Details for CHD7:c.2824A>G, p.Thr942Ala

CHROMOSOME 8
GENOMIC COORDINATES
hg19hg38
6173447560821916
VARIANT EFFECT None
ANNOTATION FLAG None
GENE CHD7
REFERENCE ALLELE A
ALTERNATE ALLELE G
TRANSCRIPT N.A.
CDNA CHANGE c.2824A>G
PROTEIN CHANGE p.Thr942Ala
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
0.00013710.00.00.00.0019020.00.00.00.0

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
ToleratedBenign2.179921Polymorphism
DBSNP ID NA
1 combination linked to CHD7:c.2824A>G, p.Thr942Ala OLI1335
1 disease linked to CHD7:c.2824A>G, p.Thr942Ala Kallmann syndrome

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