ClinVar Miner

Submissions for variant NM_194248.3(OTOF):c.32C>T (p.Ser11Leu)

dbSNP: rs200972155
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001575943 SCV001803036 uncertain significance not provided 2020-08-18 criteria provided, single submitter clinical testing In silico analysis, which includes protein predictors and evolutionary conservation, supports that this variant does not alter protein structure/function; Has not been previously published as pathogenic or benign to our knowledge
Labcorp Genetics (formerly Invitae), Labcorp RCV001575943 SCV004511297 benign not provided 2024-03-07 criteria provided, single submitter clinical testing

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