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Details for FGFR1:c.1016A>G, p.Tyr339Cys

CHROMOSOME

8

GENOMIC COORDINATES

hg19	hg38
38279380	38421862

VARIANT EFFECT

None

ANNOTATION FLAG

None

GENE

REFERENCE ALLELE

T

ALTERNATE ALLELE

C

TRANSCRIPT

N.A.

CDNA CHANGE

c.1016A>G

PROTEIN CHANGE

p.Tyr339Cys

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	4.235437	Disease causing

DBSNP ID

1 combination linked to FGFR1:c.1016A>G, p.Tyr339Cys

1 disease linked to FGFR1:c.1016A>G, p.Tyr339Cys

Hypogonadotropic hypogonadism with absent puberty phenotype

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