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 DUOX2:c.4156G>A, p.Gly1386Ser

CHROMOSOME

15

GENOMIC COORDINATES

hg19	hg38
45387718	45095520

VARIANT EFFECT

None

ANNOTATION FLAG

None

GENE

REFERENCE ALLELE

C

ALTERNATE ALLELE

T

TRANSCRIPT

N.A.

CDNA CHANGE

c.4156G>A

PROTEIN CHANGE

p.Gly1386Ser

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
1.193e-05	0.0	2.891e-05	0.0	0.0	0.0	1.758e-05	0.0	0.0

ESP
AA	EA
0.0	0.0001163

PREDICTORS

sift	pp2 hvar	cadd	mutationtaster
Deleterious	Damaging	4.154212	Disease causing

DBSNP ID

1 combination linked to DUOX2:c.4156G>A, p.Gly1386Ser

1 disease linked to DUOX2:c.4156G>A, p.Gly1386Ser

Congenital hypothyroidism

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