ClinVar Miner

Submissions for variant NM_000388.4(CASR):c.205C>A (p.Arg69Ser)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetics and Molecular Pathology, SA Pathology RCV002466850 SCV002761656 likely pathogenic Neonatal severe primary hyperparathyroidism 2020-05-29 criteria provided, single submitter clinical testing The CASR:c.205C>A variant is a single base change which substitutes the amino acid at position 69 in exon 3 from arginine to serine. The variant has not been described in the literature to date and is absent from population databases (PM2). It is not present in ClinVar or HGMD (2020.1). Computational algorithms predict a deleterious effect. Three different missense substitutions at amino acid position 69 have been reported previously in the literature (PMID: 22422767, PMID: 24947037, PMID: 26855056) (PM5). This variant is located within a highly conserved functional domain which is important for receptor functioning (PMID: 27434672) (PM1).

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