Details for NR5A1:c.86C>A, p.Thr29Lys

CHROMOSOME 9
GENOMIC COORDINATES
hg19hg38
127265589124503310
VARIANT EFFECT None
ANNOTATION FLAG None
GENE NR5A1
REFERENCE ALLELE G
ALTERNATE ALLELE T
TRANSCRIPT NM_004959.5
CDNA CHANGE c.86C>A
PROTEIN CHANGE p.Thr29Lys
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
DeleteriousPossibly Damaging3.867825Disease causing
DBSNP ID NA
1 combination linked to NR5A1:c.86C>A, p.Thr29Lys OLI998
2 diseases linked to NR5A1:c.86C>A, p.Thr29Lys Androgen insensitivity syndrome; 46,XY disorder of sex development

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