ClinVar Miner

Submissions for variant NM_005228.5(EGFR):c.322A>G (p.Arg108Gly)

dbSNP: rs1057519888
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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) RCV000440142 SCV000506078 likely pathogenic Brainstem glioma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000424206 SCV000506079 likely pathogenic Glioblastoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000434481 SCV000506080 likely pathogenic Neoplasm of brain 2016-05-31 no assertion criteria provided literature only

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