List of variants in gene combination LOC130004109, VCL reported as likely benign for Dilated cardiomyopathy 1W

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: 16

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_014000.3(VCL):c.45G>A (p.Pro15=)	rs775062250	0.00004
NM_014000.3(VCL):c.99C>T (p.Asp33=)	rs568175141	0.00002
NM_014000.3(VCL):c.30G>A (p.Glu10=)	rs146750460	0.00001
NM_014000.3(VCL):c.36C>T (p.Ile12=)	rs774195260	0.00001
NM_014000.3(VCL):c.6A>C (p.Pro2=)	rs753870747	0.00001
NM_014000.3(VCL):c.120C>T (p.Leu40=)	rs144080529
NM_014000.3(VCL):c.126G>T (p.Ala42=)	rs1031820588
NM_014000.3(VCL):c.129C>T (p.Pro43=)	rs1169961162
NM_014000.3(VCL):c.135C>A (p.Ala45=)
NM_014000.3(VCL):c.135C>T (p.Ala45=)	rs1840154950
NM_014000.3(VCL):c.18G>A (p.Thr6=)	rs1247615898
NM_014000.3(VCL):c.24G>A (p.Thr8=)	rs1411168963
NM_014000.3(VCL):c.27C>T (p.Ile9=)	rs2136218230
NM_014000.3(VCL):c.51A>G (p.Ala17=)	rs1591641682
NM_014000.3(VCL):c.69G>C (p.Leu23=)	rs1591641692
NM_014000.3(VCL):c.87G>A (p.Glu29=)	rs2136218290

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.