ClinVar Miner

Submissions for variant NM_004119.3(FLT3):c.2962G>C (p.Ala988Pro)

gnomAD frequency: 0.00749  dbSNP: rs74041526
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 RCV000884013 SCV001027364 benign not provided 2019-12-31 criteria provided, single submitter clinical testing
ITMI RCV000121123 SCV000085291 not provided not specified 2013-09-19 no assertion provided reference population

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