ClinVar Miner

Submissions for variant NM_147686.4(TRAF3IP2):c.1082G>A (p.Cys361Tyr)

gnomAD frequency: 0.00001  dbSNP: rs773316350
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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 RCV001062539 SCV001227346 uncertain significance Candidiasis, familial, 8 2021-09-02 criteria provided, single submitter clinical testing This sequence change replaces cysteine with tyrosine at codon 361 of the TRAF3IP2 protein (p.Cys361Tyr). The cysteine residue is weakly conserved and there is a large physicochemical difference between cysteine and tyrosine. This variant is present in population databases (rs773316350, ExAC 0.001%). 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 output the following: SIFT: "Tolerated"; PolyPhen-2: "Benign"; Align-GVGD: "Class C0". The tyrosine amino acid residue is found in multiple mammalian species, which suggests that this missense change does not adversely affect protein function. 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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