ClinVar Miner

Submissions for variant NM_001376.5(DYNC1H1):c.13071C>T (p.Tyr4357=)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000720715 SCV000851596 likely benign History of neurodevelopmental disorder 2017-03-08 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: Synonymous alterations with insufficient evidence to classify as benign

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