Details for PROK2:c.137G>T, p.Cys45Phe

CHROMOSOME 3
GENOMIC COORDINATES
hg19hg38
7183070371781552
VARIANT EFFECT None
ANNOTATION FLAG None
GENE PROK2
REFERENCE ALLELE C
ALTERNATE ALLELE A
TRANSCRIPT NM_001126128.2
CDNA CHANGE c.137G>T
PROTEIN CHANGE p.Cys45Phe
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
DeleteriousDamaging4.257107Disease causing
DBSNP ID NA
1 combination linked to PROK2:c.137G>T, p.Cys45Phe OLI1297
1 disease linked to PROK2:c.137G>T, p.Cys45Phe Kallmann syndrome

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