Details for NR5A1:c.1114_1116del, p.Lys372del

CHROMOSOME 9
GENOMIC COORDINATES
hg19hg38
127253381124491102
VARIANT EFFECT deletion
ANNOTATION FLAG manually_attributed
GENE NR5A1
REFERENCE ALLELE ACTT
ALTERNATE ALLELE A
TRANSCRIPT NM_004959.5
CDNA CHANGE c.1114_1116del
PROTEIN CHANGE p.Lys372del
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
NoneNone2.175203Disease causing
DBSNP ID NA
1 combination linked to NR5A1:c.1114_1116del, p.Lys372del OLI401
2 diseases linked to NR5A1:c.1114_1116del, p.Lys372del 46,XY disorder of sex development; 46,XY partial gonadal dysgenesis

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