List of variants in gene VCL reported as uncertain significance for not specified

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 52

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HGVS	dbSNP	gnomAD frequency
NM_014000.3(VCL):c.2521G>C (p.Asp841His)	rs150385900	0.00051
NM_014000.3(VCL):c.1294C>G (p.Leu432Val)	rs144146254	0.00025
NM_014000.3(VCL):c.787A>T (p.Thr263Ser)	rs142233726	0.00022
NM_014000.3(VCL):c.2969C>T (p.Ala990Val)	rs150595117	0.00019
NM_014000.3(VCL):c.590C>T (p.Thr197Ile)	rs189242810	0.00019
NM_014000.3(VCL):c.688C>T (p.Arg230Cys)	rs139312390	0.00010
NM_014000.3(VCL):c.1490T>C (p.Ile497Thr)	rs572757800	0.00008
NM_014000.3(VCL):c.1621C>G (p.Leu541Val)	rs370229150	0.00008
NM_014000.3(VCL):c.2444A>G (p.Lys815Arg)	rs373010557	0.00008
NM_014000.3(VCL):c.185T>C (p.Val62Ala)	rs769799445	0.00004
NM_014000.3(VCL):c.2046A>T (p.Leu682Phe)	rs565398652	0.00004
NM_014000.3(VCL):c.3092G>A (p.Arg1031Gln)	rs397517238	0.00004
NM_014000.3(VCL):c.3373C>T (p.Arg1125Cys)	rs373317423	0.00004
NM_014000.3(VCL):c.1844C>T (p.Ala615Val)	rs148669762	0.00003
NM_014000.3(VCL):c.2875A>C (p.Asn959His)	rs758969419	0.00003
NM_014000.3(VCL):c.2746-14C>T	rs367598954	0.00002
NM_014000.3(VCL):c.1292T>G (p.Ile431Ser)	rs766192312	0.00001
NM_014000.3(VCL):c.163G>T (p.Val55Phe)	rs755441334	0.00001
NM_014000.3(VCL):c.1798A>C (p.Ser600Arg)	rs397517236	0.00001
NM_014000.3(VCL):c.2005C>T (p.Arg669Ter)	rs780856981	0.00001
NM_014000.3(VCL):c.313C>T (p.Arg105Ter)	rs397517239	0.00001
NM_014000.3(VCL):c.3226C>T (p.Arg1076Trp)	rs397517241	0.00001
NM_014000.3(VCL):c.610G>C (p.Val204Leu)	rs727504585	0.00001
NM_014000.3(VCL):c.625A>T (p.Met209Leu)	rs144683137	0.00001
NM_014000.3(VCL):c.854G>A (p.Arg285His)	rs397517246	0.00001
NM_014000.3(VCL):c.952C>T (p.Arg318Cys)	rs397517247	0.00001
GRCh37/hg19 10q22.2(chr10:75712146-75856710)
NM_014000.3(VCL):c.1198G>T (p.Gly400Cys)	rs201361282
NM_014000.3(VCL):c.1225C>T (p.Arg409Ter)	rs202005455
NM_014000.3(VCL):c.1390A>C (p.Lys464Gln)	rs200710859
NM_014000.3(VCL):c.151G>T (p.Val51Phe)	rs1565628951
NM_014000.3(VCL):c.1559G>A (p.Arg520Gln)	rs757009736
NM_014000.3(VCL):c.1575A>C (p.Glu525Asp)	rs548487697
NM_014000.3(VCL):c.1639C>T (p.Arg547Ter)	rs397517234
NM_014000.3(VCL):c.1792G>A (p.Val598Ile)	rs397517235
NM_014000.3(VCL):c.1888G>A (p.Ala630Thr)	rs727503739
NM_014000.3(VCL):c.1973T>C (p.Val658Ala)	rs372691803
NM_014000.3(VCL):c.2185G>A (p.Ala729Thr)	rs957518574
NM_014000.3(VCL):c.2362G>C (p.Asp788His)
NM_014000.3(VCL):c.2455G>A (p.Asp819Asn)
NM_014000.3(VCL):c.2672G>C (p.Gly891Ala)	rs727503740
NM_014000.3(VCL):c.2775_2780del (p.Gly926_Val927del)	rs757018106
NM_014000.3(VCL):c.2823_2824delinsGT (p.Pro942Ser)	rs1060502196
NM_014000.3(VCL):c.2827C>A (p.Pro943Thr)	rs71579375
NM_014000.3(VCL):c.2949+1del	rs2131937426
NM_014000.3(VCL):c.3115C>T (p.Gln1039Ter)	rs727503741
NM_014000.3(VCL):c.3163C>T (p.Arg1055Ter)	rs727505159
NM_014000.3(VCL):c.3236T>C (p.Ile1079Thr)	rs727503742
NM_014000.3(VCL):c.500-5C>G	rs397517243
NM_014000.3(VCL):c.565G>C (p.Val189Leu)	rs151045204
NM_014000.3(VCL):c.622+4C>G	rs201020802
NM_014000.3(VCL):c.649A>G (p.Asn217Asp)	rs727505216

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