ClinVar Miner

Submissions for variant NM_002168.4(IDH2):c.515G>T (p.Arg172Met)

dbSNP: 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) RCV000431159 SCV000504556 pathogenic Acute myeloid leukemia 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000440163 SCV000504557 likely pathogenic Neoplasm of brain 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000422933 SCV000504558 likely pathogenic Hepatocellular carcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000433618 SCV000504559 likely pathogenic Neoplasm of the large intestine 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000440790 SCV000504560 likely pathogenic Brainstem glioma 2016-05-31 no assertion criteria provided literature only
Clinical Pathology, Faculty of Medicine, Tanta University RCV002254523 SCV002047545 risk factor Acute myocardial infarction no assertion criteria provided case-control

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