ClinVar Miner

List of variants in gene FLT3 reported as not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 22
Download table as spreadsheet
HGVS dbSNP
NM_004119.2(FLT3):c.1073A>T (p.Asp358Val) rs34172843
NM_004119.2(FLT3):c.1181A>G (p.Gln394Arg) rs587778372
NM_004119.2(FLT3):c.1249A>C (p.Ile417Leu) rs56090538
NM_004119.2(FLT3):c.1669G>A (p.Val557Ile) rs35958982
NM_004119.2(FLT3):c.190G>A (p.Gly64Arg) rs376895552
NM_004119.2(FLT3):c.2050T>C (p.Ser684Pro) rs199906407
NM_004119.2(FLT3):c.2211G>C (p.Met737Ile)
NM_004119.2(FLT3):c.2858C>T (p.Ala953Val) rs145998293
NM_004119.2(FLT3):c.2888C>T (p.Ser963Leu) rs138003347
NM_004119.2(FLT3):c.2918G>A (p.Arg973Gln) rs144397269
NM_004119.2(FLT3):c.2957C>T (p.Pro986Leu) rs587778369
NM_004119.2(FLT3):c.2962G>C (p.Ala988Pro) rs74041526
NM_004119.2(FLT3):c.2971G>A (p.Glu991Lys) rs573326027
NM_004119.2(FLT3):c.452A>G (p.Asn151Ser) rs560052209
NM_004119.2(FLT3):c.46G>C (p.Val16Leu) rs62636526
NM_004119.2(FLT3):c.580G>A (p.Val194Met) rs146030737
NM_004119.2(FLT3):c.605A>G (p.Gln202Arg) rs551777447
NM_004119.2(FLT3):c.680C>T (p.Thr227Met) rs1933437
NM_004119.2(FLT3):c.784C>T (p.Leu262Phe) rs587778370
NM_004119.2(FLT3):c.833A>C (p.Asn278Thr) rs550878210
NM_004119.2(FLT3):c.844G>A (p.Gly282Arg) rs587778371
NM_004119.2(FLT3):c.970G>A (p.Asp324Asn) rs35602083

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.