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Details for DUOX2:p.Ala1206Thr

CHROMOSOME

15

GENOMIC COORDINATES

hg19	hg38
45389889	45097691

VARIANT EFFECT

missense

ANNOTATION FLAG

automatically_attributed

GENE

REFERENCE ALLELE

C

ALTERNATE ALLELE

T

TRANSCRIPT

N.A.

CDNA CHANGE

None

PROTEIN CHANGE

p.Ala1206Thr

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	0.0001631	0.0	0.0	0.0	6.533e-05

ESP
AA	EA
None	None

PREDICTORS

sift	pp2 hvar	cadd	mutationtaster
Deleterious	Damaging	4.050849	Disease causing

DBSNP ID

1 combination linked to DUOX2:p.Ala1206Thr

1 disease linked to DUOX2:p.Ala1206Thr

Congenital hypothyroidism

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