ClinVar Miner

Submissions for variant NM_000059.4(BRCA2):c.10094T>C (p.Val3365Ala)

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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 RCV002437085 SCV002745389 uncertain significance Hereditary cancer-predisposing syndrome 2021-09-16 criteria provided, single submitter clinical testing The p.V3365A variant (also known as c.10094T>C), located in coding exon 26 of the BRCA2 gene, results from a T to C substitution at nucleotide position 10094. The valine at codon 3365 is replaced by alanine, an amino acid with similar properties. This amino acid position is conserved. In addition, this alteration is predicted to be tolerated by in silico analysis. Since supporting evidence is limited at this time, the clinical significance of this alteration remains unclear.

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