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. Author manuscript; available in PMC: 2019 Jun 1.
Published in final edited form as: Ann Neurol. 2018 May 16;83(6):1133–1146. doi: 10.1002/ana.25243

Figure 5.

Figure 5

Novel and previously reported rare functional variation in SLC35A2. Somatic mutations identified in this study are shown in red, those previously implicated in congenital disorders of glycosylation are shown in green, and those previously implicated in epileptic encephalopathies in blue. Six Polyphen2 probably damaging ultra-rare missense mutations identified in gnomAD in the canonical transcript are shown in yellow.