ttype patient gene classification type chr pos ref_allele newbase context65 cons46 HNSC HN_62854 RFX5 SNP Missense 1 151315497 G A 45 60 LUAD LUAD-S01409 RFX5 SNP Missense_Mutation 1 151314769 T C 64 56 MEL ME017 RFX5 DNP Missense_Mutation 1 151317619 GG AA 35 91 MEL MEL-13600 RFX5 SNP Silent 1 151315457 G T 43 66 MEL MEL-Ma-Mel-122 RFX5 SNP Missense_Mutation 1 151314837 G A 43 57 MEL MEL-Ma-Mel-48 RFX5 SNP Silent 1 151317611 G T 41 48 MM MM-0503 RFX5 SNP Missense_Mutation 1 151316184 G A 47 71 LUAD TCGA-05-4396 RFX5 SNP Missense_Mutation 1 151316261 C A 23 96 LUAD TCGA-05-4424 RFX5 SNP Missense_Mutation 1 151314798 C T 32 53 LUAD TCGA-05-4424 RFX5 SNP Missense_Mutation 1 151314850 C T 32 74 LUAD TCGA-05-4427 RFX5 DEL Frame_Shift_Del 1 151315112 C - 26 50 OV TCGA-13-1498 RFX5 SNP Missense_Mutation 1 151314685 C T 32 76 LUAD TCGA-35-3621 RFX5 SNP Missense_Mutation 1 151318693 C G 31 71 LUAD TCGA-38-4625 RFX5 SNP Silent 1 151316173 C T 24 66 GBM TCGA-41-3393 RFX5 SNP Nonsense_Mutation 1 151315095 G C 45 59 LUAD TCGA-49-4486 RFX5 SNP Splice_Site 1 151316755 C G 32 72 LUAD TCGA-49-6742 RFX5 SNP Missense_Mutation 1 151314991 C T 30 57 OV TCGA-61-2095 RFX5 SNP Synonymous 1 151314767 C T 24 52 LUAD TCGA-91-6829 RFX5 SNP Silent 1 151314767 C T 24 52 LUAD TCGA-91-6836 RFX5 SNP Silent 1 151315028 G T 35 58 CRC TCGA-AA-3518 RFX5 SNP Nonsense_Mutation 1 151316199 G A 39 83 CRC TCGA-AA-A01Q RFX5 SNP Silent 1 151315328 T C 58 39 UCEC TCGA-AP-A051 RFX5 SNP Missense_Mutation 1 151315507 C T 26 64 UCEC TCGA-AP-A056 RFX5 SNP Missense_Mutation 1 151315110 C T 27 79 UCEC TCGA-AP-A059 RFX5 SNP Nonsense_Mutation 1 151317006 G T 36 63 UCEC TCGA-AP-A059 RFX5 SNP Splice_Site 1 151318403 C T 18 86 UCEC TCGA-AP-A0LM RFX5 SNP Nonsense_Mutation 1 151316921 G A 37 66 UCEC TCGA-AP-A0LM RFX5 SNP Missense_Mutation 1 151317625 G T 33 91 UCEC TCGA-AP-A0LM RFX5 SNP Splice_site 1 151318681 G A 37 85 UCEC TCGA-B5-A11E RFX5 SNP Missense_Mutation 1 151315145 C A 24 50 HNSC TCGA-BA-5152 RFX5 SNP Silent 1 151317305 C A 29 48 HNSC TCGA-BA-7269 RFX5 SNP Missense_Mutation 1 151316211 G T 33 64 HNSC TCGA-BB-7866 RFX5 SNP Missense_Mutation 1 151315612 C T 27 57 BRCA TCGA-BH-A1FC RFX5 SNP Missense_Mutation 1 151315882 T C 64 58 KIRC TCGA-BP-4961 RFX5 INS Frame_Shift_Ins 1 151315565 - C 54 54 UCEC TCGA-BS-A0UM RFX5 SNP Missense_Mutation 1 151316273 C T 23 64 BLCA TCGA-BT-A3PH RFX5 SNP Silent 1 151316209 G A 45 75 KIRC TCGA-CJ-5680 RFX5 SNP Silent 1 151315361 G T 33 64 HNSC TCGA-CV-6935 RFX5 SNP Nonsense_Mutation 1 151315026 G C 45 55 UCEC TCGA-D1-A17Q RFX5 SNP Missense_Mutation 1 151315125 T G 64 56 HNSC TCGA-D6-6516 RFX5 SNP Missense_Mutation 1 151316355 C T 32 82 KIRC TCGA-DV-5574 RFX5 SNP Splice_site 1 151317012 C A 30 68