ClinVar Miner

List of variants in gene VCL reported by Ambry Genetics

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Gene type:
ClinVar version:
Total variants: 47
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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.1290C>T (p.Asp430=) rs576271894
NM_014000.2(VCL):c.1317T>C (p.Ser439=) rs71579355
NM_014000.2(VCL):c.1382C>G (p.Ala461Gly) rs886038800
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.1534C>T (p.Arg512Cys) rs781079975
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.1621C>G (p.Leu541Val) rs370229150
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.1856C>A (p.Ala619Glu) rs771628544
NM_014000.2(VCL):c.1907A>G (p.His636Arg) rs71579374
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.2159A>T (p.Lys720Ile) rs1554818881
NM_014000.2(VCL):c.2388G>A (p.Pro796=) rs767809
NM_014000.2(VCL):c.2399A>T (p.Asp800Val) rs919509789
NM_014000.2(VCL):c.2418A>G (p.Gly806=) rs538142998
NM_014000.2(VCL):c.2427C>T (p.Ser809=) rs183739128
NM_014000.2(VCL):c.2444A>G (p.Lys815Arg) rs373010557
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.2814C>G (p.Gly938=) rs2131956
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.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.3246G>A (p.Glu1082=) rs988135144
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.404T>C (p.Ile135Thr) rs373744314
NM_014000.2(VCL):c.492T>G (p.Leu164=) rs143702799
NM_014000.2(VCL):c.590C>T (p.Thr197Ile) rs189242810
NM_014000.2(VCL):c.622+4C>T rs201020802
NM_014000.2(VCL):c.660C>T (p.Asn220=) rs56264452
NM_014000.2(VCL):c.731T>A (p.Ile244Lys) rs886038819
NM_014000.2(VCL):c.768T>C (p.Asp256=) rs56413529
NM_014000.2(VCL):c.789T>C (p.Thr263=) rs538002543
NM_014000.2(VCL):c.81C>T (p.His27=) rs200733607
NM_014000.2(VCL):c.829C>A (p.Leu277Met) rs71579353
NM_014000.2(VCL):c.945C>A (p.Gly315=) rs61731180

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