ClinVar Miner

List of variants in gene VCL reported by Biesecker Lab/Human Development Section,National Institutes of Health

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Gene type:
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Total variants: 19
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HGVS dbSNP
NM_014000.2(VCL):c.1157A>G (p.Lys386Arg) rs200342284
NM_014000.2(VCL):c.1192C>T (p.Pro398Ser) rs201528612
NM_014000.2(VCL):c.1198G>T (p.Gly400Cys) rs201361282
NM_014000.2(VCL):c.1225C>T (p.Arg409Ter) rs202005455
NM_014000.2(VCL):c.1237G>A (p.Ala413Thr) rs146278697
NM_014000.2(VCL):c.1294C>G (p.Leu432Val) rs144146254
NM_014000.2(VCL):c.1555A>C (p.Ile519Leu) rs141033098
NM_014000.2(VCL):c.1607C>A (p.Pro536His) rs200624351
NM_014000.2(VCL):c.1798A>C (p.Ser600Arg) rs397517236
NM_014000.2(VCL):c.1907A>G (p.His636Arg) rs71579374
NM_014000.2(VCL):c.2521G>C (p.Asp841His) rs150385900
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.2862_2864del (p.Leu955del) rs397517237
NM_014000.2(VCL):c.2893C>T (p.Pro965Ser) rs749236817
NM_014000.2(VCL):c.404T>C (p.Ile135Thr) rs373744314
NM_014000.2(VCL):c.590C>T (p.Thr197Ile) rs189242810
NM_014000.2(VCL):c.688C>T (p.Arg230Cys) rs139312390
NM_014000.2(VCL):c.695T>A (p.Phe232Tyr) rs200956572

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