ClinVar Miner

Submissions for variant NM_032043.2(BRIP1):c.2617A>T (p.Thr873Ser) (rs758444508)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000216067 SCV000279730 uncertain significance not provided 2015-12-28 criteria provided, single submitter clinical testing This variant is denoted BRIP1 c.2617A>T at the cDNA level, p.Thr873Ser (T873S) at the protein level, and results in the change of a Threonine to a Serine (ACC>TCC). This variant has not, to our knowledge, been published in the literature as pathogenic or benign. BRIP1 Thr873Ser was not observed in approximately 6,500 individuals of European and African American ancestry in the NHLBI Exome Sequencing Project, suggesting it is not a common benign variant in these populations. Since Threonine and Serine share similar properties, this is considered a conservative amino acid substitution. BRIP1 Thr873Ser occurs at a position that is not conserved and is located in the Helicase domain (Cantor 2011). In silico analyses predict that this variant is unlikely to alter protein structure or function. Based on currently available evidence, it is unclear whether BRIP1 Thr873Ser is pathogenic or benign. We consider it to be a variant of uncertain significance.

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