ClinVar Miner

List of variants in gene VCL reported by CHEO Genetics Diagnostic Laboratory,Children's Hospital of Eastern Ontario

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Gene type:
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Total variants: 22
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HGVS dbSNP
NM_014000.2(VCL):c.120C>T (p.Leu40=) rs144080529
NM_014000.2(VCL):c.1317T>C (p.Ser439=) rs71579355
NM_014000.2(VCL):c.1521C>T (p.Pro507=) rs1564529609
NM_014000.2(VCL):c.1557C>A (p.Ile519=) rs150120464
NM_014000.2(VCL):c.1621C>G (p.Leu541Val) rs370229150
NM_014000.2(VCL):c.1671C>T (p.Asp557=) rs137877092
NM_014000.2(VCL):c.1798A>C (p.Ser600Arg) rs397517236
NM_014000.2(VCL):c.2025G>A (p.Val675=) rs140766884
NM_014000.2(VCL):c.2046A>T (p.Leu682Phe) rs565398652
NM_014000.2(VCL):c.2143G>A (p.Glu715Lys) rs1022329091
NM_014000.2(VCL):c.255C>T (p.Cys85=) rs117384664
NM_014000.2(VCL):c.2801C>T (p.Ala934Val) rs16931179
NM_014000.2(VCL):c.2827C>G (p.Pro943Ala) rs71579375
NM_014000.2(VCL):c.2867T>G (p.Met956Arg) rs765717598
NM_014000.2(VCL):c.3258+10A>T rs71579379
NM_014000.2(VCL):c.3267G>C (p.Glu1089Asp) rs149300310
NM_014000.2(VCL):c.404T>C (p.Ile135Thr) rs373744314
NM_014000.2(VCL):c.500G>A (p.Gly167Glu) rs1564523552
NM_014000.2(VCL):c.625A>T (p.Met209Leu) rs144683137
NM_014000.2(VCL):c.626T>A (p.Met209Lys) rs751243981
NM_014000.2(VCL):c.945C>A (p.Gly315=) rs61731180
NM_014000.2(VCL):c.963del (p.Leu322fs) rs1564526327

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