ttype patient gene classification type chr pos ref_allele newbase context65 cons46 BRCA BR-MEX-191 IFNA21 SNP Silent 9 21166243 C T 29 52 LUAD LUAD-S01357 IFNA21 SNP Silent 9 21166605 G A 35 46 MEL ME024 IFNA21 SNP Missense_Mutation 9 21166214 G A 43 48 MEL MEL-13600 IFNA21 SNP Silent 9 21166204 A G 8 29 MEL MEL-Ma-Mel-48 IFNA21 SNP Missense_Mutation 9 21166133 C T 28 57 LUAD TCGA-05-4427 IFNA21 SNP Silent 9 21166573 C A 25 70 GBM TCGA-15-0742 IFNA21 SNP Missense_Mutation 9 21166247 C G 25 74 LUAD TCGA-17-Z046 IFNA21 SNP Missense_Mutation 9 21166424 T A 55 51 LUAD TCGA-38-4625 IFNA21 SNP Missense_Mutation 9 21166379 G A 33 53 LUAD TCGA-49-4510 IFNA21 SNP Silent 9 21166213 G T 43 60 LUAD TCGA-49-4514 IFNA21 SNP Missense_Mutation 9 21166475 C A 32 59 CRC TCGA-AA-A02J IFNA21 SNP Missense_Mutation 9 21166548 G T 33 59 UCEC TCGA-B5-A0JY IFNA21 SNP Missense_Mutation 9 21166075 T G 64 39 KIRC TCGA-BP-5176 IFNA21 SNP Missense_Mutation 9 21166125 C A 25 74 UCEC TCGA-BS-A0UF IFNA21 SNP Silent 9 21166381 G T 33 43 HNSC TCGA-CR-6471 IFNA21 SNP Missense_Mutation 9 21166295 T G 62 54 BRCA TCGA-E2-A1L9 IFNA21 SNP Missense_Mutation 9 21166507 C A 30 48