ttype patient gene classification type chr pos ref_allele newbase context65 cons46 DLBCL DLBCL-Ls1921 FAM13B SNP Missense_Mutation 5 137288323 T C 52 72 ESO ESO-105 FAM13B SNP Nonsense_Mutation 5 137277661 C A 29 98 ESO ESO-224 FAM13B SNP Missense_Mutation 5 137281968 T A 56 67 LUAD LUAD-B00416 FAM13B SNP Nonsense_Mutation 5 137295398 C A 24 73 LUAD LUAD-CHTN-MAD08-00104 FAM13B SNP Missense_Mutation 5 137295860 T A 50 51 LUAD LUAD-S01345 FAM13B SNP Missense_Mutation 5 137281995 C T 29 81 LUAD LUAD-S01468 FAM13B SNP Missense_Mutation 5 137284800 G C 34 73 LUAD LUAD_E00522 FAM13B SNP Silent 5 137278650 T C 51 49 MEL ME029 FAM13B SNP Missense_Mutation 5 137323987 A C 12 57 MEL ME032 FAM13B SNP Missense_Mutation 5 137290020 C T 30 91 MEL MEL-JWCI-27 FAM13B SNP Missense_Mutation 5 137354099 C T 30 100 MEL MEL-Ma-Mel-48 FAM13B SNP Missense_Mutation 5 137354760 G A 41 94 MEL MEL-Ma-Mel-94 FAM13B SNP Missense_Mutation 5 137284808 G A 41 95 LUAD TCGA-05-4396 FAM13B SNP Missense_Mutation 5 137284709 G T 35 73 GBM TCGA-26-5139 FAM13B SNP Silent 5 137275998 C T 20 63 LUSC TCGA-37-3789 FAM13B SNP Missense_Mutation 5 137347574 G T 35 72 LUSC TCGA-43-6771 FAM13B SNP Silent 5 137284746 G T 45 56 LUAD TCGA-44-2657 FAM13B SNP Silent 5 137346774 G A 33 66 LUAD TCGA-44-3918 FAM13B SNP Silent 5 137354124 G A 38 49 LUSC TCGA-85-6561 FAM13B SNP Silent 5 137346823 C A 21 76 BRCA TCGA-A7-A13D FAM13B SNP Missense_Mutation 5 137289955 G A 41 91 BRCA TCGA-A8-A084 FAM13B SNP Missense_Mutation 5 137354686 G A 41 99 CRC TCGA-AA-3715 FAM13B SNP Silent 5 137281636 C T 26 48 CRC TCGA-AA-3947 FAM13B SNP Missense_Mutation 5 137346786 T G 52 73 CRC TCGA-AA-A010 FAM13B SNP Missense_Mutation 5 137284652 C A 32 82 CRC TCGA-AA-A01D FAM13B SNP Missense_Mutation 5 137354113 A G 6 91 CRC TCGA-AG-3892 FAM13B SNP Missense_Mutation 5 137281985 G T 45 66 CRC TCGA-AG-A002 FAM13B SNP Missense_Mutation 5 137275930 G T 33 82 CRC TCGA-AG-A002 FAM13B SNP Missense_Mutation 5 137342688 G A 40 49 CRC TCGA-AG-A002 FAM13B SNP Nonsense_Mutation 5 137354051 C A 32 100 UCEC TCGA-AP-A059 FAM13B SNP Missense_Mutation 5 137275968 C A 28 56 UCEC TCGA-AP-A059 FAM13B SNP Silent 5 137346763 G A 36 55 UCEC TCGA-AP-A059 FAM13B SNP Nonsense_Mutation 5 137347509 C A 32 84 UCEC TCGA-AP-A059 FAM13B SNP Missense_Mutation 5 137354001 C A 28 52 UCEC TCGA-AP-A0LD FAM13B SNP Missense_Mutation 5 137289931 C A 32 91 UCEC TCGA-AP-A0LM FAM13B SNP Missense_Mutation 5 137288366 C A 24 64 UCEC TCGA-AP-A0LM FAM13B SNP Missense_Mutation 5 137292177 C T 32 89 UCEC TCGA-AP-A0LM FAM13B SNP Silent 5 137295432 A G 6 68 UCEC TCGA-AX-A0J0 FAM13B SNP Nonsense_Mutation 5 137289150 G A 37 74 UCEC TCGA-AX-A0J0 FAM13B SNP Silent 5 137342825 A C 1 61 UCEC TCGA-AX-A0J1 FAM13B SNP Missense_Mutation 5 137284829 G A 40 95 KIRC TCGA-B0-4838 FAM13B SNP Missense_Mutation 5 137347568 T G 52 89 KIRC TCGA-B2-5641 FAM13B SNP Silent 5 137278882 C T 22 50 UCEC TCGA-B5-A11O FAM13B SNP Missense_Mutation 5 137295364 G A 38 56 HNSC TCGA-BA-5555 FAM13B SNP Missense_Mutation 5 137346746 T A 52 60 HNSC TCGA-BB-4223 FAM13B SNP Silent 5 137354085 G A 35 61 UCEC TCGA-BS-A0UF FAM13B SNP Missense_Mutation 5 137323294 C A 32 83 BRCA TCGA-C8-A12K FAM13B SNP Missense_Mutation 5 137284667 T C 54 63 HNSC TCGA-CN-4723 FAM13B SNP Missense_Mutation 5 137275949 G C 33 97 UCEC TCGA-D1-A0ZO FAM13B SNP Missense_Mutation 5 137342768 C A 24 44 UCEC TCGA-D1-A17Q FAM13B SNP Nonsense_Mutation 5 137289150 G A 37 74 BRCA TCGA-D8-A1X9 FAM13B SNP Missense_Mutation 5 137289986 C G 29 91 BRCA TCGA-E9-A22E FAM13B SNP Missense_Mutation 5 137292177 C G 32 89 BRCA TCGA-EW-A1J5 FAM13B SNP Missense_Mutation 5 137289107 C G 32 72 BLCA TCGA-GV-A3QI FAM13B SNP Missense_Mutation 5 137347541 C G 32 75