ClinVar Miner

Submissions for variant NM_000546.6(TP53):c.393del (p.Asn131fs)

dbSNP: rs1567554408
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
German Consortium for Hereditary Breast and Ovarian Cancer, University Hospital Cologne RCV000785315 SCV000923883 pathogenic Ovarian neoplasm 2018-12-01 no assertion criteria provided research
Laboratory of Virology, Oncology, Biosciences and Environment, Faculty of Sciences and Techniques, Mohammedia- University Hassan II of Casablanca RCV003483721 SCV004232075 uncertain significance Prostate cancer, hereditary, 1 2024-01-01 no assertion criteria provided clinical testing

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