ClinVar Miner

List of variants in gene VCP reported as uncertain significance for amyotrophic lateral sclerosis type 14

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 21
Download table as spreadsheet
NM_007126.5(VCP):c.1180G>A (p.Val394Met)
NM_007126.5(VCP):c.1327A>C (p.Asn443His) rs770514866
NM_007126.5(VCP):c.1360-4C>G rs769279961
NM_007126.5(VCP):c.1374G>C (p.Gln458His) rs1060499674
NM_007126.5(VCP):c.1984C>T (p.Arg662Cys)
NM_007126.5(VCP):c.2014T>G (p.Leu672Val)
NM_007126.5(VCP):c.2266G>A (p.Glu756Lys)
NM_007126.5(VCP):c.2397C>G (p.Asp799Glu) rs1329151473
NM_007126.5(VCP):c.278G>A (p.Arg93His) rs779959657
NM_007126.5(VCP):c.303-3C>T rs1183711292
NM_007126.5(VCP):c.320A>T (p.Asp107Val) rs1563980440
NM_007126.5(VCP):c.340A>G (p.Ile114Val)
NM_007126.5(VCP):c.374G>A (p.Gly125Asp) rs1563980403
NM_007126.5(VCP):c.463C>G (p.Arg155Gly) rs121909330
NM_007126.5(VCP):c.478G>C (p.Ala160Pro) rs1554668805
NM_007126.5(VCP):c.479C>T (p.Ala160Val) rs1554668804
NM_007126.5(VCP):c.512G>T (p.Ser171Ile)
NM_007126.5(VCP):c.553G>A (p.Glu185Lys) rs864309501
NM_007126.5(VCP):c.811+2_811+3inv rs1554668584
NM_007126.5(VCP):c.84T>A (p.Val28=)

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.