ClinVar Miner

List of variants in gene FUS reported by Neuberg Centre For Genomic Medicine, NCGM

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_004960.4(FUS):c.1169G>T (p.Gly390Val)	rs2144135361
NM_004960.4(FUS):c.1562G>A (p.Arg521His)	rs121909671
NM_004960.4(FUS):c.1562G>T (p.Arg521Leu)	rs121909671
NM_004960.4(FUS):c.1573C>G (p.Pro525Ala)	rs1555509699

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