Submissions for variant NM_032043.2(BRIP1):c.1609C>G (p.Leu537Val) (rs864622208)

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Total submissions: 1

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Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
Invitae	RCV000205999	SCV000259700	uncertain significance	Familial cancer of breast; Fanconi anemia, complementation group J	2018-10-17	criteria provided, single submitter	clinical testing	This sequence change replaces leucine with valine at codon 537 of the BRIP1 protein (p.Leu537Val). The leucine residue is highly conserved and there is a small physicochemical difference between leucine and valine. 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 disease. ClinVar contains an entry for this variant (Variation ID: 219688). 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: "Tolerated"; PolyPhen-2: "Probably Damaging"; Align-GVGD: "Class C0"). 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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