ClinVar Miner

Submissions for variant NC_000005.9:g.(?_87976333)_(88057095_?)del

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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 RCV004580499 SCV005063030 uncertain significance Intellectual disability, autosomal dominant 20 2019-12-21 criteria provided, single submitter clinical testing Experimental studies and prediction algorithms are not available or were not evaluated, and the functional significance of this variant is currently unknown. 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. This variant has not been reported in the literature in individuals with MEF2C-related conditions. This variant results in the deletion of exon(s) 5-11 and part of exon 4 (c.309_*42088del) of the MEF2C gene. While this is not anticipated to result in nonsense mediated decay, it likely alters RNA splicing and results in a disrupted protein product.

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