ClinVar Miner

Submissions for variant NM_000455.4(STK11):c.237C>T (p.Ile79=) (rs751859508)

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Total submissions: 6
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000163362 SCV000213899 likely benign Hereditary cancer-predisposing syndrome 2015-02-05 criteria provided, single submitter clinical testing
Counsyl RCV000412380 SCV000488349 likely benign Peutz-Jeghers syndrome 2016-03-02 criteria provided, single submitter clinical testing
GeneDx RCV000430082 SCV000514791 likely benign not specified 2017-08-21 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Invitae RCV000858747 SCV000554117 likely benign not provided 2019-01-15 criteria provided, single submitter clinical testing
Color RCV000163362 SCV000911293 likely benign Hereditary cancer-predisposing syndrome 2018-04-11 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000858747 SCV001134841 likely benign not provided 2019-01-09 criteria provided, single submitter clinical testing

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