ClinVar Miner

List of variants in gene F11 studied for coagulation protein disease

Included ClinVar conditions (43):
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Gene type:
ClinVar version:
Total variants: 169
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HGVS dbSNP
F11, DEL
NM_000128.3(F11):c.*1033A>G rs886059305
NM_000128.3(F11):c.*262A>G rs886059300
NM_000128.3(F11):c.*265A>G rs4253429
NM_000128.3(F11):c.*296G>C rs4253430
NM_000128.3(F11):c.*322G>A rs4253865
NM_000128.3(F11):c.*479A>T rs1062547
NM_000128.3(F11):c.*576G>A rs886059301
NM_000128.3(F11):c.*584A>T rs766777099
NM_000128.3(F11):c.*636A>G rs886059302
NM_000128.3(F11):c.*728T>C rs566734345
NM_000128.3(F11):c.*822A>G rs558079340
NM_000128.3(F11):c.*852G>A rs4253431
NM_000128.3(F11):c.*885G>A rs4253432
NM_000128.3(F11):c.*902G>A rs555668089
NM_000128.3(F11):c.*928G>A rs556465646
NM_000128.3(F11):c.*952G>A rs886059303
NM_000128.3(F11):c.*977_*979delATT rs886059304
NM_000128.3(F11):c.-183T>C rs886059297
NM_000128.3(F11):c.-2G>C
NM_000128.3(F11):c.-300C>T rs886059296
NM_000128.3(F11):c.-316C>G rs3733403
NM_000128.3(F11):c.-326C>G rs753031984
NM_000128.3(F11):c.-456G>A rs1004061199
NM_000128.3(F11):c.-54G>A rs4253814
NM_000128.3(F11):c.1016G>T (p.Cys339Phe) rs5967
NM_000128.3(F11):c.1028+1G>A rs1316806485
NM_000128.3(F11):c.1028+9T>C rs376630194
NM_000128.3(F11):c.1075del (p.Ile359fs) rs786204429
NM_000128.3(F11):c.1084G>A (p.Gly362Arg) rs142096488
NM_000128.3(F11):c.1103G>C (p.Gly368Ala) rs748926718
NM_000128.3(F11):c.1106A>G (p.Tyr369Cys)
NM_000128.3(F11):c.1107C>A (p.Tyr369Ter) rs773905328
NM_000128.3(F11):c.1118T>C (p.Leu373Ser)
NM_000128.3(F11):c.1120T>C (p.Cys374Arg)
NM_000128.3(F11):c.1135+5G>A rs758515608
NM_000128.3(F11):c.1136-7_1136-4del rs1439195599
NM_000128.3(F11):c.1137G>C (p.Glu379Asp)
NM_000128.3(F11):c.1171G>A (p.Gly391Arg) rs1554083456
NM_000128.3(F11):c.1186C>T (p.Arg396Cys) rs771896253
NM_000128.3(F11):c.1191T>C (p.Gly397=) rs5970
NM_000128.3(F11):c.1192G>A (p.Glu398Lys)
NM_000128.3(F11):c.1199C>T (p.Pro400Leu) rs533335580
NM_000128.3(F11):c.1200G>A (p.Pro400=) rs150377265
NM_000128.3(F11):c.1207G>A (p.Val403Met) rs281875266
NM_000128.3(F11):c.1211C>A (p.Thr404Asn) rs121965067
NM_000128.3(F11):c.1217A>C (p.His406Pro) rs901732635
NM_000128.3(F11):c.1232_1235del (p.Thr411fs) rs1057517446
NM_000128.3(F11):c.1234C>T (p.Gln412Ter) rs538083600
NM_000128.3(F11):c.1247G>A (p.Cys416Tyr) rs779802284
NM_000128.3(F11):c.1253G>T (p.Gly418Val) rs121965071
NM_000128.3(F11):c.1273T>A (p.Trp425Arg) rs1554083512
NM_000128.3(F11):c.1275G>C (p.Trp425Cys) rs533626812
NM_000128.3(F11):c.1283C>T (p.Thr428Ile) rs1554083516
NM_000128.3(F11):c.1288G>A (p.Ala430Thr) rs753909969
NM_000128.3(F11):c.1289C>T (p.Ala430Val) rs121965068
NM_000128.3(F11):c.1304+25_1304+28delAGTT rs778294619
NM_000128.3(F11):c.1305-1G>A rs1057517204
NM_000128.3(F11):c.1305-5C>T
NM_000128.3(F11):c.1313C>A (p.Ser438Ter) rs786204724
NM_000128.3(F11):c.1325del (p.Leu442fs) rs757530565
NM_000128.3(F11):c.1328G>A (p.Arg443His)
NM_000128.3(F11):c.1329del (p.Val444fs) rs1554083727
NM_000128.3(F11):c.1362_1375del (p.Lys455fs) rs1554083734
NM_000128.3(F11):c.1376_1379CTTT[1] (p.Phe460fs) rs1554083736
NM_000128.3(F11):c.1378T>G (p.Phe460Val) rs121965065
NM_000128.3(F11):c.1390C>T (p.Gln464Ter) rs1057517035
NM_000128.3(F11):c.1431C>T (p.Ser477=) rs149568223
NM_000128.3(F11):c.1432G>A (p.Gly478Arg) rs542967227
NM_000128.3(F11):c.1472dup (p.Asn491fs) rs1554083753
NM_000128.3(F11):c.1478C>T (p.Thr493Ile) rs1554083754
NM_000128.3(F11):c.1480+2T>C rs1554083758
NM_000128.3(F11):c.1481-1G>C rs1057516506
NM_000128.3(F11):c.1481-1G>T rs1057516506
NM_000128.3(F11):c.1489C>T (p.Arg497Ter) rs375422404
NM_000128.3(F11):c.1517A>G (p.Asp506Gly) rs281875258
NM_000128.3(F11):c.1546G>A (p.Val516Met) rs200622588
NM_000128.3(F11):c.1556G>A (p.Trp519Ter) rs201007090
NM_000128.3(F11):c.155dup (p.Tyr52Ter) rs1554081886
NM_000128.3(F11):c.1560dup (p.Tyr521fs) rs1057516777
NM_000128.3(F11):c.1613C>T (p.Pro538Leu) rs139695003
NM_000128.3(F11):c.1620_1621dup (p.Thr541fs) rs1554084031
NM_000128.3(F11):c.1627G>A (p.Glu543Lys) rs142952627
NM_000128.3(F11):c.1646A>G (p.Tyr549Cys)
NM_000128.3(F11):c.166T>C (p.Cys56Arg) rs121965069
NM_000128.3(F11):c.1676_1682del (p.Ile559fs) rs1057517171
NM_000128.3(F11):c.1693G>A (p.Glu565Lys) rs281875275
NM_000128.3(F11):c.1699G>A (p.Gly567Arg)
NM_000128.3(F11):c.16C>T (p.Gln6Ter) rs1554081288
NM_000128.3(F11):c.1707C>T (p.Asp569=) rs5975
NM_000128.3(F11):c.1716+1G>A rs373297713
NM_000128.3(F11):c.1718G>A (p.Gly573Glu) rs754109115
NM_000128.3(F11):c.1724C>A (p.Ser575Ter) rs281875250
NM_000128.3(F11):c.1724C>T (p.Ser575Leu) rs281875250
NM_000128.3(F11):c.1741T>C (p.Cys581Arg) rs1554084164
NM_000128.3(F11):c.1751A>T (p.Asn584Ile)
NM_000128.3(F11):c.1760G>C (p.Trp587Ser) rs121965072
NM_000128.3(F11):c.1772G>C (p.Gly591Ala)
NM_000128.3(F11):c.1778C>T (p.Thr593Met) rs145906668
NM_000128.3(F11):c.1782C>A (p.Ser594Arg) rs28934609
NM_000128.3(F11):c.1789G>A (p.Glu597Lys) rs281875251
NM_000128.3(F11):c.1789G>T (p.Glu597Ter) rs281875251
NM_000128.3(F11):c.1812G>T (p.Arg604=) rs5971
NM_000128.3(F11):c.1839G>A (p.Glu613=) rs5976
NM_000128.3(F11):c.188C>T (p.Ala63Val) rs281875244
NM_000128.3(F11):c.218+1G>A rs1057516738
NM_000128.3(F11):c.218+4A>G rs767240420
NM_000128.3(F11):c.219-11T>A rs886059298
NM_000128.3(F11):c.219G>A (p.Trp73Ter) rs762013077
NM_000128.3(F11):c.25_28del (p.His9fs) rs1057516616
NM_000128.3(F11):c.291del (p.Tyr98fs) rs1057517151
NM_000128.3(F11):c.2T>A (p.Met1Lys) rs1554081281
NM_000128.3(F11):c.302A>G (p.Lys101Arg) rs281875272
NM_000128.3(F11):c.325+5G>T rs372102736
NM_000128.3(F11):c.325G>A (p.Ala109Thr) rs768474112
NM_000128.3(F11):c.326-1G>A rs1057517364
NM_000128.3(F11):c.343del (p.Tyr115fs)
NM_000128.3(F11):c.345T>C (p.Tyr115=) rs766137229
NM_000128.3(F11):c.359T>C (p.Met120Thr)
NM_000128.3(F11):c.365G>A (p.Gly122Asp)
NM_000128.3(F11):c.374A>G (p.Tyr125Cys) rs1554082187
NM_000128.3(F11):c.400C>T (p.Gln134Ter) rs756908183
NM_000128.3(F11):c.403G>T (p.Glu135Ter) rs121965063
NM_000128.3(F11):c.408C>A (p.Cys136Ter) rs143648758
NM_000128.3(F11):c.422C>T (p.Thr141Met) rs200593979
NM_000128.3(F11):c.429C>T (p.Asp143=) rs5973
NM_000128.3(F11):c.438C>A (p.Cys146Ter) rs121965066
NM_000128.3(F11):c.449C>T (p.Thr150Met) rs1340928778
NM_000128.3(F11):c.478G>T (p.Glu160Ter) rs376961859
NM_000128.3(F11):c.484C>T (p.Arg162Cys) rs748139184
NM_000128.3(F11):c.486-2A>G rs1057516695
NM_000128.3(F11):c.499C>T (p.Leu167=) rs374761594
NM_000128.3(F11):c.55+6delinsGAG rs1554081299
NM_000128.3(F11):c.596-7_600del rs1057517116
NM_000128.3(F11):c.599G>A (p.Cys200Tyr) rs757817254
NM_000128.3(F11):c.634G>A (p.Asp212Asn)
NM_000128.3(F11):c.644_649del (p.Ile215_Asp216del) rs1459304265
NM_000128.3(F11):c.664G>T (p.Asp222Tyr) rs281875245
NM_000128.3(F11):c.67C>T (p.Gln23Ter) rs768409400
NM_000128.3(F11):c.680G>A (p.Gly227Asp) rs1489595409
NM_000128.3(F11):c.682C>T (p.Arg228Ter) rs752907087
NM_000128.3(F11):c.683G>A (p.Arg228Gln) rs281875246
NM_000128.3(F11):c.723C>G (p.Phe241Leu) rs281875265
NM_000128.3(F11):c.728C>T (p.Ser243Phe)
NM_000128.3(F11):c.730C>T (p.Gln244Ter) rs747702749
NM_000128.3(F11):c.731A>G (p.Gln244Arg)
NM_000128.3(F11):c.751C>T (p.Gln251Ter) rs754087775
NM_000128.3(F11):c.755+2T>C rs1220869989
NM_000128.3(F11):c.756A>T (p.Arg252Ser) rs1441160252
NM_000128.3(F11):c.769del (p.Thr259fs) rs1554082832
NM_000128.3(F11):c.783G>C (p.Glu261Asp) rs201079681
NM_000128.3(F11):c.801A>G (p.Thr267=) rs5974
NM_000128.3(F11):c.802C>T (p.Arg268Cys)
NM_000128.3(F11):c.803G>A (p.Arg268His) rs201688862
NM_000128.3(F11):c.809A>T (p.Lys270Ile) rs121965070
NM_000128.3(F11):c.841C>T (p.Gln281Ter) rs770505620
NM_000128.3(F11):c.865+1G>C rs1349655563
NM_000128.3(F11):c.901T>C (p.Phe301Leu) rs121965064
NM_000128.3(F11):c.908del (p.Gly303fs) rs786204722
NM_000128.3(F11):c.943G>A (p.Glu315Lys) rs281875257
NM_000128.3(F11):c.959_960TG[1] (p.Cys321fs) rs786204449
NM_000128.3(F11):c.964_965del (p.Thr322fs) rs1057516431
NM_000128.3(F11):c.976C>T (p.Arg326Cys) rs28934608
NM_000128.3(F11):c.977G>A (p.Arg326His) rs1554082932
NM_000128.3(F11):c.990del (p.Phe330fs) rs1554082938
NM_000128.3(F11):c.990dup (p.Thr331fs) rs1554082938
NM_000128.3:c.1029-2A>G
NM_001354804.2(F11):c.*1G>C
Single allele

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