Details for FUS:p.Arg269Trp

CHROMOSOME 16
GENOMIC COORDINATES
hg19hg38
3119965131188330
VARIANT EFFECT missense
ANNOTATION FLAG automatically_attributed
GENE FUS
REFERENCE ALLELE C
ALTERNATE ALLELE T
TRANSCRIPT N.A.
CDNA CHANGE None
PROTEIN CHANGE p.Arg269Trp
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
1.196e-056.179e-050.00.00.00.01.765e-050.00.0

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
DeleteriousBenign4.311881Polymorphism
DBSNP ID rs755018172
1 combination linked to FUS:p.Arg269Trp OLI776
1 disease linked to FUS:p.Arg269Trp Amyotrophic lateral sclerosis

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