ClinVar Miner

Submissions for variant NM_016239.4(MYO15A):c.950C>T (p.Ala317Val)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV002284850 SCV002574487 uncertain significance not provided 2022-03-15 criteria provided, single submitter clinical testing In silico analysis supports that this missense variant does not alter protein structure/function; Has not been previously published as pathogenic or benign to our knowledge
Labcorp Genetics (formerly Invitae), Labcorp RCV002284850 SCV003493271 benign not provided 2023-12-31 criteria provided, single submitter clinical testing

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