ClinVar Miner

Submissions for variant NM_005228.5(EGFR):c.783G>A (p.Lys261=)

dbSNP: rs1584172465
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
Labcorp Genetics (formerly Invitae), Labcorp RCV000974215 SCV001122030 likely benign EGFR-related lung cancer 2023-10-11 criteria provided, single submitter clinical testing

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