ClinVar Miner

Submissions for variant NM_000059.4(BRCA2):c.779A>T (p.Glu260Val)

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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 RCV004602376 SCV005097536 uncertain significance Hereditary cancer-predisposing syndrome 2024-05-22 criteria provided, single submitter clinical testing The p.E260V variant (also known as c.779A>T), located in coding exon 8 of the BRCA2 gene, results from an A to T substitution at nucleotide position 779. The glutamic acid at codon 260 is replaced by valine, an amino acid with dissimilar properties. This amino acid position is conserved. In addition, this alteration is predicted to be tolerated by in silico analysis. Based on the available evidence, the clinical significance of this variant remains unclear.

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