ClinVar Miner

Submissions for variant NM_000038.6(APC):c.7089A>G (p.Lys2363=) (rs864622761)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000204711 SCV000262360 likely benign not provided 2018-03-13 criteria provided, single submitter clinical testing
Ambry Genetics RCV000565724 SCV000667637 likely benign Hereditary cancer-predisposing syndrome 2017-08-01 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: Synonymous alterations with insufficient evidence to classify as benign
Color RCV000565724 SCV000681846 likely benign Hereditary cancer-predisposing syndrome 2017-05-01 criteria provided, single submitter clinical testing
Mendelics RCV000987582 SCV001136941 likely benign Familial adenomatous polyposis 1 2019-05-28 criteria provided, single submitter clinical testing

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