ClinVar Miner

Submissions for variant NM_006031.6(PCNT):c.4597C>T (p.Gln1533Ter)

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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 RCV003711186 SCV004492044 pathogenic not provided 2022-11-29 criteria provided, single submitter clinical testing This sequence change creates a premature translational stop signal (p.Gln1533*) in the PCNT gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in PCNT are known to be pathogenic (PMID: 18174396, 22821869). This variant is present in population databases (no rsID available, gnomAD 0.0009%). For these reasons, this variant has been classified as Pathogenic. This variant has not been reported in the literature in individuals affected with PCNT-related conditions.

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