ClinVar Miner

Submissions for variant NM_005228.5(EGFR):c.1793G>C (p.Gly598Ala) (rs139236063)

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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) RCV000440786 SCV000506075 likely pathogenic Glioblastoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000423114 SCV000506076 likely pathogenic Neoplasm of brain 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000429899 SCV000506077 likely pathogenic Brainstem glioma 2016-05-31 no assertion criteria provided literature only

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