ClinVar Miner

Submissions for variant NM_000254.3(MTR):c.3681T>C (p.Tyr1227=)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV005193734 SCV005824979 likely benign Methylcobalamin deficiency type cblG 2024-11-27 criteria provided, single submitter clinical testing

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