ClinVar Miner

Submissions for variant NM_058216.3(RAD51C):c.959del (p.Lys320fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Myriad Genetics, Inc. RCV003450528 SCV004189601 likely pathogenic Breast-ovarian cancer, familial, susceptibility to, 3 2023-12-06 criteria provided, single submitter clinical testing This variant is considered likely pathogenic. This variant creates a frameshift predicted to result in premature protein truncation.

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