ClinVar Miner

Submissions for variant NM_000455.4(STK11):c.1035C>T (p.His345=) (rs751619208)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000163094 SCV000213600 likely benign Hereditary cancer-predisposing syndrome 2015-08-06 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: Synonymous alterations with insufficient evidence to classify as benign
Invitae RCV000229278 SCV000284839 likely benign Peutz-Jeghers syndrome 2017-12-21 criteria provided, single submitter clinical testing
Counsyl RCV000229278 SCV000489394 likely benign Peutz-Jeghers syndrome 2016-09-29 criteria provided, single submitter clinical testing
Color RCV000163094 SCV000686576 likely benign Hereditary cancer-predisposing syndrome 2016-03-04 criteria provided, single submitter clinical testing

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