ClinVar Miner

Submissions for variant NM_001130965.3(SUN1):c.2168A>C (p.Gln723Pro)

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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 RCV005122724 SCV005737488 uncertain significance Emery-Dreifuss muscular dystrophy 2024-07-01 criteria provided, single submitter clinical testing This sequence change replaces glutamine, which is neutral and polar, with proline, which is neutral and non-polar, at codon 723 of the SUN1 protein (p.Gln723Pro). This variant is present in population databases (rs534832884, gnomAD 0.01%). This variant has not been reported in the literature in individuals affected with SUN1-related conditions. An algorithm developed to predict the effect of missense changes on protein structure and function (PolyPhen-2) suggests that this variant is likely to be disruptive. 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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