ClinVar Miner

Submissions for variant NM_001242897.2(DEPDC5):c.3383T>C (p.Ile1128Thr) (rs200653339)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000476223 SCV000558202 benign Familial focal epilepsy with variable foci 2019-12-31 criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV000518528 SCV000613080 benign not specified 2017-04-14 criteria provided, single submitter clinical testing
Mendelics RCV000990425 SCV001141411 likely benign Epilepsy, familial focal, with variable foci 1 2019-05-28 criteria provided, single submitter clinical testing

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