"Genome-Nilou Lab"[submitter] AND "VCP"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 260124	NM_007126.5(VCP):c.1695+8A>G	VCP	Single nucleotide variant (intron variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +5 more	GBenign
Select item 260123	NM_007126.5(VCP):c.1360-35A>G	VCP	Single nucleotide variant (intron variant)	not specified +4 more	GBenign
Select item 260128	NM_007126.5(VCP):c.811+3G>A	VCP	Single nucleotide variant (intron variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +5 more	GBenign
Select item 260121	NM_007126.5(VCP):c.129+47G>A	VCP	Single nucleotide variant (intron variant)	not specified +4 more	GBenign
Select item 259477	NM_004629.2(FANCG):c.1636+7A>G	FANCG, VCP	Single nucleotide variant (intron variant)	Fanconi anemia complementation group G +5 more	GBenign
Select item 134361	NM_004629.2(FANCG):c.1538G>A (p.Arg513Gln)	FANCG, VCP (R513Q)	Single nucleotide variant (missense variant)	not provided +5 more	GConflicting classifications of pathogenicity

ClinVar