ClinVar Miner

Submissions for variant NM_153460.4(IL17RC):c.565C>G (p.Gln189Glu)

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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 RCV003041718 SCV003318874 uncertain significance Candidiasis, familial, 9 2022-02-28 criteria provided, single submitter clinical testing The frequency data for this variant in the population databases is considered unreliable, as metrics indicate poor data quality at this position in the gnomAD database. This sequence change replaces glutamine, which is neutral and polar, with glutamic acid, which is acidic and polar, at codon 260 of the IL17RC protein (p.Gln260Glu). This variant has not been reported in the literature in individuals affected with IL17RC-related conditions. 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").

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