ttype patient gene classification type chr pos ref_allele newbase context65 cons46 LUAD LUAD-D02185 LMAN2L SNP Missense_Mutation 2 97403716 T A 64 59 LUAD LUAD-RT-S01707 LMAN2L SNP Silent 2 97373011 G A 42 55 MEL ME020 LMAN2L SNP Missense_Mutation 2 97399270 C G 30 86 MEL ME044 LMAN2L DNP Missense_Mutation 2 97377439 GG AA 43 54 GBM TCGA-14-0871 LMAN2L SNP Missense_Mutation 2 97400183 G C 34 71 LUAD TCGA-91-6836 LMAN2L SNP Silent 2 97405754 A T 5 44 UCEC TCGA-AP-A051 LMAN2L SNP Missense_Mutation 2 97373561 T G 50 88 UCEC TCGA-AP-A051 LMAN2L SNP Missense_Mutation 2 97403763 T C 63 68 UCEC TCGA-AP-A059 LMAN2L SNP Missense_Mutation 2 97377498 C A 30 100 UCEC TCGA-AP-A059 LMAN2L SNP Missense_Mutation 2 97405695 A G 11 71 BRCA TCGA-AR-A251 LMAN2L SNP Silent 2 97405748 C G 19 70 UCEC TCGA-AX-A0J1 LMAN2L SNP Missense_Mutation 2 97373088 C T 19 64 UCEC TCGA-AX-A0J1 LMAN2L SNP Missense_Mutation 2 97377666 C A 28 100 UCEC TCGA-BS-A0TC LMAN2L SNP Nonsense_Mutation 2 97400201 C A 32 75 UCEC TCGA-BS-A0UV LMAN2L SNP Missense_Mutation 2 97377656 C T 27 100 BLCA TCGA-BT-A2LA LMAN2L SNP Missense_Mutation 2 97405625 C G 29 54 HNSC TCGA-CR-6472 LMAN2L SNP Missense_Mutation 2 97400156 C G 30 51 HNSC TCGA-CR-7390 LMAN2L SNP Missense_Mutation 2 97377727 G A 40 53 UCEC TCGA-D1-A16E LMAN2L SNP Splice_site 2 97377602 G A 40 88 BLCA TCGA-DK-A1AB LMAN2L SNP Missense_Mutation 2 97373526 C G 30 65 CARC Carc-H55 LMAN2L SNP Missense_Mutation 2 97403788 A T 2 52