ClinVar Miner

Submissions for variant NM_002168.3(IDH2):c.515G>A (p.Arg172Lys) (rs121913503)

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Total submissions: 6
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Database of Curated Mutations (DoCM) RCV000421863 SCV000504561 pathogenic Acute myeloid leukemia 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000432566 SCV000504562 not provided Myelodysplastic syndrome 2016-03-10 no assertion provided literature only
Database of Curated Mutations (DoCM) RCV000445068 SCV000504563 likely pathogenic Brainstem glioma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000426009 SCV000504564 likely pathogenic Hepatocellular carcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000431485 SCV000504565 likely pathogenic Neoplasm of brain 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000444071 SCV000504566 likely pathogenic Neoplasm of the large intestine 2016-05-31 no assertion criteria provided literature only

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