ClinVar Miner

Submissions for variant NM_153252.5(BRWD3):c.3578G>A (p.Arg1193Gln)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV003010635 SCV003711896 likely benign Inborn genetic diseases 2022-08-31 criteria provided, single submitter clinical testing This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.
Labcorp Genetics (formerly Invitae), Labcorp RCV003565607 SCV004325994 benign not provided 2024-04-10 criteria provided, single submitter clinical testing

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