ClinVar Miner

Submissions for variant NM_006005.3(WFS1):c.2552T>G (p.Met851Arg)

gnomAD frequency: 0.00006  dbSNP: rs758613421
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001961582 SCV002250165 uncertain significance not provided 2022-11-15 criteria provided, single submitter clinical testing This variant has not been reported in the literature in individuals affected with WFS1-related conditions. This variant is present in population databases (rs758613421, gnomAD 0.02%). This sequence change replaces methionine, which is neutral and non-polar, with arginine, which is basic and polar, at codon 851 of the WFS1 protein (p.Met851Arg). 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. Advanced modeling of protein sequence and biophysical properties (such as structural, functional, and spatial information, amino acid conservation, physicochemical variation, residue mobility, and thermodynamic stability) performed at Invitae indicates that this missense variant is not expected to disrupt WFS1 protein function. ClinVar contains an entry for this variant (Variation ID: 1469462).
Fulgent Genetics, Fulgent Genetics RCV002479614 SCV002781070 uncertain significance Cataract 41; Wolfram syndrome 1; Autosomal dominant nonsyndromic hearing loss 6; Type 2 diabetes mellitus; Wolfram-like syndrome 2021-10-19 criteria provided, single submitter clinical testing
GeneDx RCV001961582 SCV004169364 uncertain significance not provided 2023-10-16 criteria provided, single submitter clinical testing In silico analysis supports that this missense variant does not alter protein structure/function; Has not been previously published as pathogenic or benign to our knowledge

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