ttype patient gene classification type chr pos ref_allele newbase context65 cons46 CLL CW223 OR4A47 SNP Missense_Mutation 11 48510703 G T 46 66 DLBCL DLBCL-Ls3866 OR4A47 SNP Missense_Mutation 11 48510699 G A 45 93 DLBCL DLBCL-MAYO_DLBCL_234 OR4A47 SNP Silent 11 48510848 C G 26 33 ESO ESO-189 OR4A47 SNP Missense_Mutation 11 48511083 T G 56 50 LUAD LUAD-CHTN-MAD06-00490 OR4A47 SNP Nonsense_Mutation 11 48510629 C A 25 51 LUAD LUAD-LIP77 OR4A47 DNP Missense_Mutation 11 48511183 TG CT 55 82 LUAD LUAD-RT-S01818 OR4A47 SNP Missense_Mutation 11 48511032 G T 35 54 LUAD LUAD-S01315 OR4A47 SNP Missense_Mutation 11 48510687 G C 44 60 LUAD LUAD-S01346 OR4A47 SNP Silent 11 48510659 C T 31 57 MEL ME009 OR4A47 SNP Silent 11 48510371 C T 20 44 MEL ME018 OR4A47 SNP Missense_Mutation 11 48510946 G A 41 53 MEL ME024 OR4A47 SNP Silent 11 48510356 G A 41 45 MEL ME032 OR4A47 SNP Silent 11 48511199 C T 17 52 MEL ME033 OR4A47 SNP Missense_Mutation 11 48510927 C T 24 48 MEL MEL-13567 OR4A47 SNP Silent 11 48510506 C T 28 48 MEL MEL-JWCI-14 OR4A47 SNP Missense_Mutation 11 48510378 C T 24 67 MEL MEL-JWCI-14 OR4A47 SNP Missense_Mutation 11 48510538 C T 29 74 MEL MEL-JWCI-WGS-1 OR4A47 SNP Silent 11 48510872 C T 32 47 MEL MEL-JWCI-WGS-12 OR4A47 SNP Missense_Mutation 11 48510601 G A 43 59 MEL MEL-JWCI-WGS-39 OR4A47 SNP Missense_Mutation 11 48510781 C T 30 69 MEL MEL-JWCI-WGS-7 OR4A47 SNP Missense_Mutation 11 48510538 C T 29 74 MEL MEL-JWCI-WGS-7 OR4A47 SNP Missense_Mutation 11 48510562 C T 29 81 MEL MEL-JWCI-WGS-7 OR4A47 SNP Missense_Mutation 11 48510886 C T 22 64 MEL MEL-Ma-Mel-114 OR4A47 SNP Missense_Mutation 11 48510588 G A 35 52 MEL MEL-Ma-Mel-114 OR4A47 SNP Missense_Mutation 11 48511033 G A 43 57 MEL MEL-Ma-Mel-59 OR4A47 SNP Silent 11 48510713 C T 21 57 MEL MEL-Ma-Mel-65 OR4A47 SNP Silent 11 48510389 C T 29 50 MEL MEL-UKRV-Mel-6 OR4A47 SNP Missense_Mutation 11 48511249 G A 33 47 LUAD TCGA-05-4382 OR4A47 SNP Missense_Mutation 11 48510574 C A 22 81 LUAD TCGA-05-4398 OR4A47 SNP Missense_Mutation 11 48511074 G T 48 76 GBM TCGA-06-0744 OR4A47 SNP Missense_Mutation 11 48510526 T C 56 66 GBM TCGA-14-3476 OR4A47 SNP Missense_Mutation 11 48511019 C A 18 57 LUAD TCGA-17-Z031 OR4A47 SNP Missense_Mutation 11 48510568 T G 52 59 LUAD TCGA-17-Z049 OR4A47 SNP Missense_Mutation 11 48511077 G A 44 60 LUAD TCGA-17-Z060 OR4A47 SNP Missense_Mutation 11 48510588 G C 35 52 LUSC TCGA-18-3409 OR4A47 SNP Silent 11 48511133 C T 30 52 OV TCGA-24-1422 OR4A47 SNP Missense_Mutation 11 48510886 C T 22 64 GBM TCGA-28-2509 OR4A47 SNP Missense_Mutation 11 48510660 G A 39 77 LUSC TCGA-33-4583 OR4A47 SNP Silent 11 48510770 G C 46 55 LUAD TCGA-38-4628 OR4A47 SNP Missense_Mutation 11 48510483 G A 40 44 LUAD TCGA-38-4631 OR4A47 SNP Missense_Mutation 11 48510487 C T 20 52 LUAD TCGA-44-2655 OR4A47 SNP Silent 11 48510590 C A 28 47 LUAD TCGA-44-3918 OR4A47 SNP Missense_Mutation 11 48510594 T A 60 51 LUAD TCGA-44-6774 OR4A47 DNP Missense_Mutation 11 48510784 GG TT 47 67 LUAD TCGA-50-5941 OR4A47 SNP Silent 11 48511136 C T 21 54 LUSC TCGA-51-4079 OR4A47 INS Frame_Shift_Ins 11 48510847 - C 42 62 LUSC TCGA-51-4081 OR4A47 SNP Silent 11 48510836 C A 30 48 LUSC TCGA-66-2759 OR4A47 SNP Silent 11 48510827 T C 64 47 LUSC TCGA-66-2783 OR4A47 SNP Missense_Mutation 11 48511193 A T 13 44 LUAD TCGA-75-6211 OR4A47 SNP Missense_Mutation 11 48511031 A T 3 49 BRCA TCGA-A8-A09I OR4A47 SNP Silent 11 48511196 C A 32 50 CRC TCGA-AA-A010 OR4A47 SNP Missense_Mutation 11 48510780 T C 58 51 CRC TCGA-AG-A002 OR4A47 SNP Missense_Mutation 11 48510852 A T 5 60 UCEC TCGA-AP-A0LM OR4A47 SNP Missense_Mutation 11 48510395 G T 33 49 BRCA TCGA-AR-A251 OR4A47 SNP Missense_Mutation 11 48511007 C A 20 57 UCEC TCGA-B5-A11E OR4A47 SNP Missense_Mutation 11 48511251 G T 33 61 UCEC TCGA-BS-A0UF OR4A47 SNP Silent 11 48510533 C A 28 52 UCEC TCGA-BS-A0UF OR4A47 SNP Missense_Mutation 11 48510546 G T 33 61 HNSC TCGA-CN-4730 OR4A47 SNP Missense_Mutation 11 48510955 C A 28 55 HNSC TCGA-CV-6935 OR4A47 SNP Missense_Mutation 11 48511249 G T 33 47 HNSC TCGA-CV-6961 OR4A47 INS Frame_Shift_Ins 11 48510865 - T 8 56 UCEC TCGA-D1-A0ZO OR4A47 SNP Silent 11 48510665 G A 44 21 BLCA TCGA-DK-A1A3 OR4A47 SNP Missense_Mutation 11 48510885 C G 30 55 BLCA TCGA-DK-A1A5 OR4A47 SNP Nonsense_Mutation 11 48511051 C G 29 55 BLCA TCGA-DK-A2I2 OR4A47 SNP Missense_Mutation 11 48511224 A G 3 70