ClinVar Miner

Submissions for variant NM_004448.4(ERBB2):c.2326_2327insTGT (p.Gly776delinsValCys)

dbSNP: rs397516979
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Total submissions: 2
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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 RCV000038127 SCV000061793 likely pathogenic Non-small cell lung carcinoma 2011-06-30 criteria provided, single submitter clinical testing
Database of Curated Mutations (DoCM) RCV000431743 SCV000505685 likely pathogenic Breast neoplasm 2015-07-14 no assertion criteria provided literature only

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