ClinVar Miner

Submissions for variant NM_004119.3(FLT3):c.1249A>C (p.Ile417Leu)

gnomAD frequency: 0.01006  dbSNP: rs56090538
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000965256 SCV001112519 benign not provided 2019-12-31 criteria provided, single submitter clinical testing
ITMI RCV000121115 SCV000085283 not provided not specified 2013-09-19 no assertion provided reference population

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