ClinVar Miner

Submissions for variant NM_003079.5(SMARCE1):c.84C>T (p.Tyr28=)

dbSNP: rs2144009223
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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 RCV001399150 SCV001600934 likely benign Familial meningioma 2020-08-11 criteria provided, single submitter clinical testing
Ambry Genetics RCV002449095 SCV002678531 likely benign Hereditary cancer-predisposing syndrome 2022-07-05 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.

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