ClinVar Miner

Submissions for variant NM_005163.2(AKT1):c.1251C>T (p.Tyr417=) (rs139297659)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000205490 SCV000262349 benign Cowden syndrome 6 2019-12-31 criteria provided, single submitter clinical testing
Genetic Services Laboratory,University of Chicago RCV000503783 SCV000593082 likely benign not specified 2016-05-23 criteria provided, single submitter clinical testing

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