ClinVar Miner

Submissions for variant NM_000314.7(PTEN):c.411A>G (p.Ala137=) (rs144545031)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000165610 SCV000216344 likely benign Hereditary cancer-predisposing syndrome 2014-09-08 criteria provided, single submitter clinical testing
Invitae RCV000232763 SCV000284591 likely benign not provided 2018-12-28 criteria provided, single submitter clinical testing
Color RCV000165610 SCV000686289 likely benign Hereditary cancer-predisposing syndrome 2017-04-06 criteria provided, single submitter clinical testing

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