ClinVar Miner

Submissions for variant NM_000314.7(PTEN):c.265C>T (p.Pro89Ser) (rs587783059)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics, Eurofins Clinical Diagnostics RCV000178755 SCV000230906 uncertain significance not provided 2015-04-16 criteria provided, single submitter clinical testing
Pathway Genomics RCV000144659 SCV000189988 uncertain significance Cowden syndrome 1 2014-07-24 no assertion criteria provided clinical testing

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