ClinVar Miner

List of variants in gene VCL reported as uncertain significance for Cardiovascular phenotype

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Total variants: 20
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HGVS dbSNP
NM_014000.2(VCL):c.1001_1015del (p.Gln334_Leu338del) rs1554817370
NM_014000.2(VCL):c.1223T>C (p.Ile408Thr) rs878854969
NM_014000.2(VCL):c.1237G>A (p.Ala413Thr) rs146278697
NM_014000.2(VCL):c.1382C>G (p.Ala461Gly) rs886038800
NM_014000.2(VCL):c.1534C>T (p.Arg512Cys) rs781079975
NM_014000.2(VCL):c.1621C>G (p.Leu541Val) rs370229150
NM_014000.2(VCL):c.1856C>A (p.Ala619Glu) rs771628544
NM_014000.2(VCL):c.1907A>G (p.His636Arg) rs71579374
NM_014000.2(VCL):c.2046A>T (p.Leu682Phe) rs565398652
NM_014000.2(VCL):c.2159A>T (p.Lys720Ile) rs1554818881
NM_014000.2(VCL):c.2399A>T (p.Asp800Val) rs919509789
NM_014000.2(VCL):c.2444A>G (p.Lys815Arg) rs373010557
NM_014000.2(VCL):c.2875A>C (p.Asn959His) rs758969419
NM_014000.2(VCL):c.2893C>T (p.Pro965Ser) rs749236817
NM_014000.2(VCL):c.2923C>T (p.Arg975Trp) rs121917776
NM_014000.2(VCL):c.2969C>T (p.Ala990Val) rs150595117
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.731T>A (p.Ile244Lys) rs886038819
NM_014000.2(VCL):c.829C>A (p.Leu277Met) rs71579353

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