ClinVar Miner

Submissions for variant NM_005228.5(EGFR):c.2412A>G (p.Glu804=)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002588428 SCV003495055 likely benign EGFR-related lung cancer 2022-08-03 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV005248950 SCV005899542 benign Lung cancer 2024-10-16 criteria provided, single submitter clinical testing This variant is considered benign. This variant is a silent/synonymous amino acid change and it is not expected to impact splicing.

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