ClinVar Miner

List of variants in gene VCL reported as uncertain significance for not specified

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Gene type:
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Total variants: 40
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HGVS dbSNP
NM_014000.2(VCL):c.1198G>T (p.Gly400Cys) rs201361282
NM_014000.2(VCL):c.1294C>G (p.Leu432Val) rs144146254
NM_014000.2(VCL):c.1390A>C (p.Lys464Gln) rs200710859
NM_014000.2(VCL):c.1490T>C (p.Ile497Thr) rs572757800
NM_014000.2(VCL):c.151G>T (p.Val51Phe) rs1565628951
NM_014000.2(VCL):c.1559G>A (p.Arg520Gln) rs757009736
NM_014000.2(VCL):c.1575A>C (p.Glu525Asp) rs548487697
NM_014000.2(VCL):c.1639C>T (p.Arg547Ter) rs397517234
NM_014000.2(VCL):c.163G>T (p.Val55Phe) rs755441334
NM_014000.2(VCL):c.1792G>A (p.Val598Ile) rs397517235
NM_014000.2(VCL):c.1798A>C (p.Ser600Arg) rs397517236
NM_014000.2(VCL):c.1844C>T (p.Ala615Val) rs148669762
NM_014000.2(VCL):c.185T>C (p.Val62Ala) rs769799445
NM_014000.2(VCL):c.1888G>A (p.Ala630Thr) rs727503739
NM_014000.2(VCL):c.1973T>C (p.Val658Ala) rs372691803
NM_014000.2(VCL):c.2005C>T (p.Arg669Ter) rs780856981
NM_014000.2(VCL):c.2046A>T (p.Leu682Phe) rs565398652
NM_014000.2(VCL):c.2444A>G (p.Lys815Arg) rs373010557
NM_014000.2(VCL):c.2521G>C (p.Asp841His) rs150385900
NM_014000.2(VCL):c.2672G>C (p.Gly891Ala) rs727503740
NM_014000.2(VCL):c.2746-14C>T rs367598954
NM_014000.2(VCL):c.2875A>C (p.Asn959His) rs758969419
NM_014000.2(VCL):c.2969C>T (p.Ala990Val) rs150595117
NM_014000.2(VCL):c.3092G>A (p.Arg1031Gln) rs397517238
NM_014000.2(VCL):c.313C>T (p.Arg105Ter) rs397517239
NM_014000.2(VCL):c.3163C>T (p.Arg1055Ter) rs727505159
NM_014000.2(VCL):c.31A>G (p.Ser11Gly) rs397517240
NM_014000.2(VCL):c.3226C>T (p.Arg1076Trp) rs397517241
NM_014000.2(VCL):c.3236T>C (p.Ile1079Thr) rs727503742
NM_014000.2(VCL):c.3373C>T (p.Arg1125Cys) rs373317423
NM_014000.2(VCL):c.500-5C>G rs397517243
NM_014000.2(VCL):c.565G>C (p.Val189Leu) rs151045204
NM_014000.2(VCL):c.590C>T (p.Thr197Ile) rs189242810
NM_014000.2(VCL):c.610G>C (p.Val204Leu) rs727504585
NM_014000.2(VCL):c.622+4C>G rs201020802
NM_014000.2(VCL):c.649A>G (p.Asn217Asp) rs727505216
NM_014000.2(VCL):c.688C>T (p.Arg230Cys) rs139312390
NM_014000.2(VCL):c.787A>T (p.Thr263Ser) rs142233726
NM_014000.2(VCL):c.854G>A (p.Arg285His) rs397517246
NM_014000.2(VCL):c.952C>T (p.Arg318Cys) rs397517247

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