ClinVar Miner

Submissions for variant NM_183357.3(ADCY5):c.471G>T (p.Glu157Asp)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003002243 SCV003293020 benign not provided 2022-04-10 criteria provided, single submitter clinical testing
GeneDx RCV003002243 SCV003842673 uncertain significance not provided 2022-09-19 criteria provided, single submitter clinical testing In silico analysis supports that this missense variant does not alter protein structure/function; Has not been previously published as pathogenic or benign to our knowledge

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