ClinVar Miner

Submissions for variant NM_001242896.3(DEPDC5):c.4386C>T (p.Pro1462=)

dbSNP: rs754105028
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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 RCV000528035 SCV000642199 likely benign Familial focal epilepsy with variable foci 2024-10-24 criteria provided, single submitter clinical testing
GeneDx RCV001562861 SCV001785698 likely benign not provided 2019-02-08 criteria provided, single submitter clinical testing

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