ttype patient gene classification type chr pos ref_allele newbase context65 cons46 BRCA BR-0032 CTR9 SNP Splice_Site 11 10783602 G A 44 98 LUAD LUAD-CHTN-3090346 CTR9 SNP Missense_Mutation 11 10781785 G A 42 100 LUAD LUAD-CHTN-MAD06-00490 CTR9 SNP Missense_Mutation 11 10793114 G C 36 73 LUAD LUAD-LC15C CTR9 SNP Silent 11 10785932 C T 29 59 LUAD LUAD-RT-S01477 CTR9 SNP Missense_Mutation 11 10800624 C T 29 76 LUAD LUAD-S01405 CTR9 SNP Missense_Mutation 11 10796819 G A 37 64 MED MD-286 CTR9 SNP Missense_Mutation 11 10794726 G A 39 86 MEL MEL-JWCI-WGS-1 CTR9 SNP Missense_Mutation 11 10781728 C T 31 80 MEL MEL-JWCI-WGS-12 CTR9 SNP Silent 11 10785974 G A 43 46 MEL MEL-JWCI-WGS-34 CTR9 SNP Missense_Mutation 11 10774252 G A 43 99 MEL MEL-JWCI-WGS-6 CTR9 DNP Missense_Mutation 11 10776719 CC TT 26 100 MEL MEL-Ma-Mel-63 CTR9 SNP Missense_Mutation 11 10797176 G A 45 97 MEL MEL-Ma-Mel-67 CTR9 SNP Silent 11 10791810 C T 32 50 LUAD TCGA-05-4396 CTR9 SNP Silent 11 10789520 C A 21 66 GBM TCGA-06-0192 CTR9 SNP Missense_Mutation 11 10774300 A G 8 78 LUSC TCGA-21-5786 CTR9 SNP Missense_Mutation 11 10785972 G T 35 100 LUSC TCGA-22-5474 CTR9 SNP Missense_Mutation 11 10794075 C T 32 96 OV TCGA-24-1565 CTR9 SNP Missense_Mutation 11 10800398 C T 26 62 OV TCGA-24-1604 CTR9 SNP Missense_Mutation 11 10778347 A G 14 90 LUAD TCGA-44-6777 CTR9 SNP Splice_site 11 10781721 G A 39 49 LUAD TCGA-55-6712 CTR9 SNP Nonsense_Mutation 11 10800533 G T 41 97 LUAD TCGA-64-1677 CTR9 SNP Missense_Mutation 11 10800443 G A 45 97 LUSC TCGA-66-2744 CTR9 SNP Missense_Mutation 11 10776627 G T 47 64 LUAD TCGA-67-3770 CTR9 INS Frame_Shift_Ins 11 10785261 - T 8 38 BRCA TCGA-A8-A06O CTR9 SNP Missense_Mutation 11 10791787 C G 25 84 CRC TCGA-AA-3864 CTR9 SNP Missense_Mutation 11 10800495 G A 38 59 CRC TCGA-AA-3930 CTR9 SNP Silent 11 10786265 T A 53 49 CRC TCGA-AA-3966 CTR9 SNP Missense_Mutation 11 10786161 G A 38 100 CRC TCGA-AA-3971 CTR9 SNP Missense_Mutation 11 10789503 C A 21 100 CRC TCGA-AA-A00N CTR9 SNP Missense_Mutation 11 10789919 C T 31 79 CRC TCGA-AA-A00N CTR9 SNP Missense_Mutation 11 10792152 C T 28 100 CRC TCGA-AA-A010 CTR9 SNP Missense_Mutation 11 10774310 C A 28 98 AML TCGA-AB-2828 CTR9 SNP Missense_Mutation 11 10781825 G A 41 99 AML TCGA-AB-2863 CTR9 SNP Missense_Mutation 11 10778376 G C 35 84 UCEC TCGA-AP-A051 CTR9 SNP Silent 11 10785276 A G 10 53 UCEC TCGA-AP-A051 CTR9 SNP Missense_Mutation 11 10794117 G A 38 98 UCEC TCGA-AP-A054 CTR9 SNP Missense_Mutation 11 10789383 A C 5 92 UCEC TCGA-AP-A059 CTR9 SNP Missense_Mutation 11 10781765 A C 1 91 UCEC TCGA-AP-A059 CTR9 SNP Missense_Mutation 11 10785662 C T 21 100 UCEC TCGA-AP-A059 CTR9 SNP Nonsense_Mutation 11 10788010 G A 44 87 UCEC TCGA-AP-A059 CTR9 SNP Missense_Mutation 11 10789934 G A 48 89 UCEC TCGA-AP-A0LM CTR9 SNP Missense_Mutation 11 10800647 G A 45 95 BRCA TCGA-AR-A0TZ CTR9 SNP Missense_Mutation 11 10777333 G A 34 100 BRCA TCGA-AR-A256 CTR9 SNP Missense_Mutation 11 10792118 G A 33 100 UCEC TCGA-AX-A05Z CTR9 SNP Missense_Mutation 11 10795636 G T 33 74 UCEC TCGA-B5-A0JV CTR9 SNP Silent 11 10797148 G A 39 28 UCEC TCGA-B5-A0JY CTR9 SNP Missense_Mutation 11 10776609 G T 45 100 UCEC TCGA-B5-A0JY CTR9 SNP Missense_Mutation 11 10776662 A T 3 92 UCEC TCGA-B5-A11E CTR9 SNP Silent 11 10789903 C A 22 51 HNSC TCGA-BB-7871 CTR9 INS Frame_Shift_Ins 11 10772990 - G 23 75 UCEC TCGA-BS-A0UF CTR9 SNP Missense_Mutation 11 10792055 G T 45 100 UCEC TCGA-BS-A0UF CTR9 SNP Missense_Mutation 11 10797072 A C 3 88 UCEC TCGA-BS-A0UL CTR9 SNP Missense_Mutation 11 10786162 C T 26 100 KIRC TCGA-CJ-4901 CTR9 SNP Splice_site 11 10785191 A G 9 80 KIRC TCGA-CJ-5671 CTR9 SNP Missense_Mutation 11 10789686 T G 50 52 HNSC TCGA-CN-6013 CTR9 SNP Missense_Mutation 11 10794110 C T 23 69 KIRC TCGA-CZ-5986 CTR9 SNP Missense_Mutation 11 10785039 T A 51 93 UCEC TCGA-D1-A103 CTR9 SNP Missense_Mutation 11 10776737 A G 16 92 UCEC TCGA-D1-A17Q CTR9 SNP Silent 11 10774236 C T 31 58 UCEC TCGA-DI-A0WH CTR9 SNP Missense_Mutation 11 10789525 G A 37 100