ttype patient gene classification type chr pos ref_allele newbase context65 cons46 BRCA BR-MEX-110 SRFBP1 SNP Missense_Mutation 5 121356038 C T 32 56 ESO ESO-669 SRFBP1 SNP Silent 5 121356441 C T 21 50 LUAD LUAD-B02077 SRFBP1 SNP Missense_Mutation 5 121356338 C T 29 82 LUAD LUAD-CHTN-Z4716A SRFBP1 SNP Missense_Mutation 5 121356014 C T 24 50 LUAD LUAD-D02085 SRFBP1 SNP Missense_Mutation 5 121356166 A C 13 53 MEL ME048 SRFBP1 SNP Missense_Mutation 5 121362735 C T 30 95 MM MM-0510 SRFBP1 SNP Nonsense_Mutation 5 121355882 C G 29 74 NB NB-1199 SRFBP1 SNP Missense_Mutation 5 121355902 T G 64 63 LUAD TCGA-17-Z062 SRFBP1 SNP Silent 5 121355925 C T 29 50 LUSC TCGA-18-3409 SRFBP1 SNP Missense_Mutation 5 121356383 A T 12 51 LUSC TCGA-37-5819 SRFBP1 SNP Missense_Mutation 5 121356226 G C 33 85 LUAD TCGA-49-4486 SRFBP1 SNP Silent 5 121355964 G A 33 65 LUAD TCGA-50-6594 SRFBP1 SNP Silent 5 121311046 G T 43 33 LUAD TCGA-64-5781 SRFBP1 SNP Missense_Mutation 5 121356095 C T 24 64 LUSC TCGA-66-2771 SRFBP1 SNP Missense_Mutation 5 121356289 A G 8 62 UCEC TCGA-A5-A0G9 SRFBP1 SNP Missense_Mutation 5 121356274 G A 39 81 CRC TCGA-AA-3672 SRFBP1 SNP Silent 5 121354991 C T 20 50 CRC TCGA-AG-3892 SRFBP1 SNP Missense_Mutation 5 121356324 T G 57 55 CRC TCGA-AG-A002 SRFBP1 SNP Missense_Mutation 5 121355985 G T 35 51 CRC TCGA-AG-A002 SRFBP1 SNP Missense_Mutation 5 121356488 G T 34 53 CRC TCGA-AG-A002 SRFBP1 SNP Nonsense_Mutation 5 121362759 C T 27 61 UCEC TCGA-AP-A051 SRFBP1 SNP Missense_Mutation 5 121355908 C T 27 56 UCEC TCGA-AP-A056 SRFBP1 SNP Missense_Mutation 5 121356184 G A 33 56 UCEC TCGA-AP-A059 SRFBP1 SNP Missense_Mutation 5 121356235 T A 60 90 UCEC TCGA-AP-A0LM SRFBP1 SNP Missense_Mutation 5 121356074 C A 30 50 UCEC TCGA-BS-A0UF SRFBP1 SNP Missense_Mutation 5 121309919 G T 33 58 UCEC TCGA-BS-A0UF SRFBP1 SNP Missense_Mutation 5 121356127 A G 2 50 HNSC TCGA-CR-7371 SRFBP1 SNP Missense_Mutation 5 121355833 T A 58 51 HNSC TCGA-CV-7099 SRFBP1 SNP Nonsense_Mutation 5 121309963 C T 23 56