ClinVar Miner

Submissions for variant NM_005228.5(EGFR):c.2200G>A (p.Glu734Lys) (rs121913420)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Database of Curated Mutations (DoCM) RCV000424211 SCV000505060 likely pathogenic Non-small cell lung cancer 2015-07-14 no assertion criteria provided literature only

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