ClinVar Miner

Submissions for variant NM_032043.3(BRIP1):c.77T>G (p.Leu26Arg)

dbSNP: rs1603368414
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001344944 SCV001539030 uncertain significance Familial cancer of breast; Fanconi anemia complementation group J 2023-06-29 criteria provided, single submitter clinical testing ClinVar contains an entry for this variant (Variation ID: 1041181). This variant has not been reported in the literature in individuals affected with BRIP1-related conditions. This variant is not present in population databases (gnomAD no frequency). This sequence change replaces leucine, which is neutral and non-polar, with arginine, which is basic and polar, at codon 26 of the BRIP1 protein (p.Leu26Arg). Advanced modeling of protein sequence and biophysical properties (such as structural, functional, and spatial information, amino acid conservation, physicochemical variation, residue mobility, and thermodynamic stability) performed at Invitae indicates that this missense variant is expected to disrupt BRIP1 protein function. 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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