ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 97
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HGVS dbSNP
NM_014000.2(VCL):c.1017T>C (p.Arg339=) rs876657632
NM_014000.2(VCL):c.1157A>G (p.Lys386Arg) rs200342284
NM_014000.2(VCL):c.1177-15C>T rs115083446
NM_014000.2(VCL):c.1198G>T (p.Gly400Cys) rs201361282
NM_014000.2(VCL):c.120C>T (p.Leu40=) rs144080529
NM_014000.2(VCL):c.1237G>A (p.Ala413Thr) rs146278697
NM_014000.2(VCL):c.1275T>C (p.Pro425=) rs397517233
NM_014000.2(VCL):c.1290C>T (p.Asp430=) rs576271894
NM_014000.2(VCL):c.1294C>G (p.Leu432Val) rs144146254
NM_014000.2(VCL):c.1317T>C (p.Ser439=) rs71579355
NM_014000.2(VCL):c.1337C>G (p.Ala446Gly) rs727504675
NM_014000.2(VCL):c.1348A>C (p.Arg450=) rs142128712
NM_014000.2(VCL):c.1390A>C (p.Lys464Gln) rs200710859
NM_014000.2(VCL):c.1407C>T (p.Ala469=) rs2229507
NM_014000.2(VCL):c.1490T>C (p.Ile497Thr) rs572757800
NM_014000.2(VCL):c.1506G>A (p.Arg502=) rs2228373
NM_014000.2(VCL):c.1542C>T (p.Val514=) rs7904077
NM_014000.2(VCL):c.1543+15G>A rs759560099
NM_014000.2(VCL):c.1544-2A>G rs727503738
NM_014000.2(VCL):c.1555A>C (p.Ile519Leu) rs141033098
NM_014000.2(VCL):c.1557C>A (p.Ile519=) rs150120464
NM_014000.2(VCL):c.1572C>T (p.Ala524=) rs138566234
NM_014000.2(VCL):c.1575A>C (p.Glu525Asp) rs548487697
NM_014000.2(VCL):c.1626C>T (p.Leu542=) rs150402791
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.1671C>T (p.Asp557=) rs137877092
NM_014000.2(VCL):c.168+9G>T rs997516030
NM_014000.2(VCL):c.1713del (p.Ala573fs) rs779488376
NM_014000.2(VCL):c.1716T>G (p.Leu572=) rs189781480
NM_014000.2(VCL):c.1762C>T (p.Gln588Ter) rs727504381
NM_014000.2(VCL):c.1788A>C (p.Ser596=) rs199582103
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.1842G>A (p.Thr614=) rs144117013
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.1907A>G (p.His636Arg) rs71579374
NM_014000.2(VCL):c.1973T>C (p.Val658Ala) rs372691803
NM_014000.2(VCL):c.2025G>A (p.Val675=) rs140766884
NM_014000.2(VCL):c.2046A>T (p.Leu682Phe) rs565398652
NM_014000.2(VCL):c.2142C>T (p.Asp714=) rs373790383
NM_014000.2(VCL):c.2388= (p.Pro796=) rs767809
NM_014000.2(VCL):c.2388G>A (p.Pro796=) rs767809
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.2796T>C (p.Asp932=) rs140308982
NM_014000.2(VCL):c.2799G>A (p.Ala933=) rs199507346
NM_014000.2(VCL):c.2801C>T (p.Ala934Val) rs16931179
NM_014000.2(VCL):c.2814= (p.Gly938=) rs2131956
NM_014000.2(VCL):c.2814C>G (p.Gly938=) rs2131956
NM_014000.2(VCL):c.2828_2829del (p.Pro943fs) rs781036800
NM_014000.2(VCL):c.2841C>T (p.Asp947=) rs566296495
NM_014000.2(VCL):c.2852C>G (p.Pro951Arg) rs368570586
NM_014000.2(VCL):c.2862_2864del (p.Leu955del) rs397517237
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.3066C>T (p.Ile1022=) rs138619320
NM_014000.2(VCL):c.3092G>A (p.Arg1031Gln) rs397517238
NM_014000.2(VCL):c.3115C>T (p.Gln1039Ter) rs727503741
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.3258+10A>T rs71579379
NM_014000.2(VCL):c.3327T>C (p.Ala1109=) rs397517242
NM_014000.2(VCL):c.3333T>C (p.Ala1111=) rs147415627
NM_014000.2(VCL):c.3373C>T (p.Arg1125Cys) rs373317423
NM_014000.2(VCL):c.339G>A (p.Arg113=) rs56314318
NM_014000.2(VCL):c.366G>A (p.Leu122=) rs199562976
NM_014000.2(VCL):c.378C>T (p.Phe126=) rs148966602
NM_014000.2(VCL):c.390+11T>G rs764668318
NM_014000.2(VCL):c.492T>G (p.Leu164=) rs143702799
NM_014000.2(VCL):c.500-5C>G rs397517243
NM_014000.2(VCL):c.562C>T (p.Arg188Ter) rs397517244
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.622+4C>T rs201020802
NM_014000.2(VCL):c.649A>G (p.Asn217Asp) rs727505216
NM_014000.2(VCL):c.659dup (p.Asn220fs) rs397517245
NM_014000.2(VCL):c.660C>T (p.Asn220=) rs56264452
NM_014000.2(VCL):c.670dup (p.Glu224fs) rs876657674
NM_014000.2(VCL):c.688C>T (p.Arg230Cys) rs139312390
NM_014000.2(VCL):c.768T>C (p.Asp256=) rs56413529
NM_014000.2(VCL):c.808T>C (p.Leu270=) rs727505339
NM_014000.2(VCL):c.854G>A (p.Arg285His) rs397517246
NM_014000.2(VCL):c.874+13T>C rs777617736
NM_014000.2(VCL):c.874+7C>G rs727503737
NM_014000.2(VCL):c.874+9C>G rs756064535
NM_014000.2(VCL):c.945C>A (p.Gly315=) rs61731180
NM_014000.2(VCL):c.952C>T (p.Arg318Cys) rs397517247

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