ClinVar Miner

Submissions for variant NM_147686.4(TRAF3IP2):c.1021C>G (p.Gln341Glu)

dbSNP: rs1239436121
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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 RCV001903252 SCV002164881 uncertain significance Candidiasis, familial, 8 2022-09-07 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 (SIFT, PolyPhen-2, Align-GVGD) all suggest that this variant is likely to be tolerated. ClinVar contains an entry for this variant (Variation ID: 1396934). This variant has not been reported in the literature in individuals affected with TRAF3IP2-related conditions. This variant is present in population databases (no rsID available, gnomAD 0.0009%). This sequence change replaces glutamine, which is neutral and polar, with glutamic acid, which is acidic and polar, at codon 341 of the TRAF3IP2 protein (p.Gln341Glu).

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