Details for CHD7:c.6379G>A, p.Ala2127Thr

CHROMOSOME 8
GENOMIC COORDINATES
hg19hg38
6176566360853104
VARIANT EFFECT None
ANNOTATION FLAG None
GENE CHD7
REFERENCE ALLELE G
ALTERNATE ALLELE A
TRANSCRIPT N.A.
CDNA CHANGE c.6379G>A
PROTEIN CHANGE p.Ala2127Thr
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
1.607e-050.00.00.00.00022260.00.00.00.0

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
DeleteriousBenign2.876004Polymorphism
DBSNP ID NA
1 combination linked to CHD7:c.6379G>A, p.Ala2127Thr OLI1346
1 disease linked to CHD7:c.6379G>A, p.Ala2127Thr Kallmann syndrome

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