ClinVar Miner

Submissions for variant NM_000535.7(PMS2):c.1011T>C (p.Thr337=) (rs1353232685)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000528606 SCV000625494 likely benign not provided 2018-02-17 criteria provided, single submitter clinical testing
Ambry Genetics RCV001016947 SCV001177956 likely benign Hereditary cancer-predisposing syndrome 2019-12-07 criteria provided, single submitter clinical testing In silico models in agreement (benign);Synonymous alterations with insufficient evidence to classify as benign

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