Details for WNT9B:c.*158C>T, None

CHROMOSOME 17
GENOMIC COORDINATES
hg19hg38
4495424246876876
VARIANT EFFECT 3'-UTR variant
ANNOTATION FLAG manually_attributed
GENE WNT9B
REFERENCE ALLELE C
ALTERNATE ALLELE T
TRANSCRIPT NM_003396.4
CDNA CHANGE c.*158C>T
PROTEIN CHANGE None
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
NoneNone0.218162Polymorphism
DBSNP ID rs1233082195
1 combination linked to WNT9B:c.*158C>T, None OLI344
1 disease linked to WNT9B:c.*158C>T, None 46,XY disorder of sex development

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