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 LHX4:c.913G>T, p.Gly305Trp

CHROMOSOME

1

GENOMIC COORDINATES

hg19	hg38
180243454	180274319

VARIANT EFFECT

None

ANNOTATION FLAG

None

GENE

REFERENCE ALLELE

G

ALTERNATE ALLELE

T

TRANSCRIPT

N.A.

CDNA CHANGE

c.913G>T

PROTEIN CHANGE

p.Gly305Trp

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
7.956e-06	0.0	0.0	0.0	0.0	0.0	1.759e-05	0.0	0.0

ESP
AA	EA
None	None

PREDICTORS

sift	pp2 hvar	cadd	mutationtaster
Deleterious	Damaging	4.160252	Disease causing

DBSNP ID

1 combination linked to LHX4:c.913G>T, p.Gly305Trp

1 disease linked to LHX4:c.913G>T, p.Gly305Trp

Kallmann syndrome

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