ClinVar Miner

List of variants in gene F11 reported by Illumina Clinical Services Laboratory,Illumina

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Gene type:
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Total variants: 85
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HGVS dbSNP
NC_000004.12:g.186266064C>T
NC_000004.12:g.186266133G>A
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.-300C>T rs886059296
NM_000128.3(F11):c.-316C>G rs3733403
NM_000128.3(F11):c.-326C>G rs753031984
NM_000128.3(F11):c.-54G>A rs4253814
NM_000128.3(F11):c.1016G>T (p.Cys339Phe) rs5967
NM_000128.3(F11):c.1028+9T>C rs376630194
NM_000128.3(F11):c.1191T>C (p.Gly397=) rs5970
NM_000128.3(F11):c.1200G>A (p.Pro400=) rs150377265
NM_000128.3(F11):c.1247G>A (p.Cys416Tyr) rs779802284
NM_000128.3(F11):c.1305-9G>T rs4253426
NM_000128.3(F11):c.1325del (p.Leu442fs) rs757530565
NM_000128.3(F11):c.1431C>T (p.Ser477=) rs149568223
NM_000128.3(F11):c.1481-1G>T rs1057516506
NM_000128.3(F11):c.1707C>T (p.Asp569=) rs5975
NM_000128.3(F11):c.1716+1G>A rs373297713
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.219-11T>A rs886059298
NM_000128.3(F11):c.325G>A (p.Ala109Thr) rs768474112
NM_000128.3(F11):c.345T>C (p.Tyr115=) rs766137229
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.429C>T (p.Asp143=) rs5973
NM_000128.3(F11):c.478G>T (p.Glu160Ter) rs376961859
NM_000128.3(F11):c.499C>T (p.Leu167=) rs374761594
NM_000128.3(F11):c.731A>G (p.Gln244Arg) rs5969
NM_000128.3(F11):c.801A>G (p.Thr267=) rs5974
NM_000128.3(F11):c.809A>T (p.Lys270Ile) rs121965070
NM_000128.3(F11):c.901T>C (p.Phe301Leu) rs121965064
NM_000128.4(F11):c.*1039G>A
NM_000128.4(F11):c.*174C>T
NM_000128.4(F11):c.*175C>T
NM_000128.4(F11):c.*186C>T
NM_000128.4(F11):c.*1A>G
NM_000128.4(F11):c.*346A>G
NM_000128.4(F11):c.*404A>G
NM_000128.4(F11):c.*445C>T
NM_000128.4(F11):c.*448A>G
NM_000128.4(F11):c.*551A>T
NM_000128.4(F11):c.*609C>A
NM_000128.4(F11):c.*763T>A
NM_000128.4(F11):c.*817A>G
NM_000128.4(F11):c.*846T>C
NM_000128.4(F11):c.*884C>T
NM_000128.4(F11):c.*933C>G
NM_000128.4(F11):c.-57G>A
NM_000128.4(F11):c.-70G>A
NM_000128.4(F11):c.1020C>T (p.Asn340=) rs149052026
NM_000128.4(F11):c.1029-11T>C
NM_000128.4(F11):c.1219A>G (p.Thr407Ala)
NM_000128.4(F11):c.1304+12G>A
NM_000128.4(F11):c.1305-14T>C
NM_000128.4(F11):c.1416T>C (p.Tyr472=)
NM_000128.4(F11):c.1480+4C>T
NM_000128.4(F11):c.1777A>G (p.Thr593Ala)
NM_000128.4(F11):c.1836C>T (p.Val612=)
NM_000128.4(F11):c.1842C>T (p.Tyr614=)
NM_000128.4(F11):c.1843G>A (p.Val615Met) rs202061241
NM_000128.4(F11):c.453C>T (p.Tyr151=) rs34807019
NM_000128.4(F11):c.539A>G (p.Lys180Arg) rs190283743
NM_000128.4(F11):c.56-6T>C
NM_000128.4(F11):c.596-6G>A rs369721182
NM_000128.4(F11):c.642C>T (p.Asn214=)
NM_000128.4(F11):c.696T>C (p.His232=) rs746382259
NM_000128.4(F11):c.861C>T (p.Ile287=) rs5964

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