ClinVar Miner

Submissions for variant NM_001242896.3(DEPDC5):c.4197C>T (p.Phe1399=)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003060471 SCV003448913 likely benign Familial focal epilepsy with variable foci 2022-11-23 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV004598233 SCV005092527 likely benign not provided 2024-07-01 criteria provided, single submitter clinical testing DEPDC5: BP4, BP7

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