ClinVar Miner

Submissions for variant NM_003824.4(FADD):c.419G>A (p.Arg140His)

gnomAD frequency: 0.00001  dbSNP: rs1371367785
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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 RCV001327787 SCV001518876 uncertain significance FADD-related immunodeficiency 2021-08-26 criteria provided, single submitter clinical testing This sequence change replaces arginine with histidine at codon 140 of the FADD protein (p.Arg140His). The arginine residue is moderately conserved and there is a small physicochemical difference between arginine and histidine. This variant is not present in population databases (ExAC no frequency). This variant has not been reported in the literature in individuals affected with FADD-related conditions. 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: "Tolerated"; PolyPhen-2: "Possibly Damaging"; Align-GVGD: "Class C0"). 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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