ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-141 AICDA SNP Splice_site 12 8756932 G C 43 78 ESO ESO-160 AICDA SNP Missense_Mutation 12 8757883 G A 39 49 LUAD LUAD-CHTN-MAD06-00668 AICDA SNP Missense_Mutation 12 8757907 C T 27 77 LUAD LUAD-CHTN-Z4716A AICDA SNP Missense_Mutation 12 8757971 G T 36 57 LUAD LUAD-S01356 AICDA SNP Missense_Mutation 12 8758017 C A 27 68 MED MD-277 AICDA SNP Missense_Mutation 12 8758050 C T 27 72 MEL ME009 AICDA SNP Silent 12 8759590 C T 30 56 MEL MEL-JWCI-WGS-18 AICDA SNP Missense_Mutation 12 8759549 C A 18 94 MEL MEL-Ma-Mel-08a AICDA SNP Missense_Mutation 12 8757447 C T 29 70 GBM TCGA-06-5418 AICDA SNP Missense_Mutation 12 8758006 C T 19 64 OV TCGA-13-1510 AICDA SNP Missense_Mutation 12 8757516 A G 13 87 LUAD TCGA-17-Z008 AICDA SNP Silent 12 8758007 G T 38 32 LUSC TCGA-60-2709 AICDA SNP Missense_Mutation 12 8757847 G C 39 62 LUSC TCGA-60-2724 AICDA SNP Missense_Mutation 12 8757847 G C 39 62 LUSC TCGA-66-2794 AICDA SNP Silent 12 8758043 G A 33 62 GBM TCGA-76-6283 AICDA SNP Missense_Mutation 12 8759510 C T 19 94 KIRC TCGA-A3-3382 AICDA SNP Missense_Mutation 12 8758017 C T 27 68 CRC TCGA-AA-3856 AICDA SNP Missense_Mutation 12 8758025 G T 44 60 CRC TCGA-AA-3971 AICDA SNP Silent 12 8758007 G A 38 32 CRC TCGA-AA-3984 AICDA SNP Missense_Mutation 12 8759562 G A 39 72 CRC TCGA-AA-A010 AICDA SNP Missense_Mutation 12 8757408 G T 35 78 CRC TCGA-AG-3892 AICDA SNP Missense_Mutation 12 8757906 G A 38 94 UCEC TCGA-AP-A051 AICDA SNP Silent 12 8757905 C T 27 49 UCEC TCGA-AP-A056 AICDA SNP Silent 12 8757968 A G 6 49 UCEC TCGA-AP-A0LJ AICDA SNP Missense_Mutation 12 8757952 C A 31 64 UCEC TCGA-B5-A11E AICDA SNP Missense_Mutation 12 8757814 T C 63 87 BRCA TCGA-BH-A0W3 AICDA SNP Missense_Mutation 12 8759472 G T 33 94 HNSC TCGA-CV-7261 AICDA SNP Missense_Mutation 12 8757850 G A 46 63 HNSC TCGA-CV-7406 AICDA SNP Missense_Mutation 12 8758041 G A 37 82 UCEC TCGA-D1-A103 AICDA SNP Splice_Site 12 8756935 T C 55 73 UCEC TCGA-D1-A103 AICDA SNP Missense_Mutation 12 8757480 C T 31 67 UCEC TCGA-D1-A17U AICDA SNP Missense_Mutation 12 8757858 C T 23 94