ClinVar Miner

List of variants in gene F10 reported as uncertain significance for congenital vitamin K-dependent coagulation factors deficiency

Included ClinVar conditions (11):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 44
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HGVS dbSNP gnomAD frequency
NM_000504.4(F10):c.60C>T (p.Leu20=) rs3211718 0.00507
NM_000504.4(F10):c.424G>A (p.Glu142Lys) rs61753266 0.00347
NM_000504.4(F10):c.1032C>T (p.Pro344=) rs41286610 0.00106
NM_000504.4(F10):c.646G>A (p.Asp216Asn) rs144711550 0.00031
NM_000504.4(F10):c.947A>G (p.Lys316Arg) rs144679674 0.00030
NM_000504.4(F10):c.872G>A (p.Arg291Gln) rs149212700 0.00028
NM_000504.4(F10):c.57G>A (p.Leu19=) rs370154986 0.00021
NM_000504.4(F10):c.460G>A (p.Gly154Arg) rs149285827 0.00016
NM_000504.4(F10):c.747+11G>A rs376728587 0.00016
NM_000504.4(F10):c.747+8T>C rs200618182 0.00016
NM_000504.4(F10):c.257-12C>T rs372691873 0.00010
NM_000504.4(F10):c.142A>C (p.Met48Leu) rs201731360 0.00009
NM_000504.4(F10):c.7C>T (p.Arg3Cys) rs149972574 0.00008
NM_000504.4(F10):c.1226C>T (p.Thr409Ile) rs775241064 0.00006
NM_000504.4(F10):c.878C>T (p.Thr293Met) rs752412971 0.00005
NM_000504.4(F10):c.1415C>T (p.Pro472Leu) rs1315933127 0.00004
NM_000504.3(F10):c.-60G>A rs3212993 0.00003
NM_000504.4(F10):c.348C>T (p.Phe116=) rs747030511 0.00003
NM_000504.4(F10):c.1215C>T (p.Ala405=) rs770904651 0.00001
NM_000504.4(F10):c.261C>T (p.Gly87=) rs763365831 0.00001
NM_000504.4(F10):c.318G>C (p.Gly106=) rs567909277 0.00001
NM_000504.4(F10):c.535C>T (p.Arg179Cys) rs1277295882 0.00001
NM_000504.4(F10):c.80G>A (p.Arg27His) rs1263735827 0.00001
NM_000504.4(F10):c.-10C>G rs757542867
NM_000504.4(F10):c.1043G>A (p.Trp348Ter) rs1566922655
NM_000504.4(F10):c.107C>A (p.Ala36Glu) rs2036405879
NM_000504.4(F10):c.1237G>A (p.Asp413Asn) rs1595099677
NM_000504.4(F10):c.1321G>A (p.Glu441Lys) rs1305872315
NM_000504.4(F10):c.1325G>A (p.Gly442Asp) rs1233330150
NM_000504.4(F10):c.1347C>T (p.Tyr449=) rs1432439347
NM_000504.4(F10):c.1387G>C (p.Asp463His) rs1476602298
NM_000504.4(F10):c.1406G>A (p.Arg469Lys) rs771971250
NM_000504.4(F10):c.152G>A (p.Gly51Glu) rs751782758
NM_000504.4(F10):c.160G>A (p.Glu54Lys) rs121964939
NM_000504.4(F10):c.231G>C (p.Thr77=) rs201932014
NM_000504.4(F10):c.241T>G (p.Trp81Gly) rs1595092916
NM_000504.4(F10):c.28C>T (p.Leu10Phe) rs2142244681
NM_000504.4(F10):c.584C>G (p.Pro195Arg) rs886050002
NM_000504.4(F10):c.633C>G (p.Thr211=) rs140852978
NM_000504.4(F10):c.702G>C (p.Arg234Ser) rs1595096266
NM_000504.4(F10):c.829T>A (p.Cys277Ser) rs2138554252
NM_000504.4(F10):c.84G>T (p.Arg28Ser) rs1212018525
NM_000504.4(F10):c.89A>G (p.Gln30Arg) rs2142252077
NM_000504.4(F10):c.916G>A (p.Glu306Lys) rs1366354349

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