ClinVar Miner

Submissions for variant NM_001127500.3(MET):c.71G>A (p.Gly24Glu) (rs180985111)

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Total submissions: 6
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000167873 SCV000218519 likely benign Renal cell carcinoma, papillary, 1 2019-12-31 criteria provided, single submitter clinical testing
Vantari Genetics RCV000210818 SCV000267041 uncertain significance Hereditary cancer-predisposing syndrome 2015-12-07 criteria provided, single submitter clinical testing
Ambry Genetics RCV000210818 SCV000673696 benign Hereditary cancer-predisposing syndrome 2018-12-21 criteria provided, single submitter clinical testing Insufficient or conflicting evidence;In silico models in agreement (benign);Co-occurence with a mutation in another gene that clearly explains a proband's phenotype;Other data supporting benign classification
Mendelics RCV000167873 SCV000838226 likely benign Renal cell carcinoma, papillary, 1 2018-07-02 criteria provided, single submitter clinical testing
ITMI RCV000121347 SCV000085525 not provided not specified 2013-09-19 no assertion provided reference population
CSER _CC_NCGL, University of Washington RCV000148614 SCV000190329 likely benign Lymphoedema 2014-06-01 no assertion criteria provided research

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