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Details for TWNK:c.1031G>A, p.Arg334Gln

CHROMOSOME

10

GENOMIC COORDINATES

hg19	hg38
102748968	100989211

VARIANT EFFECT

missense

ANNOTATION FLAG

automatically_attributed

GENE

REFERENCE ALLELE

G

ALTERNATE ALLELE

A

TRANSCRIPT

N.A.

CDNA CHANGE

c.1031G>A

PROTEIN CHANGE

p.Arg334Gln

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
None	None	None	None	None	None	None	None	None

ESP
AA	EA
None	None

PREDICTORS

sift	pp2 hvar	cadd	mutationtaster
Deleterious	Possibly Damaging	2.850411	Disease causing

DBSNP ID

1 combination linked to TWNK:c.1031G>A, p.Arg334Gln

1 disease linked to TWNK:c.1031G>A, p.Arg334Gln

Progressive external ophthalmoplegia

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