ClinVar Miner

List of variants in gene VCL reported as likely benign by Ambry Genetics

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Gene type:
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Total variants: 14
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HGVS dbSNP
NM_014000.2(VCL):c.1290C>T (p.Asp430=) rs576271894
NM_014000.2(VCL):c.1555A>C (p.Ile519Leu) rs141033098
NM_014000.2(VCL):c.1716T>G (p.Leu572=) rs189781480
NM_014000.2(VCL):c.2025G>A (p.Val675=) rs140766884
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.2827C>G (p.Pro943Ala) rs71579375
NM_014000.2(VCL):c.2862_2864delGTT (p.Leu955del) rs397517237
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.622+4C>T rs201020802
NM_014000.2(VCL):c.660C>T (p.Asn220=) rs56264452
NM_014000.2(VCL):c.789T>C (p.Thr263=) rs538002543
NM_014000.2(VCL):c.81C>T (p.His27=) rs200733607

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