ClinVar Miner

Submissions for variant NM_001242897.2(DEPDC5):c.2622T>C (p.Cys874=) (rs115299174)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001079624 SCV000558177 benign Familial focal epilepsy with variable foci 2019-12-31 criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV000711434 SCV000841799 benign not provided 2018-01-25 criteria provided, single submitter clinical testing
Ambry Genetics RCV000716156 SCV000846993 benign Seizures 2016-07-28 criteria provided, single submitter clinical testing Synonymous alterations with insufficient evidence to classify as benign

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