ttype patient gene classification type chr pos ref_allele newbase context65 cons46 MEL MEL-Ma-Mel-53 ROPN1B SNP Silent 3 125690999 C T 30 53 LUAD TCGA-05-4250 ROPN1B SNP Missense_Mutation 3 125694456 C A 32 66 LUAD TCGA-17-Z026 ROPN1B SNP Missense_Mutation 3 125701153 C T 29 63 LUSC TCGA-39-5027 ROPN1B SNP Silent 3 125701208 C T 32 55 BRCA TCGA-A8-A07W ROPN1B SNP Silent 3 125690996 C T 29 52 BRCA TCGA-A8-A07W ROPN1B SNP Missense_Mutation 3 125694476 A T 13 64 CRC TCGA-AA-3856 ROPN1B SNP Missense_Mutation 3 125690980 C A 27 68 CRC TCGA-AG-A002 ROPN1B SNP Silent 3 125694436 G A 38 50 UCEC TCGA-AP-A051 ROPN1B SNP Splice_Site 3 125701290 T C 57 62 BRCA TCGA-AR-A250 ROPN1B SNP Silent 3 125694466 C T 31 22 KIRC TCGA-B0-5701 ROPN1B SNP Silent 3 125702160 G A 36 46 BRCA TCGA-C8-A12T ROPN1B SNP Missense_Mutation 3 125701143 G A 45 63 KIRC TCGA-CJ-5682 ROPN1B SNP Missense_Mutation 3 125690967 G T 34 68 HNSC TCGA-CV-7095 ROPN1B SNP Missense_Mutation 3 125694519 C G 32 56 UCEC TCGA-D1-A163 ROPN1B SNP Silent 3 125702136 C T 22 52 BLCA TCGA-DK-A3IN ROPN1B SNP Splice_site 3 125690896 C T 29 68