ClinVar Miner

Submissions for variant NM_000254.3(MTR):c.1305T>C (p.Ile435=)

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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 RCV003628958 SCV004512019 benign Methylcobalamin deficiency type cblG 2023-11-15 criteria provided, single submitter clinical testing

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