ttype patient gene classification type chr pos ref_allele newbase context65 cons46 BRCA BR-0043 CEP192 SNP Silent 18 13056510 T C 55 41 ESO ESO-0015 CEP192 SNP Splice_Site 18 13105079 G A 36 83 ESO ESO-037 CEP192 SNP Missense_Mutation 18 13114192 G A 33 58 ESO ESO-147 CEP192 SNP Missense_Mutation 18 13068145 C T 24 79 HNSC HN_00190 CEP192 SNP Missense 18 13096256 G T 42 95 HNSC HN_62426 CEP192 SNP Synonymous 18 13073085 C T 29 54 LUAD LUAD-CHTN-MAD06-00668 CEP192 SNP Missense_Mutation 18 13049024 C T 18 50 LUAD LUAD-CHTN-MAD06-00678 CEP192 SNP Splice_site 18 13092525 A G 3 61 LUAD LUAD-E00897 CEP192 SNP Missense_Mutation 18 13087029 G T 41 97 LUAD LUAD-RT-S01769 CEP192 SNP Nonsense_Mutation 18 13059091 C G 29 60 LUAD LUAD-RT-S01774 CEP192 SNP Missense_Mutation 18 13068228 G T 45 57 LUAD LUAD-S01478 CEP192 SNP Missense_Mutation 18 13059246 G C 40 68 LUAD LUAD_E00565 CEP192 SNP Missense_Mutation 18 13087561 G A 33 59 MEL ME009 CEP192 SNP Missense_Mutation 18 13008571 C T 17 51 MEL ME024 CEP192 SNP Missense_Mutation 18 13056190 C T 30 55 MEL ME043 CEP192 DNP Missense_Mutation 18 13095624 CC TT 30 87 MEL MEL-JWCI-WGS-32 CEP192 SNP Missense_Mutation 18 13068913 C T 22 83 MEL MEL-JWCI-WGS-33 CEP192 SNP Silent 18 13071095 C T 27 58 MEL MEL-JWCI-WGS-34 CEP192 SNP Missense_Mutation 18 13053037 C T 21 44 MEL MEL-Ma-Mel-35 CEP192 SNP Silent 18 13056276 C T 21 44 MEL MEL-Ma-Mel-67 CEP192 SNP Silent 18 13073085 C T 29 54 MEL MEL-Ma-Mel-67 CEP192 SNP Silent 18 13092488 C T 30 51 MM MM-0308 CEP192 SNP Splice_site 18 13059082 T G 59 75 MM MM-0339 CEP192 SNP Splice_site 18 13059082 T G 59 75 NB NB-1194 CEP192 SNP Splice_Site_SNP 18 13103589 T G 58 79 LUAD TCGA-05-4389 CEP192 SNP Missense_Mutation 18 13049425 G A 48 48 LUAD TCGA-05-4390 CEP192 SNP Missense_Mutation 18 13030600 A T 12 57 LUAD TCGA-05-4396 CEP192 SNP Missense_Mutation 18 13056638 C A 23 49 LUAD TCGA-05-4396 CEP192 SNP Silent 18 13068180 C A 31 58 LUAD TCGA-05-4396 CEP192 SNP Silent 18 13068921 C A 23 45 LUAD TCGA-05-4396 CEP192 SNP Splice_Site 18 13114128 G T 33 62 LUAD TCGA-05-4430 CEP192 SNP Silent 18 13095519 G T 43 54 OV TCGA-13-0904 CEP192 SNP Missense_Mutation 18 13056284 C G 17 49 LUAD TCGA-17-Z008 CEP192 SNP Silent 18 13059281 C T 29 54 LUAD TCGA-17-Z014 CEP192 SNP Missense_Mutation 18 13049233 A G 5 60 LUAD TCGA-17-Z016 CEP192 SNP Missense_Mutation 18 13040877 G A 46 67 LUAD TCGA-17-Z041 CEP192 SNP Missense_Mutation 18 13116441 G A 36 50 LUAD TCGA-17-Z045 CEP192 SNP Silent 18 13087592 A G 16 51 LUAD TCGA-17-Z062 CEP192 SNP Missense_Mutation 18 13105032 G T 33 59 LUSC TCGA-21-5787 CEP192 SNP Missense_Mutation 18 13059268 G A 34 54 OV TCGA-23-1031 CEP192 SNP Splice_site 18 13114130 G C 34 69 OV TCGA-24-1425 CEP192 SNP Synonymous 18 13056381 G T 44 54 OV TCGA-24-2281 CEP192 SNP Missense_Mutation 18 13049205 G T 48 50 LUSC TCGA-33-4532 CEP192 SNP Silent 18 13048935 C T 29 49 LUSC TCGA-34-5231 CEP192 SNP Nonsense_Mutation 18 13056424 C T 29 72 LUSC TCGA-34-5239 CEP192 SNP Missense_Mutation 18 13092463 G A 33 58 LUSC TCGA-37-3783 CEP192 SNP Missense_Mutation 18 13056361 G T 38 50 LUAD TCGA-49-4514 CEP192 SNP Missense_Mutation 18 13124735 T G 52 79 LUAD TCGA-50-5931 CEP192 SNP Missense_Mutation 18 13059303 G A 48 49 LUAD TCGA-50-5946 CEP192 SNP Missense_Mutation 18 13056289 C T 29 54 LUAD TCGA-50-6592 CEP192 SNP Missense_Mutation 18 13124693 C G 28 55 LUSC TCGA-56-5898 CEP192 SNP Missense_Mutation 18 13089487 A C 7 54 OV TCGA-57-1993 CEP192 SNP Missense_Mutation 18 13059273 G A 40 96 LUSC TCGA-60-2720 CEP192 SNP Missense_Mutation 18 13113642 G C 45 84 LUSC TCGA-60-2724 CEP192 SNP Missense_Mutation 18 13104996 G C 36 64 LUSC TCGA-63-5131 CEP192 SNP Missense_Mutation 18 13048922 C G 32 71 LUSC TCGA-63-6202 CEP192 SNP Missense_Mutation 18 13104999 G C 41 72 LUSC TCGA-66-2734 CEP192 SNP Silent 18 13073110 C A 31 73 LUSC TCGA-66-2766 CEP192 SNP Missense_Mutation 18 13049582 G C 33 52 LUAD TCGA-73-4668 CEP192 DNP Missense_Mutation 18 13073170 GG TT 35 98 LUAD TCGA-75-6211 CEP192 SNP Missense_Mutation 18 13049430 G T 33 56 LUAD TCGA-91-6828 CEP192 SNP Missense_Mutation 18 13087217 G C 41 84 UCEC TCGA-A5-A0GH CEP192 SNP Silent 18 13096262 G A 38 49 BRCA TCGA-A8-A06Q CEP192 SNP Splice_Site 18 13099581 G A 44 76 BRCA TCGA-A8-A06X CEP192 SNP Missense_Mutation 18 13117605 G A 33 83 CRC TCGA-AA-3516 CEP192 SNP Missense_Mutation 18 13096300 C T 27 53 CRC TCGA-AA-3877 CEP192 SNP Nonsense_Mutation 18 13049590 C T 29 57 CRC TCGA-AA-3877 CEP192 SNP Nonsense_Mutation 18 13116476 C T 27 52 CRC TCGA-AA-3947 CEP192 DEL Frame_Shift_Del 18 13049146 A - 13 72 CRC TCGA-AA-3947 CEP192 SNP Silent 18 13100360 T G 60 50 CRC TCGA-AA-3966 CEP192 SNP Nonsense_Mutation 18 13056463 G T 35 65 CRC TCGA-AA-3977 CEP192 SNP Missense_Mutation 18 13114135 G A 37 55 CRC TCGA-AA-3984 CEP192 SNP Missense_Mutation 18 13049508 T G 60 52 CRC TCGA-AA-A01R CEP192 SNP Missense_Mutation 18 13055897 C T 17 54 CRC TCGA-AA-A01R CEP192 SNP Splice_site 18 13069738 T C 58 69 AML TCGA-AB-2833 CEP192 SNP Missense_Mutation 18 13049366 G A 33 52 CRC TCGA-AG-A002 CEP192 SNP Silent 18 13071155 G A 37 10 CRC TCGA-AG-A02N CEP192 SNP Missense_Mutation 18 13095600 G A 38 40 UCEC TCGA-AP-A051 CEP192 SNP Missense_Mutation 18 13049296 G A 42 53 UCEC TCGA-AP-A054 CEP192 SNP Silent 18 13067922 T C 51 52 UCEC TCGA-AP-A056 CEP192 SNP Missense_Mutation 18 13049191 T G 62 59 UCEC TCGA-AP-A056 CEP192 SNP Missense_Mutation 18 13068895 G A 37 96 UCEC TCGA-AP-A059 CEP192 SNP Missense_Mutation 18 13114146 T A 51 47 UCEC TCGA-AP-A059 CEP192 SNP Nonsense_Mutation 18 13116476 C T 27 52 UCEC TCGA-AP-A059 CEP192 SNP Missense_Mutation 18 13124693 C T 28 55 UCEC TCGA-AP-A0LM CEP192 SNP Nonsense_Mutation 18 13042241 G T 35 63 UCEC TCGA-AP-A0LM CEP192 SNP Missense_Mutation 18 13087116 G A 42 83 BRCA TCGA-AR-A255 CEP192 SNP Missense_Mutation 18 13056429 C G 26 55 UCEC TCGA-AX-A06B CEP192 SNP Silent 18 13056360 C T 27 51 UCEC TCGA-AX-A0J0 CEP192 SNP Missense_Mutation 18 13069848 G A 37 65 UCEC TCGA-AX-A0J0 CEP192 SNP Nonsense_Mutation 18 13092456 G T 33 81 UCEC TCGA-AX-A0J0 CEP192 SNP Missense_Mutation 18 13092465 G T 33 62 UCEC TCGA-AX-A0J0 CEP192 SNP Missense_Mutation 18 13099491 C A 32 89 UCEC TCGA-AX-A0J1 CEP192 SNP Silent 18 13092441 C A 20 77 UCEC TCGA-B5-A11E CEP192 SNP Missense_Mutation 18 13015346 G A 41 61 UCEC TCGA-B5-A11E CEP192 SNP Silent 18 13059101 T C 60 53 UCEC TCGA-B5-A11N CEP192 SNP Missense_Mutation 18 13008504 G A 46 57 UCEC TCGA-B5-A11Y CEP192 SNP Missense_Mutation 18 13049261 C T 23 47 HNSC TCGA-BA-5555 CEP192 SNP Nonsense_Mutation 18 13069788 A T 13 61 HNSC TCGA-BB-7862 CEP192 SNP Silent 18 13087592 A G 16 51 BRCA TCGA-BH-A0BZ CEP192 SNP Missense_Mutation 18 13087076 T C 50 57 BRCA TCGA-BH-A18I CEP192 SNP Missense_Mutation 18 13059100 G A 40 64 KIRC TCGA-BP-4967 CEP192 SNP Missense_Mutation 18 13114196 A C 8 48 UCEC TCGA-BS-A0UF CEP192 SNP Nonsense_Mutation 18 13049566 G T 33 62 UCEC TCGA-BS-A0UF CEP192 SNP Missense_Mutation 18 13056355 C A 32 42 UCEC TCGA-BS-A0UJ CEP192 SNP Missense_Mutation 18 13049107 A G 3 79 UCEC TCGA-BS-A0UV CEP192 SNP Missense_Mutation 18 13015396 T G 56 52 UCEC TCGA-BS-A0UV CEP192 SNP Missense_Mutation 18 13029915 G A 41 49 BRCA TCGA-C8-A1HJ CEP192 SNP Missense_Mutation 18 13057640 G A 38 81 HNSC TCGA-CN-5369 CEP192 SNP Missense_Mutation 18 13095576 C T 32 80 HNSC TCGA-CV-5431 CEP192 SNP Silent 18 13056573 C T 32 52 HNSC TCGA-CV-5441 CEP192 SNP Silent 18 13053023 G T 40 39 HNSC TCGA-CV-7253 CEP192 SNP Missense_Mutation 18 13057679 C T 23 62 UCEC TCGA-D1-A103 CEP192 SNP Missense_Mutation 18 13049796 C T 19 50 UCEC TCGA-D1-A103 CEP192 SNP Missense_Mutation 18 13071106 C A 32 58 UCEC TCGA-D1-A16J CEP192 SNP Missense_Mutation 18 13015357 G A 45 57 UCEC TCGA-D1-A17H CEP192 SNP Missense_Mutation 18 13095639 C T 20 60 UCEC TCGA-D1-A17L CEP192 SNP Missense_Mutation 18 13056337 C G 20 65 UCEC TCGA-D1-A17Q CEP192 SNP Missense_Mutation 18 13095626 G A 37 56 BLCA TCGA-G2-A2ES CEP192 SNP Silent 18 13059227 G C 37 47 BLCA TCGA-G2-A2ES CEP192 SNP Silent 18 13069784 C T 30 48 BLCA TCGA-GV-A3JZ CEP192 SNP Silent 18 13092445 C T 29 93