ClinVar Miner

Submissions for variant NM_000255.4(MMUT):c.1146T>A (p.Thr382=)

dbSNP: rs2127417956
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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 RCV002146868 SCV002417335 likely benign not provided 2021-09-05 criteria provided, single submitter clinical testing

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