ClinVar Miner

Submissions for variant NM_005228.5(EGFR):c.866C>A (p.Ala289Asp)

dbSNP: rs149840192
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Database of Curated Mutations (DoCM) RCV000434840 SCV000506063 likely pathogenic Glioblastoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000443311 SCV000506064 likely pathogenic Squamous cell carcinoma of the head and neck 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000427425 SCV000506065 likely pathogenic Neoplasm of brain 2016-05-31 no assertion criteria provided literature only

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