List of variants in gene VCP reported by OMIM

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 14

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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.476G>A (p.Arg159His)	rs121909335	0.00001
NM_007126.5(VCP):c.1184A>G (p.Asp395Gly)	rs1828721782
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.283C>G (p.Arg95Gly)	rs121909332
NM_007126.5(VCP):c.290G>A (p.Gly97Glu)	rs864309502
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.475C>A (p.Arg159Ser)	rs387906789
NM_007126.5(VCP):c.475C>G (p.Arg159Gly)	rs387906789
NM_007126.5(VCP):c.553G>A (p.Glu185Lys)	rs864309501
NM_007126.5(VCP):c.695C>A (p.Ala232Glu)	rs121909331

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