ClinVar Miner

Submissions for variant NM_001111307.2(PDE4A):c.991C>T (p.Pro331Ser)

gnomAD frequency: 0.00286  dbSNP: rs150660796
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics RCV000513702 SCV000609674 likely benign not provided 2017-06-20 criteria provided, single submitter clinical testing
Invitae RCV000513702 SCV001023610 benign not provided 2019-12-31 criteria provided, single submitter clinical testing

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