"Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, E - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 194756	NM_007126.5(VCP):c.2406T>C (p.Asp802=)	VCP	Single nucleotide variant (synonymous variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +5 more	GBenign/Likely benign
Select item 742604	NM_007126.5(VCP):c.2160+8T>G	VCP	Single nucleotide variant (intron variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GBenign
Select item 1096276	NM_007126.5(VCP):c.2109C>T (p.Ile703=)	VCP	Single nucleotide variant (synonymous variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GLikely benign
Select item 260125	NM_007126.5(VCP):c.1704A>G (p.Gln568=)	VCP	Single nucleotide variant (synonymous variant)	VCP-related condition +6 more	GBenign/Likely benign
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 283215	NM_007126.5(VCP):c.1584C>T (p.Ala528=)	VCP	Single nucleotide variant (synonymous variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +6 more	GConflicting classifications of pathogenicity
Select item 366718	NM_007126.5(VCP):c.1092C>T (p.Asp364=)	VCP	Single nucleotide variant (synonymous variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +5 more	GBenign/Likely benign
Select item 260119	NM_007126.5(VCP):c.1082-18_1082-8dup	VCP	Duplication (intron variant)	VCP-related condition +6 more	GBenign
Select item 464103	NM_007126.5(VCP):c.1082-9G>T	VCP	Single nucleotide variant (intron variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +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