Additional file 4: Table S3. of Pathogenic variant burden in the ExAC database: an empirical approach to evaluating population data for clinical variant interpretation
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List of clinically relevant transcripts for hereditary cancer, PCD, and cardiology genes. For each gene examined, a single clinically relevant transcript was selected to make NMD predictions. PCD primary ciliary dyskinesia. (XLSX 47 kb)
创建时间：
2017-02-07
