ClinVar Miner

List of variants in gene VCL reported as likely benign by CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario

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Total variants: 10
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HGVS dbSNP gnomAD frequency
NM_014000.3(VCL):c.1237G>A (p.Ala413Thr) rs146278697 0.00044
NM_014000.3(VCL):c.366G>A (p.Leu122=) rs199562976 0.00029
NM_014000.3(VCL):c.2827C>G (p.Pro943Ala) rs71579375 0.00013
NM_014000.3(VCL):c.2799G>A (p.Ala933=) rs199507346 0.00009
NM_014000.3(VCL):c.2349G>A (p.Val783=) rs558040780 0.00006
NM_014000.3(VCL):c.255C>T (p.Cys85=) rs117384664 0.00004
NM_014000.3(VCL):c.1857G>A (p.Ala619=) rs1402201354 0.00002
NM_014000.3(VCL):c.2520T>G (p.Pro840=) rs777218777 0.00001
NM_014000.3(VCL):c.3363A>C (p.Gly1121=) rs771949807 0.00001
NM_014000.3(VCL):c.2247G>A (p.Leu749=) rs1840111616

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