ClinVar Miner

Submissions for variant NM_005228.5(EGFR):c.1263G>A (p.Glu421=)

dbSNP: rs2128939704
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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 RCV001408025 SCV001610012 likely benign EGFR-related lung cancer 2019-12-22 criteria provided, single submitter clinical testing

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