ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-122 SIX3 SNP Missense_Mutation 2 45169803 C T 23 78 LUAD LUAD-B01246 SIX3 SNP Silent 2 45169909 G T 43 70 LUAD LUAD-B02050 SIX3 SNP Missense_Mutation 2 45169295 A G 1 79 LUAD LUAD-CHTN-Z4716A SIX3 SNP Missense_Mutation 2 45169680 G A 38 90 LUAD LUAD-NYU408 SIX3 SNP Missense_Mutation 2 45169935 C A 22 92 MEL ME033 SIX3 SNP Silent 2 45169300 C T 31 72 LUAD TCGA-05-4397 SIX3 SNP Missense_Mutation 2 45170024 G T 37 92 LUSC TCGA-33-4586 SIX3 SNP Missense_Mutation 2 45169617 T C 50 83 LUSC TCGA-37-3789 SIX3 SNP Missense_Mutation 2 45169910 G C 41 92 LUAD TCGA-44-2657 SIX3 SNP Silent 2 45169954 C T 27 64 LUAD TCGA-44-2662 SIX3 DEL Frame_Shift_Del 2 45171841 CA - 25 70 LUAD TCGA-50-5049 SIX3 SNP Silent 2 45169936 C A 21 58 CRC TCGA-AA-A022 SIX3 SNP Missense_Mutation 2 45171841 C T 25 70 UCEC TCGA-AP-A0LM SIX3 SNP Missense_Mutation 2 45169297 C A 20 73 CRC TCGA-AY-4070 SIX3 SNP Missense_Mutation 2 45169343 G C 39 63 KIRC TCGA-B2-4098 SIX3 SNP Silent 2 45171737 C A 25 58 HNSC TCGA-BA-5152 SIX3 DNP Missense_Mutation 2 45169452 CC AT 30 67 HNSC TCGA-BB-7871 SIX3 SNP Missense_Mutation 2 45170030 G A 38 78 HNSC TCGA-CV-6934 SIX3 SNP Nonsense_Mutation 2 45169584 C A 31 69 UCEC TCGA-D1-A103 SIX3 SNP Silent 2 45169813 G A 36 78 UCEC TCGA-D1-A160 SIX3 SNP Silent 2 45171839 C T 27 68 HNSC TCGA-D6-6516 SIX3 DNP Missense_Mutation 2 45169459 CC TT 22 50 BLCA TCGA-G2-A2EO SIX3 SNP Missense_Mutation 2 45169727 C T 29 78 BLCA TCGA-H4-A2HQ SIX3 SNP Missense_Mutation 2 45171878 C G 27 73