ClinVar Miner

List of variants in gene VCL reported as likely benign by GeneDx

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Gene type:
ClinVar version:
Total variants: 85
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HGVS dbSNP gnomAD frequency
NM_014000.3(VCL):c.2022+167C>T rs12416686 0.01784
NM_014000.3(VCL):c.*292G>C rs77295081 0.01549
NM_014000.3(VCL):c.240-146C>T rs35828059 0.01357
NM_014000.3(VCL):c.239+148A>T rs71535783 0.01118
NM_014000.3(VCL):c.2950-22C>G rs71579378 0.00753
NM_014000.3(VCL):c.783+250C>T rs146236857 0.00439
NM_014000.3(VCL):c.3259-144G>C rs140785696 0.00429
NM_014000.3(VCL):c.1873-183C>T rs149008791 0.00309
NM_014000.3(VCL):c.1907A>G (p.His636Arg) rs71579374 0.00240
NM_014000.3(VCL):c.2950-201T>C rs187870650 0.00206
NM_014000.3(VCL):c.1572C>T (p.Ala524=) rs138566234 0.00086
NM_014000.3(VCL):c.1555A>C (p.Ile519Leu) rs141033098 0.00064
NM_014000.3(VCL):c.1237G>A (p.Ala413Thr) rs146278697 0.00044
NM_014000.3(VCL):c.1176+20G>A rs370298549 0.00025
NM_014000.3(VCL):c.571T>C (p.Leu191=) rs370334093 0.00021
NM_014000.3(VCL):c.1716T>G (p.Leu572=) rs189781480 0.00016
NM_014000.3(VCL):c.2827C>G (p.Pro943Ala) rs71579375 0.00013
NM_014000.3(VCL):c.378C>T (p.Phe126=) rs148966602 0.00012
NM_014000.3(VCL):c.2655C>T (p.Phe885=) rs149196315 0.00011
NM_014000.3(VCL):c.2142C>T (p.Asp714=) rs373790383 0.00009
NM_014000.3(VCL):c.3066C>T (p.Ile1022=) rs138619320 0.00009
NM_014000.3(VCL):c.1176+13A>G rs758133739 0.00007
NM_014000.3(VCL):c.2802C>T (p.Ala934=) rs372381809 0.00007
NM_014000.3(VCL):c.168+20C>A rs368934323 0.00006
NM_014000.3(VCL):c.169-7C>G rs370213146 0.00006
NM_014000.3(VCL):c.1743+6A>T rs370709860 0.00006
NM_014000.3(VCL):c.2349G>A (p.Val783=) rs558040780 0.00006
NM_014000.3(VCL):c.2748G>A (p.Pro916=) rs761794669 0.00006
NM_014000.3(VCL):c.404T>C (p.Ile135Thr) rs373744314 0.00006
NM_014000.3(VCL):c.1177-14G>A rs778137720 0.00004
NM_014000.3(VCL):c.1177-5T>C rs370860265 0.00004
NM_014000.3(VCL):c.1206G>A (p.Pro402=) rs779265817 0.00004
NM_014000.3(VCL):c.2472C>G (p.Ile824Met) rs140381835 0.00004
NM_014000.3(VCL):c.2746-8C>T rs532645343 0.00004
NM_014000.3(VCL):c.1164C>T (p.Ile388=) rs370852950 0.00003
NM_014000.3(VCL):c.225A>G (p.Pro75=) rs759937112 0.00003
NM_014000.3(VCL):c.2823C>T (p.Val941=) rs747647927 0.00003
NM_014000.3(VCL):c.1170T>C (p.Ala390=) rs201459260 0.00002
NM_014000.3(VCL):c.2746-14C>T rs367598954 0.00002
NM_014000.3(VCL):c.582G>A (p.Ser194=) rs773725513 0.00002
NM_014000.3(VCL):c.783+5G>A rs767694507 0.00002
NM_014000.3(VCL):c.1177-18C>T rs1336724326 0.00001
NM_014000.3(VCL):c.1347A>G (p.Arg449=) rs781535174 0.00001
NM_014000.3(VCL):c.1433A>G (p.Asn478Ser) rs763235691 0.00001
NM_014000.3(VCL):c.1563G>C (p.Gly521=) rs747932867 0.00001
NM_014000.3(VCL):c.2322C>T (p.Ser774=) rs202184524 0.00001
NM_014000.3(VCL):c.239+11G>A rs918332199 0.00001
NM_014000.3(VCL):c.2760C>T (p.Ala920=) rs138594604 0.00001
NM_014000.3(VCL):c.2841C>T (p.Asp947=) rs566296495 0.00001
NM_014000.3(VCL):c.2904C>T (p.Ala968=) rs558112511 0.00001
NM_014000.3(VCL):c.3154-8C>G rs376690719 0.00001
NM_014000.3(VCL):c.3189C>T (p.Leu1063=) rs765020779 0.00001
NM_014000.3(VCL):c.3259-5T>C rs1057523095 0.00001
NM_014000.3(VCL):c.3381T>C (p.Val1127=) rs943734765 0.00001
NM_014000.3(VCL):c.622+18T>C rs1218431325 0.00001
NM_014000.3(VCL):c.780C>T (p.Ser260=) rs774377548 0.00001
NM_014000.3(VCL):c.874+7C>G rs727503737 0.00001
NM_014000.3(VCL):c.1022+172TTTA[3] rs199705227
NM_014000.3(VCL):c.1074G>A (p.Gln358=) rs1057520879
NM_014000.3(VCL):c.1092A>G (p.Thr364=) rs1057521557
NM_014000.3(VCL):c.1157A>G (p.Lys386Arg) rs200342284
NM_014000.3(VCL):c.169-10delinsTG rs1554814892
NM_014000.3(VCL):c.169-11del rs753900484
NM_014000.3(VCL):c.169-18T>A rs1057521827
NM_014000.3(VCL):c.169-290A>G rs144295868
NM_014000.3(VCL):c.1743+19T>C rs542039663
NM_014000.3(VCL):c.1743+310del rs66999390
NM_014000.3(VCL):c.1743+310dup rs66999390
NM_014000.3(VCL):c.1800C>T (p.Ser600=) rs1341597341
NM_014000.3(VCL):c.1872+12A>G rs1057522638
NM_014000.3(VCL):c.1973T>C (p.Val658Ala) rs372691803
NM_014000.3(VCL):c.2256G>C (p.Gly752=) rs1057522615
NM_014000.3(VCL):c.2275C>A (p.Arg759=) rs774477633
NM_014000.3(VCL):c.2435-10T>C rs201207594
NM_014000.3(VCL):c.2435-3T>C rs1554819048
NM_014000.3(VCL):c.2559+18T>C rs1314406001
NM_014000.3(VCL):c.261G>A (p.Lys87=) rs1057523799
NM_014000.3(VCL):c.2769G>A (p.Val923=) rs1057521313
NM_014000.3(VCL):c.2862_2864del (p.Leu955del) rs397517237
NM_014000.3(VCL):c.3153+22GT[18] rs3037359
NM_014000.3(VCL):c.3153+51_3153+54dup rs1554819657
NM_014000.3(VCL):c.3153+54_3153+55insCATG rs764616052
NM_014000.3(VCL):c.622+35A>G rs181991376
NM_014000.3(VCL):c.622+4C>G rs201020802
NM_014000.3(VCL):c.789T>C (p.Thr263=) rs538002543

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