ClinVar Miner

List of variants in gene F9 studied for not specified

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Gene type:
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Total variants: 68
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HGVS dbSNP gnomAD frequency
NM_000133.4(F9):c.580A>G (p.Thr194Ala) rs6048 0.22614
NM_000133.4(F9):c.1095A>G (p.Ser365=) rs112057482 0.01021
NM_000133.4(F9):c.1110G>A (p.Gln370=) rs34698779 0.00833
NM_000133.4(F9):c.967G>A (p.Glu323Lys) rs150351950 0.00294
NM_000133.4(F9):c.391+10T>G rs375734226 0.00116
NM_000133.4(F9):c.8G>A (p.Arg3His) rs148060786 0.00042
NM_000133.4(F9):c.1345C>T (p.Arg449Trp) rs757996262 0.00009
NM_000133.4(F9):c.1346G>A (p.Arg449Gln) rs143018900 0.00007
NM_000133.4(F9):c.1150C>T (p.Arg384Ter) rs137852261 0.00001
NM_000133.4(F9):c.354G>A (p.Trp118Ter) rs1234002716 0.00001
NM_000133.4(F9):c.459G>A (p.Val153=) rs144314232 0.00001
NM_000133.4(F9):c.1032C>T (p.Ile344=) rs886038243
NM_000133.4(F9):c.1078T>A (p.Phe360Ile) rs1603267386
NM_000133.4(F9):c.1105C>T (p.Leu369Phe) rs2148367939
NM_000133.4(F9):c.1106_1113del (p.Leu369fs) rs1603267391
NM_000133.4(F9):c.1113C>A (p.Tyr371Ter) rs1603267398
NM_000133.4(F9):c.1120G>T (p.Val374Phe) rs137852271
NM_000133.4(F9):c.1135C>T (p.Arg379Ter) rs137852258
NM_000133.4(F9):c.1136G>A (p.Arg379Gln) rs137852259
NM_000133.4(F9):c.1144T>A (p.Cys382Ser) rs137852260
NM_000133.4(F9):c.1148T>C (p.Leu383Pro) rs1387119011
NM_000133.4(F9):c.1173T>A (p.Tyr391Ter) rs1603267411
NM_000133.4(F9):c.1174A>G (p.Asn392Asp) rs1603267412
NM_000133.4(F9):c.1186T>A (p.Cys396Ser) rs1603267420
NM_000133.4(F9):c.1241C>T (p.Pro414Leu) rs1603267443
NM_000133.4(F9):c.1256T>G (p.Val419Gly) rs137852280
NM_000133.4(F9):c.127C>T (p.Arg43Trp) rs1603264205
NM_000133.4(F9):c.128G>A (p.Arg43Gln) rs1275708479
NM_000133.4(F9):c.1290C>A (p.Ser430Arg) rs762229532
NM_000133.4(F9):c.1304G>A (p.Cys435Tyr) rs1385141619
NM_000133.4(F9):c.1325G>A (p.Gly442Glu) rs1603267474
NM_000133.4(F9):c.1361T>C (p.Ile454Thr) rs1603267486
NM_000133.4(F9):c.189A>C (p.Glu63Asp) rs762447016
NM_000133.4(F9):c.190T>C (p.Cys64Arg) rs137852224
NM_000133.4(F9):c.226G>A (p.Glu76Lys) rs1603264236
NM_000133.4(F9):c.252+5G>A rs1266788575
NM_000133.4(F9):c.260T>G (p.Phe87Cys) rs1603264299
NM_000133.4(F9):c.304T>C (p.Cys102Arg) rs1603264719
NM_000133.4(F9):c.344A>G (p.Tyr115Cys) rs1603264727
NM_000133.4(F9):c.374G>A (p.Gly125Glu)
NM_000133.4(F9):c.38del (p.Gly13fs) rs1603263376
NM_000133.4(F9):c.392-1G>C rs1603265480
NM_000133.4(F9):c.392-7_392-4del rs2148361119
NM_000133.4(F9):c.416G>A (p.Gly139Asp) rs1216516070
NM_000133.4(F9):c.422G>A (p.Cys141Tyr) rs1351675410
NM_000133.4(F9):c.424G>C (p.Glu142Gln)
NM_000133.4(F9):c.427C>T (p.Gln143Ter) rs1603265487
NM_000133.4(F9):c.466T>C (p.Ser156Pro)
NM_000133.4(F9):c.484C>T (p.Arg162Ter) rs137852272
NM_000133.4(F9):c.509G>A (p.Cys170Tyr) rs1603265500
NM_000133.4(F9):c.520+19T>C
NM_000133.4(F9):c.520G>A (p.Val174Met) rs1603265504
NM_000133.4(F9):c.533G>T (p.Cys178Phe) rs1603265779
NM_000133.4(F9):c.613A>G (p.Thr205Ala) rs1603265805
NM_000133.4(F9):c.682G>A (p.Val228Ile)
NM_000133.4(F9):c.719G>A (p.Trp240Ter) rs1603265827
NM_000133.4(F9):c.720G>A (p.Trp240Ter) rs1603265830
NM_000133.4(F9):c.723+1G>A rs1603265832
NM_000133.4(F9):c.731T>C (p.Leu244Ser) rs1603267171
NM_000133.4(F9):c.803G>T (p.Cys268Phe) rs1603267195
NM_000133.4(F9):c.839-20dup rs773613916
NM_000133.4(F9):c.88+1G>T rs1603263397
NM_000133.4(F9):c.88+5_88+8del rs1603263399
NM_000133.4(F9):c.880C>T (p.Arg294Ter) rs137852248
NM_000133.4(F9):c.892C>T (p.Arg298Ter) rs137852250
NM_000133.4(F9):c.947T>C (p.Ile316Thr) rs1603267344
NM_000133.4(F9):c.971C>A (p.Pro324His)
NM_000133.4(F9):c.997C>T (p.Pro333Ser) rs2148367784

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