ClinVar Miner

Submissions for variant NM_000059.4(BRCA2):c.9257-14T>C

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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 RCV004018399 SCV004848935 uncertain significance Hereditary cancer-predisposing syndrome 2015-03-09 criteria provided, single submitter clinical testing The c.9257-14T>C intronic alteration consists of a T to C substitution 14 nucleotides before coding exon 24 in the BRCA2 gene. Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear.

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