ClinVar Miner

Submissions for variant NM_000465.4(BARD1):c.1677A>G (p.Val559=)

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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. RCV004440086 SCV004930360 likely benign Familial cancer of breast 2023-12-13 criteria provided, single submitter clinical testing This variant is considered likely benign. This variant is a silent/synonymous amino acid change and it is not expected to impact splicing.

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