ClinVar Miner

Submissions for variant NM_000314.8(PTEN):c.462C>T (p.Phe154=)

dbSNP: rs1859982800
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001176180 SCV001340060 likely benign Hereditary cancer-predisposing syndrome 2019-01-07 criteria provided, single submitter clinical testing
Laboratory of Virology, Oncology, Biosciences and Environment, Faculty of Sciences and Techniques, Mohammedia- University Hassan II of Casablanca RCV003483782 SCV004231952 uncertain significance Prostate cancer, hereditary, 1 2024-01-01 no assertion criteria provided clinical testing

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