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Details for FGFR1:c.2057T>C, p.Phe686Ser

CHROMOSOME

8

GENOMIC COORDINATES

hg19	hg38
38271799	38414281

VARIANT EFFECT

None

ANNOTATION FLAG

None

GENE

REFERENCE ALLELE

A

ALTERNATE ALLELE

G

TRANSCRIPT

N.A.

CDNA CHANGE

c.2057T>C

PROTEIN CHANGE

p.Phe686Ser

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	Possibly Damaging	4.186801	Disease causing

DBSNP ID

1 combination linked to FGFR1:c.2057T>C, p.Phe686Ser

1 disease linked to FGFR1:c.2057T>C, p.Phe686Ser

Hypogonadotropic hypogonadism with absent puberty phenotype

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