Details for CXCR4:c.236A>C, p.His79Pro

CHROMOSOME 2
GENOMIC COORDINATES
hg19hg38
136873262136115692
VARIANT EFFECT missense
ANNOTATION FLAG automatically_attributed
GENE CXCR4
REFERENCE ALLELE T
ALTERNATE ALLELE G
TRANSCRIPT NM_003467.2
CDNA CHANGE c.236A>C
PROTEIN CHANGE p.His79Pro
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
DeleteriousDamaging3.875737Disease causing
DBSNP ID rs1573614635
1 combination linked to CXCR4:c.236A>C, p.His79Pro OLI422
1 disease linked to CXCR4:c.236A>C, p.His79Pro Normosmic congenital hypogonadotropic hypogonadism

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