Related gene-specific medical variations for Gene (Select 2521) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2671949	NM_004960.4(FUS):c.1573C>T (p.Pro525Ser)	FUS (P521S +2 more)	Single nucleotide variant (missense variant +1 more)	Amyotrophic lateral sclerosis type 6	GUncertain significance
Select item 2503053	t(12;16)(q13.13;p11.2)	FUS, TFCP2	Translocation	Adrenal cortex carcinoma	GUncertain significance
Select item 2441593	NM_004960.4(FUS):c.936+9G>A	FUS	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2441591	NM_004960.4(FUS):c.1576T>A (p.Tyr526Asn)	FUS (Y522N +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 994880	NM_004960.4(FUS):c.1527C>T (p.Gly509=)	FUS	Single nucleotide variant (synonymous variant +1 more)	not provided	GUncertain significance
Select item 873231	NM_004960.4(FUS):c.1555C>T (p.Gln519Ter)	FUS (Q515* +2 more)	Single nucleotide variant (nonsense +1 more)	Amyotrophic lateral sclerosis type 6	GPathogenic
Select item 549702	NM_004960.3(FUS):c.*2201dup	FUS	Duplication (3 prime UTR variant +1 more)	Distal spinal muscular atrophy	GUncertain significance
Select item 259597	NM_004960.4(FUS):c.191-41T>C	FUS	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 259592	NM_004960.4(FUS):c.1394-16G>T	FUS	Single nucleotide variant (intron variant)	not specified	GLikely benign

ClinVar