ClinVar Miner

List of variants in gene VCL reported as benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 71
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HGVS dbSNP gnomAD frequency
NM_014000.3(VCL):c.2814C>G (p.Gly938=) rs2131956 0.74148
NM_014000.3(VCL):c.1743+229C>T rs4746172 0.73246
NM_014000.3(VCL):c.1353-233C>T rs10824069 0.72697
NM_014000.3(VCL):c.1743+295_1743+297dup rs59287851 0.72392
NM_014000.3(VCL):c.875-24T>A rs1908339 0.65590
NM_014000.3(VCL):c.2131+64C>T rs2270552 0.62645
NM_014000.3(VCL):c.2950-50C>T rs10824072 0.51206
NM_014000.3(VCL):c.2435-59C>A rs2131957 0.51170
NM_014000.3(VCL):c.2745+151T>C rs2270551 0.47070
NM_014000.3(VCL):c.2388G>A (p.Pro796=) rs767809 0.42862
NM_014000.3(VCL):c.3153+47T>C rs2270550 0.42070
NM_014000.3(VCL):c.784-60G>A rs2270548 0.40906
NM_014000.3(VCL):c.875-324dup rs5786133 0.40792
NM_014000.3(VCL):c.2559+81G>T rs2279648 0.12795
NM_014000.3(VCL):c.1177-158_1177-157insCA rs10652052 0.07596
NM_014000.3(VCL):c.623-181A>C rs60563569 0.06798
NM_014000.3(VCL):c.500-281T>C rs74146314 0.06797
NM_014000.3(VCL):c.500-236A>G rs74146315 0.06791
NM_014000.3(VCL):c.2434+159G>A rs57050827 0.06780
NM_014000.3(VCL):c.768T>C (p.Asp256=) rs56413529 0.06776
NM_014000.3(VCL):c.339G>A (p.Arg113=) rs56314318 0.06767
NM_014000.3(VCL):c.622+211T>C rs111609277 0.06762
NM_014000.3(VCL):c.622+191C>T rs71524384 0.06748
NM_014000.3(VCL):c.1407C>T (p.Ala469=) rs2229507 0.06739
NM_014000.3(VCL):c.1506G>A (p.Arg502=) rs2228373 0.06736
NM_014000.3(VCL):c.622+158G>A rs71524373 0.06722
NM_014000.3(VCL):c.622+88C>G rs79479684 0.06687
NM_014000.3(VCL):c.1177-278T>C rs7073889 0.05881
NM_014000.3(VCL):c.1872+197G>C rs12243178 0.05370
NM_014000.3(VCL):c.1872+199A>C rs74146325 0.04163
NM_014000.3(VCL):c.2434+48C>T rs55984079 0.03928
NM_014000.3(VCL):c.945C>A (p.Gly315=) rs61731180 0.02850
NM_014000.3(VCL):c.1352+35C>A rs73280468 0.02489
NM_014000.3(VCL):c.3153+49T>C rs868668365 0.01918
NM_014000.3(VCL):c.1353-203A>G rs7900388 0.01820
NM_014000.3(VCL):c.3154-138A>G rs1874148 0.01806
NM_014000.3(VCL):c.2801C>T (p.Ala934Val) rs16931179 0.00658
NM_014000.3(VCL):c.1557C>A (p.Ile519=) rs150120464 0.00466
NM_014000.3(VCL):c.1317T>C (p.Ser439=) rs71579355 0.00442
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.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.1671C>T (p.Asp557=) rs137877092 0.00228
NM_014000.3(VCL):c.2434+19T>C rs188216596 0.00198
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.1348A>C (p.Arg450=) rs142128712 0.00075
NM_014000.3(VCL):c.2521G>C (p.Asp841His) rs150385900 0.00051
NM_014000.3(VCL):c.492T>G (p.Leu164=) rs143702799 0.00033
NM_014000.3(VCL):c.1626C>T (p.Leu542=) rs150402791 0.00031
NM_014000.3(VCL):c.366G>A (p.Leu122=) rs199562976 0.00029
NM_014000.3(VCL):c.1744-19T>G rs201488697 0.00022
NM_014000.3(VCL):c.1842G>A (p.Thr614=) rs144117013 0.00016
NM_014000.3(VCL):c.2796T>C (p.Asp932=) rs140308982 0.00012
NM_014000.3(VCL):c.1290C>T (p.Asp430=) rs576271894 0.00009
NM_014000.3(VCL):c.2799G>A (p.Ala933=) rs199507346 0.00009
NM_014000.3(VCL):c.3333T>C (p.Ala1111=) rs147415627 0.00008
NM_014000.3(VCL):c.1743+309_1743+310dup rs66999390
NM_014000.3(VCL):c.1744-192del rs150514819
NM_014000.3(VCL):c.2022+186dup rs199610574
NM_014000.3(VCL):c.2022+239dup rs946868220
NM_014000.3(VCL):c.239+210dup rs142336119
NM_014000.3(VCL):c.3153+22GT[10] rs3037359
NM_014000.3(VCL):c.3153+22GT[11] rs3037359
NM_014000.3(VCL):c.3153+22GT[15] rs3037359
NM_014000.3(VCL):c.3153+48_3153+49insCG rs60917222
NM_014000.3(VCL):c.622+107dup rs369560544
NM_014000.3(VCL):c.622+4C>T rs201020802
NM_014000.3(VCL):c.623-83T>C rs58026892

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