ClinVar Miner

Submissions for variant NM_002878.4(RAD51D):c.787_791del (p.Ala263fs)

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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. RCV003450540 SCV004189628 likely pathogenic Breast-ovarian cancer, familial, susceptibility to, 4 2023-11-30 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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