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Details for FUS:c.*59G>A, None

CHROMOSOME

16

GENOMIC COORDINATES

hg19	hg38
31202818	31191497

VARIANT EFFECT

3'-UTR variant

ANNOTATION FLAG

automatically_attributed_and_verified

GENE

REFERENCE ALLELE

G

ALTERNATE ALLELE

A

TRANSCRIPT

CDNA CHANGE

c.*59G>A

PROTEIN CHANGE

None

ALLELE FREQUENCY

1KGP
Global	AFR	AMR	EAS	EUR	SAS
None	None	None	None	None	None

Gnomad
Global	AFR	AMR	ASJ	EAS	FIN	NFE	OTH	SAS
0.0	0.0	0.0	0.0	0.0	0.0	0.0	0.0	0.0

ESP
AA	EA
None	None

PREDICTORS

sift	pp2 hvar	cadd	mutationtaster
None	None	0.440795	Disease causing

DBSNP ID

1 combination linked to FUS:c.*59G>A, None

1 disease linked to FUS:c.*59G>A, None

Amyotrophic lateral sclerosis

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