ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 80
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HGVS dbSNP gnomAD frequency
NM_014000.3(VCL):c.1506G>A (p.Arg502=) rs2228373 0.06736
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.2801C>T (p.Ala934Val) rs16931179 0.00658
NM_014000.3(VCL):c.1317T>C (p.Ser439=) rs71579355 0.00442
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.1177-15C>T rs115083446 0.00414
NM_014000.3(VCL):c.1542C>T (p.Val514=) rs7904077 0.00380
NM_014000.3(VCL):c.1873-183C>T rs149008791 0.00309
NM_014000.3(VCL):c.3258+10A>T rs71579379 0.00267
NM_014000.3(VCL):c.2025G>A (p.Val675=) rs140766884 0.00256
NM_014000.3(VCL):c.2023-20A>G rs143756084 0.00247
NM_014000.3(VCL):c.1907A>G (p.His636Arg) rs71579374 0.00240
NM_014000.3(VCL):c.1671C>T (p.Asp557=) rs137877092 0.00228
NM_014000.3(VCL):c.2950-201T>C rs187870650 0.00206
NM_014000.3(VCL):c.1353-19G>A rs145537824 0.00193
NM_014000.3(VCL):c.660C>T (p.Asn220=) rs56264452 0.00091
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.2521G>C (p.Asp841His) rs150385900 0.00051
NM_014000.3(VCL):c.1237G>A (p.Ala413Thr) rs146278697 0.00044
NM_014000.3(VCL):c.492T>G (p.Leu164=) rs143702799 0.00033
NM_014000.3(VCL):c.366G>A (p.Leu122=) rs199562976 0.00029
NM_014000.3(VCL):c.571T>C (p.Leu191=) rs370334093 0.00021
NM_014000.3(VCL):c.590C>T (p.Thr197Ile) rs189242810 0.00019
NM_014000.3(VCL):c.1716T>G (p.Leu572=) rs189781480 0.00016
NM_014000.3(VCL):c.1842G>A (p.Thr614=) rs144117013 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.2802C>T (p.Ala934=) rs372381809 0.00007
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.404T>C (p.Ile135Thr) rs373744314 0.00006
NM_014000.3(VCL):c.528C>T (p.Asp176=) rs746453891 0.00005
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.2265T>C (p.Ser755=) rs147887754 0.00004
NM_014000.3(VCL):c.2472C>G (p.Ile824Met) rs140381835 0.00004
NM_014000.3(VCL):c.1164C>T (p.Ile388=) rs370852950 0.00003
NM_014000.3(VCL):c.2823C>T (p.Val941=) rs747647927 0.00003
NM_014000.3(VCL):c.783+5G>A rs767694507 0.00002
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.2322C>T (p.Ser774=) rs202184524 0.00001
NM_014000.3(VCL):c.2760C>T (p.Ala920=) rs138594604 0.00001
NM_014000.3(VCL):c.2904C>T (p.Ala968=) rs558112511 0.00001
NM_014000.3(VCL):c.3154-6C>T rs371257509 0.00001
NM_014000.3(VCL):c.3189C>T (p.Leu1063=) rs765020779 0.00001
NM_014000.3(VCL):c.424T>C (p.Leu142=) rs762497815 0.00001
NM_014000.3(VCL):c.875-5T>C rs1225977039 0.00001
NM_014000.3(VCL):c.1022+172TTTA[3] rs199705227
NM_014000.3(VCL):c.1157A>G (p.Lys386Arg) rs200342284
NM_014000.3(VCL):c.1294C>T (p.Leu432=) rs144146254
NM_014000.3(VCL):c.1296A>G (p.Leu432=)
NM_014000.3(VCL):c.168+9G>T rs997516030
NM_014000.3(VCL):c.169-290A>G rs144295868
NM_014000.3(VCL):c.1743+310del rs66999390
NM_014000.3(VCL):c.1743+310dup rs66999390
NM_014000.3(VCL):c.1973T>C (p.Val658Ala) rs372691803
NM_014000.3(VCL):c.2091C>T (p.Thr697=) rs775493699
NM_014000.3(VCL):c.2434+10G>A rs1591713338
NM_014000.3(VCL):c.2529G>A (p.Pro843=) rs1591714816
NM_014000.3(VCL):c.2559+18T>C rs1314406001
NM_014000.3(VCL):c.2862_2864del (p.Leu955del) rs397517237
NM_014000.3(VCL):c.3099C>T (p.Ala1033=)
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.622+4C>T rs201020802

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