ClinVar Miner

Submissions for variant NM_001077242.2(DEPDC7):c.763A>T (p.Lys255Ter)

gnomAD frequency: 0.00005  dbSNP: rs201199439
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
New York Genome Center RCV001281562 SCV001468872 uncertain significance Autism 2019-07-25 criteria provided, single submitter clinical testing

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