ttype patient gene classification type chr pos ref_allele newbase context65 cons46 BRCA BR-0031 CTCF DNP Missense_Mutation 16 67662337 GC CT 46 100 HNSC HN_63021 CTCF SNP Missense 16 67660496 G A 35 100 LUAD LUAD-B02594 CTCF SNP Missense_Mutation 16 67644974 G T 42 78 LUAD LUAD-RT-S01810 CTCF SNP Silent 16 67654647 G T 40 49 MEL MEL-Ma-Mel-36 CTCF SNP Missense_Mutation 16 67654624 C T 31 100 MM MM-0421-FIX CTCF SNP Synonymous 16 67650676 C T 27 46 LUAD TCGA-05-4395 CTCF SNP Silent 16 67645894 G C 40 23 OV TCGA-13-1497 CTCF SNP Missense_Mutation 16 67645945 G C 33 63 LUSC TCGA-18-3409 CTCF SNP Missense_Mutation 16 67662408 C T 22 100 OV TCGA-24-2035 CTCF SNP Synonymous 16 67663345 C T 27 48 LUAD TCGA-35-5375 CTCF SNP Missense_Mutation 16 67660607 G A 38 85 LUAD TCGA-44-2655 CTCF SNP Silent 16 67662413 G T 39 43 LUAD TCGA-44-2655 CTCF SNP Silent 16 67663408 C T 28 44 LUAD TCGA-44-3918 CTCF SNP Missense_Mutation 16 67654636 G A 47 100 LUSC TCGA-60-2698 CTCF SNP Silent 16 67671757 C G 29 54 LUSC TCGA-60-2726 CTCF SNP Silent 16 67645107 A G 14 55 LUAD TCGA-64-5781 CTCF SNP Splice_site 16 67670753 G T 34 71 LUSC TCGA-66-2786 CTCF SNP Silent 16 67662443 A G 8 65 BRCA TCGA-A2-A0CQ CTCF SNP Missense_Mutation 16 67654645 C G 30 100 BRCA TCGA-A2-A0YF CTCF INS Splice_Site 16 67645853 - TAC 35 100 UCEC TCGA-A5-A0GA CTCF SNP Missense_Mutation 16 67654642 C T 27 100 UCEC TCGA-A5-A0GH CTCF DEL Frame_Shift_Del 16 67645967 TG - 55 91 UCEC TCGA-A5-A0GI CTCF SNP Nonsense_Mutation 16 67655479 C T 23 63 UCEC TCGA-A5-A0GM CTCF SNP Nonsense_Mutation 16 67645291 C T 21 74 UCEC TCGA-A5-A0GM CTCF SNP Splice_Site 16 67645517 G A 44 100 UCEC TCGA-A5-A0GP CTCF SNP Nonsense_Mutation 16 67655479 C T 23 63 UCEC TCGA-A5-A0R9 CTCF SNP Missense_Mutation 16 67654646 C T 23 100 UCEC TCGA-A5-A0VO CTCF SNP Nonsense_Mutation 16 67660616 C T 17 100 CRC TCGA-A6-2672 CTCF SNP Missense_Mutation 16 67663406 C T 27 79 CRC TCGA-A6-2676 CTCF SNP Missense_Mutation 16 67650719 C T 31 99 BRCA TCGA-A8-A0AD CTCF SNP Missense_Mutation 16 67645922 C T 29 99 CRC TCGA-AA-3518 CTCF SNP Missense_Mutation 16 67662412 C T 27 100 CRC TCGA-AA-3667 CTCF SNP Missense_Mutation 16 67660607 G T 38 85 CRC TCGA-AA-3845 CTCF SNP Missense_Mutation 16 67660580 C T 27 84 CRC TCGA-AA-A00D CTCF SNP Missense_Mutation 16 67644779 C G 20 70 CRC TCGA-AA-A010 CTCF SNP Missense_Mutation 16 67650729 A G 6 90 AML TCGA-AB-3009 CTCF SNP Nonsense_Mutation 16 67660469 C T 27 58 CRC TCGA-AG-A002 CTCF SNP Missense_Mutation 16 67650710 C T 31 84 CRC TCGA-AG-A026 CTCF SNP Missense_Mutation 16 67644806 C G 20 94 BRCA TCGA-AN-A0AT CTCF SNP Nonsense_Mutation 16 67645308 G A 42 100 BRCA TCGA-AN-A0FS CTCF SNP Missense_Mutation 16 67645507 A G 13 92 BRCA TCGA-AO-A12B CTCF DEL Frame_Shift_Del 16 67644796 GAGA - 41 94 UCEC TCGA-AP-A051 CTCF SNP Missense_Mutation 16 67645223 G A 43 100 UCEC TCGA-AP-A059 CTCF SNP Missense_Mutation 16 67654607 A C 1 94 UCEC TCGA-AP-A059 CTCF SNP Silent 16 67660564 A G 6 53 UCEC TCGA-AP-A0LL CTCF INS Frame_Shift_Ins 16 67670599 - T 28 87 UCEC TCGA-AP-A0LM CTCF SNP Missense_Mutation 16 67670668 C T 24 61 UCEC TCGA-AP-A0LP CTCF SNP Missense_Mutation 16 67654643 G A 40 100 UCEC TCGA-AX-A05T CTCF DEL Frame_Shift_Del 16 67645502 AAATT - 1 79 UCEC TCGA-AX-A05Y CTCF SNP Missense_Mutation 16 67654643 G A 40 100 UCEC TCGA-AX-A05Z CTCF SNP Missense_Mutation 16 67645102 A G 10 68 UCEC TCGA-AX-A05Z CTCF SNP Nonsense_Mutation 16 67645270 G T 33 87 UCEC TCGA-AX-A06H CTCF INS Frame_Shift_Ins 16 67646012 - AC 13 91 UCEC TCGA-AX-A0J0 CTCF SNP Nonsense_Mutation 16 67645069 G T 33 83 UCEC TCGA-B5-A0JV CTCF SNP Missense_Mutation 16 67662451 G A 40 100 UCEC TCGA-B5-A0K7 CTCF SNP Nonsense_Mutation 16 67662323 C A 19 46 UCEC TCGA-B5-A11R CTCF SNP Nonsense_Mutation 16 67645273 C T 17 100 UCEC TCGA-B5-A11X CTCF DEL Frame_Shift_Del 16 67644787 A - 13 86 UCEC TCGA-B5-A11Y CTCF SNP Nonsense_Mutation 16 67655479 C T 23 63 BRCA TCGA-B6-A0RI CTCF SNP Splice_Site 16 67645518 T G 57 91 BRCA TCGA-B6-A0WZ CTCF SNP Missense_Mutation 16 67655464 G C 45 100 KIRC TCGA-B8-4151 CTCF SNP Missense_Mutation 16 67660544 C A 24 100 HNSC TCGA-BA-5151 CTCF INS Frame_Shift_Ins 16 67645241 - G 59 92 UCEC TCGA-BG-A0LX CTCF SNP Nonsense_Mutation 16 67644949 C T 29 94 UCEC TCGA-BG-A0M4 CTCF INS Frame_Shift_Ins 16 67646012 - AC 13 91 UCEC TCGA-BG-A0M4 CTCF SNP Nonsense_Mutation 16 67655479 C T 23 63 UCEC TCGA-BG-A0M9 CTCF SNP Nonsense_Mutation 16 67645273 C T 17 100 UCEC TCGA-BG-A0MC CTCF SNP Missense_Mutation 16 67654646 C T 23 100 UCEC TCGA-BG-A0MO CTCF DEL Frame_Shift_Del 16 67670650 T - 52 81 UCEC TCGA-BG-A0MQ CTCF SNP Missense_Mutation 16 67646007 A G 6 90 UCEC TCGA-BG-A0VV CTCF SNP Nonsense_Mutation 16 67660469 C T 27 58 UCEC TCGA-BG-A186 CTCF SNP Missense_Mutation 16 67654642 C T 27 100 BRCA TCGA-BH-A0BP CTCF SNP Silent 16 67644837 A G 3 53 BRCA TCGA-BH-A0DH CTCF SNP Missense_Mutation 16 67645922 C A 29 99 BRCA TCGA-BH-A0W4 CTCF SNP Missense_Mutation 16 67645919 C T 31 100 BRCA TCGA-BH-A0W5 CTCF SNP Missense_Mutation 16 67645923 A C 6 91 UCEC TCGA-BK-A0C9 CTCF SNP Nonsense_Mutation 16 67645326 T A 50 71 UCEC TCGA-BK-A0C9 CTCF SNP Nonsense_Mutation 16 67645327 C T 29 76 KIRC TCGA-BP-4775 CTCF SNP Nonsense_Mutation 16 67644949 C T 29 94 UCEC TCGA-BS-A0T9 CTCF SNP Nonsense_Mutation 16 67655479 C T 23 63 UCEC TCGA-BS-A0T9 CTCF SNP Missense_Mutation 16 67662303 C T 21 100 UCEC TCGA-BS-A0U5 CTCF SNP Missense_Mutation 16 67650722 T C 61 90 UCEC TCGA-BS-A0UJ CTCF SNP Missense_Mutation 16 67645354 A C 2 76 UCEC TCGA-BS-A0UM CTCF SNP Nonsense_Mutation 16 67663367 G T 33 79 UCEC TCGA-BS-A0V6 CTCF SNP Nonsense_Mutation 16 67662338 C A 27 58 BLCA TCGA-BT-A0YX CTCF SNP Silent 16 67662356 G A 33 87 BLCA TCGA-BT-A2LB CTCF SNP Missense_Mutation 16 67650746 T C 52 91 BRCA TCGA-C8-A12T CTCF SNP Nonsense_Mutation 16 67655431 G T 33 100 BRCA TCGA-C8-A134 CTCF SNP Silent 16 67645098 T A 55 44 HNSC TCGA-CQ-5327 CTCF SNP Missense_Mutation 16 67662366 C G 32 87 HNSC TCGA-CQ-5327 CTCF SNP Missense_Mutation 16 67662427 C G 32 77 HNSC TCGA-CQ-5334 CTCF SNP Silent 16 67650751 G A 36 64 HNSC TCGA-CQ-5334 CTCF SNP Nonsense_Mutation 16 67655479 C T 23 63 HNSC TCGA-CQ-6228 CTCF SNP Nonsense_Mutation 16 67670700 A T 5 81 HNSC TCGA-CR-7382 CTCF SNP Missense_Mutation 16 67650717 G A 40 99 HNSC TCGA-CV-6938 CTCF SNP Nonsense_Mutation 16 67670670 C T 29 61 HNSC TCGA-CV-7102 CTCF SNP Missense_Mutation 16 67660529 C T 29 100 HNSC TCGA-CV-7242 CTCF SNP Missense_Mutation 16 67660581 G T 38 87 HNSC TCGA-CV-7253 CTCF SNP Missense_Mutation 16 67650762 G T 46 99 UCEC TCGA-D1-A0ZR CTCF SNP Splice_Site 16 67663300 G C 33 94 UCEC TCGA-D1-A0ZV CTCF SNP Nonsense_Mutation 16 67645168 G T 33 85 UCEC TCGA-D1-A0ZV CTCF SNP Missense_Mutation 16 67650756 C T 30 99 UCEC TCGA-D1-A161 CTCF INS Frame_Shift_Ins 16 67654681 - GT 41 100 UCEC TCGA-D1-A163 CTCF SNP Splice_site 16 67663303 T A 49 50 UCEC TCGA-D1-A163 CTCF SNP Missense_Mutation 16 67663337 C A 22 65 UCEC TCGA-D1-A16D CTCF INS Frame_Shift_Ins 16 67650765 - T 12 91 UCEC TCGA-D1-A16Q CTCF SNP Nonsense_Mutation 16 67655479 C T 23 63 UCEC TCGA-D1-A16X CTCF SNP Missense_Mutation 16 67644740 A G 9 71 UCEC TCGA-D1-A16X CTCF SNP Nonsense_Mutation 16 67670646 G T 33 87 UCEC TCGA-D1-A17D CTCF SNP Missense_Mutation 16 67662298 G A 38 100 UCEC TCGA-D1-A17S CTCF SNP Missense_Mutation 16 67654607 A C 1 94 UCEC TCGA-D1-A17U CTCF DEL Frame_Shift_Del 16 67663409 T - 54 72 BRCA TCGA-D8-A1JC CTCF SNP Silent 16 67662443 A T 8 65 BRCA TCGA-D8-A1X6 CTCF SNP Splice_site 16 67644736 A G 4 71 BRCA TCGA-E2-A156 CTCF SNP Nonsense_Mutation 16 67644796 G T 41 94 BRCA TCGA-E2-A15T CTCF SNP Nonsense_Mutation 16 67670628 G T 45 87 BRCA TCGA-E2-A1L9 CTCF DEL Frame_Shift_Del 16 67644817 CGCCGGGAAGGGGG - 19 71 BRCA TCGA-E9-A1R0 CTCF SNP Missense_Mutation 16 67645418 T C 64 92 BRCA TCGA-E9-A227 CTCF SNP Missense_Mutation 16 67645934 C G 21 99 BRCA TCGA-EW-A1IY CTCF SNP Missense_Mutation 16 67645412 A G 14 92 BLCA TCGA-FD-A3B3 CTCF SNP Silent 16 67662347 C A 24 58 BLCA TCGA-G2-A2EJ CTCF SNP Missense_Mutation 16 67654676 G A 34 100 HNSC TCGA-H7-7774 CTCF DEL Frame_Shift_Del 16 67663349 GAGGGGGAAAATG - 33 94 HNSC TCGA-HL-7533 CTCF SNP Missense_Mutation 16 67670652 G A 45 87 HNSC TCGA-HL-7533 CTCF SNP Missense_Mutation 16 67671611 G C 45 100