ttype patient gene classification type chr pos ref_allele newbase context65 cons46 CLL CW139 C1QL3 SNP Silent 10 16562924 G T 39 43 HNSC HN_62756 C1QL3 SNP Synonymous 10 16556596 G A 38 42 OV TCGA-04-1338 C1QL3 SNP Missense_Mutation 10 16556654 C G 20 88 LUAD TCGA-05-4396 C1QL3 SNP Missense_Mutation 10 16556595 C A 23 100 LUSC TCGA-18-3415 C1QL3 SNP Missense_Mutation 10 16562655 T A 51 86 LUSC TCGA-33-4533 C1QL3 SNP Missense_Mutation 10 16563058 G T 34 93 UCEC TCGA-AP-A0LE C1QL3 SNP Missense_Mutation 10 16562694 A C 6 73 HNSC TCGA-BA-6869 C1QL3 SNP Silent 10 16562732 G A 40 72 UCEC TCGA-D1-A0ZP C1QL3 SNP Missense_Mutation 10 16562683 C A 27 93 UCEC TCGA-FI-A2EW C1QL3 SNP Silent 10 16562750 G A 39 52