ClinVar Miner

Submissions for variant NM_007294.4(BRCA1):c.4342del (p.Ser1448fs)

dbSNP: rs886040225
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Precision Medicine, Meizhou People's Hospital RCV002250815 SCV002520855 pathogenic Familial cancer of breast no assertion criteria provided curation

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