ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 35
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HGVS dbSNP
NM_014000.2(VCL):c.1177-15C>T rs115083446
NM_014000.2(VCL):c.120C>T (p.Leu40=) rs144080529
NM_014000.2(VCL):c.1290C>T (p.Asp430=) rs576271894
NM_014000.2(VCL):c.1317T>C (p.Ser439=) rs71579355
NM_014000.2(VCL):c.1353-19G>A rs145537824
NM_014000.2(VCL):c.1407C>T (p.Ala469=) rs2229507
NM_014000.2(VCL):c.1506G>A (p.Arg502=) rs2228373
NM_014000.2(VCL):c.1542C>T (p.Val514=) rs7904077
NM_014000.2(VCL):c.1555A>C (p.Ile519Leu) rs141033098
NM_014000.2(VCL):c.1557C>A (p.Ile519=) rs150120464
NM_014000.2(VCL):c.1626C>T (p.Leu542=) rs150402791
NM_014000.2(VCL):c.1671C>T (p.Asp557=) rs137877092
NM_014000.2(VCL):c.1716T>G (p.Leu572=) rs189781480
NM_014000.2(VCL):c.1842G>A (p.Thr614=) rs144117013
NM_014000.2(VCL):c.2023-20A>G rs143756084
NM_014000.2(VCL):c.2025G>A (p.Val675=) rs140766884
NM_014000.2(VCL):c.2388= (p.Pro796=) rs767809
NM_014000.2(VCL):c.2388G>A (p.Pro796=) rs767809
NM_014000.2(VCL):c.2434+19T>C rs188216596
NM_014000.2(VCL):c.2521G>C (p.Asp841His) rs150385900
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.2801C>T (p.Ala934Val) rs16931179
NM_014000.2(VCL):c.2814= (p.Gly938=) rs2131956
NM_014000.2(VCL):c.2814C>G (p.Gly938=) rs2131956
NM_014000.2(VCL):c.3258+10A>T rs71579379
NM_014000.2(VCL):c.3333T>C (p.Ala1111=) rs147415627
NM_014000.2(VCL):c.339G>A (p.Arg113=) rs56314318
NM_014000.2(VCL):c.366G>A (p.Leu122=) rs199562976
NM_014000.2(VCL):c.622+4C>T rs201020802
NM_014000.2(VCL):c.660C>T (p.Asn220=) rs56264452
NM_014000.2(VCL):c.768T>C (p.Asp256=) rs56413529
NM_014000.2(VCL):c.81C>T (p.His27=) rs200733607
NM_014000.2(VCL):c.875-24T>A rs1908339
NM_014000.2(VCL):c.945C>A (p.Gly315=) rs61731180

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