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Details for GH1:c.440T>C, p.Ile147Thr

CHROMOSOME

17

GENOMIC COORDINATES

hg19	hg38
61995136	63917776

VARIANT EFFECT

missense

ANNOTATION FLAG

automatically_attributed

GENE

REFERENCE ALLELE

A

ALTERNATE ALLELE

G

TRANSCRIPT

CDNA CHANGE

c.440T>C

PROTEIN CHANGE

p.Ile147Thr

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
None	None	None	None	None	None	None	None	None

ESP
AA	EA
None	None

PREDICTORS

sift	pp2 hvar	cadd	mutationtaster
Deleterious	Damaging	2.811747	Disease causing

DBSNP ID

1 combination linked to GH1:c.440T>C, p.Ile147Thr

1 disease linked to GH1:c.440T>C, p.Ile147Thr

Normosmic congenital hypogonadotropic hypogonadism

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