ClinVar Miner

Submissions for variant NM_000388.4(CASR):c.659G>C (p.Arg220Pro)

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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 RCV002651722 SCV003525562 pathogenic Familial hypocalciuric hypercalcemia; Autosomal dominant hypocalcemia 1 2022-04-24 criteria provided, single submitter clinical testing For these reasons, this variant has been classified as Pathogenic. This variant disrupts the p.Arg220 amino acid residue in CASR. Other variant(s) that disrupt this residue have been determined to be pathogenic (PMID: 1889203, 10885494, 11763315, 11889203, 17974727, 22142470, 22192860, 22422767). This suggests that this residue is clinically significant, and that variants that disrupt this residue are likely to be disease-causing. 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 disruptive. This missense change has been observed in individual(s) with familial hypocalciuric hypercalcemia (PMID: 22422767, 23081733). It has also been observed to segregate with disease in related individuals. This variant is not present in population databases (gnomAD no frequency). This sequence change replaces arginine, which is basic and polar, with proline, which is neutral and non-polar, at codon 220 of the CASR protein (p.Arg220Pro).

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