ttype patient gene classification type chr pos ref_allele newbase context65 cons46 HNSC HN_00466 MAP3K8 SNP Missense 10 30748284 G T 38 95 LUAD LUAD-RT-S01840 MAP3K8 SNP Missense_Mutation 10 30747064 G C 33 96 MEL MEL-JWCI-14 MAP3K8 SNP Missense_Mutation 10 30736748 C T 30 80 MEL MEL-JWCI-WGS-12 MAP3K8 SNP Silent 10 30747150 C T 24 49 GBM TCGA-06-0141 MAP3K8 SNP Silent 10 30739369 A G 1 54 LUAD TCGA-17-Z049 MAP3K8 SNP Silent 10 30747105 G A 39 49 LUAD TCGA-17-Z057 MAP3K8 SNP Missense_Mutation 10 30748380 G A 38 63 LUAD TCGA-49-6745 MAP3K8 SNP Nonsense_Mutation 10 30740626 C T 29 68 LUAD TCGA-67-3772 MAP3K8 SNP Silent 10 30748249 G C 45 64 LUAD TCGA-67-3772 MAP3K8 SNP Silent 10 30748321 G C 45 60 UCEC TCGA-A5-A0GH MAP3K8 SNP Missense_Mutation 10 30749641 C T 31 96 CRC TCGA-AA-3555 MAP3K8 SNP Missense_Mutation 10 30739439 G T 45 97 CRC TCGA-AA-3715 MAP3K8 SNP Silent 10 30739282 T C 59 44 CRC TCGA-AA-3811 MAP3K8 SNP Silent 10 30747105 G A 39 49 CRC TCGA-AA-3864 MAP3K8 SNP Silent 10 30747087 G A 38 36 CRC TCGA-AA-3947 MAP3K8 SNP Missense_Mutation 10 30739388 C T 25 97 BRCA TCGA-AN-A0AR MAP3K8 SNP Missense_Mutation 10 30728142 C G 30 86 UCEC TCGA-AP-A051 MAP3K8 SNP Missense_Mutation 10 30749709 G A 38 96 UCEC TCGA-AP-A059 MAP3K8 SNP Missense_Mutation 10 30736868 C T 27 97 UCEC TCGA-AP-A0LM MAP3K8 SNP Missense_Mutation 10 30727964 C A 32 67 UCEC TCGA-AP-A0LM MAP3K8 SNP Missense_Mutation 10 30728172 G A 37 59 UCEC TCGA-AX-A0J0 MAP3K8 SNP Missense_Mutation 10 30727958 G A 41 87 UCEC TCGA-AX-A0J1 MAP3K8 SNP Missense_Mutation 10 30749686 G A 38 96 UCEC TCGA-B5-A0JY MAP3K8 SNP Missense_Mutation 10 30748379 C T 27 63 UCEC TCGA-B5-A0JZ MAP3K8 SNP Missense_Mutation 10 30749707 G C 42 96 HNSC TCGA-BB-4223 MAP3K8 SNP Missense_Mutation 10 30749691 C G 32 79 BRCA TCGA-BH-A0HA MAP3K8 SNP Missense_Mutation 10 30747044 G T 35 96 HNSC TCGA-CN-4730 MAP3K8 SNP Silent 10 30749693 C T 32 54 UCEC TCGA-D1-A0ZQ MAP3K8 SNP Silent 10 30728035 C T 19 36 UCEC TCGA-D1-A103 MAP3K8 SNP Silent 10 30728029 T C 50 50 UCEC TCGA-D1-A15X MAP3K8 SNP Silent 10 30748327 G A 38 44 UCEC TCGA-D1-A177 MAP3K8 SNP Missense_Mutation 10 30747080 G C 43 96