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 TRHR:c.504T>G, p.Ile168Met

CHROMOSOME

8

GENOMIC COORDINATES

hg19	hg38
110100245	109088016

VARIANT EFFECT

missense

ANNOTATION FLAG

manually_attributed

GENE

REFERENCE ALLELE

T

ALTERNATE ALLELE

G

TRANSCRIPT

CDNA CHANGE

c.504T>G

PROTEIN CHANGE

p.Ile168Met

ALLELE FREQUENCY

1KGP
Global	AFR	AMR	EAS	EUR	SAS
0.0014	0.0	0.0	0.0069	0.0	0.0

Gnomad
Global	AFR	AMR	ASJ	EAS	FIN	NFE	OTH	SAS
0.000191	6.152e-05	2.892e-05	0.0	0.002392	0.0	0.0	0.0003264	0.0

ESP
AA	EA
None	None

PREDICTORS

sift	pp2 hvar	cadd	mutationtaster
Tolerated	Benign	0.81526	Polymorphism

DBSNP ID

1 combination linked to TRHR:c.504T>G, p.Ile168Met

1 disease linked to TRHR:c.504T>G, p.Ile168Met

Congenital hypothyroidism

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