Details for IFNW1:c.58G>A,

CHROMOSOME 9
GENOMIC COORDINATES
hg19hg38
2114151221141513
VARIANT EFFECT None
ANNOTATION FLAG None
GENE IFNW1
REFERENCE ALLELE C
ALTERNATE ALLELE T
TRANSCRIPT NM_002177.3
CDNA CHANGE c.58G>A
PROTEIN CHANGE None
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
0.0010.00.00.00.0050.0

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
0.0030480.00049290.00069890.0031280.00.0099560.0041930.0018120.0

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
ToleratedBenign0.124532Polymorphism
DBSNP ID NA
1 combination linked to IFNW1:c.58G>A, OLI1332
1 disease linked to IFNW1:c.58G>A, Primary immunodeficiency

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