ClinVar Miner

Submissions for variant NM_001242896.3(DEPDC5):c.1625A>C (p.Gln542Pro)

dbSNP: rs886039279
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneReviews RCV000254585 SCV000321054 not provided Epilepsy, familial focal, with variable foci 1 no assertion provided literature only

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