ClinVar Miner

List of variants in gene VCP reported as benign 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: 10
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NM_007126.5(VCP):c.1082-18_1082-8dup rs11272867
NM_007126.5(VCP):c.1082-9G>T rs12349922
NM_007126.5(VCP):c.1092C>T (p.Asp364=) rs61752947
NM_007126.5(VCP):c.1584C>T (p.Ala528=) rs147623367
NM_007126.5(VCP):c.1704A>G (p.Gln568=) rs142577424
NM_007126.5(VCP):c.18-5T>C rs114256093
NM_007126.5(VCP):c.1875G>T (p.Arg625=) rs201410035
NM_007126.5(VCP):c.2214A>G (p.Glu738=) rs374391034
NM_007126.5(VCP):c.79A>G (p.Ile27Val) rs140913250
NM_007126.5(VCP):c.927C>T (p.Ile309=) rs34097935

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