ttype patient gene classification type chr pos ref_allele newbase context65 cons46 LUAD LUAD-E01278 IFNB1 SNP Missense_Mutation 9 21077388 G T 45 48 LUAD LUAD-NYU284 IFNB1 SNP Missense_Mutation 9 21077693 A T 1 58 MEL ME010 IFNB1 SNP Silent 9 21077350 C T 30 57 MEL MEL-JWCI-WGS-39 IFNB1 SNP Missense_Mutation 9 21077649 C T 30 61 LUAD TCGA-05-4398 IFNB1 SNP Missense_Mutation 9 21077760 G T 45 50 LUAD TCGA-05-4417 IFNB1 SNP Missense_Mutation 9 21077501 A G 7 63 LUAD TCGA-05-4424 IFNB1 SNP Missense_Mutation 9 21077762 A G 1 34 OV TCGA-13-1509 IFNB1 SNP Missense_Mutation 9 21077536 A T 8 48 GBM TCGA-19-2619 IFNB1 SNP Silent 9 21077338 G A 45 51 GBM TCGA-27-1834 IFNB1 SNP Missense_Mutation 9 21077465 C A 30 41 LUAD TCGA-50-6592 IFNB1 SNP Missense_Mutation 9 21077565 C T 29 57 LUSC TCGA-60-2698 IFNB1 SNP Missense_Mutation 9 21077455 C G 29 54 LUSC TCGA-60-2720 IFNB1 SNP Missense_Mutation 9 21077471 G A 44 51 CRC TCGA-AA-3710 IFNB1 SNP Missense_Mutation 9 21077312 C T 31 52 UCEC TCGA-AP-A051 IFNB1 SNP Missense_Mutation 9 21077786 C T 30 46 KIRC TCGA-B0-4822 IFNB1 SNP Missense_Mutation 9 21077712 G A 35 66 UCEC TCGA-B5-A11E IFNB1 SNP Missense_Mutation 9 21077444 T G 59 28 BRCA TCGA-BH-A0BZ IFNB1 SNP Silent 9 21077514 G A 33 61 BRCA TCGA-BH-A0HW IFNB1 SNP Missense_Mutation 9 21077643 C T 27 47 KIRC TCGA-BP-4787 IFNB1 SNP Missense_Mutation 9 21077494 T A 64 49 UCEC TCGA-D1-A17Q IFNB1 SNP Missense_Mutation 9 21077435 C A 32 47 UCEC TCGA-D1-A17Q IFNB1 SNP Silent 9 21077806 G T 47 51