ClinVar Miner

Submissions for variant NM_001322934.2(NFKB2):c.292C>A (p.His98Asn)

dbSNP: rs1589859604
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000816983 SCV000957516 uncertain significance Immunodeficiency, common variable, 10 2018-11-17 criteria provided, single submitter clinical testing 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. Algorithms developed to predict the effect of missense changes on protein structure and function are either unavailable or do not agree on the potential impact of this missense change (SIFT: "Deleterious"; PolyPhen-2: "Benign"; Align-GVGD: "Class C0"). This variant has not been reported in the literature in individuals with NFKB2-related disease. This variant is not present in population databases (ExAC no frequency). This sequence change replaces histidine with asparagine at codon 98 of the NFKB2 protein (p.His98Asn). The histidine residue is highly conserved and there is a small physicochemical difference between histidine and asparagine.

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