ClinVar Miner

Submissions for variant NM_032415.7(CARD11):c.3010T>G (p.Cys1004Gly)

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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 RCV002676084 SCV002989065 uncertain significance Severe combined immunodeficiency due to CARD11 deficiency; BENTA disease 2022-03-26 criteria provided, single submitter clinical testing This sequence change replaces cysteine, which is neutral and slightly polar, with glycine, which is neutral and non-polar, at codon 1004 of the CARD11 protein (p.Cys1004Gly). This variant is present in population databases (rs757199275, gnomAD 0.01%). This variant has not been reported in the literature in individuals affected with CARD11-related conditions. Algorithms developed to predict the effect of missense changes on protein structure and function (SIFT, PolyPhen-2, Align-GVGD) all suggest that this variant is likely to be tolerated. 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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