ClinVar Miner

List of variants reported as uncertain significance for Factor X deficiency

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Total variants: 20
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HGVS dbSNP
NM_000504.4(F10):c.1043G>A (p.Trp348Ter) rs1566922655
NM_000504.4(F10):c.1215C>T (p.Ala405=) rs770904651
NM_000504.4(F10):c.1226C>T (p.Thr409Ile) rs775241064
NM_000504.4(F10):c.1237G>A (p.Asp413Asn)
NM_000504.4(F10):c.1321G>A (p.Glu441Lys)
NM_000504.4(F10):c.241T>G (p.Trp81Gly)
NM_000504.4(F10):c.257-12C>T rs372691873
NM_000504.4(F10):c.348C>T (p.Phe116=) rs747030511
NM_000504.4(F10):c.396C>T (p.Asp132=) rs111737184
NM_000504.4(F10):c.424G>A (p.Glu142Lys) rs61753266
NM_000504.4(F10):c.535C>T (p.Arg179Cys)
NM_000504.4(F10):c.57G>A (p.Leu19=) rs370154986
NM_000504.4(F10):c.584C>G (p.Pro195Arg) rs886050002
NM_000504.4(F10):c.60C>T (p.Leu20=) rs3211718
NM_000504.4(F10):c.633C>G (p.Thr211=) rs140852978
NM_000504.4(F10):c.702G>C (p.Arg234Ser)
NM_000504.4(F10):c.747+11G>A rs376728587
NM_000504.4(F10):c.7C>T (p.Arg3Cys) rs149972574
NM_000504.4(F10):c.872G>A (p.Arg291Gln) rs149212700
NM_000504.4(F10):c.878C>T (p.Thr293Met) rs752412971

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