ClinVar Miner

Submissions for variant NM_001042646.3(TRAK1):c.620A>G (p.Tyr207Cys)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV002308872 SCV002601102 uncertain significance not provided 2024-08-08 criteria provided, single submitter clinical testing In silico analysis supports that this missense variant has a deleterious effect on protein structure/function; Has not been previously published as pathogenic or benign to our knowledge
Labcorp Genetics (formerly Invitae), Labcorp RCV002308872 SCV005776721 likely benign not provided 2024-09-05 criteria provided, single submitter clinical testing

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