Details for HOXA13:c.1024G>A, p.Ala342Thr

CHROMOSOME 7
GENOMIC COORDINATES
hg19hg38
2723796027198341
VARIANT EFFECT None
ANNOTATION FLAG None
GENE HOXA13
REFERENCE ALLELE C
ALTERNATE ALLELE T
TRANSCRIPT NM_000522
CDNA CHANGE c.1024G>A
PROTEIN CHANGE p.Ala342Thr
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
ToleratedBenign2.919792Disease causing
DBSNP ID NA
1 combination linked to HOXA13:c.1024G>A, p.Ala342Thr OLI1565
1 disease linked to HOXA13:c.1024G>A, p.Ala342Thr Syndrome with 46,XY disorder of sex development

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