ClinVar Miner

Submissions for variant NM_000059.4(BRCA2):c.7572A>T (p.Lys2524Asn)

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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 RCV003187241 SCV003853798 uncertain significance Hereditary cancer-predisposing syndrome 2023-02-01 criteria provided, single submitter clinical testing The p.K2524N variant (also known as c.7572A>T), located in coding exon 14 of the BRCA2 gene, results from an A to T substitution at nucleotide position 7572. The lysine at codon 2524 is replaced by asparagine, an amino acid with similar properties. This amino acid position is conserved. In addition, the in silico prediction for this alteration is inconclusive. Since supporting evidence is limited at this time, the clinical significance of this alteration remains unclear.

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