Details for XIAP:c.1057-2A>G,

CHROMOSOME X
GENOMIC COORDINATES
hg19hg38
123026579123892729
VARIANT EFFECT splicing
ANNOTATION FLAG automatically_attributed_and_verified
GENE XIAP
REFERENCE ALLELE A
ALTERNATE ALLELE G
TRANSCRIPT NM_001167.3
CDNA CHANGE c.1057-2A>G
PROTEIN CHANGE None
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
NoneNone4.501279None
DBSNP ID NA
1 combination linked to XIAP:c.1057-2A>G, OLI056
1 disease linked to XIAP:c.1057-2A>G, Primary hemophagocytic lymphohistiocytosis

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