ClinVar Miner

Submissions for variant NM_002168.3(IDH2):c.514A>G (p.Arg172Gly) (rs1057519906)

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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) RCV000438062 SCV000506613 likely pathogenic Brainstem glioma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000419393 SCV000506614 likely pathogenic Neoplasm of the large intestine 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000429662 SCV000506615 likely pathogenic Acute myeloid leukemia 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000440787 SCV000506616 likely pathogenic Hepatocellular carcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000423117 SCV000506617 likely pathogenic Neoplasm of brain 2016-05-31 no assertion criteria provided literature only

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