ClinVar Miner

Submissions for variant NM_002878.4(RAD51D):c.522C>T (p.Asp174=)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV005190969 SCV005823854 likely benign Breast-ovarian cancer, familial, susceptibility to, 4 2024-11-11 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV005190969 SCV006095735 benign Breast-ovarian cancer, familial, susceptibility to, 4 2025-02-24 criteria provided, single submitter clinical testing This variant is considered benign. This variant is a silent/synonymous amino acid change and it is not expected to impact splicing.

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