ttype patient gene classification type chr pos ref_allele newbase context65 cons46 LUAD LUAD-RT-S01702 OR4S1 SNP Missense_Mutation 11 48328207 G A 42 59 LUAD LUAD-S00488 OR4S1 SNP Missense_Mutation 11 48328637 G C 35 79 MEL MEL-JWCI-27 OR4S1 SNP Missense_Mutation 11 48328235 C T 30 77 MEL MEL-JWCI-WGS-12 OR4S1 SNP Missense_Mutation 11 48328397 C T 30 48 MEL MEL-JWCI-WGS-34 OR4S1 SNP Missense_Mutation 11 48328418 C T 30 92 MEL MEL-JWCI-WGS-42 OR4S1 SNP Silent 11 48327864 C T 30 42 MEL MEL-Ma-Mel-67 OR4S1 SNP Missense_Mutation 11 48328211 C T 30 66 MM MM-0553 OR4S1 SNP Silent 11 48328626 C T 32 46 LUAD TCGA-05-5428 OR4S1 SNP Missense_Mutation 11 48328531 A G 8 53 GBM TCGA-06-5417 OR4S1 SNP Missense_Mutation 11 48328474 G T 42 82 OV TCGA-13-0726 OR4S1 SNP Missense_Mutation 11 48328640 A T 2 63 LUAD TCGA-17-Z023 OR4S1 SNP Silent 11 48328563 G T 47 48 LUAD TCGA-17-Z052 OR4S1 SNP Nonsense_Mutation 11 48328542 C A 17 47 LUSC TCGA-18-3414 OR4S1 SNP Silent 11 48328071 C G 32 50 LUSC TCGA-22-5471 OR4S1 SNP Missense_Mutation 11 48328546 C T 31 57 LUSC TCGA-37-4135 OR4S1 SNP Missense_Mutation 11 48328166 C A 17 51 LUAD TCGA-49-6743 OR4S1 SNP Silent 11 48328183 C A 23 48 LUSC TCGA-66-2754 OR4S1 SNP Silent 11 48328449 C T 26 54 LUAD TCGA-73-4662 OR4S1 SNP Nonsense_Mutation 11 48328454 C A 29 55 LUAD TCGA-91-6831 OR4S1 SNP Missense_Mutation 11 48328205 G A 43 51 BRCA TCGA-A8-A07W OR4S1 SNP Missense_Mutation 11 48328672 T C 60 77 CRC TCGA-AA-3977 OR4S1 SNP Missense_Mutation 11 48328086 C A 32 53 CRC TCGA-AA-A00N OR4S1 SNP Silent 11 48328629 T C 49 48 CRC TCGA-AA-A02H OR4S1 SNP Missense_Mutation 11 48328664 G T 35 47 AML TCGA-AB-2808 OR4S1 SNP Silent 11 48328335 T C 59 50 UCEC TCGA-AP-A0LM OR4S1 SNP Silent 11 48327822 T C 63 49 UCEC TCGA-AX-A0J1 OR4S1 SNP Missense_Mutation 11 48328291 G T 33 55 CRC TCGA-AY-4070 OR4S1 SNP Missense_Mutation 11 48327983 G T 48 52 UCEC TCGA-BS-A0UJ OR4S1 SNP Missense_Mutation 11 48328456 T C 50 55 HNSC TCGA-CR-7365 OR4S1 SNP Splice_site 11 48328704 A G 10 75 HNSC TCGA-CR-7370 OR4S1 SNP Silent 11 48327915 C A 29 66 HNSC TCGA-CV-5444 OR4S1 DEL Frame_Shift_Del 11 48328525 C - 26 61 BRCA TCGA-E9-A1R4 OR4S1 SNP Missense_Mutation 11 48328481 C G 30 63 BLCA TCGA-GD-A2C5 OR4S1 SNP Missense_Mutation 11 48328337 C T 25 51