ttype patient gene classification type chr pos ref_allele newbase context65 cons46 BRCA BR-0027 PAAF1 SNP Missense_Mutation 11 73620606 C G 30 81 HNSC HN_62505 PAAF1 SNP Missense 11 73589855 C T 29 74 LUAD LUAD-74TBW PAAF1 SNP Splice_Site 11 73625456 A T 7 76 LUAD LUAD-F00121 PAAF1 SNP Missense_Mutation 11 73589838 A T 11 70 MEL MEL-Ma-Mel-119 PAAF1 SNP Silent 11 73610262 C A 32 61 LUAD TCGA-05-4396 PAAF1 SNP Missense_Mutation 11 73611402 C A 21 83 LUAD TCGA-05-4424 PAAF1 SNP Silent 11 73620586 G T 39 51 GBM TCGA-06-0648 PAAF1 SNP Missense_Mutation 11 73627614 G A 38 82 OV TCGA-29-2427 PAAF1 SNP Missense_Mutation 11 73611394 T A 51 78 LUSC TCGA-66-2767 PAAF1 SNP Missense_Mutation 11 73620469 T A 50 52 LUSC TCGA-66-2793 PAAF1 SNP Missense_Mutation 11 73638345 A C 9 71 BRCA TCGA-A2-A0D2 PAAF1 SNP Silent 11 73627700 T C 58 52 BRCA TCGA-A8-A06Q PAAF1 SNP Silent 11 73611344 G A 45 63 CRC TCGA-AA-3516 PAAF1 SNP Silent 11 73611329 A G 10 55 CRC TCGA-AA-A00N PAAF1 SNP Silent 11 73598466 A C 7 54 AML TCGA-AB-2828 PAAF1 SNP Silent 11 73635709 G A 34 58 CRC TCGA-AG-A020 PAAF1 DEL In_Frame_Del 11 73610216 GAG - 33 79 UCEC TCGA-AX-A0J0 PAAF1 SNP Missense_Mutation 11 73610259 A C 1 49 UCEC TCGA-B5-A0JY PAAF1 SNP Silent 11 73611329 A T 10 55 HNSC TCGA-BB-7871 PAAF1 SNP Missense_Mutation 11 73625542 G T 35 82 KIRC TCGA-BP-4768 PAAF1 SNP Missense_Mutation 11 73620605 T A 54 64 KIRC TCGA-BP-4989 PAAF1 SNP Missense_Mutation 11 73638349 A T 7 71 UCEC TCGA-BS-A0UF PAAF1 SNP Missense_Mutation 11 73610256 G T 45 80 BLCA TCGA-BT-A20J PAAF1 SNP Silent 11 73627688 G A 47 63 BLCA TCGA-BT-A20N PAAF1 SNP Missense_Mutation 11 73620513 G A 37 81 HNSC TCGA-CV-7440 PAAF1 SNP Missense_Mutation 11 73620473 G A 43 81 BRCA TCGA-E2-A1LH PAAF1 DEL Frame_Shift_Del 11 73627677 ATTT - 8 59