ClinVar Miner

Submissions for variant NM_000038.6(APC):c.2385C>T (p.Leu795=) (rs80188155)

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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000574420 SCV000667241 likely benign Hereditary cancer-predisposing syndrome 2017-06-13 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: Synonymous alterations with insufficient evidence to classify as benign
Color RCV000574420 SCV000686889 likely benign Hereditary cancer-predisposing syndrome 2016-06-15 criteria provided, single submitter clinical testing
Counsyl RCV000410266 SCV000489146 likely benign Familial adenomatous polyposis 1 2016-08-29 criteria provided, single submitter clinical testing
Invitae RCV000410266 SCV000768389 likely benign Familial adenomatous polyposis 1 2017-12-14 criteria provided, single submitter clinical testing
Systems Biology Platform Zhejiang California International NanoSystems Institute RCV000074225 SCV000105818 cancer Familial colorectal cancer no assertion criteria provided not provided Converted during submission to other.

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