ClinVar Miner

Submissions for variant NM_032043.3(BRIP1):c.3492C>A (p.Cys1164Ter)

gnomAD frequency: 0.00001  dbSNP: rs2061304701
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001239012 SCV001411857 uncertain significance Familial cancer of breast; Fanconi anemia complementation group J 2019-10-18 criteria provided, single submitter clinical testing This sequence change results in a premature translational stop signal in the BRIP1 gene (p.Cys1164*). While this is not anticipated to result in nonsense mediated decay, it is expected to disrupt the last 86 amino acids of the BRIP1 protein. This variant is not present in population databases (ExAC no frequency). This variant has not been reported in the literature in individuals with BRIP1-related conditions. Experimental studies and prediction algorithms are not available or were not evaluated, and the functional significance of this variant is currently unknown. In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance.

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