ClinVar Miner

Submissions for variant NM_000535.7(PMS2):c.33T>A (p.Pro11=) (rs780178572)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000871219 SCV001012833 likely benign Hereditary nonpolyposis colon cancer 2019-12-31 criteria provided, single submitter clinical testing
Ambry Genetics RCV001020203 SCV001181651 likely benign Hereditary cancer-predisposing syndrome 2017-09-30 criteria provided, single submitter clinical testing Synonymous alterations with insufficient evidence to classify as benign
Color RCV001020203 SCV001341148 likely benign Hereditary cancer-predisposing syndrome 2019-01-02 criteria provided, single submitter clinical testing

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