Extended Data Table 3 Shared splicing outlier events

From: De novo variants in the RNU4-2 snRNA cause a frequent neurodevelopmental syndrome

  1. Splicing outlier events detected by FRASER2 that are shared between two or more individuals with RNU4-2 variants. None of the events were observed in any of the 378 control individuals. *Genes identified as associated with NDD in Fu et al. Nature Genetics 202322 (PubMed ID 35982160). DDG2P: Developmental disorders gene 2 phenotype database.
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