ClinVar Miner

Submissions for variant NM_005228.5(EGFR):c.2192G>A (p.Trp731Ter)

dbSNP: rs397517089
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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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 RCV000038384 SCV000062056 uncertain significance not specified 2008-03-01 no assertion criteria provided clinical testing

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