List of variants in gene VCP reported as pathogenic for amyotrophic lateral sclerosis

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: 20

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HGVS	dbSNP	gnomAD frequency
NM_007126.5(VCP):c.572G>A (p.Arg191Gln)	rs121909334	0.00002
NM_007126.5(VCP):c.1460G>A (p.Arg487His)	rs767379602	0.00001
NM_007126.5(VCP):c.476G>A (p.Arg159His)	rs121909335	0.00001
NM_007126.5(VCP):c.1774G>A (p.Asp592Asn)	rs387906790
NM_007126.5(VCP):c.271A>T (p.Asn91Tyr)	rs863225291
NM_007126.5(VCP):c.277C>T (p.Arg93Cys)	rs1554669087
NM_007126.5(VCP):c.283C>T (p.Arg95Cys)	rs121909332
NM_007126.5(VCP):c.290G>A (p.Gly97Glu)	rs864309502
NM_007126.5(VCP):c.463C>A (p.Arg155Ser)	rs121909330
NM_007126.5(VCP):c.463C>T (p.Arg155Cys)	rs121909330
NM_007126.5(VCP):c.464G>A (p.Arg155His)	rs121909329
NM_007126.5(VCP):c.464G>C (p.Arg155Pro)	rs121909329
NM_007126.5(VCP):c.466G>A (p.Gly156Ser)
NM_007126.5(VCP):c.469G>A (p.Gly157Arg)	rs1554668814
NM_007126.5(VCP):c.472A>G (p.Met158Val)	rs1554668813
NM_007126.5(VCP):c.475C>A (p.Arg159Ser)	rs387906789
NM_007126.5(VCP):c.475C>G (p.Arg159Gly)	rs387906789
NM_007126.5(VCP):c.475C>T (p.Arg159Cys)	rs387906789
NM_007126.5(VCP):c.478G>C (p.Ala160Pro)	rs1554668805
NM_007126.5(VCP):c.572G>C (p.Arg191Pro)	rs121909334

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