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Details for GNRHR:c.784C>T, p.Arg262Trp

CHROMOSOME

4

GENOMIC COORDINATES

hg19	hg38
68606401	67740683

VARIANT EFFECT

None

ANNOTATION FLAG

None

GENE

REFERENCE ALLELE

G

ALTERNATE ALLELE

A

TRANSCRIPT

N.A.

CDNA CHANGE

c.784C>T

PROTEIN CHANGE

p.Arg262Trp

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
1.595e-05	0.0	0.0	0.0	0.0001087	0.0	1.768e-05	0.0	0.0

ESP
AA	EA
None	None

PREDICTORS

sift	pp2 hvar	cadd	mutationtaster
Deleterious	Possibly Damaging	4.524368	Disease causing

DBSNP ID

1 combination linked to GNRHR:c.784C>T, p.Arg262Trp

1 disease linked to GNRHR:c.784C>T, p.Arg262Trp

Normosmic congenital hypogonadotropic hypogonadism

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