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Details for TG:p.Asp1767Gly

CHROMOSOME

8

GENOMIC COORDINATES

hg19	hg38
133961087	132948842

VARIANT EFFECT

missense

ANNOTATION FLAG

automatically_attributed

GENE

REFERENCE ALLELE

A

ALTERNATE ALLELE

G

TRANSCRIPT

N.A.

CDNA CHANGE

None

PROTEIN CHANGE

p.Asp1767Gly

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	0.0	0.0	0.0	0.0	0.0	3.518e-05	0.0001629	0.0

ESP
AA	EA
None	None

PREDICTORS

sift	pp2 hvar	cadd	mutationtaster
Tolerated	Benign	0.424496	Polymorphism

DBSNP ID

1 combination linked to TG:p.Asp1767Gly

1 disease linked to TG:p.Asp1767Gly

Congenital hypothyroidism

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