ClinVar Miner

Submissions for variant NM_000203.5(IDUA):c.1509_1511del (p.Met504del)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Revvity Omics, Revvity RCV003487914 SCV004235549 uncertain significance not provided 2023-03-22 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003755047 SCV004463099 uncertain significance Mucopolysaccharidosis type 1 2023-06-03 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. Experimental studies and prediction algorithms are not available or were not evaluated, and the functional significance of this variant is currently unknown. This variant has not been reported in the literature in individuals affected with IDUA-related conditions. This variant is not present in population databases (gnomAD no frequency). This variant, c.1509_1511del, results in the deletion of 1 amino acid(s) of the IDUA protein (p.Met504del), but otherwise preserves the integrity of the reading frame.

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