ClinVar Miner

Submissions for variant NM_001366385.1(CARD14):c.376G>C (p.Glu126Gln)

dbSNP: rs377568726
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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 RCV001884666 SCV002158105 uncertain significance Pityriasis rubra pilaris; Psoriasis 2 2022-12-15 criteria provided, single submitter clinical testing ClinVar contains an entry for this variant (Variation ID: 1393957). 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. 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 not expected to disrupt CARD14 protein function. This variant has not been reported in the literature in individuals affected with CARD14-related conditions. This variant is not present in population databases (gnomAD no frequency). This sequence change replaces glutamic acid, which is acidic and polar, with glutamine, which is neutral and polar, at codon 126 of the CARD14 protein (p.Glu126Gln).

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