ClinVar Miner

Submissions for variant NM_005228.5(EGFR):c.2370G>T (p.Thr790=)

dbSNP: rs376452156
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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 RCV001425934 SCV001628572 likely benign EGFR-related lung cancer 2024-10-09 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV005245952 SCV005895771 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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