ClinVar Miner

Submissions for variant NM_004119.3(FLT3):c.2503G>T (p.Asp835Tyr) (rs121913488)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000017665 SCV000037942 pathogenic Acute myeloid leukemia 2004-05-01 no assertion criteria provided literature only
OMIM RCV000017666 SCV000037943 pathogenic Acute lymphoid leukemia 2004-05-01 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000017665 SCV000504507 pathogenic Acute myeloid leukemia 2014-10-02 no assertion criteria provided literature only
Hematopathology,The University of Texas M.D. Anderson Cancer Center RCV000017665 SCV001571656 pathogenic Acute myeloid leukemia 2018-03-30 no assertion criteria provided clinical testing

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