ClinVar Miner

Submissions for variant NM_003072.5(SMARCA4):c.1230G>T (p.Leu410=)

dbSNP: rs2086356109
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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 RCV002100613 SCV002389663 likely benign Rhabdoid tumor predisposition syndrome 2 2020-11-22 criteria provided, single submitter clinical testing
Ambry Genetics RCV003289437 SCV004007532 likely benign Hereditary cancer-predisposing syndrome 2023-04-19 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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