Details for FUS:c.41G>A,

CHROMOSOME 16
GENOMIC COORDINATES
hg19hg38
3120280031191479
VARIANT EFFECT unknown
ANNOTATION FLAG manually_attributed
GENE FUS
REFERENCE ALLELE G
ALTERNATE ALLELE A
TRANSCRIPT ENST00000254108.7
CDNA CHANGE c.41G>A
PROTEIN CHANGE None
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
0.00440.00080.00580.00.01290.0041

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
0.0066910.0010470.0067440.014590.00.0011550.0079830.007660.009967

ESP
AAEA
0.0015930.005814
PREDICTORS
siftpp2 hvarcaddmutationtaster
NoneNone1.294523Polymorphism
DBSNP ID rs80301724
1 combination linked to FUS:c.41G>A, OLI627
1 disease linked to FUS:c.41G>A, Amyotrophic lateral sclerosis
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