ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.3877A>C (p.Ile1293Leu) (rs876659799)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000221273 SCV000276637 uncertain significance Hereditary cancer-predisposing syndrome 2016-03-03 criteria provided, single submitter clinical testing
GeneDx RCV000480203 SCV000566632 uncertain significance not provided 2015-05-20 criteria provided, single submitter clinical testing This variant is denoted BRCA2 c.3877A>C at the cDNA level, p.Ile1293Leu (I1293L) at the protein level, and results in the change of an Isoleucine to a Leucine (ATA>CTA). Using alternate nomenclature, this variant would be defined as BRCA2 4105A>C. This variant has not, to our knowledge, been published in the literature as pathogenic or benign. BRCA2 Ile1293Leu was not observed in approximately 6,500 individuals of European and African American ancestry in the NHLBI Exome Sequencing Project, indicating it is not a common benign variant in these populations. Since Isoleucine and Leucine share similar properties, this is considered a conservative amino acid substitution. BRCA2 Ile1293Leu occurs at a position that is not conserved and is not located in a known functional domain (Narod 2004, Borg 2010, Roy 2012). In silico analyses predict that this variant is unlikely to alter protein structure or function. Based on currently available information, it is unclear whether BRCA2 Ile1293Leu is pathogenic or benign. We consider it to be a variant of uncertain significance.

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