ClinVar Miner

Submissions for variant NM_000314.7(PTEN):c.294A>G (p.Leu98=) (rs770224289)

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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 RCV000213647 SCV000277053 likely benign Hereditary cancer-predisposing syndrome 2018-04-11 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: Synonymous alterations with insufficient evidence to classify as benign
Invitae RCV000645096 SCV000766838 likely benign PTEN hamartoma tumor syndrome 2017-09-20 criteria provided, single submitter clinical testing
Color RCV000213647 SCV000912945 likely benign Hereditary cancer-predisposing syndrome 2018-02-06 criteria provided, single submitter clinical testing

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