ClinVar Miner

Submissions for variant NM_001366385.1(CARD14):c.827C>A (p.Ser276Ter)

gnomAD frequency: 0.00006  dbSNP: rs149318654
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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 RCV000695378 SCV000823873 uncertain significance Pityriasis rubra pilaris; Psoriasis 2 2023-11-27 criteria provided, single submitter clinical testing This sequence change creates a premature translational stop signal (p.Ser276*) in the CARD14 gene. It is expected to result in an absent or disrupted protein product. However, the current clinical and genetic evidence is not sufficient to establish whether loss-of-function variants in CARD14 cause disease. This variant is present in population databases (rs149318654, gnomAD 0.03%). This variant has not been reported in the literature in individuals affected with CARD14-related conditions. ClinVar contains an entry for this variant (Variation ID: 573655). 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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