ClinVar Miner

Submissions for variant NM_006231.3(POLE):c.3090C>T (p.Phe1030=) (rs766306895)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000988942 SCV000556339 likely benign Colorectal cancer, susceptibility to, 12 2019-12-31 criteria provided, single submitter clinical testing
Ambry Genetics RCV000566320 SCV000671318 likely benign Hereditary cancer-predisposing syndrome 2016-01-22 criteria provided, single submitter clinical testing Synonymous alterations with insufficient evidence to classify as benign
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000759281 SCV000888518 benign not provided 2017-11-22 criteria provided, single submitter clinical testing
Mendelics RCV000988942 SCV001138879 likely benign Colorectal cancer, susceptibility to, 12 2019-05-28 criteria provided, single submitter clinical testing

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