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Details for GRN:c.*78C>T,

CHROMOSOME

17

GENOMIC COORDINATES

hg19	hg38
42430244	44352876

VARIANT EFFECT

None

ANNOTATION FLAG

None

GENE

REFERENCE ALLELE

C

ALTERNATE ALLELE

T

TRANSCRIPT

N.A.

CDNA CHANGE

c.*78C>T

PROTEIN CHANGE

None

ALLELE FREQUENCY

1KGP
Global	AFR	AMR	EAS	EUR	SAS
0.4245	0.7345	0.2421	0.38	0.3012	0.3078

Gnomad
Global	AFR	AMR	ASJ	EAS	FIN	NFE	OTH	SAS
None	None	None	None	None	None	None	None	None

ESP
AA	EA
None	None

PREDICTORS

sift	pp2 hvar	cadd	mutationtaster
None	None	0.421735	Polymorphism

DBSNP ID

5 combinations linked to GRN:c.*78C>T,

OLI965; OLI966; OLI967; OLI968; OLI969

1 disease linked to GRN:c.*78C>T,

Amyotrophic lateral sclerosis

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