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Details for CHD7:c.7861C>G, p.Gln2621Glu

CHROMOSOME

8

GENOMIC COORDINATES

hg19	hg38
61774785	60862226

VARIANT EFFECT

None

ANNOTATION FLAG

None

GENE

REFERENCE ALLELE

C

ALTERNATE ALLELE

G

TRANSCRIPT

N.A.

CDNA CHANGE

c.7861C>G

PROTEIN CHANGE

p.Gln2621Glu

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
4.098e-06	0.0	2.938e-05	0.0	0.0	0.0	0.0	0.0	0.0

ESP
AA	EA
None	None

PREDICTORS

sift	pp2 hvar	cadd	mutationtaster
Tolerated	Benign	2.836257	Disease causing

DBSNP ID

1 combination linked to CHD7:c.7861C>G, p.Gln2621Glu

1 disease linked to CHD7:c.7861C>G, p.Gln2621Glu

Hypogonadotropic hypogonadism with absent puberty phenotype

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