ClinVar Miner

Submissions for variant NM_003072.5(SMARCA4):c.675G>A (p.Val225=)

dbSNP: rs1599952186
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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 RCV001025622 SCV001187848 likely benign Hereditary cancer-predisposing syndrome 2019-10-18 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 RCV001410514 SCV001612563 likely benign Rhabdoid tumor predisposition syndrome 2 2021-07-13 criteria provided, single submitter clinical testing

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