Details for FOXP1:c.1762G>A, p.Ala588Thr

CHROMOSOME 11
GENOMIC COORDINATES
hg19hg38
7101516871304122
VARIANT EFFECT None
ANNOTATION FLAG None
GENE FOXP1
REFERENCE ALLELE C
ALTERNATE ALLELE T
TRANSCRIPT NM_032682.5
CDNA CHANGE c.1762G>A
PROTEIN CHANGE p.Ala588Thr
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
NoneNone-0.052374None
DBSNP ID NA
1 combination linked to FOXP1:c.1762G>A, p.Ala588Thr OLI1246
2 diseases linked to FOXP1:c.1762G>A, p.Ala588Thr Progressive non-fluent aphasia; Corticobasal syndrome
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