Additional file 1 of Performance of in silico prediction tools for the classification of rare BRCA1/2 missense variants in clinical diagnostics
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Table S1. List of all variants (n=236) from the Classified Variant Set, including reference, functional impact and number of families affected within the cohort of patients from the German Consortium of Hereditary Breast and Ovarian Cancer (as of September 2016). (XLSX 28 kb)
补充表S1：分类变异集（Classified Variant Set）中全部236个变异位点的列表，涵盖参考信息、功能影响，以及2016年9月时来自德国遗传性乳腺癌和卵巢癌联盟（German Consortium of Hereditary Breast and Ovarian Cancer）的患者队列中受该变异影响的家系数目。（XLSX格式，28 KB）
创建时间：
2018-03-27
