ttype patient gene classification type chr pos ref_allele newbase context65 cons46 MM MM-0598 MRPS10 SNP Missense_Mutation 6 42179631 T G 51 75 MM MM-0598 MRPS10 SNP Missense_Mutation 6 42179649 T C 52 47 LUAD TCGA-44-6778 MRPS10 SNP Missense_Mutation 6 42185578 G A 38 78 UCEC TCGA-AX-A0J1 MRPS10 SNP Silent 6 42181891 G A 40 44 HNSC TCGA-BA-6868 MRPS10 SNP Missense_Mutation 6 42179587 C G 24 67 UCEC TCGA-BS-A0UF MRPS10 SNP Nonsense_Mutation 6 42179541 C A 32 96 HNSC TCGA-CN-4726 MRPS10 SNP Missense_Mutation 6 42185571 G A 38 49