List of variants in gene VCL reported as benign for cardiovascular disorder

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: 46

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_014000.3(VCL):c.*1584T>A	rs703258	0.74527
NM_014000.3(VCL):c.2814C>G (p.Gly938=)	rs2131956	0.74148
NM_014000.3(VCL):c.875-24T>A	rs1908339	0.65590
NM_014000.3(VCL):c.2388G>A (p.Pro796=)	rs767809	0.42862
NM_014000.3(VCL):c.3153+47T>C	rs2270550	0.42070
NM_014000.3(VCL):c.*1823G>A	rs8255	0.20084
NM_014000.3(VCL):c.*1854A>C	rs3829204	0.11656
NM_014000.3(VCL):c.768T>C (p.Asp256=)	rs56413529	0.06776
NM_014000.3(VCL):c.339G>A (p.Arg113=)	rs56314318	0.06767
NM_014000.3(VCL):c.1407C>T (p.Ala469=)	rs2229507	0.06739
NM_014000.3(VCL):c.1506G>A (p.Arg502=)	rs2228373	0.06736
NM_014000.3(VCL):c.*1853A>C	rs554923257	0.04999
NM_014000.3(VCL):c.945C>A (p.Gly315=)	rs61731180	0.02850
NM_014000.3(VCL):c.2801C>T (p.Ala934Val)	rs16931179	0.00658
NM_014000.3(VCL):c.1557C>A (p.Ile519=)	rs150120464	0.00466
NM_014000.3(VCL):c.1317T>C (p.Ser439=)	rs71579355	0.00442
NM_014000.3(VCL):c.1177-15C>T	rs115083446	0.00414
NM_014000.3(VCL):c.1542C>T (p.Val514=)	rs7904077	0.00380
NM_014000.3(VCL):c.3258+10A>T	rs71579379	0.00267
NM_014000.3(VCL):c.2025G>A (p.Val675=)	rs140766884	0.00256
NM_014000.3(VCL):c.2023-20A>G	rs143756084	0.00247
NM_014000.3(VCL):c.1907A>G (p.His636Arg)	rs71579374	0.00240
NM_014000.3(VCL):c.1671C>T (p.Asp557=)	rs137877092	0.00228
NM_014000.3(VCL):c.2434+19T>C	rs188216596	0.00198
NM_014000.3(VCL):c.1353-19G>A	rs145537824	0.00193
NM_014000.3(VCL):c.660C>T (p.Asn220=)	rs56264452	0.00091
NM_014000.3(VCL):c.1572C>T (p.Ala524=)	rs138566234	0.00086
NM_014000.3(VCL):c.1348A>C (p.Arg450=)	rs142128712	0.00075
NM_014000.3(VCL):c.1555A>C (p.Ile519Leu)	rs141033098	0.00064
NM_014000.3(VCL):c.2521G>C (p.Asp841His)	rs150385900	0.00051
NM_014000.3(VCL):c.492T>G (p.Leu164=)	rs143702799	0.00033
NM_014000.3(VCL):c.1176+20G>A	rs370298549	0.00025
NM_014000.3(VCL):c.1744-19T>G	rs201488697	0.00022
NM_014000.3(VCL):c.1788A>C (p.Ser596=)	rs199582103	0.00021
NM_014000.3(VCL):c.1716T>G (p.Leu572=)	rs189781480	0.00016
NM_014000.3(VCL):c.378C>T (p.Phe126=)	rs148966602	0.00012
NM_014000.3(VCL):c.1352+20dup	rs570134112	0.00011
NM_014000.3(VCL):c.1290C>T (p.Asp430=)	rs576271894	0.00009
NM_014000.3(VCL):c.3333T>C (p.Ala1111=)	rs147415627	0.00008
NM_014000.3(VCL):c.404T>C (p.Ile135Thr)	rs373744314	0.00006
NM_014000.3(VCL):c.1164C>T (p.Ile388=)	rs370852950	0.00003
NM_014000.3(VCL):c.1157A>G (p.Lys386Arg)	rs200342284
NM_014000.3(VCL):c.169-11del	rs753900484
NM_014000.3(VCL):c.1744-4del	rs1187225391
NM_014000.3(VCL):c.2862_2864del (p.Leu955del)	rs397517237
NM_014000.3(VCL):c.622+4C>T	rs201020802

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.