ttype patient gene classification type chr pos ref_allele newbase context65 cons46 BRCA BR-0036 FAM107B SNP Silent 10 14816300 C G 21 51 ESO ESO-224 FAM107B SNP Silent 10 14816258 C T 27 61 HNSC HN_62739 FAM107B SNP Synonymous 10 14816282 G A 41 48 LUAD LUAD-S01315 FAM107B SNP Silent 10 14816392 G T 37 52 LUAD LUAD-S01357 FAM107B SNP Missense_Mutation 10 14816438 T A 64 54 MEL MEL-Ma-Mel-65 FAM107B SNP Silent 10 14709654 G A 34 47 LUAD TCGA-05-4410 FAM107B SNP Silent 10 14816390 C A 30 55 GBM TCGA-14-0817 FAM107B SNP Missense_Mutation 10 14816316 G A 38 49 LUAD TCGA-17-Z010 FAM107B SNP Missense_Mutation 10 14816535 G A 41 83 GBM TCGA-27-1834 FAM107B SNP Missense_Mutation 10 14564008 G C 41 97 LUSC TCGA-39-5037 FAM107B SNP Missense_Mutation 10 14572388 A G 14 87 LUSC TCGA-60-2708 FAM107B SNP Missense_Mutation 10 14816587 C G 28 71 LUAD TCGA-67-3771 FAM107B SNP Silent 10 14563219 G C 42 62 BRCA TCGA-A2-A04R FAM107B SNP Missense_Mutation 10 14816305 C A 28 53 BRCA TCGA-A2-A0T6 FAM107B SNP Silent 10 14816537 C T 20 58 CRC TCGA-A6-2676 FAM107B SNP Missense_Mutation 10 14816377 G A 39 80 CRC TCGA-AA-3525 FAM107B SNP Missense_Mutation 10 14563262 G T 42 78 CRC TCGA-AA-3949 FAM107B SNP Missense_Mutation 10 14816460 C T 28 51 CRC TCGA-AG-A002 FAM107B SNP Missense_Mutation 10 14563226 C A 32 79 UCEC TCGA-AP-A056 FAM107B SNP Missense_Mutation 10 14563916 T G 52 56 UCEC TCGA-AP-A0LM FAM107B SNP Splice_site 10 14816252 C T 24 79 UCEC TCGA-AP-A0LM FAM107B SNP Missense_Mutation 10 14816595 G T 39 83 UCEC TCGA-AX-A0J0 FAM107B SNP Missense_Mutation 10 14563968 C A 32 97 KIRC TCGA-BP-5010 FAM107B SNP Missense_Mutation 10 14816481 C T 26 52 UCEC TCGA-BS-A0UJ FAM107B SNP Missense_Mutation 10 14572385 T A 64 87 BLCA TCGA-BT-A20T FAM107B SNP Missense_Mutation 10 14572359 G C 45 94 HNSC TCGA-CQ-5326 FAM107B SNP Nonsense_Mutation 10 14816385 G C 45 55 UCEC TCGA-D1-A103 FAM107B SNP Silent 10 14816465 G A 44 58 UCEC TCGA-D1-A17Q FAM107B SNP Missense_Mutation 10 14816578 C T 27 55