ClinVar Miner

Submissions for variant NM_004119.3(FLT3):c.1775T>C (p.Val592Ala)

dbSNP: rs1057520025
Minimum review status: Collection method:
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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) RCV000435462 SCV000510443 likely pathogenic Acute myeloid leukemia 2016-05-13 no assertion criteria provided literature only

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