ClinVar Miner

Submissions for variant NM_006254.4(PRKCD):c.1857T>C (p.Pro619=)

gnomAD frequency: 0.94337  dbSNP: rs900495
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Total submissions: 7
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine RCV000455503 SCV000540118 benign not specified 2016-03-29 criteria provided, single submitter clinical testing Variant identified in a genome or exome case(s) and assessed due to predicted null impact of the variant or pathogenic assertions in the literature or databases. Disclaimer: This variant has not undergone full assessment. The following are preliminary notes: Frequency
Labcorp Genetics (formerly Invitae), Labcorp RCV001515317 SCV001723368 benign Autoimmune lymphoproliferative syndrome, type III caused by mutation in PRKCD 2024-02-01 criteria provided, single submitter clinical testing
GeneDx RCV001613284 SCV001836209 benign not provided 2021-05-04 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001515317 SCV002031857 benign Autoimmune lymphoproliferative syndrome, type III caused by mutation in PRKCD 2021-10-25 criteria provided, single submitter clinical testing
Unidad de Genómica Garrahan, Hospital de Pediatría Garrahan RCV000455503 SCV004102604 benign not specified 2023-11-12 criteria provided, single submitter clinical testing This variant is classified as Benign based on local population frequency. This variant was detected in 100% of patients studied by a panel of primary immunodeficiencies. Number of patients: 96. Only high quality variants are reported.
Breakthrough Genomics, Breakthrough Genomics RCV001613284 SCV005301853 benign not provided criteria provided, single submitter not provided
GenomeConnect, ClinGen RCV001613284 SCV002074734 not provided not provided no assertion provided phenotyping only Variant interpreted as Benign and reported on 04-27-2020 by Lab or GTR ID 500031. GenomeConnect assertions are reported exactly as they appear on the patient-provided report from the testing laboratory. GenomeConnect staff make no attempt to reinterpret the clinical significance of the variant. This variant was reported in an individual referred for clinical diagnostic genetic testing.

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