ClinVar Miner

Submissions for variant NM_005228.5(EGFR):c.1793G>T (p.Gly598Val) (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) RCV000434448 SCV000505293 likely pathogenic Neoplasm of brain 2014-12-26 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000436167 SCV000506072 likely pathogenic Glioblastoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000418494 SCV000506073 likely pathogenic Brainstem glioma 2016-05-31 no assertion criteria provided literature only

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