ClinVar Miner

List of variants in gene F13A1 studied for coagulation protein disease

Included ClinVar conditions (45):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 66
Download table as spreadsheet
HGVS dbSNP
F13A1, 1-BP INS, 1286C
F13A1, 2-BP DEL, 210AG
NM_000129.3(F13A1):c.*1030G>T rs548323382
NM_000129.3(F13A1):c.*112G>T rs3024463
NM_000129.3(F13A1):c.*1167T>G rs886061655
NM_000129.3(F13A1):c.*126T>C rs1050782
NM_000129.3(F13A1):c.*160G>A rs1050783
NM_000129.3(F13A1):c.*221G>A rs3024464
NM_000129.3(F13A1):c.*270C>T rs568780978
NM_000129.3(F13A1):c.*417G>T rs886061658
NM_000129.3(F13A1):c.*42G>A rs886061659
NM_000129.3(F13A1):c.*443G>A rs3024486
NM_000129.3(F13A1):c.*587G>A rs75981686
NM_000129.3(F13A1):c.*619C>T rs191569585
NM_000129.3(F13A1):c.*627G>A rs886061657
NM_000129.3(F13A1):c.*628G>A rs886061656
NM_000129.3(F13A1):c.*67C>T rs182425546
NM_000129.3(F13A1):c.*743G>A rs12862
NM_000129.3(F13A1):c.*89A>G rs3024462
NM_000129.3(F13A1):c.*927G>A rs746364189
NM_000129.3(F13A1):c.*945T>C rs774737661
NM_000129.3(F13A1):c.*995G>T rs3024466
NM_000129.3(F13A1):c.-18-5dup rs750373197
NM_000129.3(F13A1):c.-19+12= rs2815822
NM_000129.3(F13A1):c.-19+12A>C rs2815822
NM_000129.3(F13A1):c.-28G>A rs886061662
NM_000129.3(F13A1):c.102C>T (p.Gly34=) rs187027323
NM_000129.3(F13A1):c.103G>T (p.Val35Leu) rs5985
NM_000129.3(F13A1):c.1112+11T>C rs758486753
NM_000129.3(F13A1):c.1243G>T (p.Val415Phe) rs121913070
NM_000129.3(F13A1):c.1326C>A (p.Tyr442Ter) rs121913066
NM_000129.3(F13A1):c.1352_1353del (p.His451fs) rs1561645895
NM_000129.3(F13A1):c.1504G>A (p.Gly502Arg) rs121913068
NM_000129.3(F13A1):c.160T>A (p.Phe54Ile) rs138690353
NM_000129.3(F13A1):c.1687G>A (p.Gly563Arg) rs121913069
NM_000129.3(F13A1):c.1694C>T (p.Pro565Leu) rs5982
NM_000129.3(F13A1):c.1704A>G (p.Glu568=) rs5986
NM_000129.3(F13A1):c.1731G>C (p.Thr577=) rs137945179
NM_000129.3(F13A1):c.1777G>A (p.Gly593Ser)
NM_000129.3(F13A1):c.1804C>T (p.Gln602Ter)
NM_000129.3(F13A1):c.1817del (p.His606fs) rs1561641262
NM_000129.3(F13A1):c.183C>A (p.Asn61Lys) rs121913067
NM_000129.3(F13A1):c.1860G>C (p.Leu620=) rs138943514
NM_000129.3(F13A1):c.1951G>A (p.Val651Ile) rs5987
NM_000129.3(F13A1):c.1954G>C (p.Glu652Gln) rs5988
NM_000129.3(F13A1):c.1984C>T (p.Arg662Ter) rs267606789
NM_000129.3(F13A1):c.2029A>G (p.Met677Val) rs371964182
NM_000129.3(F13A1):c.2045G>A (p.Arg682His) rs121913064
NM_000129.3(F13A1):c.2067C>T (p.Thr689=) rs750971578
NM_000129.3(F13A1):c.2110C>T (p.Arg704Trp) rs267606787
NM_000129.3(F13A1):c.233G>T (p.Arg78Leu)
NM_000129.3(F13A1):c.327C>T (p.Tyr109=) rs886061661
NM_000129.3(F13A1):c.514C>T (p.Arg172Ter) rs121913065
NM_000129.3(F13A1):c.563G>T (p.Trp188Leu) rs1561673120
NM_000129.3(F13A1):c.728T>C (p.Met243Thr) rs267606788
NM_000129.3(F13A1):c.782G>A (p.Arg261His) rs121913071
NM_000129.3(F13A1):c.799-13C>T rs188094485
NM_000129.3(F13A1):c.851A>G (p.Tyr284Cys) rs121913074
NM_000129.3(F13A1):c.888C>G (p.Ser296Arg)
NM_000129.3(F13A1):c.889G>A (p.Val297Ile) rs199564311
NM_000129.3(F13A1):c.949G>T (p.Val317Phe) rs121913073
NM_000129.3(F13A1):c.980G>A (p.Arg327Gln) rs121913072
NM_000129.3(F13A1):c.990A>T (p.Gly330=) rs886061660
NM_000129.3(F13A1):c.996A>C (p.Pro332=) rs5981
NM_000129.3:c.603_606delAAGA
NM_000129.3:c.691-1G>A

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.