ttype patient gene classification type chr pos ref_allele newbase context65 cons46 MEL MEL-JWCI-WGS-43 CCDC149 SNP Missense_Mutation 4 24854773 G T 33 70 NB NB-2074 CCDC149 SNP Missense_Mutation 4 24836600 C T 25 76 LUAD TCGA-05-4396 CCDC149 SNP Missense_Mutation 4 24878201 C A 23 100 LUAD TCGA-05-4410 CCDC149 SNP Silent 4 24838915 C A 29 46 GBM TCGA-06-0221 CCDC149 SNP Missense_Mutation 4 24838869 C T 27 100 LUAD TCGA-17-Z022 CCDC149 SNP Missense_Mutation 4 24838087 G T 35 61 GBM TCGA-76-6656 CCDC149 SNP Missense_Mutation 4 24878210 T C 52 90 CRC TCGA-AA-3949 CCDC149 SNP Silent 4 24839844 G A 38 38 CRC TCGA-AA-A00N CCDC149 SNP Missense_Mutation 4 24839881 G A 40 100 UCEC TCGA-AP-A054 CCDC149 SNP Silent 4 24854703 G A 38 28 UCEC TCGA-AP-A059 CCDC149 SNP Missense_Mutation 4 24878171 T C 57 77 UCEC TCGA-AP-A0LM CCDC149 SNP Missense_Mutation 4 24839809 A G 5 93 KIRC TCGA-B0-4815 CCDC149 SNP Silent 4 24810062 G A 40 41 UCEC TCGA-B5-A0JY CCDC149 SNP Missense_Mutation 4 24839827 G A 42 100 UCEC TCGA-B5-A11U CCDC149 SNP Missense_Mutation 4 24810258 C A 24 62 UCEC TCGA-BS-A0UA CCDC149 DEL Frame_Shift_Del 4 24838064 T - 52 50 UCEC TCGA-BS-A0UF CCDC149 SNP Missense_Mutation 4 24824158 A C 4 69 HNSC TCGA-CR-7377 CCDC149 SNP Missense_Mutation 4 24854761 T C 52 65