ClinVar Miner

Submissions for variant NM_022552.5(DNMT3A):c.2644C>G (p.Arg882Gly)

dbSNP: rs377577594
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Database of Curated Mutations (DoCM) RCV000427931 SCV000503766 pathogenic Acute myeloid leukemia 2014-10-02 no assertion criteria provided literature only

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