Details for PROKR2:c.390C>T, p.Ser130=

CHROMOSOME 20
GENOMIC COORDINATES
hg19hg38
52946265313980
VARIANT EFFECT None
ANNOTATION FLAG None
GENE PROKR2
REFERENCE ALLELE G
ALTERNATE ALLELE A
TRANSCRIPT N.A.
CDNA CHANGE c.390C>T
PROTEIN CHANGE p.Ser130=
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
0.0005290.00018460.00054940.00.00.00023110.00087940.00081593.266e-05

ESP
AAEA
0.0002270.0006977
PREDICTORS
siftpp2 hvarcaddmutationtaster
NoneNone0.309191Polymorphism
DBSNP ID NA
1 combination linked to PROKR2:c.390C>T, p.Ser130= OLI1171
1 disease linked to PROKR2:c.390C>T, p.Ser130= Kallmann syndrome

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