This site uses cookies!

We use cookies for security, analytics and session persistence reasons. Please refer to our Cookie Policy for more information.

Select Cookie Preferences (Hover for info)

Details for FIG4:c.2116G>A, p.Val706Ile

CHROMOSOME

6

GENOMIC COORDINATES

hg19	hg38
110110816	109789613

VARIANT EFFECT

None

ANNOTATION FLAG

None

GENE

REFERENCE ALLELE

G

ALTERNATE ALLELE

A

TRANSCRIPT

CDNA CHANGE

c.2116G>A

PROTEIN CHANGE

p.Val706Ile

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
1.989e-05	6.152e-05	2.892e-05	0.0	0.0	0.0	1.759e-05	0.0	3.267e-05

ESP
AA	EA
None	None

PREDICTORS

sift	pp2 hvar	cadd	mutationtaster
Tolerated	Benign	1.66303	Polymorphism

DBSNP ID

1 combination linked to FIG4:c.2116G>A, p.Val706Ile

1 disease linked to FIG4:c.2116G>A, p.Val706Ile

Amyotrophic lateral sclerosis

Found any issues with the data on this page? Report this entry.