ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-164 SLC25A22 SNP Silent 11 792311 G T 35 50 MEL ME011 SLC25A22 SNP Silent 11 793585 C T 32 62 MEL MEL-Ma-Mel-94 SLC25A22 SNP Missense_Mutation 11 792364 A C 10 75 LUAD TCGA-64-1678 SLC25A22 SNP Missense_Mutation 11 792399 C A 27 55 UCEC TCGA-A5-A0R9 SLC25A22 SNP Silent 11 792389 G A 39 36 UCEC TCGA-AP-A059 SLC25A22 SNP Missense_Mutation 11 792882 C T 25 94 UCEC TCGA-AP-A059 SLC25A22 SNP Missense_Mutation 11 792924 C T 19 94 BRCA TCGA-AR-A1AU SLC25A22 SNP Silent 11 793561 G A 40 51 BRCA TCGA-BH-A18P SLC25A22 SNP Missense_Mutation 11 792383 C G 32 44 BLCA TCGA-BL-A13J SLC25A22 SNP Silent 11 792032 C T 29 55 UCEC TCGA-BS-A0UF SLC25A22 SNP Missense_Mutation 11 792318 A G 10 87 HNSC TCGA-CQ-7065 SLC25A22 SNP Missense_Mutation 11 791950 A G 10 56 HNSC TCGA-CR-6470 SLC25A22 SNP Missense_Mutation 11 792587 C T 23 80 HNSC TCGA-CV-7101 SLC25A22 SNP Missense_Mutation 11 792580 T C 57 86 HNSC TCGA-CV-7414 SLC25A22 SNP Missense_Mutation 11 794488 G A 39 90