Details for FOXP2:

CHROMOSOME 7
GENOMIC COORDINATES
hg19hg38
114329917114689862
VARIANT EFFECT missense
ANNOTATION FLAG manually_attributed
GENE FOXP2
REFERENCE ALLELE A
ALTERNATE ALLELE C
TRANSCRIPT N.A.
CDNA CHANGE None
PROTEIN CHANGE None
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
1.994e-050.08.687e-050.00.00.08.827e-060.00016360.0

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
ToleratedDamaging3.332022Disease causing
DBSNP ID NA
1 combination linked to FOXP2: OLI486
1 disease linked to FOXP2: Rare pervasive developmental disorder

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