ClinVar Miner

Submissions for variant NM_005228.5(EGFR):c.2260A>G (p.Lys754Glu)

dbSNP: rs397517101
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 RCV000038397 SCV000062069 uncertain significance not specified 2006-10-28 no assertion criteria provided clinical testing

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