ClinVar Miner

Submissions for variant NM_004456.4(EZH2):c.1937A>C (p.Tyr646Ser) (rs267601394)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Database of Curated Mutations (DoCM) RCV000433156 SCV000505310 likely pathogenic Non-Hodgkin lymphoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000441670 SCV000505311 likely pathogenic Malignant melanoma of skin 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000423969 SCV000505312 likely pathogenic Lymphoma 2014-12-26 no assertion criteria provided literature only

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