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De novo mutation data sourced from supplementary table 1 from: Lelieveld et al. (2016) Nature Neuroscience 19:1194-1196 doi: 10.1038/nn.4352
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Note that the paper says that the variants were aligned to hg19, but their table of de novo variants is definitely for hg18 (GRCh37).
data frame of de novos, including gene symbol, functional consequence (VEP format), chromosome, nucleotide position and SNV or INDEL type
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