ClinVar Miner

List of variants in gene F7 reported as uncertain significance for coagulation protein disease

Included ClinVar conditions (43):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 38
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HGVS dbSNP
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.1003T>C (p.Phe335Leu) rs762858015
NM_000131.4(F7):c.1054G>A (p.Ala352Thr) rs3093267
NM_000131.4(F7):c.130+11A>T rs886049986
NM_000131.4(F7):c.169C>A (p.Arg57=) rs886049987
NM_000131.4(F7):c.215C>G (p.Ser72Cys)
NM_000131.4(F7):c.283G>A (p.Glu95Lys)
NM_000131.4(F7):c.682-11C>A rs750680622
NM_000131.4(F7):c.805+7_805+43del
NM_000131.4(F7):c.879G>A (p.Thr293=) rs148965964
NM_000131.4(F7):c.996G>A (p.Thr332=) rs202240468

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