ClinVar Miner

List of variants in gene F11 reported as uncertain significance for coagulation protein disease

Included ClinVar conditions (43):
Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 69
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HGVS dbSNP
NM_000128.3(F11):c.*1033A>G rs886059305
NM_000128.3(F11):c.*262A>G rs886059300
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.*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.-326C>G rs753031984
NM_000128.3(F11):c.-456G>A rs1004061199
NM_000128.3(F11):c.1028+9T>C rs376630194
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.1135+5G>A rs758515608
NM_000128.3(F11):c.1137G>C (p.Glu379Asp)
NM_000128.3(F11):c.1171G>A (p.Gly391Arg) rs1554083456
NM_000128.3(F11):c.1192G>A (p.Glu398Lys)
NM_000128.3(F11):c.1200G>A (p.Pro400=) rs150377265
NM_000128.3(F11):c.1217A>C (p.His406Pro) rs901732635
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.1305-5C>T
NM_000128.3(F11):c.1325del (p.Leu442fs) rs757530565
NM_000128.3(F11):c.1328G>A (p.Arg443His)
NM_000128.3(F11):c.1431C>T (p.Ser477=) rs149568223
NM_000128.3(F11):c.1481-1G>T rs1057516506
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.1627G>A (p.Glu543Lys) rs142952627
NM_000128.3(F11):c.1646A>G (p.Tyr549Cys)
NM_000128.3(F11):c.1699G>A (p.Gly567Arg)
NM_000128.3(F11):c.1718G>A (p.Gly573Glu) rs754109115
NM_000128.3(F11):c.1741T>C (p.Cys581Arg) rs1554084164
NM_000128.3(F11):c.1751A>T (p.Asn584Ile)
NM_000128.3(F11):c.1772G>C (p.Gly591Ala)
NM_000128.3(F11):c.1789G>A (p.Glu597Lys) rs281875251
NM_000128.3(F11):c.188C>T (p.Ala63Val) rs281875244
NM_000128.3(F11):c.218+4A>G rs767240420
NM_000128.3(F11):c.219-11T>A rs886059298
NM_000128.3(F11):c.302A>G (p.Lys101Arg) rs281875272
NM_000128.3(F11):c.325+5G>T rs372102736
NM_000128.3(F11):c.345T>C (p.Tyr115=) rs766137229
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.422C>T (p.Thr141Met) rs200593979
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.499C>T (p.Leu167=) rs374761594
NM_000128.3(F11):c.55+6delinsGAG rs1554081299
NM_000128.3(F11):c.599G>A (p.Cys200Tyr) rs757817254
NM_000128.3(F11):c.634G>A (p.Asp212Asn)
NM_000128.3(F11):c.680G>A (p.Gly227Asp) rs1489595409
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.731A>G (p.Gln244Arg)
NM_000128.3(F11):c.756A>T (p.Arg252Ser) rs1441160252
NM_000128.3(F11):c.783G>C (p.Glu261Asp) rs201079681
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.977G>A (p.Arg326His) rs1554082932

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