ClinVar Miner

Submissions for variant NM_000255.4(MMUT):c.414T>C (p.Phe138=)

dbSNP: rs2127420068
Minimum review status: Collection method:
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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 RCV002109519 SCV002399344 likely benign not provided 2021-07-20 criteria provided, single submitter clinical testing

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