ClinVar Miner

Submissions for variant NM_015965.7(NDUFA13):c.2T>C (p.Met1Thr)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Revvity Omics, Revvity RCV003132860 SCV003813517 uncertain significance Mitochondrial complex 1 deficiency, nuclear type 28 2021-09-02 criteria provided, single submitter clinical testing

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