ClinVar Miner

Submissions for variant NM_000546.6(TP53):c.158_163delinsAT (p.Trp53fs)

dbSNP: rs2151042609
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
National Health Laboratory Service, Universitas Academic Hospital and University of the Free State RCV002226330 SCV002505077 pathogenic Hereditary breast ovarian cancer syndrome 2022-04-19 criteria provided, single submitter clinical testing

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