ClinVar Miner

List of variants in gene VCL reported as uncertain significance

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Gene type:
ClinVar version:
Total variants: 248
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HGVS dbSNP
NC_000010.10:g.(?_75757946)_(75758153_?)del
NM_014000.2(VCL):c.*1143A>G rs886047224
NM_014000.2(VCL):c.*1203A>C rs149551128
NM_014000.2(VCL):c.*1282C>T rs529687198
NM_014000.2(VCL):c.*1285C>T rs879813349
NM_014000.2(VCL):c.*1403C>T rs886047225
NM_014000.2(VCL):c.*145del rs756151016
NM_014000.2(VCL):c.*148A>G rs528724911
NM_014000.2(VCL):c.*1540A>C rs886047226
NM_014000.2(VCL):c.*1659C>T rs1804893
NM_014000.2(VCL):c.*1665_*1669dup rs886047227
NM_014000.2(VCL):c.*1708A>G rs886047229
NM_014000.2(VCL):c.*1709_*1712dupAAGA rs1554820063
NM_014000.2(VCL):c.*1761A>G rs886047230
NM_014000.2(VCL):c.*1841_*1842insA rs886047231
NM_014000.2(VCL):c.*1841_*1842insAA rs886047231
NM_014000.2(VCL):c.*212C>A rs757322860
NM_014000.2(VCL):c.*355_*356delCT rs144115212
NM_014000.2(VCL):c.*652T>C rs79816413
NM_014000.2(VCL):c.*698C>A rs182637339
NM_014000.2(VCL):c.*709del rs886047223
NM_014000.2(VCL):c.*864C>T rs536381894
NM_014000.2(VCL):c.-62T>G rs886047215
NM_014000.2(VCL):c.1001_1015del (p.Gln334_Leu338del) rs1554817370
NM_014000.2(VCL):c.1015C>T (p.Arg339Cys) rs759961842
NM_014000.2(VCL):c.1031G>C (p.Gly344Ala) rs778875353
NM_014000.2(VCL):c.1039C>T (p.Pro347Ser)
NM_014000.2(VCL):c.1040C>T (p.Pro347Leu) rs148619523
NM_014000.2(VCL):c.1046C>T (p.Ala349Val)
NM_014000.2(VCL):c.1050G>A (p.Met350Ile)
NM_014000.2(VCL):c.1115G>A (p.Arg372His) rs377289804
NM_014000.2(VCL):c.113C>T (p.Pro38Leu) rs1060502194
NM_014000.2(VCL):c.1157A>G (p.Lys386Arg) rs200342284
NM_014000.2(VCL):c.1192C>T (p.Pro398Ser) rs201528612
NM_014000.2(VCL):c.1195A>C (p.Asn399His) rs377228795
NM_014000.2(VCL):c.1198G>T (p.Gly400Cys) rs201361282
NM_014000.2(VCL):c.1223T>C (p.Ile408Thr) rs878854969
NM_014000.2(VCL):c.1225C>T (p.Arg409Ter) rs202005455
NM_014000.2(VCL):c.1229G>A (p.Gly410Asp) rs1064796607
NM_014000.2(VCL):c.1237G>A (p.Ala413Thr) rs146278697
NM_014000.2(VCL):c.1238C>T (p.Ala413Val) rs794729190
NM_014000.2(VCL):c.1247G>A (p.Arg416Gln) rs758811315
NM_014000.2(VCL):c.1268A>G (p.Asp423Gly) rs769504902
NM_014000.2(VCL):c.1287T>A (p.Asp429Glu) rs139371702
NM_014000.2(VCL):c.1290C>T (p.Asp430=) rs576271894
NM_014000.2(VCL):c.1292T>G (p.Ile431Ser) rs766192312
NM_014000.2(VCL):c.1294C>G (p.Leu432Val) rs144146254
NM_014000.2(VCL):c.1296_1297inv (p.Arg433Cys)
NM_014000.2(VCL):c.1297C>T (p.Arg433Cys) rs139559937
NM_014000.2(VCL):c.1298G>A (p.Arg433His) rs754046223
NM_014000.2(VCL):c.1319C>T (p.Ala440Val) rs1554817862
NM_014000.2(VCL):c.1346G>A (p.Arg449Gln) rs755234443
NM_014000.2(VCL):c.1352+5G>A rs374522164
NM_014000.2(VCL):c.1379G>A (p.Arg460Gln) rs753026034
NM_014000.2(VCL):c.1382C>A (p.Ala461Asp)
NM_014000.2(VCL):c.1382C>G (p.Ala461Gly) rs886038800
NM_014000.2(VCL):c.1390A>C (p.Lys464Gln) rs200710859
NM_014000.2(VCL):c.1403C>T (p.Thr468Met) rs147957747
NM_014000.2(VCL):c.1490T>C (p.Ile497Thr) rs572757800
NM_014000.2(VCL):c.1511T>C (p.Ile504Thr) rs745343813
NM_014000.2(VCL):c.151G>T (p.Val51Phe) rs1565628951
NM_014000.2(VCL):c.1521C>T (p.Pro507=) rs1564529609
NM_014000.2(VCL):c.1534C>T (p.Arg512Cys) rs781079975
NM_014000.2(VCL):c.1535G>A (p.Arg512His) rs367568441
NM_014000.2(VCL):c.1542C>T (p.Val514=) rs7904077
NM_014000.2(VCL):c.1543+8C>G rs886047218
NM_014000.2(VCL):c.1543G>A (p.Gly515Ser) rs1215494764
NM_014000.2(VCL):c.1555A>C (p.Ile519Leu) rs141033098
NM_014000.2(VCL):c.1559G>A (p.Arg520Gln) rs757009736
NM_014000.2(VCL):c.155G>C (p.Ser52Thr) rs886047216
NM_014000.2(VCL):c.1575A>C (p.Glu525Asp) rs548487697
NM_014000.2(VCL):c.1582C>T (p.Arg528Cys) rs923960592
NM_014000.2(VCL):c.1583G>A (p.Arg528His) rs746095066
NM_014000.2(VCL):c.158A>G (p.Asn53Ser) rs751938777
NM_014000.2(VCL):c.1607C>A (p.Pro536His) rs200624351
NM_014000.2(VCL):c.1612C>T (p.Arg538Trp)
NM_014000.2(VCL):c.1613G>A (p.Arg538Gln) rs566596830
NM_014000.2(VCL):c.1620T>A (p.Asp540Glu)
NM_014000.2(VCL):c.1621C>G (p.Leu541Val) rs370229150
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.1648C>G (p.Gln550Glu) rs1406371942
NM_014000.2(VCL):c.1652T>C (p.Leu551Pro) rs1057524278
NM_014000.2(VCL):c.166C>T (p.Arg56Trp) rs1555112641
NM_014000.2(VCL):c.1671C>T (p.Asp557=) rs137877092
NM_014000.2(VCL):c.1708C>T (p.Arg570Ter) rs794729191
NM_014000.2(VCL):c.1713del (p.Ala573fs) rs779488376
NM_014000.2(VCL):c.1715T>C (p.Leu572Pro) rs1060502197
NM_014000.2(VCL):c.1716T>G (p.Leu572=) rs189781480
NM_014000.2(VCL):c.1743+6A>G
NM_014000.2(VCL):c.1744-1G>T rs1057524654
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.1803T>A (p.Asp601Glu)
NM_014000.2(VCL):c.1814C>G (p.Pro605Arg) rs960761223
NM_014000.2(VCL):c.1819A>C (p.Lys607Gln) rs794729192
NM_014000.2(VCL):c.1835C>T (p.Ala612Val)
NM_014000.2(VCL):c.1844C>T (p.Ala615Val) rs148669762
NM_014000.2(VCL):c.1856C>A (p.Ala619Glu) rs771628544
NM_014000.2(VCL):c.1856C>T (p.Ala619Val)
NM_014000.2(VCL):c.185T>C (p.Val62Ala) rs769799445
NM_014000.2(VCL):c.1861A>C (p.Asn621His) rs374309823
NM_014000.2(VCL):c.1863C>G (p.Asn621Lys) rs746293391
NM_014000.2(VCL):c.1865G>A (p.Arg622Lys) rs771590749
NM_014000.2(VCL):c.1868A>C (p.Glu623Ala) rs1060502193
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.1917G>T (p.Lys639Asn) rs915381122
NM_014000.2(VCL):c.1918C>T (p.Leu640Phe) rs886047219
NM_014000.2(VCL):c.1928C>T (p.Thr643Met) rs150643310
NM_014000.2(VCL):c.1940C>T (p.Ala647Val) rs534449109
NM_014000.2(VCL):c.1961A>G (p.Asn654Ser)
NM_014000.2(VCL):c.1973T>C (p.Val658Ala) rs372691803
NM_014000.2(VCL):c.1998G>T (p.Lys666Asn) rs886047220
NM_014000.2(VCL):c.1999A>G (p.Thr667Ala)
NM_014000.2(VCL):c.2000C>T (p.Thr667Met) rs794729187
NM_014000.2(VCL):c.2005C>T (p.Arg669Ter) rs780856981
NM_014000.2(VCL):c.2006G>A (p.Arg669Gln) rs759771302
NM_014000.2(VCL):c.2022+5G>T rs1050797785
NM_014000.2(VCL):c.2035G>T (p.Ala679Ser) rs375392559
NM_014000.2(VCL):c.2046A>T (p.Leu682Phe) rs565398652
NM_014000.2(VCL):c.2050A>G (p.Arg684Gly) rs730880249
NM_014000.2(VCL):c.2050A>T (p.Arg684Trp) rs730880249
NM_014000.2(VCL):c.2069C>A (p.Ala690Asp) rs1057524826
NM_014000.2(VCL):c.20G>T (p.Arg7Leu)
NM_014000.2(VCL):c.2143G>A (p.Glu715Lys) rs1022329091
NM_014000.2(VCL):c.2159A>T (p.Lys720Ile) rs1554818881
NM_014000.2(VCL):c.2173G>A (p.Ala725Thr) rs1554818884
NM_014000.2(VCL):c.2182G>A (p.Glu728Lys)
NM_014000.2(VCL):c.2237C>A (p.Pro746His) rs746821947
NM_014000.2(VCL):c.224C>T (p.Pro75Leu) rs373830664
NM_014000.2(VCL):c.2267T>C (p.Ile756Thr) rs1554818898
NM_014000.2(VCL):c.2273G>A (p.Arg758His)
NM_014000.2(VCL):c.2275C>A (p.Arg759=) rs774477633
NM_014000.2(VCL):c.2276G>A (p.Arg759Gln) rs1425397914
NM_014000.2(VCL):c.2285G>A (p.Arg762Gln)
NM_014000.2(VCL):c.2330C>T (p.Pro777Leu) rs1564532927
NM_014000.2(VCL):c.2365G>A (p.Glu789Lys) rs745419923
NM_014000.2(VCL):c.2387C>T (p.Pro796Leu) rs1364541925
NM_014000.2(VCL):c.2387del (p.Pro796fs) rs1241654679
NM_014000.2(VCL):c.238A>C (p.Lys80Gln) rs775532257
NM_014000.2(VCL):c.2399A>T (p.Asp800Val) rs919509789
NM_014000.2(VCL):c.2427C>T (p.Ser809=) rs183739128
NM_014000.2(VCL):c.2428G>A (p.Asp810Asn) rs751458490
NM_014000.2(VCL):c.2435-1G>A rs794729188
NM_014000.2(VCL):c.2443A>G (p.Lys815Glu) rs960017518
NM_014000.2(VCL):c.2444A>G (p.Lys815Arg) rs373010557
NM_014000.2(VCL):c.2453T>A (p.Leu818Gln) rs794727192
NM_014000.2(VCL):c.2468G>A (p.Arg823Gln) rs759202535
NM_014000.2(VCL):c.2472C>G (p.Ile824Met) rs140381835
NM_014000.2(VCL):c.248A>T (p.Asn83Ile) rs1554816646
NM_014000.2(VCL):c.2521G>C (p.Asp841His) rs150385900
NM_014000.2(VCL):c.2528C>T (p.Pro843Leu) rs764302249
NM_014000.2(VCL):c.2531C>T (p.Pro844Leu) rs145393322
NM_014000.2(VCL):c.2539C>T (p.Pro847Ser) rs372711612
NM_014000.2(VCL):c.2543A>G (p.Asp848Gly)
NM_014000.2(VCL):c.2566G>A (p.Asp856Asn) rs1554819202
NM_014000.2(VCL):c.2649A>C (p.Glu883Asp) rs752902180
NM_014000.2(VCL):c.2652G>A (p.Glu884=) rs371187988
NM_014000.2(VCL):c.2672G>C (p.Gly891Ala) rs727503740
NM_014000.2(VCL):c.2699T>C (p.Met900Thr) rs1554819236
NM_014000.2(VCL):c.2746-14C>T rs367598954
NM_014000.2(VCL):c.2746-8C>T rs532645343
NM_014000.2(VCL):c.2802C>T (p.Ala934=) rs372381809
NM_014000.2(VCL):c.2803G>A (p.Asp935Asn) rs746658025
NM_014000.2(VCL):c.2807C>T (p.Ala936Val) rs754681045
NM_014000.2(VCL):c.2823_2824delinsGT (p.Pro942Ser) rs1060502196
NM_014000.2(VCL):c.2827C>G (p.Pro943Ala) rs71579375
NM_014000.2(VCL):c.2828_2829del (p.Pro943fs) rs781036800
NM_014000.2(VCL):c.2852C>G (p.Pro951Arg) rs368570586
NM_014000.2(VCL):c.2853del (p.Glu952fs) rs878854972
NM_014000.2(VCL):c.2862_2864del (p.Leu955del) rs397517237
NM_014000.2(VCL):c.2866A>G (p.Met956Val) rs761830073
NM_014000.2(VCL):c.2867T>G (p.Met956Arg) rs765717598
NM_014000.2(VCL):c.2875A>C (p.Asn959His) rs758969419
NM_014000.2(VCL):c.2875A>G (p.Asn959Asp) rs758969419
NM_014000.2(VCL):c.2887A>G (p.Asn963Asp) rs777702397
NM_014000.2(VCL):c.2893C>T (p.Pro965Ser) rs749236817
NM_014000.2(VCL):c.2905G>A (p.Ala969Thr) rs199751261
NM_014000.2(VCL):c.2923C>T (p.Arg975Trp) rs121917776
NM_014000.2(VCL):c.2924G>A (p.Arg975Gln) rs767325003
NM_014000.2(VCL):c.292G>A (p.Asp98Asn) rs794729193
NM_014000.2(VCL):c.2935A>G (p.Lys979Glu)
NM_014000.2(VCL):c.2969C>T (p.Ala990Val) rs150595117
NM_014000.2(VCL):c.2978G>T (p.Arg993Leu) rs1554819624
NM_014000.2(VCL):c.3008G>A (p.Arg1003Gln) rs1085307604
NM_014000.2(VCL):c.3019G>C (p.Gly1007Arg) rs1554819630
NM_014000.2(VCL):c.3039_3043dup (p.Leu1015fs)
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.3164G>A (p.Arg1055Gln)
NM_014000.2(VCL):c.3186G>A (p.Gln1062=) rs761534024
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.3245A>C (p.Glu1082Ala) rs1554819693
NM_014000.2(VCL):c.3258+10A>T rs71579379
NM_014000.2(VCL):c.3258+4T>C rs1268605937
NM_014000.2(VCL):c.3267G>C (p.Glu1089Asp) rs149300310
NM_014000.2(VCL):c.32G>A (p.Ser11Asn) rs777811020
NM_014000.2(VCL):c.3358G>A (p.Ala1120Thr)
NM_014000.2(VCL):c.3373C>T (p.Arg1125Cys) rs373317423
NM_014000.2(VCL):c.3379G>A (p.Val1127Ile) rs1312868617
NM_014000.2(VCL):c.378C>A (p.Phe126Leu) rs148966602
NM_014000.2(VCL):c.378C>T (p.Phe126=) rs148966602
NM_014000.2(VCL):c.379G>A (p.Asp127Asn) rs1554816666
NM_014000.2(VCL):c.390+4G>A rs1060502195
NM_014000.2(VCL):c.404T>C (p.Ile135Thr) rs373744314
NM_014000.2(VCL):c.437C>A (p.Thr146Lys) rs1421034616
NM_014000.2(VCL):c.458C>T (p.Thr153Ile) rs1554816691
NM_014000.2(VCL):c.45G>A (p.Pro15=) rs775062250
NM_014000.2(VCL):c.492T>G (p.Leu164=) rs143702799
NM_014000.2(VCL):c.500-5C>G rs397517243
NM_014000.2(VCL):c.500G>A (p.Gly167Glu) rs1564523552
NM_014000.2(VCL):c.50C>A (p.Ala17Glu) rs794729189
NM_014000.2(VCL):c.511A>G (p.Met171Val)
NM_014000.2(VCL):c.536A>C (p.Gln179Pro) rs1564523578
NM_014000.2(VCL):c.550C>T (p.His184Tyr) rs1321660809
NM_014000.2(VCL):c.562C>T (p.Arg188Ter) rs397517244
NM_014000.2(VCL):c.565G>A (p.Val189Met) rs151045204
NM_014000.2(VCL):c.565G>C (p.Val189Leu) rs151045204
NM_014000.2(VCL):c.565G>T (p.Val189Leu) rs151045204
NM_014000.2(VCL):c.590C>T (p.Thr197Ile) rs189242810
NM_014000.2(VCL):c.592G>A (p.Val198Met) rs760340545
NM_014000.2(VCL):c.610G>C (p.Val204Leu) rs727504585
NM_014000.2(VCL):c.622+4C>A
NM_014000.2(VCL):c.622+4C>G rs201020802
NM_014000.2(VCL):c.625A>T (p.Met209Leu) rs144683137
NM_014000.2(VCL):c.626T>A (p.Met209Lys) rs751243981
NM_014000.2(VCL):c.649A>G (p.Asn217Asp) rs727505216
NM_014000.2(VCL):c.676G>A (p.Ala226Thr) rs146910007
NM_014000.2(VCL):c.688C>T (p.Arg230Cys) rs139312390
NM_014000.2(VCL):c.695T>A (p.Phe232Tyr) rs200956572
NM_014000.2(VCL):c.701T>C (p.Val234Ala)
NM_014000.2(VCL):c.731T>A (p.Ile244Lys) rs886038819
NM_014000.2(VCL):c.736C>T (p.Arg246Cys) rs794729194
NM_014000.2(VCL):c.737G>A (p.Arg246His) rs746577068
NM_014000.2(VCL):c.768T>A (p.Asp256Glu) rs56413529
NM_014000.2(VCL):c.780C>T (p.Ser260=) rs774377548
NM_014000.2(VCL):c.783+5G>A
NM_014000.2(VCL):c.787A>T (p.Thr263Ser) rs142233726
NM_014000.2(VCL):c.789T>C (p.Thr263=) rs538002543
NM_014000.2(VCL):c.829C>A (p.Leu277Met) rs71579353
NM_014000.2(VCL):c.853C>T (p.Arg285Cys) rs757517552
NM_014000.2(VCL):c.854G>A (p.Arg285His) rs397517246
NM_014000.2(VCL):c.901C>T (p.Gln301Ter) rs886047217
NM_014000.2(VCL):c.952C>T (p.Arg318Cys) rs397517247

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