ClinVar Miner

Submissions for variant NM_001197104.2(KMT2A):c.10804T>C (p.Ser3602Pro)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV004762697 SCV005368996 uncertain significance not provided 2023-06-27 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

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