ClinVar Miner

Submissions for variant NM_002739.5(PRKCG):c.955C>A (p.Pro319Thr)

gnomAD frequency: 0.00001  dbSNP: rs367543214
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV001814973 SCV002062026 uncertain significance not specified 2018-11-07 criteria provided, single submitter clinical testing
Psychiatry Genetics Yale University RCV000084807 SCV000116943 not provided not provided no assertion provided not provided

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