ClinVar Miner

List of variants in gene F10 studied for congenital vitamin K-dependent coagulation factors deficiency

Included ClinVar conditions (6):
Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 68
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HGVS dbSNP
D282N
E14K
E32Q
E7G
F10, G-A, -20
F10, PRO343SER
F10, SER334PRO
F10, THR318MET
F10, VAL298MET
Factor X Ketchikan
NC_000013.11:g.113122796G>A
NM_000504.4(F10):c.-10C>G
NM_000504.4(F10):c.1032C>T (p.Pro344=)
NM_000504.4(F10):c.1043G>A (p.Trp348Ter) rs1566922655
NM_000504.4(F10):c.107C>A (p.Ala36Glu)
NM_000504.4(F10):c.1087G>A (p.Gly363Ser) rs1595099527
NM_000504.4(F10):c.1096C>T (p.Arg366Cys) rs104894392
NM_000504.4(F10):c.1115G>C (p.Arg372Pro) rs142699098
NM_000504.4(F10):c.111G>A (p.Arg37=) rs115112448
NM_000504.4(F10):c.1210T>C (p.Cys404Arg) rs1595099645
NM_000504.4(F10):c.1215C>T (p.Ala405=) rs770904651
NM_000504.4(F10):c.1226C>T (p.Thr409Ile) rs775241064
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)
NM_000504.4(F10):c.1347C>T (p.Tyr449=)
NM_000504.4(F10):c.1348G>A (p.Gly450Arg) rs1595099844
NM_000504.4(F10):c.1387G>C (p.Asp463His)
NM_000504.4(F10):c.1406G>A (p.Arg469Lys)
NM_000504.4(F10):c.1415C>T (p.Pro472Leu)
NM_000504.4(F10):c.142A>C (p.Met48Leu)
NM_000504.4(F10):c.152G>A (p.Gly51Glu)
NM_000504.4(F10):c.160G>A (p.Glu54Lys) rs121964939
NM_000504.4(F10):c.161A>G (p.Glu54Gly) rs121964944
NM_000504.4(F10):c.241T>G (p.Trp81Gly) rs1595092916
NM_000504.4(F10):c.257-12C>T rs372691873
NM_000504.4(F10):c.261C>T (p.Gly87=)
NM_000504.4(F10):c.28C>T (p.Leu10Phe)
NM_000504.4(F10):c.318G>C (p.Gly106=)
NM_000504.4(F10):c.348C>T (p.Phe116=) rs747030511
NM_000504.4(F10):c.396C>T (p.Asp132=) rs111737184
NM_000504.4(F10):c.399C>T (p.Asn133=) rs5962
NM_000504.4(F10):c.400G>A (p.Gly134Arg) rs368225671
NM_000504.4(F10):c.424G>A (p.Glu142Lys) rs61753266
NM_000504.4(F10):c.460G>A (p.Gly154Arg)
NM_000504.4(F10):c.513del (p.Cys172fs)
NM_000504.4(F10):c.535C>T (p.Arg179Cys) rs1277295882
NM_000504.4(F10):c.574G>A (p.Gly192Arg) rs3211783
NM_000504.4(F10):c.57G>A (p.Leu19=) rs370154986
NM_000504.4(F10):c.584C>G (p.Pro195Arg) rs886050002
NM_000504.4(F10):c.60C>T (p.Leu20=) rs3211718
NM_000504.4(F10):c.633C>G (p.Thr211=) rs140852978
NM_000504.4(F10):c.646G>A (p.Asp216Asn)
NM_000504.4(F10):c.702G>C (p.Arg234Ser) rs1595096266
NM_000504.4(F10):c.71-8C>T rs374210821
NM_000504.4(F10):c.747+11G>A rs376728587
NM_000504.4(F10):c.792C>T (p.Thr264=) rs5960
NM_000504.4(F10):c.7C>T (p.Arg3Cys) rs149972574
NM_000504.4(F10):c.80G>A (p.Arg27His)
NM_000504.4(F10):c.814del (p.Ile271_Leu272insTer) rs387906506
NM_000504.4(F10):c.829T>A (p.Cys277Ser)
NM_000504.4(F10):c.84G>T (p.Arg28Ser)
NM_000504.4(F10):c.859A>T (p.Arg287Trp) rs121964948
NM_000504.4(F10):c.872G>A (p.Arg291Gln) rs149212700
NM_000504.4(F10):c.878C>T (p.Thr293Met) rs752412971
NM_000504.4(F10):c.89A>G (p.Gln30Arg)
NM_000504.4(F10):c.90G>C (p.Gln30His) rs5961
NM_000504.4(F10):c.916G>A (p.Glu306Lys)

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