ClinVar Miner

Submissions for variant NM_001029883.3(PCARE):c.2112_2113inv (p.Ala705Thr)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001298793 SCV001487860 uncertain significance not provided 2020-06-26 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. Experimental studies and prediction algorithms are not available or were not evaluated, and the functional significance of this variant is currently unknown. This variant has not been reported in the literature in individuals with PCARE-related conditions. The frequency data for this variant in the population databases is not available, as this variant may be reported as separate entries in the ExAC database. This sequence change replaces alanine with threonine at codon 705 of the PCARE protein (p.Ala705Thr). The alanine residue is moderately conserved and there is a small physicochemical difference between alanine and threonine.

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