ClinVar Miner

List of variants in gene VCL reported as likely pathogenic

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Total variants: 11
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HGVS dbSNP
NM_014000.2(VCL):c.1531G>T (p.Asp511Tyr) rs863225121
NM_014000.2(VCL):c.1544-2A>G rs727503738
NM_014000.2(VCL):c.1639C>T (p.Arg547Ter) rs397517234
NM_014000.2(VCL):c.1713delA (p.Ala573Hisfs) rs779488376
NM_014000.2(VCL):c.1762C>T (p.Gln588Ter) rs727504381
NM_014000.2(VCL):c.2828_2829delCT (p.Pro943Argfs) rs781036800
NM_014000.2(VCL):c.3115C>T (p.Gln1039Ter) rs727503741
NM_014000.2(VCL):c.562C>T (p.Arg188Ter) rs397517244
NM_014000.2(VCL):c.659_660insA (p.Asn220Lysfs) rs397517245
NM_014000.2(VCL):c.670_671insG (p.Glu224Glyfs) rs876657674
NM_014000.2:c.963del

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