107367156 G T 33 56 CRC TCGA-AG-A002 OR13C2 SNP Missense_Mutation 9 107366971 C A 32 42 CRC TCGA-AG-A002 OR13C2 SNP Missense_Mutation 9 107367639 C A 32 48 CRC TCGA-AG-A002 OR13C2 SNP Missense_Mutation 9 107367844 C A 32 43 UCEC TCGA-AP-A051 OR13C2 SNP Missense_Mutation 9 107367842 G T 36 58 UCEC TCGA-AX-A0J0 OR13C2 SNP Missense_Mutation 9 107367643 C A 32 44 BRCA TCGA-B6-A0IK OR13C2 SNP Missense_Mutation 9 107367603 G C 41 54 BRCA TCGA-C8-A12T OR13C2 SNP Missense_Mutation 9 107367609 C G 32 60 HNSC TCGA-CV-7245 OR13C2 SNP Missense_Mutation 9 107367190 G C 44 88 HNSC TCGA-CV-7409 OR13C2 SNP Missense_Mutation 9 107367223 C A 28 51 KIRC TCGA-CZ-5457 OR13C2 SNP Silent 9 107367525 G A 44 49 BLCA TCGA-GV-A3JX OR13C2 SNP Missense_Mutation 9 107367631 G A 41 88