Details for CHD7:c.2613+5G>A,

CHROMOSOME 8
GENOMIC COORDINATES
hg19hg38
6172906560816506
VARIANT EFFECT None
ANNOTATION FLAG None
GENE CHD7
REFERENCE ALLELE G
ALTERNATE ALLELE A
TRANSCRIPT N.A.
CDNA CHANGE c.2613+5G>A
PROTEIN CHANGE None
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
0.00020.00080.00.00.00.0

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
1.396e-050.00022240.00.00.00.00.00.00.0

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
NoneNone1.672314Disease causing
DBSNP ID NA
1 combination linked to CHD7:c.2613+5G>A, OLI1606
1 disease linked to CHD7:c.2613+5G>A, Normosmic congenital hypogonadotropic hypogonadism

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