ClinVar Miner

Submissions for variant NM_032043.3(BRIP1):c.1643A>C (p.Tyr548Ser)

dbSNP: rs587782405
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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 RCV001305467 SCV001494802 uncertain significance Familial cancer of breast; Fanconi anemia complementation group J 2020-12-10 criteria provided, single submitter clinical testing 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. Algorithms developed to predict the effect of missense changes on protein structure and function are either unavailable or do not agree on the potential impact of this missense change (SIFT: "Deleterious"; PolyPhen-2: "Probably Damaging"; Align-GVGD: "Class C0"). This variant has not been reported in the literature in individuals with BRIP1-related conditions. This variant is not present in population databases (ExAC no frequency). This sequence change replaces tyrosine with serine at codon 548 of the BRIP1 protein (p.Tyr548Ser). The tyrosine residue is highly conserved and there is a large physicochemical difference between tyrosine and serine.

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