Additional file 4 of Molecular basis of a new ovine model for human 3M syndrome-2

Additional file 4: Table S4. List of 103 private whole genome sequencing variants identified in an affected lamb (BCRHS3) after filtering based on segregation, predicted protein impact, removal of known SNPs and duplicates.

附加文件4：表S4。本表格收录了103个私有全基因组测序变异位点，这些变异是在患病羔羊（BCRHS3）中，经遗传分离筛选、预测蛋白质影响、移除已知单核苷酸多态性（Single Nucleotide Polymorphism，SNPs）及重复变异后鉴定得到的。