Details for NCF2:p.Phe116Ser

CHROMOSOME 1
GENOMIC COORDINATES
hg19hg38
183546753183577618
VARIANT EFFECT None
ANNOTATION FLAG None
GENE NCF2
REFERENCE ALLELE A
ALTERNATE ALLELE G
TRANSCRIPT N.A.
CDNA CHANGE None
PROTEIN CHANGE p.Phe116Ser
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
DeleteriousDamaging4.141303Polymorphism
DBSNP ID NA
1 combination linked to NCF2:p.Phe116Ser OLI1716
1 disease linked to NCF2:p.Phe116Ser Common variable immunodeficiency

Found any issues with the data on this page? Report this entry.