ttype patient gene classification type chr pos ref_allele newbase context65 cons46 MEL MEL-JWCI-WGS-8 LRRC58 SNP Missense_Mutation 3 120054732 G A 33 59 MEL MEL-Ma-Mel-86 LRRC58 SNP Missense_Mutation 3 120054735 G A 35 91 MM MM-0338 LRRC58 SNP Synonymous 3 120053755 A G 13 54 MM MM-0338 LRRC58 SNP Synonymous 3 120053860 A G 13 56 NB NB-1599 LRRC58 INS Frame_Shift_Ins 3 120067981 - C 54 64 LUAD TCGA-05-4398 LRRC58 SNP Missense_Mutation 3 120050100 C G 32 98 LUAD TCGA-44-6776 LRRC58 SNP Missense_Mutation 3 120054769 T C 51 84 LUAD TCGA-50-5941 LRRC58 SNP Silent 3 120053875 C T 21 82 LUSC TCGA-66-2744 LRRC58 SNP Missense_Mutation 3 120054684 G T 35 91 LUSC TCGA-70-6723 LRRC58 SNP Missense_Mutation 3 120053955 T A 63 88 CRC TCGA-AA-3977 LRRC58 SNP Nonsense_Mutation 3 120053901 C A 32 95 CRC TCGA-AA-A00N LRRC58 SNP Missense_Mutation 3 120053952 T G 61 88 AML TCGA-AB-2877 LRRC58 SNP Missense_Mutation 3 120050085 C T 17 75 UCEC TCGA-AP-A056 LRRC58 SNP Missense_Mutation 3 120053798 C T 31 73 UCEC TCGA-AP-A0LM LRRC58 SNP Missense_Mutation 3 120054684 G T 35 91 HNSC TCGA-CR-7367 LRRC58 SNP Silent 3 120053967 G A 35 72 HNSC TCGA-DQ-7592 LRRC58 SNP Nonsense_Mutation 3 120053938 A C 12 62