Details for HSD17B3:c.476C>A, p.Thr159Asn

CHROMOSOME 9
GENOMIC COORDINATES
hg19hg38
9901204696249764
VARIANT EFFECT None
ANNOTATION FLAG None
GENE HSD17B3
REFERENCE ALLELE G
ALTERNATE ALLELE T
TRANSCRIPT NM_000197
CDNA CHANGE c.476C>A
PROTEIN CHANGE p.Thr159Asn
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
ToleratedBenign1.742416Polymorphism
DBSNP ID NA
1 combination linked to HSD17B3:c.476C>A, p.Thr159Asn OLI1562
1 disease linked to HSD17B3:c.476C>A, p.Thr159Asn Syndrome with 46,XY disorder of sex development

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