ttype patient gene classification type chr pos ref_allele newbase context65 cons46 LUAD LUAD-TJW61 GFI1B SNP Silent 9 135863717 C A 21 76 MEL MEL-JWCI-WGS-1 GFI1B SNP Silent 9 135863687 C T 24 48 MM MM-0424 GFI1B SNP Silent 9 135862760 G A 39 36 GBM TCGA-06-6695 GFI1B SNP Missense_Mutation 9 135866288 G A 39 97 LUAD TCGA-17-Z031 GFI1B SNP Missense_Mutation 9 135862731 C A 24 51 LUAD TCGA-17-Z060 GFI1B SNP Missense_Mutation 9 135863743 A T 6 58 GBM TCGA-26-5133 GFI1B SNP Missense_Mutation 9 135863634 G A 37 71 LUSC TCGA-33-4566 GFI1B SNP Missense_Mutation 9 135862794 G T 42 51 LUSC TCGA-33-4583 GFI1B SNP Missense_Mutation 9 135862758 C A 26 51 LUSC TCGA-33-6737 GFI1B SNP Missense_Mutation 9 135866411 C T 23 97 LUSC TCGA-37-5819 GFI1B SNP Missense_Mutation 9 135863634 G T 37 71 LUAD TCGA-38-4631 GFI1B SNP Silent 9 135864468 G T 42 46 LUSC TCGA-60-2723 GFI1B SNP Silent 9 135863681 C A 21 50 LUAD TCGA-73-4666 GFI1B DNP Missense_Mutation 9 135865147 CG TT 23 63 CRC TCGA-AA-3864 GFI1B SNP Missense_Mutation 9 135866388 G A 38 97 CRC TCGA-AA-A01Z GFI1B SNP Silent 9 135862799 G A 39 37 CRC TCGA-AG-A002 GFI1B SNP Missense_Mutation 9 135864453 C A 32 64 CRC TCGA-AG-A002 GFI1B SNP Missense_Mutation 9 135866422 G T 34 68 UCEC TCGA-AP-A056 GFI1B SNP Silent 9 135864540 C T 31 50 KIRC TCGA-B0-5695 GFI1B SNP Missense_Mutation 9 135863634 G T 37 71 UCEC TCGA-BS-A0UV GFI1B SNP Silent 9 135864471 C T 31 45 HNSC TCGA-CV-7089 GFI1B SNP Missense_Mutation 9 135862790 G C 41 60 UCEC TCGA-D1-A15X GFI1B SNP Missense_Mutation 9 135865264 G A 37 96 UCEC TCGA-D1-A17H GFI1B SNP Missense_Mutation 9 135866405 C T 27 58 BLCA TCGA-G2-A2EK GFI1B SNP Missense_Mutation 9 135866388 G A 38 97