ClinVar Miner

Submissions for variant NM_004456.5(EZH2):c.2051G>A (p.Arg684His)

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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 RCV003037266 SCV003440229 uncertain significance Weaver syndrome 2022-09-10 criteria provided, single submitter clinical testing This sequence change replaces arginine, which is basic and polar, with histidine, which is basic and polar, at codon 684 of the EZH2 protein (p.Arg684His). This variant is not present in population databases (gnomAD no frequency). This missense change has been observed in individual(s) with clinical features of EZH2-related conditions and/or Weaver syndrome (PMID: 24214728, 31785789). Advanced modeling of protein sequence and biophysical properties (such as structural, functional, and spatial information, amino acid conservation, physicochemical variation, residue mobility, and thermodynamic stability) performed at Invitae indicates that this missense variant is expected to disrupt EZH2 protein function. This variant disrupts the p.Arg684 amino acid residue in EZH2. Other variant(s) that disrupt this residue have been determined to be pathogenic (PMID: 22190405, 26694085, 29802153). This suggests that this residue is clinically significant, and that variants that disrupt this residue are likely to be disease-causing. 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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