ClinVar Miner

Submissions for variant NM_003072.5(SMARCA4):c.4872G>T (p.Pro1624=)

dbSNP: rs182644267
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000570394 SCV000672063 likely benign Hereditary cancer-predisposing syndrome 2017-02-06 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.
Eurofins Ntd Llc (ga) RCV000591456 SCV000702268 uncertain significance not provided 2016-10-27 criteria provided, single submitter clinical testing
Invitae RCV001083057 SCV001012771 likely benign Rhabdoid tumor predisposition syndrome 2 2023-11-08 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001809612 SCV002056227 likely benign Intellectual disability, autosomal dominant 16 2021-07-15 criteria provided, single submitter clinical testing

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