Details for PROP1:c.152G>T, p.Gly51Val

CHROMOSOME 5
GENOMIC COORDINATES
hg19hg38
177421297177994296
VARIANT EFFECT unknown
ANNOTATION FLAG None
GENE PROP1
REFERENCE ALLELE C
ALTERNATE ALLELE A
TRANSCRIPT NM_006261
CDNA CHANGE c.152G>T
PROTEIN CHANGE p.Gly51Val
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
0.00022220.00019390.00.00.0021550.07.389e-050.00050473.297e-05

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
ToleratedBenign-1.427696Polymorphism
DBSNP ID NA
1 combination linked to PROP1:c.152G>T, p.Gly51Val OLI1415
1 disease linked to PROP1:c.152G>T, p.Gly51Val Hypogonadotropic hypogonadism with absent puberty phenotype

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