ClinVar Miner

Submissions for variant NM_005228.5(EGFR):c.2248G>C (p.Ala750Pro)

dbSNP: rs121913229
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine RCV000038395 SCV000062067 uncertain significance not specified 2008-03-01 no assertion criteria provided clinical testing
Database of Curated Mutations (DoCM) RCV000442888 SCV000505065 likely pathogenic Lung adenocarcinoma 2015-07-14 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000425827 SCV000505066 likely pathogenic Non-small cell lung carcinoma 2015-07-14 no assertion criteria provided literature only

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