ClinVar Miner

List of variants in gene VCL reported by GeneDx

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Gene type:
ClinVar version:
Total variants: 154
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HGVS dbSNP
NC_000010.11:g.74083685_74083688del rs199705227
NM_003373.4(VCL):c.169-10delinsTG rs1554814892
NM_003373.4(VCL):c.169-11del rs753900484
NM_003373.4(VCL):c.2746-2193_2746-2192del rs781036800
NM_003373.4(VCL):c.875-324dup rs5786133
NM_014000.2(VCL):c.-13G>A rs780482320
NM_014000.2(VCL):c.-264A>G rs3812625
NM_014000.2(VCL):c.-386A>G rs3812624
NM_014000.2(VCL):c.1015C>T (p.Arg339Cys) rs759961842
NM_014000.2(VCL):c.1074G>A (p.Gln358=) rs1057520879
NM_014000.2(VCL):c.1092A>G (p.Thr364=) rs1057521557
NM_014000.2(VCL):c.1170T>C (p.Ala390=) rs201459260
NM_014000.2(VCL):c.1176+13A>G rs758133739
NM_014000.2(VCL):c.1176+20G>A rs370298549
NM_014000.2(VCL):c.1177-14G>A rs778137720
NM_014000.2(VCL):c.1177-158_1177-157insCA rs10652052
NM_014000.2(VCL):c.1177-18C>T rs1336724326
NM_014000.2(VCL):c.1177-5T>C rs370860265
NM_014000.2(VCL):c.1206G>A (p.Pro402=) rs779265817
NM_014000.2(VCL):c.1229G>A (p.Gly410Asp) rs1064796607
NM_014000.2(VCL):c.1238C>T (p.Ala413Val) rs794729190
NM_014000.2(VCL):c.1292T>G (p.Ile431Ser) rs766192312
NM_014000.2(VCL):c.1298G>A (p.Arg433His) rs754046223
NM_014000.2(VCL):c.1346G>A (p.Arg449Gln) rs755234443
NM_014000.2(VCL):c.1353-19G>A rs145537824
NM_014000.2(VCL):c.1353-233C>T rs10824069
NM_014000.2(VCL):c.1403C>T (p.Thr468Met) rs147957747
NM_014000.2(VCL):c.1535G>A (p.Arg512His) rs367568441
NM_014000.2(VCL):c.1563G>C (p.Gly521=) rs747932867
NM_014000.2(VCL):c.1583G>A (p.Arg528His) rs746095066
NM_014000.2(VCL):c.1652T>C (p.Leu551Pro) rs1057524278
NM_014000.2(VCL):c.168+20C>A rs368934323
NM_014000.2(VCL):c.169-18T>A rs1057521827
NM_014000.2(VCL):c.169-290A>G rs144295868
NM_014000.2(VCL):c.1708C>T (p.Arg570Ter) rs794729191
NM_014000.2(VCL):c.1743+19T>C rs542039663
NM_014000.2(VCL):c.1743+229C>T rs4746172
NM_014000.2(VCL):c.1743+6A>T rs370709860
NM_014000.2(VCL):c.1744-1G>T rs1057524654
NM_014000.2(VCL):c.1800C>T (p.Ser600=) rs1341597341
NM_014000.2(VCL):c.1819A>C (p.Lys607Gln) rs794729192
NM_014000.2(VCL):c.1872+12A>G rs1057522638
NM_014000.2(VCL):c.1872+197G>C rs12243178
NM_014000.2(VCL):c.1872+199A>C rs74146325
NM_014000.2(VCL):c.1940C>T (p.Ala647Val) rs534449109
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.2022+167C>T rs12416686
NM_014000.2(VCL):c.2023-20A>G rs143756084
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.2131+64C>T rs2270552
NM_014000.2(VCL):c.224C>T (p.Pro75Leu) rs373830664
NM_014000.2(VCL):c.2256G>C (p.Gly752=) rs1057522615
NM_014000.2(VCL):c.225A>G (p.Pro75=) rs759937112
NM_014000.2(VCL):c.2267T>C (p.Ile756Thr) rs1554818898
NM_014000.2(VCL):c.2275C>A (p.Arg759=) rs774477633
NM_014000.2(VCL):c.2365G>A (p.Glu789Lys) rs745419923
NM_014000.2(VCL):c.239+11G>A rs918332199
NM_014000.2(VCL):c.2428G>A (p.Asp810Asn) rs751458490
NM_014000.2(VCL):c.2434+159G>A rs57050827
NM_014000.2(VCL):c.2434+19T>C rs188216596
NM_014000.2(VCL):c.2434+48C>T rs55984079
NM_014000.2(VCL):c.2435-10T>C rs201207594
NM_014000.2(VCL):c.2435-1G>A rs794729188
NM_014000.2(VCL):c.2435-3T>C rs1554819048
NM_014000.2(VCL):c.2435-59C>A rs2131957
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.2528C>T (p.Pro843Leu) rs764302249
NM_014000.2(VCL):c.2539C>T (p.Pro847Ser) rs372711612
NM_014000.2(VCL):c.2559+18T>C rs1314406001
NM_014000.2(VCL):c.261G>A (p.Lys87=) rs1057523799
NM_014000.2(VCL):c.2655C>T (p.Phe885=) rs149196315
NM_014000.2(VCL):c.2745+151T>C rs2270551
NM_014000.2(VCL):c.2746-8C>T rs532645343
NM_014000.2(VCL):c.2748G>A (p.Pro916=) rs761794669
NM_014000.2(VCL):c.2760C>T (p.Ala920=) rs138594604
NM_014000.2(VCL):c.2769G>A (p.Val923=) rs1057521313
NM_014000.2(VCL):c.2802C>T (p.Ala934=) rs372381809
NM_014000.2(VCL):c.2823C>T (p.Val941=) rs747647927
NM_014000.2(VCL):c.2827C>G (p.Pro943Ala) rs71579375
NM_014000.2(VCL):c.292G>A (p.Asp98Asn) rs794729193
NM_014000.2(VCL):c.2950-22C>G rs71579378
NM_014000.2(VCL):c.2950-50C>T rs10824072
NM_014000.2(VCL):c.3008G>A (p.Arg1003Gln) rs1085307604
NM_014000.2(VCL):c.3154-8C>G rs376690719
NM_014000.2(VCL):c.3259-5T>C rs1057523095
NM_014000.2(VCL):c.3381T>C (p.Val1127=) rs943734765
NM_014000.2(VCL):c.379G>A (p.Asp127Asn) rs1554816666
NM_014000.2(VCL):c.500-236A>G rs74146315
NM_014000.2(VCL):c.500-281T>C rs74146314
NM_014000.2(VCL):c.50C>A (p.Ala17Glu) rs794729189
NM_014000.2(VCL):c.565G>T (p.Val189Leu) rs151045204
NM_014000.2(VCL):c.571T>C (p.Leu191=) rs370334093
NM_014000.2(VCL):c.582G>A (p.Ser194=) rs773725513
NM_014000.2(VCL):c.622+158G>A rs71524373
NM_014000.2(VCL):c.622+18T>C rs1218431325
NM_014000.2(VCL):c.622+191C>T rs71524384
NM_014000.2(VCL):c.622+211T>C rs111609277
NM_014000.2(VCL):c.623-83T>C rs58026892
NM_014000.2(VCL):c.676G>A (p.Ala226Thr) rs146910007
NM_014000.2(VCL):c.736C>T (p.Arg246Cys) rs794729194
NM_014000.2(VCL):c.780C>T (p.Ser260=) rs774377548
NM_014000.2(VCL):c.784-60G>A rs2270548
NM_014000.2(VCL):c.789T>C (p.Thr263=) rs538002543
NM_014000.2(VCL):c.81C>T (p.His27=) rs200733607
NM_014000.2(VCL):c.875-24T>A rs1908339
NM_014000.3(VCL):c.1157A>G (p.Lys386Arg) rs200342284
NM_014000.3(VCL):c.1177-15C>T rs115083446
NM_014000.3(VCL):c.120C>T (p.Leu40=) rs144080529
NM_014000.3(VCL):c.1237G>A (p.Ala413Thr) rs146278697
NM_014000.3(VCL):c.1290C>T (p.Asp430=) rs576271894
NM_014000.3(VCL):c.1294C>G (p.Leu432Val) rs144146254
NM_014000.3(VCL):c.1317T>C (p.Ser439=) rs71579355
NM_014000.3(VCL):c.1407C>T (p.Ala469=) rs2229507
NM_014000.3(VCL):c.1506G>A (p.Arg502=) rs2228373
NM_014000.3(VCL):c.1542C>T (p.Val514=) rs7904077
NM_014000.3(VCL):c.1555A>C (p.Ile519Leu) rs141033098
NM_014000.3(VCL):c.1557C>A (p.Ile519=) rs150120464
NM_014000.3(VCL):c.1572C>T (p.Ala524=) rs138566234
NM_014000.3(VCL):c.1626C>T (p.Leu542=) rs150402791
NM_014000.3(VCL):c.1671C>T (p.Asp557=) rs137877092
NM_014000.3(VCL):c.1716T>G (p.Leu572=) rs189781480
NM_014000.3(VCL):c.1798A>C (p.Ser600Arg) rs397517236
NM_014000.3(VCL):c.1842G>A (p.Thr614=) rs144117013
NM_014000.3(VCL):c.1907A>G (p.His636Arg) rs71579374
NM_014000.3(VCL):c.2025G>A (p.Val675=) rs140766884
NM_014000.3(VCL):c.2142C>T (p.Asp714=) rs373790383
NM_014000.3(VCL):c.2388G>A (p.Pro796=) rs767809
NM_014000.3(VCL):c.2521G>C (p.Asp841His) rs150385900
NM_014000.3(VCL):c.2746-14C>T rs367598954
NM_014000.3(VCL):c.2796T>C (p.Asp932=) rs140308982
NM_014000.3(VCL):c.2799G>A (p.Ala933=) rs199507346
NM_014000.3(VCL):c.2801C>T (p.Ala934Val) rs16931179
NM_014000.3(VCL):c.2814C>G (p.Gly938=) rs2131956
NM_014000.3(VCL):c.2841C>T (p.Asp947=) rs566296495
NM_014000.3(VCL):c.2852C>G (p.Pro951Arg) rs368570586
NM_014000.3(VCL):c.2862_2864del (p.Leu955del) rs397517237
NM_014000.3(VCL):c.2969C>T (p.Ala990Val) rs150595117
NM_014000.3(VCL):c.3066C>T (p.Ile1022=) rs138619320
NM_014000.3(VCL):c.3163C>T (p.Arg1055Ter) rs727505159
NM_014000.3(VCL):c.3258+10A>T rs71579379
NM_014000.3(VCL):c.3333T>C (p.Ala1111=) rs147415627
NM_014000.3(VCL):c.339G>A (p.Arg113=) rs56314318
NM_014000.3(VCL):c.366G>A (p.Leu122=) rs199562976
NM_014000.3(VCL):c.378C>T (p.Phe126=) rs148966602
NM_014000.3(VCL):c.562C>T (p.Arg188Ter) rs397517244
NM_014000.3(VCL):c.590C>T (p.Thr197Ile) rs189242810
NM_014000.3(VCL):c.622+4C>T rs201020802
NM_014000.3(VCL):c.660C>T (p.Asn220=) rs56264452
NM_014000.3(VCL):c.768T>C (p.Asp256=) rs56413529
NM_014000.3(VCL):c.874+7C>G rs727503737
NM_014000.3(VCL):c.945C>A (p.Gly315=) rs61731180

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