ClinVar Miner

Submissions for variant NM_002739.5(PRKCG):c.1899C>T (p.Pro633=)

gnomAD frequency: 0.00002  dbSNP: rs367543219
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Athena Diagnostics Inc RCV000084812 SCV000843566 likely benign not provided 2018-01-26 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV003964956 SCV004777411 likely benign PRKCG-related condition 2020-02-14 criteria provided, single submitter clinical testing This variant is classified as likely benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).
Psychiatry Genetics Yale University RCV000084812 SCV000116948 not provided not provided no assertion provided not provided

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