ClinVar Miner

Submissions for variant NM_022552.5(DNMT3A):c.2645G>C (p.Arg882Pro)

dbSNP: rs147001633
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Database of Curated Mutations (DoCM) RCV000427788 SCV000503757 likely pathogenic Myelodysplastic syndrome 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000436723 SCV000503758 pathogenic Acute myeloid leukemia 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000419470 SCV000503759 likely pathogenic Lung adenocarcinoma 2016-05-31 no assertion criteria provided literature only

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