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Details for FGFR1:c.289G>C, p.Gly97Arg

CHROMOSOME

8

GENOMIC COORDINATES

hg19	hg38
38287269	38429751

VARIANT EFFECT

missense

ANNOTATION FLAG

automatically_attributed

GENE

REFERENCE ALLELE

C

ALTERNATE ALLELE

G

TRANSCRIPT

CDNA CHANGE

c.289G>C

PROTEIN CHANGE

p.Gly97Arg

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	4.126966	Disease causing

DBSNP ID

1 combination linked to FGFR1:c.289G>C, p.Gly97Arg

1 disease linked to FGFR1:c.289G>C, p.Gly97Arg

Normosmic congenital hypogonadotropic hypogonadism

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