ClinVar Miner

Submissions for variant NM_032043.3(BRIP1):c.3225A>T (p.Ser1075=)

dbSNP: rs1291039468
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV000584276 SCV000689370 likely benign Hereditary cancer-predisposing syndrome 2015-07-22 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000636224 SCV000757656 likely benign Familial cancer of breast; Fanconi anemia complementation group J 2024-03-29 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV004787989 SCV005404341 benign Familial cancer of breast 2024-09-10 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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