ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.9191A>G (p.Asp3064Gly) (rs1064794614)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000486534 SCV000569577 uncertain significance not provided 2016-11-30 criteria provided, single submitter clinical testing This variant is denoted BRCA2 c.9191A>G at the cDNA level, p.Asp3064Gly (D3064G) at the protein level, and results in the change of an Aspartic Acid to a Glycine (GAC>GGC). Using alternate nomenclature, this variant would be defined as BRCA2 9419A>G. This variant has not, to our knowledge, been published in the literature as pathogenic or benign. BRCA2 Asp3064Gly 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 Aspartic Acid and Glycine differ in polarity, charge, size or other properties, this is considered a non-conservative amino acid substitution. BRCA2 Asp3064Gly occurs at a position that is not conserved and is located within the DNA binding domain (Yang 2002). In silico analyses are inconsistent regarding the effect this variant may have on protein structure or function. Based on currently available evidence, it is unclear whether BRCA2 Asp3064Gly is a pathogenic or benign variant. We consider it to be a variant of uncertain significance.

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