ClinVar Miner

Submissions for variant NM_032043.3(BRIP1):c.2676T>C (p.Leu892=)

dbSNP: rs2144115485
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001432456 SCV001635227 likely benign Familial cancer of breast; Fanconi anemia complementation group J 2023-01-11 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV002258253 SCV002533640 likely benign Hereditary cancer-predisposing syndrome 2021-07-26 criteria provided, single submitter curation
Ambry Genetics RCV002258253 SCV002743893 likely benign Hereditary cancer-predisposing syndrome 2021-05-11 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.
Myriad Genetics, Inc. RCV004789590 SCV005405852 benign Familial cancer of breast 2024-09-05 criteria provided, single submitter clinical testing This variant is considered benign. This variant is a silent/synonymous amino acid change and it is not expected to impact splicing.

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