ClinVar Miner

Submissions for variant NM_005228.5(EGFR):c.1536C>T (p.Pro512=)

dbSNP: rs374670788
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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 RCV000925701 SCV001071250 likely benign EGFR-related lung cancer 2023-12-29 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV002259053 SCV002537316 likely benign Hereditary cancer-predisposing syndrome 2021-12-13 criteria provided, single submitter curation

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