"Genome Diagnostics Laboratory, Amsterdam University Medical Center"[s - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 259594	NM_004960.4(FUS):c.147C>A (p.Gly49=)	FUS	Single nucleotide variant (synonymous variant +1 more)	not provided +3 more	GBenign
Select item 259595	NM_004960.4(FUS):c.153C>T (p.Gly51=)	FUS	Single nucleotide variant (synonymous variant +1 more)	not specified +3 more	GBenign
Select item 259596	NM_004960.4(FUS):c.190+9T>C	FUS	Single nucleotide variant (intron variant)	not specified +3 more	GBenign
Select item 259598	NM_004960.4(FUS):c.291C>T (p.Tyr97=)	FUS	Single nucleotide variant (synonymous variant +1 more)	Amyotrophic lateral sclerosis type 6 +3 more	GBenign
Select item 540281	NM_004960.4(FUS):c.518_523del	FUS	Microsatellite (splice donor variant)	not provided +2 more	GBenign
Select item 318986	NM_004960.4(FUS):c.669CGG[7] (p.Gly231dup)	FUS	Microsatellite (inframe_insertion +1 more)	not specified +4 more	GBenign/Likely benign
Select item 705951	NM_004960.4(FUS):c.675C>T (p.Gly225=)	FUS	Single nucleotide variant (synonymous variant +1 more)	Tremor, hereditary essential, 4 +3 more	GBenign/Likely benign
Select item 705002	NM_004960.4(FUS):c.1067-6C>T	FUS	Single nucleotide variant (intron variant)	Tremor, hereditary essential, 4 +3 more	GLikely benign
Select item 259593	NM_004960.4(FUS):c.1464C>T (p.Gly488=)	FUS	Single nucleotide variant (synonymous variant +1 more)	not provided +4 more	GBenign/Likely benign
Select item 1200398	NM_004960.4(FUS):c.1542-5dup	FUS	Duplication (intron variant)	not provided	GLikely benign
Select item 1209969	NM_004960.4(FUS):c.1542-6_1542-5del	FUS	Deletion (intron variant)	not specified +1 more	GBenign/Likely benign
Select item 540280	NM_004960.4(FUS):c.1566G>A (p.Arg522=)	FUS	Single nucleotide variant (synonymous variant +1 more)	Inborn genetic diseases +3 more	GBenign/Likely benign