ClinVar Miner

Submissions for variant NM_000059.4(BRCA2):c.8855T>C (p.Met2952Thr)

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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 RCV002373839 SCV002683919 uncertain significance Hereditary cancer-predisposing syndrome 2022-07-03 criteria provided, single submitter clinical testing The p.M2952T variant (also known as c.8855T>C), located in coding exon 21 of the BRCA2 gene, results from a T to C substitution at nucleotide position 8855. The methionine at codon 2952 is replaced by threonine, 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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