ClinVar Miner

List of variants in gene VCL reported by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 125
Download table as spreadsheet
HGVS dbSNP
NM_014000.2(VCL):c.-13G>A rs780482320
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.1157A>G (p.Lys386Arg) rs200342284
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.1177-15C>T rs115083446
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.120C>T (p.Leu40=) rs144080529
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.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.1298G>A (p.Arg433His) rs754046223
NM_014000.2(VCL):c.1317T>C (p.Ser439=) rs71579355
NM_014000.2(VCL):c.1346G>A (p.Arg449Gln) rs755234443
NM_014000.2(VCL):c.1353-19G>A rs145537824
NM_014000.2(VCL):c.1403C>T (p.Thr468Met) rs147957747
NM_014000.2(VCL):c.1407C>T (p.Ala469=) rs2229507
NM_014000.2(VCL):c.1506G>A (p.Arg502=) rs2228373
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.1555A>C (p.Ile519Leu) rs141033098
NM_014000.2(VCL):c.1557C>A (p.Ile519=) rs150120464
NM_014000.2(VCL):c.1563G>C (p.Gly521=) rs747932867
NM_014000.2(VCL):c.1572C>T (p.Ala524=) rs138566234
NM_014000.2(VCL):c.1583G>A (p.Arg528His) rs746095066
NM_014000.2(VCL):c.1626C>T (p.Leu542=) rs150402791
NM_014000.2(VCL):c.1652T>C (p.Leu551Pro) rs1057524278
NM_014000.2(VCL):c.1671C>T (p.Asp557=) rs137877092
NM_014000.2(VCL):c.168+20C>A rs368934323
NM_014000.2(VCL):c.169-10delCinsTG rs1554814892
NM_014000.2(VCL):c.169-11delT rs753900484
NM_014000.2(VCL):c.169-18T>A rs1057521827
NM_014000.2(VCL):c.1708C>T (p.Arg570Ter) rs794729191
NM_014000.2(VCL):c.1716T>G (p.Leu572=) rs189781480
NM_014000.2(VCL):c.1743+19T>C rs542039663
NM_014000.2(VCL):c.1743+6A>T rs370709860
NM_014000.2(VCL):c.1744-1G>T rs1057524654
NM_014000.2(VCL):c.1798A>C (p.Ser600Arg) rs397517236
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.1842G>A (p.Thr614=) rs144117013
NM_014000.2(VCL):c.1872+12A>G rs1057522638
NM_014000.2(VCL):c.1907A>G (p.His636Arg) rs71579374
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.2023-20A>G rs143756084
NM_014000.2(VCL):c.2025G>A (p.Val675=) rs140766884
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.2142C>T (p.Asp714=) rs373790383
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.2388G>A (p.Pro796=) rs767809
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+19T>C rs188216596
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.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.2539C>T (p.Pro847Ser) rs372711612
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.2746-14C>T rs367598954
NM_014000.2(VCL):c.2746-8C>T rs532645343
NM_014000.2(VCL):c.2748G>A (p.Pro916=) rs761794669
NM_014000.2(VCL):c.2769G>A (p.Val923=) rs1057521313
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.2802C>T (p.Ala934=) rs372381809
NM_014000.2(VCL):c.2814C>G (p.Gly938=) rs2131956
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.2828_2829delCT (p.Pro943Argfs) 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_2864delGTT (p.Leu955del) rs397517237
NM_014000.2(VCL):c.292G>A (p.Asp98Asn) rs794729193
NM_014000.2(VCL):c.2969C>T (p.Ala990Val) rs150595117
NM_014000.2(VCL):c.3008G>A (p.Arg1003Gln) rs1085307604
NM_014000.2(VCL):c.3066C>T (p.Ile1022=) rs138619320
NM_014000.2(VCL):c.3154-8C>G rs376690719
NM_014000.2(VCL):c.3163C>T (p.Arg1055Ter) rs727505159
NM_014000.2(VCL):c.3258+10A>T rs71579379
NM_014000.2(VCL):c.3259-5T>C rs1057523095
NM_014000.2(VCL):c.3333T>C (p.Ala1111=) rs147415627
NM_014000.2(VCL):c.3381T>C (p.Val1127=) rs943734765
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.379G>A (p.Asp127Asn) rs1554816666
NM_014000.2(VCL):c.50C>A (p.Ala17Glu) rs794729189
NM_014000.2(VCL):c.562C>T (p.Arg188Ter) rs397517244
NM_014000.2(VCL):c.565G>T (p.Val189Leu) rs151045204
NM_014000.2(VCL):c.582G>A (p.Ser194=) rs773725513
NM_014000.2(VCL):c.590C>T (p.Thr197Ile) rs189242810
NM_014000.2(VCL):c.622+18T>C rs1218431325
NM_014000.2(VCL):c.622+4C>T rs201020802
NM_014000.2(VCL):c.660C>T (p.Asn220=) rs56264452
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.768T>C (p.Asp256=) rs56413529
NM_014000.2(VCL):c.780C>T (p.Ser260=) rs774377548
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.874+7C>G rs727503737
NM_014000.2(VCL):c.945C>A (p.Gly315=) rs61731180

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.