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 WNT4:c.896C>T, p.Thr299Met

CHROMOSOME

1

GENOMIC COORDINATES

hg19	hg38
22446703	22120210

VARIANT EFFECT

None

ANNOTATION FLAG

None

GENE

REFERENCE ALLELE

G

ALTERNATE ALLELE

A

TRANSCRIPT

N.A.

CDNA CHANGE

c.896C>T

PROTEIN CHANGE

p.Thr299Met

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
3.983e-06	0.0	0.0	0.0	0.0	0.0	8.81e-06	0.0	0.0

ESP
AA	EA
None	None

PREDICTORS

sift	pp2 hvar	cadd	mutationtaster
Deleterious	Benign	3.252105	Polymorphism

DBSNP ID

1 combination linked to WNT4:c.896C>T, p.Thr299Met

1 disease linked to WNT4:c.896C>T, p.Thr299Met

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