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: 51
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HGVS dbSNP
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.*145delA 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_*1669dupAAGTA 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.*709delG rs886047223
NM_014000.2(VCL):c.*864C>T rs536381894
NM_014000.2(VCL):c.-62T>G rs886047215
NM_014000.2(VCL):c.1040C>T (p.Pro347Leu) rs148619523
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.1379G>A (p.Arg460Gln) rs753026034
NM_014000.2(VCL):c.1542C>T (p.Val514=) rs7904077
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.1671C>T (p.Asp557=) rs137877092
NM_014000.2(VCL):c.1716T>G (p.Leu572=) rs189781480
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.2472C>G (p.Ile824Met) rs140381835
NM_014000.2(VCL):c.2521G>C (p.Asp841His) rs150385900
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.3186G>A (p.Gln1062=) rs761534024
NM_014000.2(VCL):c.3258+10A>T rs71579379
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.45G>A (p.Pro15=) rs775062250
NM_014000.2(VCL):c.492T>G (p.Leu164=) rs143702799
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.901C>T (p.Gln301Ter) rs886047217

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