ClinVar Miner

Submissions for variant NM_001242897.2(DEPDC5):c.814G>A (p.Val272Ile) (rs187334123)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001081491 SCV000558203 benign Familial focal epilepsy with variable foci 2019-12-31 criteria provided, single submitter clinical testing
Center for Pediatric Genomic Medicine,Children's Mercy Hospital and Clinics RCV000514765 SCV000610573 likely benign not provided 2017-09-01 criteria provided, single submitter clinical testing

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