ttype patient gene classification type chr pos ref_allele newbase context65 cons46 LUAD LUAD-B01811 NPS SNP Silent 10 129350774 C A 21 51 MEL MEL-JWCI-14 NPS SNP Missense_Mutation 10 129350899 C T 29 52 MEL MEL-JWCI-WGS-1 NPS SNP Missense_Mutation 10 129347817 C T 30 85 MEL MEL-JWCI-WGS-39 NPS DNP Missense_Mutation 10 129350842 CC TT 30 86 MEL MEL-JWCI-WGS-7 NPS SNP Missense_Mutation 10 129350881 C T 30 86 LUAD TCGA-05-4396 NPS SNP Missense_Mutation 10 129347775 C A 24 54 LUAD TCGA-05-4432 NPS SNP Missense_Mutation 10 129350781 G C 41 74 LUSC TCGA-34-2596 NPS INS Frame_Shift_Ins 10 129350870 - A 45 58 LUAD TCGA-35-4122 NPS SNP Nonsense_Mutation 10 129350835 A T 9 80 LUSC TCGA-60-2722 NPS SNP Missense_Mutation 10 129350859 G C 47 73 UCEC TCGA-A5-A0GP NPS SNP Missense_Mutation 10 129350873 A C 1 80 UCEC TCGA-AP-A0LM NPS SNP Missense_Mutation 10 129350876 A C 1 62 UCEC TCGA-B5-A0JY NPS SNP Missense_Mutation 10 129350776 G T 33 63 HNSC TCGA-BB-7862 NPS SNP Silent 10 129347783 G T 48 57 UCEC TCGA-D1-A103 NPS SNP Missense_Mutation 10 129347803 T C 59 54 UCEC TCGA-D1-A16X NPS SNP Nonsense_Mutation 10 129350793 G T 33 57 CARC Carc-H54 NPS SNP Missense_Mutation 10 129350839 G T 35 86