List of variants in gene VCP reported as benign for frontotemporal dementia and/or amyotrophic lateral sclerosis 6

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: 30

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_007126.5(VCP):c.1360-35A>G	rs2258240	0.75740
NM_007126.5(VCP):c.811+3G>A	rs514492	0.75591
NM_007126.5(VCP):c.1695+8A>G	rs684562	0.54947
NM_007126.5(VCP):c.*153G>T	rs1053318	0.19091
NM_007126.5(VCP):c.129+47G>A	rs10972300	0.17835
NM_007126.5(VCP):c.*596C>T	rs55745923	0.02117
NM_007126.5(VCP):c.18-5T>C	rs114256093	0.01353
NM_007126.5(VCP):c.*906A>G	rs76360394	0.00965
NM_007126.5(VCP):c.1082-9G>T	rs12349922	0.00667
NM_007126.5(VCP):c.1092C>T (p.Asp364=)	rs61752947	0.00619
NM_007126.5(VCP):c.1360-14C>G	rs144304208	0.00311
NM_007126.5(VCP):c.1704A>G (p.Gln568=)	rs142577424	0.00296
NM_007126.5(VCP):c.927C>T (p.Ile309=)	rs34097935	0.00270
NM_007126.5(VCP):c.-267C>T	rs184152880	0.00252
NM_007126.5(VCP):c.79A>G (p.Ile27Val)	rs140913250	0.00151
NM_007126.5(VCP):c.1081+17C>T	rs200756991	0.00113
NM_007126.5(VCP):c.1584C>T (p.Ala528=)	rs147623367	0.00064
NM_007126.5(VCP):c.832T>C (p.Leu278=)	rs200670526	0.00040
NM_007126.5(VCP):c.1482+18A>G	rs370501665	0.00024
NM_007126.5(VCP):c.2193C>T (p.Ile731=)	rs186657793	0.00017
NM_007126.5(VCP):c.1875G>T (p.Arg625=)	rs201410035	0.00009
NM_007126.5(VCP):c.2229G>A (p.Ala743=)	rs200767982	0.00009
NM_007126.5(VCP):c.*438A>G	rs137953487	0.00004
NM_007126.5(VCP):c.54A>G (p.Lys18=)	rs766042571	0.00003
NM_007126.5(VCP):c.2214A>G (p.Glu738=)	rs374391034	0.00002
NM_007126.5(VCP):c.812-7C>G	rs764429197	0.00002
NM_007126.5(VCP):c.1407A>G (p.Val469=)	rs761430933	0.00001
NM_007126.5(VCP):c.2160+8T>G	rs564249854	0.00001
NM_007126.5(VCP):c.465T>G (p.Arg155=)	rs765140312	0.00001
NM_007126.5(VCP):c.1082-18_1082-8dup	rs11272867

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.