ttype patient gene classification type chr pos ref_allele newbase context65 cons46 MEL ME044 CDC42EP4 SNP Silent 17 71281713 G A 43 53 MEL MEL-JWCI-WGS-39 CDC42EP4 SNP Missense_Mutation 17 71281958 C T 30 75 MEL MEL-Ma-Mel-48 CDC42EP4 SNP Silent 17 71281815 G A 43 36 LUAD TCGA-05-4410 CDC42EP4 SNP Missense_Mutation 17 71281726 C A 23 53 GBM TCGA-06-0219 CDC42EP4 SNP Missense_Mutation 17 71282053 G A 42 57 LUAD TCGA-38-4625 CDC42EP4 SNP Silent 17 71282454 G A 38 44 LUSC TCGA-51-4081 CDC42EP4 SNP Missense_Mutation 17 71281750 C A 27 65 LUSC TCGA-60-2719 CDC42EP4 SNP Missense_Mutation 17 71281876 T C 57 17 LUSC TCGA-66-2781 CDC42EP4 SNP Missense_Mutation 17 71282411 T C 55 55 LUSC TCGA-66-2781 CDC42EP4 SNP Silent 17 71282412 G C 46 57 UCEC TCGA-A5-A0G9 CDC42EP4 SNP Silent 17 71282169 C T 23 37 CRC TCGA-AA-3949 CDC42EP4 SNP Missense_Mutation 17 71282504 C T 27 98 UCEC TCGA-AP-A056 CDC42EP4 SNP Missense_Mutation 17 71281904 C T 27 47 UCEC TCGA-BG-A18B CDC42EP4 SNP Nonsense_Mutation 17 71282585 G A 39 74 UCEC TCGA-BS-A0UV CDC42EP4 SNP Silent 17 71281908 G A 38 59 HNSC TCGA-CN-4739 CDC42EP4 SNP Missense_Mutation 17 71282368 G A 37 97 HNSC TCGA-CR-6472 CDC42EP4 SNP Silent 17 71281968 G A 45 79 BLCA TCGA-CU-A0YR CDC42EP4 SNP Silent 17 71281971 G A 46 62 HNSC TCGA-CV-5979 CDC42EP4 SNP Missense_Mutation 17 71282113 T C 58 66 UCEC TCGA-D1-A17D CDC42EP4 SNP Missense_Mutation 17 71282413 C T 27 68