ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-0129 SAT1 SNP Splice_site 23 23803544 G C 33 96 MEL ME009 SAT1 SNP Silent 23 23801813 C T 32 34 LUAD TCGA-55-1592 SAT1 SNP Missense_Mutation 23 23801932 G A 44 97 LUAD TCGA-73-4658 SAT1 SNP Silent 23 23803931 G A 33 63 CRC TCGA-AA-3866 SAT1 SNP Missense_Mutation 23 23802053 T A 57 61 BRCA TCGA-AN-A0FS SAT1 SNP Missense_Mutation 23 23801965 T C 60 87 UCEC TCGA-AP-A059 SAT1 SNP Silent 23 23802062 C A 28 52 UCEC TCGA-AP-A0LM SAT1 SNP Missense_Mutation 23 23801842 C T 27 49 BRCA TCGA-AR-A1AP SAT1 SNP Missense_Mutation 23 23803899 C A 32 83 UCEC TCGA-AX-A0J0 SAT1 SNP Missense_Mutation 23 23803448 A G 6 60 KIRC TCGA-BP-5173 SAT1 SNP Missense_Mutation 23 23803813 G A 35 75 KIRC TCGA-BP-5173 SAT1 SNP Silent 23 23803814 G A 44 55 UCEC TCGA-BS-A0TC SAT1 SNP Missense_Mutation 23 23803528 G A 40 96 UCEC TCGA-BS-A0UF SAT1 SNP Silent 23 23801480 C T 31 68 UCEC TCGA-BS-A0UV SAT1 SNP Missense_Mutation 23 23801977 C T 23 80 BLCA TCGA-BT-A0YX SAT1 SNP Splice_site 23 23803975 G C 41 51 HNSC TCGA-CR-7368 SAT1 SNP Missense_Mutation 23 23803928 C A 29 96 HNSC TCGA-CV-7091 SAT1 SNP Splice_Site 23 23801827 G A 44 96 UCEC TCGA-D1-A177 SAT1 SNP Missense_Mutation 23 23801955 C T 21 97 HNSC TCGA-DQ-5624 SAT1 SNP Missense_Mutation 23 23803921 G A 33 96