ClinVar Miner

Submissions for variant NM_147686.4(TRAF3IP2):c.1201C>T (p.Arg401Trp)

dbSNP: rs767596361
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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 RCV002024953 SCV002314150 uncertain significance Candidiasis, familial, 8 2021-09-19 criteria provided, single submitter clinical testing This sequence change replaces arginine with tryptophan at codon 401 of the TRAF3IP2 protein (p.Arg401Trp). The arginine residue is highly conserved and there is a moderate physicochemical difference between arginine and tryptophan. This variant is not present in population databases (ExAC no frequency). This variant has not been reported in the literature in individuals affected with TRAF3IP2-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 disruptive. Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant may disrupt the consensus splice site. 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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