ClinVar Miner

List of variants in gene FLNC reported by Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine

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Gene type:
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Total variants: 23
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HGVS dbSNP
NM_001458.4(FLNC):c.1032C>T (p.Val344=) rs2291562
NM_001458.4(FLNC):c.1444C>T (p.Arg482Ter) rs1420159591
NM_001458.4(FLNC):c.1458C>A (p.Pro486=) rs2291563
NM_001458.4(FLNC):c.1471G>C (p.Val491Leu) rs770264114
NM_001458.4(FLNC):c.147C>T (p.His49=) rs3734972
NM_001458.4(FLNC):c.1614C>T (p.Tyr538=) rs76046880
NM_001458.4(FLNC):c.2265+12C>G rs2291566
NM_001458.4(FLNC):c.2390-13C>T rs78086167
NM_001458.4(FLNC):c.2450T>C (p.Ile817Thr) rs200653747
NM_001458.4(FLNC):c.3297A>G (p.Val1099=) rs3734973
NM_001458.4(FLNC):c.3838C>T (p.Leu1280=) rs34180031
NM_001458.4(FLNC):c.3973C>T (p.Leu1325=) rs34373805
NM_001458.4(FLNC):c.4056C>T (p.Arg1352=) rs75770585
NM_001458.4(FLNC):c.4404= (p.Asp1468=) rs2249128
NM_001458.4(FLNC):c.4431G>A (p.Leu1477=) rs2291568
NM_001458.4(FLNC):c.4700G>A (p.Arg1567Gln) rs2291569
NM_001458.4(FLNC):c.4928-7T>C rs201957008
NM_001458.4(FLNC):c.5669-12C>T rs79790270
NM_001458.4(FLNC):c.5763T>C (p.Thr1921=) rs3816884
NM_001458.4(FLNC):c.577G>A (p.Ala193Thr) rs387906587
NM_001458.4(FLNC):c.720T>C (p.Ile240=) rs2291560
NM_001458.4(FLNC):c.7221C>T (p.Asp2407=) rs3816885
NM_001458.4(FLNC):c.795T>C (p.Gly265=) rs2291561

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