List of variants in gene VCL reported as uncertain significance by Mayo Clinic Laboratories, Mayo Clinic

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_014000.3(VCL):c.2969C>T (p.Ala990Val)	rs150595117	0.00019
NM_014000.3(VCL):c.2531C>T (p.Pro844Leu)	rs145393322	0.00007
NM_014000.3(VCL):c.1039C>T (p.Pro347Ser)	rs566961713	0.00003
NM_014000.3(VCL):c.1040C>T (p.Pro347Leu)	rs148619523	0.00003
NM_014000.3(VCL):c.1298G>A (p.Arg433His)	rs754046223	0.00001
NM_014000.3(VCL):c.1559G>A (p.Arg520Gln)	rs757009736
NM_014000.3(VCL):c.1998G>T (p.Lys666Asn)	rs886047220
NM_014000.3(VCL):c.2039G>A (p.Arg680His)	rs1840094043
NM_014000.3(VCL):c.2386C>G (p.Pro796Ala)	rs749471739
NM_014000.3(VCL):c.2387del (p.Pro796fs)	rs1241654679
NM_014000.3(VCL):c.565G>T (p.Val189Leu)	rs151045204
NM_014000.3(VCL):c.999T>A (p.Asp333Glu)

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