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Details for TPO:c.1759G>A, p.Gly587Arg

CHROMOSOME

2

GENOMIC COORDINATES

hg19	hg38
1491754	1487982

VARIANT EFFECT

missense

ANNOTATION FLAG

automatically_attributed

GENE

REFERENCE ALLELE

G

ALTERNATE ALLELE

A

TRANSCRIPT

CDNA CHANGE

c.1759G>A

PROTEIN CHANGE

p.Gly587Arg

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
3.979e-06	0.0	0.0	0.0	0.0	0.0	8.798e-06	0.0	0.0

ESP
AA	EA
None	None

PREDICTORS

sift	pp2 hvar	cadd	mutationtaster
Deleterious	Damaging	4.201137	Disease causing

DBSNP ID

1 combination linked to TPO:c.1759G>A, p.Gly587Arg

1 disease linked to TPO:c.1759G>A, p.Gly587Arg

Congenital hypothyroidism

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