ClinVar Miner

Submissions for variant NM_005228.5(EGFR):c.2862C>T (p.Asp954=)

gnomAD frequency: 0.00001  dbSNP: rs397517138
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mendelics RCV000987886 SCV001137372 likely benign Lung carcinoma 2019-05-28 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001474197 SCV001678365 likely benign EGFR-related lung cancer 2024-01-24 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV002257381 SCV002537676 likely benign Hereditary cancer-predisposing syndrome 2020-11-10 criteria provided, single submitter curation
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine RCV000038453 SCV000062125 likely benign not specified 2008-03-01 no assertion criteria provided clinical testing

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