ClinVar Miner

Submissions for variant NM_005228.5(EGFR):c.2303_2305delinsTCT (p.Ser768_Val769delinsIleLeu)

dbSNP: rs1584238193
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Core Molecular Diagnostic Lab, McGill University Health Centre RCV000790622 SCV000925976 pathogenic Non-small cell lung carcinoma 2019-07-09 criteria provided, single submitter clinical testing

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