ClinVar Miner

Submissions for variant NM_001127500.2(MET):c.2638-7del (rs587780736)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000723812 SCV000225560 uncertain significance not provided 2014-10-28 criteria provided, single submitter clinical testing
GeneDx RCV000174283 SCV000569535 likely benign not specified 2017-11-02 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Illumina Clinical Services Laboratory,Illumina RCV000123117 SCV000466453 likely benign Renal cell carcinoma, papillary, 1 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV000123117 SCV000166419 benign Renal cell carcinoma, papillary, 1 2018-01-12 criteria provided, single submitter clinical testing

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