ClinVar Miner

Submissions for variant NM_000203.5(IDUA):c.199A>G (p.Ser67Gly)

dbSNP: rs370442463
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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 RCV001950072 SCV002201094 uncertain significance Mucopolysaccharidosis type 1 2021-11-06 criteria provided, single submitter clinical testing This sequence change replaces serine, which is neutral and polar, with glycine, which is neutral and non-polar, at codon 67 of the IDUA protein (p.Ser67Gly). This variant is present in population databases (rs370442463, gnomAD 0.02%). This variant has not been reported in the literature in individuals affected with IDUA-related conditions. 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. 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.

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