ClinVar Miner

Submissions for variant NM_001287491.2(TET3):c.190C>T (p.Arg64Trp)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV004777459 SCV005391394 uncertain significance not provided 2024-04-26 criteria provided, single submitter clinical testing Has not been previously published as pathogenic or benign to our knowledge; No data available from control populations to assess the frequency of this variant; In silico analysis does not support a benign or deleterious effect of this variant on protein structure/function

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