ttype patient gene classification type chr pos ref_allele newbase context65 cons46 HNSC HN_00076 MCOLN1 SNP Missense 19 7593104 C T 21 56 LUAD LUAD-B01246 MCOLN1 SNP Missense_Mutation 19 7593738 G T 41 69 LUAD LUAD-NYU282 MCOLN1 SNP Silent 19 7593091 G T 47 51 LUAD LUAD-RT-S01818 MCOLN1 SNP Missense_Mutation 19 7589934 A T 10 63 LUAD LUAD-S00486 MCOLN1 SNP Missense_Mutation 19 7593777 A G 4 87 MEL ME009 MCOLN1 SNP Missense_Mutation 19 7593780 G A 42 81 MEL ME011 MCOLN1 SNP Missense_Mutation 19 7592424 C T 22 85 MEL MEL-13537 MCOLN1 SNP Missense_Mutation 19 7591452 G A 39 51 MEL MEL-Ma-Mel-08a MCOLN1 SNP Missense_Mutation 19 7592442 C T 23 42 MEL MEL-Ma-Mel-36 MCOLN1 SNP Missense_Mutation 19 7589912 C T 30 48 MEL MEL-Ma-Mel-48 MCOLN1 SNP Missense_Mutation 19 7589868 C T 22 74 MEL MEL-Ma-Mel-48 MCOLN1 SNP Missense_Mutation 19 7593566 C T 24 62 MEL MEL-UKRV-Mel-24 MCOLN1 SNP Missense_Mutation 19 7591692 C T 23 75 LUAD TCGA-05-4396 MCOLN1 SNP Silent 19 7594580 G T 47 61 LUAD TCGA-05-4397 MCOLN1 SNP Silent 19 7589950 C G 29 65 GBM TCGA-12-0688 MCOLN1 SNP Missense_Mutation 19 7591685 G A 40 46 GBM TCGA-14-0862 MCOLN1 SNP Splice_Site 19 7593590 G A 40 92 LUAD TCGA-17-Z001 MCOLN1 SNP Silent 19 7593514 G T 47 52 LUAD TCGA-50-5044 MCOLN1 SNP Missense_Mutation 19 7593840 T C 50 86 BRCA TCGA-A2-A0D2 MCOLN1 SNP Missense_Mutation 19 7598649 C G 22 45 BRCA TCGA-A8-A07C MCOLN1 SNP Silent 19 7593049 G A 40 30 CRC TCGA-AA-3864 MCOLN1 SNP Missense_Mutation 19 7593735 G A 39 62 CRC TCGA-AA-3947 MCOLN1 SNP Missense_Mutation 19 7591778 C T 19 39 CRC TCGA-AA-3966 MCOLN1 SNP Missense_Mutation 19 7593557 C T 23 92 CRC TCGA-AG-A002 MCOLN1 SNP Missense_Mutation 19 7593485 G T 33 78 CRC TCGA-AG-A02N MCOLN1 SNP Silent 19 7591677 C A 23 55 BRCA TCGA-AO-A124 MCOLN1 SNP Missense_Mutation 19 7589918 C A 18 54 UCEC TCGA-AP-A051 MCOLN1 SNP Missense_Mutation 19 7591758 G T 35 92 UCEC TCGA-AP-A051 MCOLN1 SNP Splice_site 19 7593142 C T 19 44 UCEC TCGA-AP-A059 MCOLN1 SNP Silent 19 7592591 C T 30 62 UCEC TCGA-AP-A059 MCOLN1 SNP Splice_site 19 7593856 G T 35 93 UCEC TCGA-AP-A0LM MCOLN1 SNP Splice_Site 19 7593144 G A 44 92 UCEC TCGA-AP-A0LM MCOLN1 SNP Silent 19 7593847 C T 31 47 UCEC TCGA-AP-A0LM MCOLN1 SNP Missense_Mutation 19 7594522 T G 62 85 UCEC TCGA-B5-A0JY MCOLN1 SNP Missense_Mutation 19 7591779 G A 37 92 UCEC TCGA-B5-A11E MCOLN1 SNP Missense_Mutation 19 7591421 G A 39 61 UCEC TCGA-BS-A0UF MCOLN1 SNP Missense_Mutation 19 7598493 C T 23 76 UCEC TCGA-BS-A0UV MCOLN1 SNP Missense_Mutation 19 7589945 C T 31 67 UCEC TCGA-BS-A0UV MCOLN1 SNP Missense_Mutation 19 7592790 A C 13 84 BLCA TCGA-BT-A0YX MCOLN1 SNP Nonsense_Mutation 19 7591755 C T 23 66 KIRC TCGA-CJ-5672 MCOLN1 DEL Frame_Shift_Del 19 7589957 T - 56 85 HNSC TCGA-CR-7388 MCOLN1 SNP Missense_Mutation 19 7594574 C G 31 48 HNSC TCGA-CV-7099 MCOLN1 SNP Missense_Mutation 19 7593497 C T 23 92 UCEC TCGA-D1-A103 MCOLN1 SNP Missense_Mutation 19 7589892 C T 27 39 UCEC TCGA-D1-A103 MCOLN1 SNP Missense_Mutation 19 7591450 G A 38 37 UCEC TCGA-D1-A167 MCOLN1 SNP Splice_site 19 7593142 C T 19 44 BRCA TCGA-E2-A10E MCOLN1 SNP Missense_Mutation 19 7591479 A T 8 58 BLCA TCGA-G2-A2EL MCOLN1 SNP Missense_Mutation 19 7591788 G C 45 76 HNSC TCGA-HD-7917 MCOLN1 SNP Missense_Mutation 19 7589892 C T 27 39