ClinVar Miner

List of variants in gene F10 studied for blood coagulation disease

Included ClinVar conditions (155):
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Gene type:
ClinVar version:
Total variants: 93
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HGVS dbSNP gnomAD frequency
NM_000504.4(F10):c.865+33A>G rs2031184 0.93642
NM_000504.4(F10):c.232-17T>C rs2251102 0.79208
NM_000504.4(F10):c.792C>T (p.Thr264=) rs5960 0.72493
NM_000504.4(F10):c.574G>A (p.Gly192Arg) rs3211783 0.02730
NM_000504.4(F10):c.399C>T (p.Asn133=) rs5962 0.01840
NM_000504.4(F10):c.90G>C (p.Gln30His) rs5961 0.01285
NM_000504.4(F10):c.111G>A (p.Arg37=) rs115112448 0.00649
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.396C>T (p.Asp132=) rs111737184 0.00287
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.1351A>C (p.Ile451Leu) rs369872236 0.00011
NM_000504.4(F10):c.257-12C>T rs372691873 0.00010
NM_000504.4(F10):c.71-8C>T rs374210821 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.1097G>A (p.Arg366His) rs143715673 0.00005
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.1012G>A (p.Val338Met) rs121964947 0.00001
NM_000504.4(F10):c.1073C>T (p.Thr358Met) rs768222784 0.00001
NM_000504.4(F10):c.1215C>T (p.Ala405=) rs770904651 0.00001
NM_000504.4(F10):c.140A>G (p.Glu47Gly) rs121964943 0.00001
NM_000504.4(F10):c.161A>G (p.Glu54Gly) rs121964944 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.400G>A (p.Gly134Arg) rs368225671 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.1036C>T (p.Arg346Cys)
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.1087G>A (p.Gly363Ser) rs1595099527
NM_000504.4(F10):c.1094G>C (p.Gly365Ala)
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.1120T>C (p.Ser374Pro) rs121964941
NM_000504.4(F10):c.119G>C (p.Arg40Thr)
NM_000504.4(F10):c.1210T>C (p.Cys404Arg) rs1595099645
NM_000504.4(F10):c.1216G>A (p.Gly406Ser) rs376163818
NM_000504.4(F10):c.1237G>A (p.Asp413Asn) rs1595099677
NM_000504.4(F10):c.1252G>C (p.Asp418His) rs2138557799
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.1331C>T (p.Ala444Val)
NM_000504.4(F10):c.1347C>T (p.Tyr449=) rs1432439347
NM_000504.4(F10):c.1348G>A (p.Gly450Arg) rs1595099844
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.162_163del (p.Glu56fs) rs749213415
NM_000504.4(F10):c.167A>G (p.Glu56Gly)
NM_000504.4(F10):c.183_184delinsTTGCTCATACGAAGAGGCCC (p.Arg68_Glu69insSerTyrGluGluAlaArg)
NM_000504.4(F10):c.205G>A (p.Glu69Lys) rs1325135019
NM_000504.4(F10):c.212T>C (p.Phe71Ser)
NM_000504.4(F10):c.214G>C (p.Glu72Gln) rs121964945
NM_000504.4(F10):c.231G>C (p.Thr77=) rs201932014
NM_000504.4(F10):c.232-2563_503-451del
NM_000504.4(F10):c.241T>G (p.Trp81Gly) rs1595092916
NM_000504.4(F10):c.248_251del (p.Lys83fs)
NM_000504.4(F10):c.256G>A (p.Asp86Asn)
NM_000504.4(F10):c.270T>A (p.Cys90Ter)
NM_000504.4(F10):c.28C>T (p.Leu10Phe) rs2142244681
NM_000504.4(F10):c.299_300del (p.Lys100fs)
NM_000504.4(F10):c.305_306del (p.Lys102fs)
NM_000504.4(F10):c.307G>C (p.Asp103His)
NM_000504.4(F10):c.513del (p.Cys172fs) rs2138548669
NM_000504.4(F10):c.584C>G (p.Pro195Arg) rs886050002
NM_000504.4(F10):c.61G>A (p.Gly21Arg) rs753790195
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.814del (p.Ile271_Leu272insTer) rs387906506
NM_000504.4(F10):c.815T>C (p.Leu272Pro)
NM_000504.4(F10):c.829T>A (p.Cys277Ser) rs2138554252
NM_000504.4(F10):c.837C>A (p.Tyr279Ter) rs1250509122
NM_000504.4(F10):c.84G>T (p.Arg28Ser) rs1212018525
NM_000504.4(F10):c.859A>T (p.Arg287Trp) rs121964948
NM_000504.4(F10):c.89A>G (p.Gln30Arg) rs2142252077
NM_000504.4(F10):c.916G>A (p.Glu306Lys) rs1366354349
NM_000504.4(F10):c.964G>A (p.Asp322Asn) rs121964942
NM_001312675.2(F10):c.*138C>T rs121964940

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