ClinVar Miner

Submissions for variant NM_000553.6(WRN):c.3281T>G (p.Val1094Gly)

dbSNP: rs1563377393
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000705901 SCV000834919 uncertain significance Werner syndrome 2018-04-11 criteria provided, single submitter clinical testing In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. Algorithms developed to predict the effect of missense changes on protein structure and function (SIFT, PolyPhen-2, Align-GVGD) all suggest that this variant is likely to be tolerated, but these predictions have not been confirmed by published functional studies and their clinical significance is uncertain. This variant has not been reported in the literature in individuals with WRN-related disease. This variant is not present in population databases (ExAC no frequency). This sequence change replaces valine with glycine at codon 1094 of the WRN protein (p.Val1094Gly). The valine residue is weakly conserved and there is a moderate physicochemical difference between valine and glycine.

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