ClinVar Miner

List of variants in gene VCL reported as likely benign by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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Total variants: 32
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HGVS dbSNP gnomAD frequency
NM_014000.3(VCL):c.1907A>G (p.His636Arg) rs71579374 0.00240
NM_014000.3(VCL):c.660C>T (p.Asn220=) rs56264452 0.00091
NM_014000.3(VCL):c.1572C>T (p.Ala524=) rs138566234 0.00086
NM_014000.3(VCL):c.1348A>C (p.Arg450=) rs142128712 0.00075
NM_014000.3(VCL):c.1237G>A (p.Ala413Thr) rs146278697 0.00044
NM_014000.3(VCL):c.492T>G (p.Leu164=) rs143702799 0.00033
NM_014000.3(VCL):c.1626C>T (p.Leu542=) rs150402791 0.00031
NM_014000.3(VCL):c.366G>A (p.Leu122=) rs199562976 0.00029
NM_014000.3(VCL):c.1788A>C (p.Ser596=) rs199582103 0.00021
NM_014000.3(VCL):c.1842G>A (p.Thr614=) rs144117013 0.00016
NM_014000.3(VCL):c.2796T>C (p.Asp932=) rs140308982 0.00012
NM_014000.3(VCL):c.378C>T (p.Phe126=) rs148966602 0.00012
NM_014000.3(VCL):c.1290C>T (p.Asp430=) rs576271894 0.00009
NM_014000.3(VCL):c.2142C>T (p.Asp714=) rs373790383 0.00009
NM_014000.3(VCL):c.2799G>A (p.Ala933=) rs199507346 0.00009
NM_014000.3(VCL):c.3066C>T (p.Ile1022=) rs138619320 0.00009
NM_014000.3(VCL):c.3333T>C (p.Ala1111=) rs147415627 0.00008
NM_014000.3(VCL):c.390+11T>G rs764668318 0.00002
NM_014000.3(VCL):c.808T>C (p.Leu270=) rs727505339 0.00002
NM_014000.3(VCL):c.1543+15G>A rs759560099 0.00001
NM_014000.3(VCL):c.2841C>T (p.Asp947=) rs566296495 0.00001
NM_014000.3(VCL):c.2852C>G (p.Pro951Arg) rs368570586 0.00001
NM_014000.3(VCL):c.3327T>C (p.Ala1109=) rs397517242 0.00001
NM_014000.3(VCL):c.874+13T>C rs777617736 0.00001
NM_014000.3(VCL):c.874+7C>G rs727503737 0.00001
NM_014000.3(VCL):c.1017T>C (p.Arg339=) rs876657632
NM_014000.3(VCL):c.1157A>G (p.Lys386Arg) rs200342284
NM_014000.3(VCL):c.1275T>C (p.Pro425=) rs397517233
NM_014000.3(VCL):c.1337C>G (p.Ala446Gly) rs727504675
NM_014000.3(VCL):c.168+9G>T rs997516030
NM_014000.3(VCL):c.2862_2864del (p.Leu955del) rs397517237
NM_014000.3(VCL):c.874+9C>G rs756064535

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