ClinVar Miner

List of variants in gene VCL reported as likely benign for not specified

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Gene type:
ClinVar version:
Total variants: 79
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HGVS dbSNP
NM_014000.2(VCL):c.-13G>A rs780482320
NM_014000.2(VCL):c.1017T>C (p.Arg339=) rs876657632
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.1177-18C>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.1237G>A (p.Ala413Thr) rs146278697
NM_014000.2(VCL):c.1275T>C (p.Pro425=) rs397517233
NM_014000.2(VCL):c.1290C>T (p.Asp430=) rs576271894
NM_014000.2(VCL):c.1337C>G (p.Ala446Gly) rs727504675
NM_014000.2(VCL):c.1348A>C (p.Arg450=) rs142128712
NM_014000.2(VCL):c.1543+15G>A rs759560099
NM_014000.2(VCL):c.1555A>C (p.Ile519Leu) rs141033098
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.1626C>T (p.Leu542=) rs150402791
NM_014000.2(VCL):c.168+20C>A rs368934323
NM_014000.2(VCL):c.168+9G>T rs997516030
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.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.1788A>C (p.Ser596=) rs199582103
NM_014000.2(VCL):c.1800C>T (p.Ser600=) rs1341597341
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.2025G>A (p.Val675=) rs140766884
NM_014000.2(VCL):c.2091C>A (p.Thr697=) rs775493699
NM_014000.2(VCL):c.2142C>T (p.Asp714=) rs373790383
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.2275C>A (p.Arg759=) rs774477633
NM_014000.2(VCL):c.239+11G>A rs918332199
NM_014000.2(VCL):c.2435-10T>C rs201207594
NM_014000.2(VCL):c.2435-3T>C rs1554819048
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.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.2802C>T (p.Ala934=) rs372381809
NM_014000.2(VCL):c.2823C>T (p.Val941=) rs747647927
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.2924G>A (p.Arg975Gln) rs767325003
NM_014000.2(VCL):c.3066C>T (p.Ile1022=) rs138619320
NM_014000.2(VCL):c.3154-8C>G rs376690719
NM_014000.2(VCL):c.3259-5T>C rs1057523095
NM_014000.2(VCL):c.3327T>C (p.Ala1109=) rs397517242
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.366G>A (p.Leu122=) rs199562976
NM_014000.2(VCL):c.378C>T (p.Phe126=) rs148966602
NM_014000.2(VCL):c.390+11T>G rs764668318
NM_014000.2(VCL):c.492T>G (p.Leu164=) rs143702799
NM_014000.2(VCL):c.582G>A (p.Ser194=) rs773725513
NM_014000.2(VCL):c.622+18T>C rs1218431325
NM_014000.2(VCL):c.660C>T (p.Asn220=) rs56264452
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.808T>C (p.Leu270=) rs727505339
NM_014000.2(VCL):c.874+13T>C rs777617736
NM_014000.2(VCL):c.874+7C>G rs727503737
NM_014000.2(VCL):c.874+9C>G rs756064535

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