"Institute of Human Genetics, University of Wuerzburg"[submitter] AND - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1329299	NM_014000.3(VCL):c.140T>G (p.Val47Gly)	VCL (V47G)	Single nucleotide variant (missense variant)	Cardiomyopathy	GUncertain significance
Select item 3255545	NM_014000.3(VCL):c.143A>C (p.Gln48Pro)	VCL (Q48P)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 2	Gnot provided
Select item 3255546	NM_014000.3(VCL):c.159C>A (p.Asn53Lys)	VCL (N53K)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 2	Gnot provided
Select item 3255547	NM_014000.3(VCL):c.168+4A>T	VCL	Single nucleotide variant (intron variant)	Hypertrophic cardiomyopathy 2	Gnot provided
Select item 3255548	NM_014000.3(VCL):c.168+15C>G	VCL	Single nucleotide variant (intron variant)	Hypertrophic cardiomyopathy 2	Gnot provided
Select item 3255549	NM_014000.3(VCL):c.1176+13A>T	VCL	Single nucleotide variant (intron variant)	Hypertrophic cardiomyopathy 2	Gnot provided
Select item 3255550	NM_014000.3(VCL):c.1176+19A>T	VCL	Single nucleotide variant (intron variant)	Hypertrophic cardiomyopathy 2	Gnot provided
Select item 689587	NM_014000.3(VCL):c.1382C>A (p.Ala461Asp)	VCL (A461D)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1W	GUncertain significance

ClinVar