ClinVar Miner

Submissions for variant NM_005228.5(EGFR):c.2236_2250del (p.Glu746_Ala750del)

dbSNP: rs727504233
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV001311279 SCV001501388 pathogenic not provided 2021-01-01 criteria provided, single submitter clinical testing
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine RCV000154199 SCV000203851 drug response Tyrosine kinase inhibitor response 2007-01-16 no assertion criteria provided clinical testing
Key Laboratory of Carcinogenesis and Cancer Invasion, Central South University RCV003998240 SCV004042728 likely pathogenic Lung adenocarcinoma no assertion criteria provided clinical testing

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