ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-931 ORM1 SNP Missense_Mutation 9 117087109 G C 35 49 LUAD LUAD-S01331 ORM1 SNP Missense_Mutation 9 117094175 C G 22 50 MEL MEL-Ma-Mel-114 ORM1 SNP Splice_site 9 117087072 G A 43 34 MM MM-0604 ORM1 SNP Missense_Mutation 9 117085980 G A 37 54 LUAD TCGA-05-4397 ORM1 SNP Missense_Mutation 9 117086000 T G 58 36 LUAD TCGA-50-5066 ORM1 SNP Missense_Mutation 9 117086345 A T 9 52 LUAD TCGA-50-5930 ORM1 SNP Missense_Mutation 9 117087141 G T 40 46 CRC TCGA-AA-3864 ORM1 SNP Missense_Mutation 9 117087392 G A 38 54 CRC TCGA-AA-A00N ORM1 SNP Silent 9 117086077 C T 18 55 CRC TCGA-AA-A00N ORM1 SNP Silent 9 117087089 C T 31 42 CRC TCGA-AG-A002 ORM1 SNP Missense_Mutation 9 117087090 G A 38 56 BRCA TCGA-AN-A0AL ORM1 DEL Frame_Shift_Del 9 117085806 CCTGCATGCG - 30 49 UCEC TCGA-AP-A056 ORM1 SNP Missense_Mutation 9 117085972 G A 39 24 UCEC TCGA-AP-A059 ORM1 SNP Missense_Mutation 9 117087354 G T 34 53 UCEC TCGA-B5-A0JY ORM1 SNP Silent 9 117086053 G A 35 35 UCEC TCGA-B5-A0K7 ORM1 SNP Missense_Mutation 9 117085972 G A 39 24 UCEC TCGA-B5-A11N ORM1 SNP Missense_Mutation 9 117086082 C T 18 74 UCEC TCGA-B5-A1MY ORM1 SNP Missense_Mutation 9 117087347 C A 18 62 HNSC TCGA-CV-5431 ORM1 SNP Missense_Mutation 9 117087155 G C 33 56 UCEC TCGA-D1-A103 ORM1 SNP Splice_site 9 117086367 C T 19 34