ClinVar Miner

Submissions for variant NM_007294.4(BRCA1):c.4459A>T (p.Lys1487Ter)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV005020353 SCV005647136 pathogenic Breast-ovarian cancer, familial, susceptibility to, 1; Pancreatic cancer, susceptibility to, 4; Fanconi anemia, complementation group S 2024-01-18 criteria provided, single submitter clinical testing

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