ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.7477A>G (p.Met2493Val) (rs1064793329)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000482631 SCV000565820 uncertain significance not provided 2016-09-12 criteria provided, single submitter clinical testing This variant is denoted BRCA2 c.7477A>G at the cDNA level, p.Met2493Val (M2493V) at the protein level, and results in the change of a Methionine to a Valine (ATG>GTG). Using alternate nomenclature, this variant would be defined as BRCA2 7705A>G. This variant has not, to our knowledge, been published in the literature as pathogenic or benign. BRCA2 Met2493Val 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 Methionine and Valine share similar properties, this is considered a conservative amino acid substitution. BRCA2 Met2493Val occurs at a position that is not conserved and is located in the DNA binding domain and the FANCD2 binding domain (Yang 2002, UniProt). In silico analyses are inconsistent regarding the effect this variant may have on protein structure and function. Based on currently available evidence, it is unclear whether BRCA2 Met2493Val is a pathogenic or benign variant. We consider it to be a variant of uncertain significance.

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