ClinVar Miner

List of variants in gene F7 studied for coagulation protein disease

Included ClinVar conditions (43):
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Gene type:
ClinVar version:
Total variants: 83
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HGVS dbSNP
F7, -55C-T
F7, -61T-G
F7, -94C-G
F7, 1-BP DEL, 11128C
F7, ALA244VAL
F7, ARG247HIS
F7, ASN57ASP
F7, CYS178TYR
F7, CYS310PHE
F7, CYS61TER
F7, GLU25LYS
F7, GLY354CYS
F7, IVS4DS, G-A, +1
F7, THR359MET
NM_000131.4(F7):c.*1054C>A rs546634569
NM_000131.4(F7):c.*1057C>T rs141219406
NM_000131.4(F7):c.*1077del rs886050000
NM_000131.4(F7):c.*1475G>A rs3093258
NM_000131.4(F7):c.*1500_*1503del rs539395699
NM_000131.4(F7):c.*1614A>C rs577978392
NM_000131.4(F7):c.*275G>A rs886049988
NM_000131.4(F7):c.*284C>T rs750831181
NM_000131.4(F7):c.*285G>A rs577927838
NM_000131.4(F7):c.*294A>C rs886049989
NM_000131.4(F7):c.*340T>C rs545497651
NM_000131.4(F7):c.*410C>T rs139474305
NM_000131.4(F7):c.*425C>T rs886049990
NM_000131.4(F7):c.*499G>A rs575689457
NM_000131.4(F7):c.*543A>G rs886049991
NM_000131.4(F7):c.*561_*562AT[1] rs886049992
NM_000131.4(F7):c.*582C>T rs886049993
NM_000131.4(F7):c.*605G>A rs144204350
NM_000131.4(F7):c.*620C>T rs151109093
NM_000131.4(F7):c.*628_*630del rs747160994
NM_000131.4(F7):c.*672_*673CA[3] rs886049995
NM_000131.4(F7):c.*703_*704AC[3] rs3093252
NM_000131.4(F7):c.*71T>A rs143748941
NM_000131.4(F7):c.*756_*770delinsCCA rs886049997
NM_000131.4(F7):c.*846_*850CTTCA[1] rs886049998
NM_000131.4(F7):c.*909C>T rs886049999
NM_000131.4(F7):c.*991G>A rs3093254
NM_000131.4(F7):c.-27C>T rs886049985
NM_000131.4(F7):c.-30A>C
NM_000131.4(F7):c.-55C>T
NM_000131.4(F7):c.-61T>G
NM_000131.4(F7):c.1003T>C (p.Phe335Leu) rs762858015
NM_000131.4(F7):c.1027G>A (p.Gly343Ser)
NM_000131.4(F7):c.1054G>A (p.Ala352Thr) rs3093267
NM_000131.4(F7):c.1061C>T (p.Ala354Val) rs36209567
NM_000131.4(F7):c.108G>A (p.Pro36=) rs3093238
NM_000131.4(F7):c.1091G>A (p.Arg364Gln) rs121964926
NM_000131.4(F7):c.1109G>T (p.Cys370Phe) rs121964927
NM_000131.4(F7):c.1114C>T (p.Gln372Ter)
NM_000131.4(F7):c.1165T>G (p.Cys389Gly) rs121964934
NM_000131.4(F7):c.1224T>G (p.His408Gln) rs121964936
NM_000131.4(F7):c.1285G>A (p.Ala429Thr) rs755377592
NM_000131.4(F7):c.130+11A>T rs886049986
NM_000131.4(F7):c.1391del (p.Pro464fs)
NM_000131.4(F7):c.169C>A (p.Arg57=) rs886049987
NM_000131.4(F7):c.215C>G (p.Ser72Cys)
NM_000131.4(F7):c.218T>A (p.Leu73Gln)
NM_000131.4(F7):c.283G>A (p.Glu95Lys)
NM_000131.4(F7):c.285G>A (p.Glu95=) rs36208758
NM_000131.4(F7):c.38T>C (p.Leu13Pro) rs387906507
NM_000131.4(F7):c.430+1G>A
NM_000131.4(F7):c.479A>G (p.Gln160Arg) rs200016360
NM_000131.4(F7):c.509G>A (p.Arg170His)
NM_000131.4(F7):c.525C>T (p.His175=) rs6042
NM_000131.4(F7):c.628C>T (p.Gln210Ter) rs267606790
NM_000131.4(F7):c.64+8C>T rs10482844
NM_000131.4(F7):c.64+9G>A rs6039
NM_000131.4(F7):c.681+1G>T
NM_000131.4(F7):c.682-11C>A rs750680622
NM_000131.4(F7):c.722C>A (p.Thr241Asn)
NM_000131.4(F7):c.805+3_805+6del rs754785708
NM_000131.4(F7):c.805+5G>A
NM_000131.4(F7):c.805+7_805+43del
NM_000131.4(F7):c.817_831del (p.Leu273_Asp277del)
NM_000131.4(F7):c.849_865del (p.Arg284fs) rs786205091
NM_000131.4(F7):c.879G>A (p.Thr293=) rs148965964
NM_000131.4(F7):c.911C>T (p.Ala304Val)
NM_000131.4(F7):c.983T>C (p.Phe328Ser) rs387906508
NM_000131.4(F7):c.996G>A (p.Thr332=) rs202240468

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