ttype patient gene classification type chr pos ref_allele newbase context65 cons46 CLL CW230 TCN2 SNP Missense_Mutation 22 31011631 C T 25 63 LUAD LUAD-B00915 TCN2 SNP Missense_Mutation 22 31006924 G T 39 27 LUAD LUAD-RT-S01777 TCN2 SNP Missense_Mutation 22 31009026 A T 8 74 LUAD LUAD-S01315 TCN2 SNP Nonsense_Mutation 22 31008988 C G 29 79 MEL MEL-Ma-Mel-94 TCN2 SNP Missense_Mutation 22 31010344 C T 29 59 LUAD TCGA-05-4398 TCN2 DEL Frame_Shift_Del 22 31013404 ACAG - 14 71 OV TCGA-13-0720 TCN2 SNP Silent 22 31011602 C T 22 48 LUSC TCGA-18-3406 TCN2 SNP Splice_site 22 31003382 G T 47 62 LUSC TCGA-22-5472 TCN2 SNP Missense_Mutation 22 31008891 C A 21 60 LUAD TCGA-44-3918 TCN2 SNP Silent 22 31018994 C G 24 51 LUSC TCGA-66-2767 TCN2 SNP Missense_Mutation 22 31019016 G A 39 61 CRC TCGA-A6-2672 TCN2 SNP Missense_Mutation 22 31013374 C T 19 47 CRC TCGA-AA-3516 TCN2 SNP Missense_Mutation 22 31006990 G A 43 68 CRC TCGA-AA-3864 TCN2 SNP Missense_Mutation 22 31019011 C T 27 42 CRC TCGA-AA-A010 TCN2 SNP Missense_Mutation 22 31019040 C A 32 53 CRC TCGA-AG-3608 TCN2 SNP Missense_Mutation 22 31007025 C A 28 53 BRCA TCGA-AN-A04D TCN2 SNP Missense_Mutation 22 31019054 C A 17 61 UCEC TCGA-AP-A0LE TCN2 SNP Splice_Site 22 31010334 A G 7 74 UCEC TCGA-AP-A0LT TCN2 SNP Missense_Mutation 22 31011718 T C 60 53 KIRC TCGA-B0-5812 TCN2 SNP Nonsense_Mutation 22 31018990 T A 61 75 UCEC TCGA-B5-A0K3 TCN2 SNP Splice_Site 22 31011586 A G 7 74 UCEC TCGA-BG-A0M4 TCN2 SNP Missense_Mutation 22 31011414 C A 22 81 BLCA TCGA-C4-A0EZ TCN2 SNP Splice_site 22 31011460 G A 35 81 HNSC TCGA-CV-6936 TCN2 SNP Missense_Mutation 22 31010483 C T 32 67 UCEC TCGA-D1-A103 TCN2 SNP Missense_Mutation 22 31013385 C A 28 47 BLCA TCGA-DK-A2I4 TCN2 SNP Silent 22 31019015 C T 23 45 BLCA TCGA-G2-A2EO TCN2 SNP Missense_Mutation 22 31011378 G C 33 39