ClinVar Miner

Submissions for variant NM_001242897.2(DEPDC5):c.2550C>T (p.Ala850=) (rs201146392)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000720834 SCV000851718 likely benign Seizures 2017-05-25 criteria provided, single submitter clinical testing Synonymous alterations with insufficient evidence to classify as benign
Invitae RCV000863965 SCV001004701 likely benign Familial focal epilepsy with variable foci 2019-12-31 criteria provided, single submitter clinical testing

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