ClinVar Miner

Submissions for variant NM_032043.3(BRIP1):c.1676C>T (p.Thr559Ile)

dbSNP: rs876658266
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001177031 SCV001341136 uncertain significance Hereditary cancer-predisposing syndrome 2020-03-06 criteria provided, single submitter clinical testing This missense variant replaces threonine with isoleucine at codon 559 of the BRIP1 protein. Computational prediction suggests that this variant may not impact protein structure and function (internally defined REVEL score threshold <= 0.5, PMID: 27666373). Splice site prediction tools suggest that this variant may not impact RNA splicing. To our knowledge, functional studies have not been reported for this variant. This variant has not been reported in individuals affected with hereditary cancer in the literature. This variant has not been identified in the general population by the Genome Aggregation Database (gnomAD). The available evidence is insufficient to determine the role of this variant in disease conclusively. Therefore, this variant is classified as a Variant of Uncertain Significance.
Baylor Genetics RCV003462647 SCV004217066 uncertain significance Familial cancer of breast 2023-06-29 criteria provided, single submitter clinical testing

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