ClinVar Miner

Submissions for variant NM_022552.5(DNMT3A):c.1676G>A (p.Cys559Tyr)

dbSNP: rs1313738991
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mendelics RCV002249029 SCV002516312 likely pathogenic Acute myeloid leukemia 2022-05-04 criteria provided, single submitter clinical testing

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