ClinVar Miner

Submissions for variant NM_007186.6(CEP250):c.545G>A (p.Arg182Gln)

gnomAD frequency: 0.00002  dbSNP: rs762645568
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV002043657 SCV002307954 uncertain significance not provided 2021-03-29 criteria provided, single submitter clinical testing This sequence change replaces arginine with glutamine at codon 182 of the CEP250 protein (p.Arg182Gln). The arginine residue is moderately conserved and there is a small physicochemical difference between arginine and glutamine. This variant is present in population databases (rs762645568, ExAC 0.01%). 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: "Not Available"; PolyPhen-2: "Probably Damaging"; Align-GVGD: "Not Available"). This variant has not been reported in the literature in individuals with CEP250-related conditions.

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