Details for FGF17:c.208G>A, p.Gly70Arg

CHROMOSOME 8
GENOMIC COORDINATES
hg19hg38
2190376022046249
VARIANT EFFECT None
ANNOTATION FLAG None
GENE FGF17
REFERENCE ALLELE G
ALTERNATE ALLELE A
TRANSCRIPT N.A.
CDNA CHANGE c.208G>A
PROTEIN CHANGE p.Gly70Arg
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
1.594e-050.02.894e-050.00.00.02.647e-050.00.0

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
DeleteriousDamaging3.980205Polymorphism
DBSNP ID NA
1 combination linked to FGF17:c.208G>A, p.Gly70Arg OLI1650
1 disease linked to FGF17:c.208G>A, p.Gly70Arg Kallmann syndrome

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