ClinVar Miner

Submissions for variant NM_080632.3(UPF3B):c.1052A>G (p.Glu351Gly)

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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 RCV002690215 SCV002991948 uncertain significance Syndromic X-linked intellectual disability 14 2022-09-05 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. This variant has not been reported in the literature in individuals affected with UPF3B-related conditions. This variant is present in population databases (rs757253031, gnomAD 0.02%), including at least one homozygous and/or hemizygous individual. This sequence change replaces glutamic acid, which is acidic and polar, with glycine, which is neutral and non-polar, at codon 351 of the UPF3B protein (p.Glu351Gly).

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