ClinVar Miner

Submissions for variant NM_025114.4(CEP290):c.4586C>G (p.Pro1529Arg)

dbSNP: rs759438587
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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 RCV001216653 SCV001388459 uncertain significance Familial aplasia of the vermis; Meckel-Gruber syndrome; Nephronophthisis 2019-08-20 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 are either unavailable or do not agree on the potential impact of this missense change (SIFT: "Deleterious"; PolyPhen-2: "Possibly Damaging"; Align-GVGD: "Class C0"). This variant has not been reported in the literature in individuals with CEP290-related conditions. This variant is present in population databases (rs759438587, ExAC 0.001%). This sequence change replaces proline with arginine at codon 1529 of the CEP290 protein (p.Pro1529Arg). The proline residue is highly conserved and there is a moderate physicochemical difference between proline and arginine.

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