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 DUSP6:c.566A>G, p.Asn189Ser

CHROMOSOME

12

GENOMIC COORDINATES

hg19	hg38
89744637	89350860

VARIANT EFFECT

missense

ANNOTATION FLAG

automatically_attributed

GENE

REFERENCE ALLELE

T

ALTERNATE ALLELE

C

TRANSCRIPT

CDNA CHANGE

c.566A>G

PROTEIN CHANGE

p.Asn189Ser

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
0.0001949	0.0	5.782e-05	0.0	0.0	0.000231	0.000352	0.0	6.533e-05

ESP
AA	EA
0.000227	0.0004651

PREDICTORS

sift	pp2 hvar	cadd	mutationtaster
Tolerated	Benign	0.975293	Disease causing

DBSNP ID

1 combination linked to DUSP6:c.566A>G, p.Asn189Ser

1 disease linked to DUSP6:c.566A>G, p.Asn189Ser

Kallmann syndrome

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