ClinVar Miner

Submissions for variant NM_005445.4(SMC3):c.3254G>C (p.Ser1085Thr)

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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 RCV005124918 SCV005745939 uncertain significance Cornelia de Lange syndrome 3 2024-11-27 criteria provided, single submitter clinical testing This sequence change replaces serine, which is neutral and polar, with threonine, which is neutral and polar, at codon 1085 of the SMC3 protein (p.Ser1085Thr). This variant is present in population databases (rs760275709, gnomAD 0.003%). This variant has not been reported in the literature in individuals affected with SMC3-related conditions. Invitae Evidence Modeling of protein sequence and biophysical properties (such as structural, functional, and spatial information, amino acid conservation, physicochemical variation, residue mobility, and thermodynamic stability) has been performed for this missense variant. However, the output from this modeling did not meet the statistical confidence thresholds required to predict the impact of this variant on SMC3 protein function. 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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