ClinVar Miner

List of variants in gene VCL reported as benign by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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Gene type:
ClinVar version:
Total variants: 23
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HGVS dbSNP gnomAD frequency
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.1557C>A (p.Ile519=) rs150120464 0.00466
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.1907A>G (p.His636Arg) rs71579374 0.00240
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.1572C>T (p.Ala524=) rs138566234 0.00086
NM_014000.3(VCL):c.1348A>C (p.Arg450=) rs142128712 0.00075
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.1788A>C (p.Ser596=) rs199582103 0.00021
NM_014000.3(VCL):c.1842G>A (p.Thr614=) rs144117013 0.00016
NM_014000.3(VCL):c.1290C>T (p.Asp430=) rs576271894 0.00009
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.874+13T>C rs777617736 0.00001
NM_014000.3(VCL):c.622+4C>T rs201020802

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