Details for FGFR1:c.1097C>T, p.Pro366Leu

CHROMOSOME 8
GENOMIC COORDINATES
hg19hg38
3827723838419720
VARIANT EFFECT None
ANNOTATION FLAG None
GENE FGFR1
REFERENCE ALLELE G
ALTERNATE ALLELE A
TRANSCRIPT N.A.
CDNA CHANGE c.1097C>T
PROTEIN CHANGE p.Pro366Leu
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
DeleteriousBenign2.964257Disease causing
DBSNP ID NA
1 combination linked to FGFR1:c.1097C>T, p.Pro366Leu OLI1419
1 disease linked to FGFR1:c.1097C>T, p.Pro366Leu Hypogonadotropic hypogonadism with absent puberty phenotype

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