ClinVar Miner

Submissions for variant NM_005228.5(EGFR):c.885T>C (p.Cys295=)

dbSNP: rs2128935175
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002126682 SCV002459494 likely benign EGFR-related lung cancer 2021-03-18 criteria provided, single submitter clinical testing

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