ClinVar Miner

Submissions for variant NM_004448.4(ERBB2):c.2324_2325insCTCCGTGATGGC (p.Ala775_Gly776insSerValMetAla)

dbSNP: rs397516976
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Total submissions: 1
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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 RCV000156384 SCV000206102 likely pathogenic Non-small cell lung carcinoma 2014-02-06 criteria provided, single submitter clinical testing

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