ClinVar Miner

Submissions for variant NM_000455.4(STK11):c.363G>A (p.Glu121=) (rs864622574)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000205084 SCV000261172 likely benign Peutz-Jeghers syndrome 2015-10-13 criteria provided, single submitter clinical testing
Ambry Genetics RCV000570726 SCV000664372 likely benign Hereditary cancer-predisposing syndrome 2016-11-17 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: Synonymous alterations with insufficient evidence to classify as benign,In silico models in agreement (benign)

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