ttype patient gene classification type chr pos ref_allele newbase context65 cons46 DLBCL DLBCL-MAYO_DLBCL_234 MYLIP SNP Silent 6 16144047 G A 39 38 ESO ESO-0280 MYLIP SNP Missense_Mutation 6 16143363 C T 27 49 HNSC HN_01000 MYLIP SNP Synonymous 6 16143972 G A 33 59 LUAD LUAD-NYU776 MYLIP SNP Missense_Mutation 6 16145436 G A 38 68 LUAD LUAD-RT-S01831 MYLIP SNP Missense_Mutation 6 16130852 G T 44 100 LUAD LUAD-YINHD MYLIP SNP Missense_Mutation 6 16141860 A T 16 57 MED MD-144 MYLIP SNP Missense_Mutation 6 16145436 G C 38 68 MED MD-343 MYLIP SNP Missense_Mutation 6 16144067 C T 27 96 MEL ME012 MYLIP SNP Missense_Mutation 6 16144032 G T 45 67 MEL ME050 MYLIP SNP Silent 6 16144083 C T 19 49 MEL MEL-Ma-Mel-59 MYLIP DNP Missense_Mutation 6 16145502 CC TT 22 98 MM MM-0546 MYLIP SNP Silent 6 16129610 G A 37 55 LUAD TCGA-05-4396 MYLIP SNP Missense_Mutation 6 16143393 G T 47 98 LUAD TCGA-05-4396 MYLIP SNP Silent 6 16145414 C A 23 48 GBM TCGA-06-0743 MYLIP SNP Missense_Mutation 6 16143302 A C 4 47 LUSC TCGA-22-1012 MYLIP SNP Silent 6 16144053 C T 27 45 GBM TCGA-28-5216 MYLIP SNP Missense_Mutation 6 16141881 G C 41 97 LUSC TCGA-39-5022 MYLIP SNP Missense_Mutation 6 16130818 G A 45 100 LUAD TCGA-49-4487 MYLIP SNP Nonsense_Mutation 6 16145361 C G 29 88 LUAD TCGA-50-5044 MYLIP SNP Missense_Mutation 6 16130890 C A 21 100 LUAD TCGA-50-5946 MYLIP SNP Missense_Mutation 6 16145328 A G 2 58 LUAD TCGA-50-6594 MYLIP SNP Missense_Mutation 6 16130898 G T 47 80 LUAD TCGA-55-5899 MYLIP SNP Missense_Mutation 6 16130937 G T 36 80 OV TCGA-61-2094 MYLIP SNP Missense_Mutation 6 16143276 G A 41 98 LUSC TCGA-66-2773 MYLIP SNP Missense_Mutation 6 16145463 T C 51 69 LUAD TCGA-67-3771 MYLIP SNP Nonsense_Mutation 6 16143378 C T 25 98 GBM TCGA-76-6282 MYLIP SNP Missense_Mutation 6 16130808 C G 29 50 GBM TCGA-76-6282 MYLIP SNP Silent 6 16130886 C T 32 57 CRC TCGA-AA-3672 MYLIP SNP Silent 6 16144086 A G 8 34 CRC TCGA-AA-3715 MYLIP SNP Silent 6 16145533 C T 27 50 CRC TCGA-AA-3984 MYLIP SNP Silent 6 16145302 C T 27 48 UCEC TCGA-AP-A0LF MYLIP SNP Missense_Mutation 6 16142016 G C 41 97 UCEC TCGA-B5-A0JY MYLIP SNP Silent 6 16145248 A G 1 52 HNSC TCGA-CV-6961 MYLIP SNP Silent 6 16141928 G T 47 64 HNSC TCGA-CV-7089 MYLIP SNP Silent 6 16143386 G T 46 50 KIRC TCGA-CW-5581 MYLIP SNP Missense_Mutation 6 16146960 T C 56 91 BRCA TCGA-D8-A1XS MYLIP SNP Missense_Mutation 6 16145378 T A 55 71