ClinVar Miner

Submissions for variant NM_005228.5(EGFR):c.2303G>T (p.Ser768Ile) (rs121913465)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine, Partners HealthCare Personalized Medicine RCV000038407 SCV000062079 pathogenic Non-small cell lung cancer 2011-03-11 criteria provided, single submitter clinical testing
Database of Curated Mutations (DoCM) RCV000038407 SCV000505071 likely pathogenic Non-small cell lung cancer 2015-07-14 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000428042 SCV000505072 likely pathogenic Carcinoma of esophagus 2015-07-14 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000435248 SCV000505073 likely pathogenic Squamous cell lung carcinoma 2014-12-26 no assertion criteria provided literature only

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