ClinVar Miner

List of variants in gene VCL reported as uncertain significance by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 83
Download table as spreadsheet
HGVS dbSNP
NC_000010.11:g.73998112C>T
NM_003373.4(VCL):c.*145del rs756151016
NM_003373.4(VCL):c.*1665_*1669dup rs886047227
NM_003373.4(VCL):c.*1705_*1708AAGA[3] rs1554820063
NM_003373.4(VCL):c.*353_*354CT[1] rs144115212
NM_003373.4(VCL):c.*709del rs886047223
NM_014000.2(VCL):c.*1143A>G rs886047224
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.*148A>G rs528724911
NM_014000.2(VCL):c.*1540A>C rs886047226
NM_014000.2(VCL):c.*1659C>T rs1804893
NM_014000.2(VCL):c.*1708A>G rs886047229
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.*652T>C rs79816413
NM_014000.2(VCL):c.*698C>A rs182637339
NM_014000.2(VCL):c.*864C>T rs536381894
NM_014000.2(VCL):c.-62T>G rs886047215
NM_014000.2(VCL):c.1015C>T (p.Arg339Cys) rs759961842
NM_014000.2(VCL):c.1040C>T (p.Pro347Leu) rs148619523
NM_014000.2(VCL):c.1177-14G>A rs778137720
NM_014000.2(VCL):c.1223T>C (p.Ile408Thr) rs878854969
NM_014000.2(VCL):c.1287T>A (p.Asp429Glu) rs139371702
NM_014000.2(VCL):c.1379G>A (p.Arg460Gln) rs753026034
NM_014000.2(VCL):c.1543+8C>G rs886047218
NM_014000.2(VCL):c.155G>C (p.Ser52Thr) rs886047216
NM_014000.2(VCL):c.1607C>A (p.Pro536His) rs200624351
NM_014000.2(VCL):c.1613G>A (p.Arg538Gln) rs566596830
NM_014000.2(VCL):c.1856C>T (p.Ala619Val) rs771628544
NM_014000.2(VCL):c.1918C>T (p.Leu640Phe) rs886047219
NM_014000.2(VCL):c.1998G>T (p.Lys666Asn) rs886047220
NM_014000.2(VCL):c.2006G>A (p.Arg669Gln) rs759771302
NM_014000.2(VCL):c.2427C>T (p.Ser809=) rs183739128
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.2746-8C>T rs532645343
NM_014000.2(VCL):c.2802C>T (p.Ala934=) rs372381809
NM_014000.2(VCL):c.2807C>T (p.Ala936Val) rs754681045
NM_014000.2(VCL):c.2924G>A (p.Arg975Gln) rs767325003
NM_014000.2(VCL):c.3186G>A (p.Gln1062=) rs761534024
NM_014000.2(VCL):c.378C>A (p.Phe126Leu) rs148966602
NM_014000.2(VCL):c.45G>A (p.Pro15=) rs775062250
NM_014000.2(VCL):c.592G>A (p.Val198Met) rs760340545
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.901C>T (p.Gln301Ter) rs886047217
NM_014000.3(VCL):c.*1526A>G
NM_014000.3(VCL):c.*1751C>T
NM_014000.3(VCL):c.*1793C>T
NM_014000.3(VCL):c.*1794G>A
NM_014000.3(VCL):c.*207G>T
NM_014000.3(VCL):c.*279T>C
NM_014000.3(VCL):c.*491C>T
NM_014000.3(VCL):c.*646C>G
NM_014000.3(VCL):c.-58G>T
NM_014000.3(VCL):c.1290C>T (p.Asp430=) rs576271894
NM_014000.3(VCL):c.1317T>C (p.Ser439=) rs71579355
NM_014000.3(VCL):c.1390A>G (p.Lys464Glu)
NM_014000.3(VCL):c.1404G>A (p.Thr468=)
NM_014000.3(VCL):c.1433A>G (p.Asn478Ser)
NM_014000.3(VCL):c.1472T>C (p.Val491Ala)
NM_014000.3(VCL):c.1555A>C (p.Ile519Leu) rs141033098
NM_014000.3(VCL):c.1599G>C (p.Met533Ile)
NM_014000.3(VCL):c.1704G>A (p.Gln568=)
NM_014000.3(VCL):c.1716T>G (p.Leu572=) rs189781480
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.2110G>A (p.Asp704Asn)
NM_014000.3(VCL):c.2338C>T (p.Arg780Cys)
NM_014000.3(VCL):c.256A>G (p.Thr86Ala)
NM_014000.3(VCL):c.2796T>C (p.Asp932=) rs140308982
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.3258+10A>T rs71579379
NM_014000.3(VCL):c.36C>T (p.Ile12=)
NM_014000.3(VCL):c.378C>T (p.Phe126=) rs148966602
NM_014000.3(VCL):c.492T>G (p.Leu164=) rs143702799
NM_014000.3(VCL):c.622+4C>T rs201020802
NM_014000.3(VCL):c.808T>C (p.Leu270=) rs727505339

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.