ClinVar Miner

Submissions for variant NM_000059.4(BRCA2):c.7982A>G (p.Asp2661Gly)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV003300656 SCV003995750 uncertain significance Hereditary cancer-predisposing syndrome 2023-05-28 criteria provided, single submitter clinical testing The p.D2661G variant (also known as c.7982A>G), located in coding exon 17 of the BRCA2 gene, results from an A to G substitution at nucleotide position 7982. The aspartic acid at codon 2661 is replaced by glycine, an amino acid with similar properties. This amino acid position is conserved. In addition, this alteration is predicted to be deleterious by in silico analysis. Since supporting evidence is limited at this time, the clinical significance of this alteration remains unclear.

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