ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-805 CHFR SNP Silent 12 133424689 G A 40 41 HNSC HN_62426 CHFR SNP Nonsense 12 133428264 G A 47 81 LUAD LUAD-RT-S01707 CHFR SNP Missense_Mutation 12 133423698 C G 24 72 LUAD LUAD-S01346 CHFR SNP Silent 12 133425261 C T 30 51 LUAD LUAD-S01354 CHFR SNP Nonsense_Mutation 12 133438098 G A 47 53 LUAD LUAD-S01356 CHFR SNP Missense_Mutation 12 133420659 C A 28 58 LUAD LUAD-S01478 CHFR SNP Missense_Mutation 12 133454228 G A 41 81 MED MD-045 CHFR SNP Missense_Mutation 12 133428224 G A 39 71 MEL MEL-JWCI-WGS-8 CHFR SNP Silent 12 133420665 G A 41 52 MEL MEL-Ma-Mel-37 CHFR SNP Silent 12 133424731 C T 21 56 LUAD TCGA-05-4396 CHFR SNP Silent 12 133433143 G T 47 50 LUAD TCGA-05-4432 CHFR SNP Missense_Mutation 12 133447364 C A 26 82 LUSC TCGA-18-3409 CHFR SNP Missense_Mutation 12 133435753 G A 44 46 LUSC TCGA-18-3417 CHFR SNP Missense_Mutation 12 133435727 C A 26 48 LUSC TCGA-18-4721 CHFR SNP Missense_Mutation 12 133435751 C T 19 40 LUSC TCGA-22-0944 CHFR SNP Silent 12 133419614 C T 29 53 LUAD TCGA-55-5899 CHFR SNP Missense_Mutation 12 133434066 G A 39 85 LUAD TCGA-75-6211 CHFR SNP Missense_Mutation 12 133420622 C G 31 84 LUAD TCGA-91-6828 CHFR SNP Missense_Mutation 12 133438086 C A 30 60 CRC TCGA-AA-3525 CHFR SNP Missense_Mutation 12 133435802 C T 29 43 CRC TCGA-AA-3715 CHFR SNP Splice_site 12 133423629 C A 21 93 CRC TCGA-AA-3984 CHFR SNP Missense_Mutation 12 133438140 G A 33 49 CRC TCGA-AG-A002 CHFR SNP Missense_Mutation 12 133448903 T C 57 88 UCEC TCGA-AP-A059 CHFR SNP Silent 12 133446260 G T 35 53 UCEC TCGA-AP-A0LM CHFR SNP Missense_Mutation 12 133419624 C T 27 84 UCEC TCGA-AX-A06H CHFR SNP Silent 12 133438075 G A 39 47 UCEC TCGA-AX-A0J1 CHFR SNP Missense_Mutation 12 133433133 G A 38 69 UCEC TCGA-AX-A0J1 CHFR SNP Missense_Mutation 12 133435699 G A 40 62 KIRC TCGA-B0-4841 CHFR SNP Missense_Mutation 12 133454224 G C 41 50 KIRC TCGA-B0-5119 CHFR SNP Missense_Mutation 12 133435664 C T 31 73 KIRC TCGA-B2-5633 CHFR SNP Missense_Mutation 12 133454165 C T 18 96 UCEC TCGA-B5-A11E CHFR SNP Missense_Mutation 12 133425242 G T 35 54 UCEC TCGA-B5-A11Y CHFR SNP Missense_Mutation 12 133438137 G T 43 51 HNSC TCGA-CR-7370 CHFR SNP Nonsense_Mutation 12 133433063 G C 45 84 HNSC TCGA-CV-7242 CHFR SNP Missense_Mutation 12 133435715 C T 32 83 UCEC TCGA-D1-A0ZO CHFR SNP Silent 12 133434124 C T 19 49 UCEC TCGA-D1-A103 CHFR SNP Missense_Mutation 12 133428251 T C 58 87 UCEC TCGA-D1-A103 CHFR SNP Silent 12 133428286 G A 40 40 UCEC TCGA-D1-A17D CHFR SNP Missense_Mutation 12 133430022 G A 40 53 HNSC TCGA-D6-6516 CHFR SNP Splice_Site 12 133423717 C A 32 93 BLCA TCGA-DK-A1A3 CHFR SNP Nonsense_Mutation 12 133428210 G A 45 93 BLCA TCGA-DK-A3IU CHFR DNP Nonsense_Mutation 12 133433091 CC AA 30 98 BLCA TCGA-FD-A3B6 CHFR SNP Missense_Mutation 12 133433181 C G 30 85 BLCA TCGA-H4-A2HQ CHFR DNP Missense_Mutation 12 133428240 CC GT 30 94