ClinVar Miner

Submissions for variant NM_000203.5(IDUA):c.247C>T (p.Arg83Cys)

dbSNP: rs771733089
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001041087 SCV001204682 uncertain significance Mucopolysaccharidosis type 1 2022-02-05 criteria provided, single submitter clinical testing This sequence change replaces arginine, which is basic and polar, with cysteine, which is neutral and slightly polar, at codon 83 of the IDUA protein (p.Arg83Cys). This variant is present in population databases (rs771733089, gnomAD 0.01%). This variant has not been reported in the literature in individuals affected with IDUA-related conditions. ClinVar contains an entry for this variant (Variation ID: 839353). Algorithms developed to predict the effect of missense changes on protein structure and function are either unavailable or do not agree on the potential impact of this missense change (SIFT: "Tolerated"; PolyPhen-2: "Possibly Damaging"; Align-GVGD: "Class C0"). 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.
GeneDx RCV001772227 SCV002001378 uncertain significance not provided 2020-12-28 criteria provided, single submitter clinical testing Has not been previously published as pathogenic or benign to our knowledge; Not observed at a significant frequency in large population cohorts (Lek et al., 2016); In silico analysis supports that this missense variant has a deleterious effect on protein structure/function
Revvity Omics, Revvity RCV001772227 SCV003809919 uncertain significance not provided 2023-01-17 criteria provided, single submitter clinical testing
Natera, Inc. RCV001041087 SCV002083091 uncertain significance Mucopolysaccharidosis type 1 2021-04-02 no assertion criteria provided clinical testing

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