ClinVar Miner

Submissions for variant NM_001164508.2(NEB):c.24772_24778delinsA (p.Tyr8258_Asp8260delinsAsn)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Baylor Genetics RCV003476524 SCV004200051 uncertain significance Arthrogryposis multiplex congenita 6 2024-12-08 criteria provided, single submitter clinical testing This variant is predicted to create a small in-frame change with uncertain consequences.

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