ClinVar Miner

Submissions for variant NM_004119.2(FLT3):c.2504A>T (p.Asp835Val) (rs121909646)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000017660 SCV000037937 pathogenic Acute myeloid leukemia 2004-05-01 no assertion criteria provided literature only
OMIM RCV000017661 SCV000037938 pathogenic Acute lymphoid leukemia 2004-05-01 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000017660 SCV000504505 pathogenic Acute myeloid leukemia 2015-07-14 no assertion criteria provided literature only

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