ClinVar Miner

Submissions for variant NM_182961.4(SYNE1):c.17229T>G (p.Tyr5743Ter) (rs377344899)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000627245 SCV000748236 pathogenic not provided 2018-04-24 criteria provided, single submitter clinical testing The Y5672X variant in the SYNE1 gene has been reported previously in the heterozygous state in an individual withataxia and polyneuropathy (Fogel et al., 2014). This variant is predicted to cause loss of normal protein functioneither through protein truncation or nonsense-mediated mRNA decay. Furthermore, the Y5672X variant is notobserved in large population cohorts (Lek et al., 2016). We interpret Y5672X as a pathogenic variant.

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