ClinVar Miner

Submissions for variant NM_001289910.1(IDH2):c.262C>T (p.Arg88Trp) (rs267606870)

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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Database of Curated Mutations (DoCM) RCV000438997 SCV000504577 likely pathogenic Multiple myeloma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000421344 SCV000504578 pathogenic Acute myeloid leukemia 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000428106 SCV000504579 likely pathogenic Myelodysplastic syndrome 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000438361 SCV000504580 likely pathogenic Squamous cell carcinoma of the head and neck 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000422389 SCV000504581 likely pathogenic Neoplasm of the large intestine 2016-05-31 no assertion criteria provided literature only

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