Details for CHD7:c.1105C>G, p.Pro369Ala

CHROMOSOME 8
GENOMIC COORDINATES
hg19hg38
6165509660742537
VARIANT EFFECT None
ANNOTATION FLAG None
GENE CHD7
REFERENCE ALLELE C
ALTERNATE ALLELE G
TRANSCRIPT N.A.
CDNA CHANGE c.1105C>G
PROTEIN CHANGE p.Pro369Ala
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
2.407e-050.00.00.00.00.05.307e-050.00.0

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
DeleteriousBenign1.768823Polymorphism
DBSNP ID NA
1 combination linked to CHD7:c.1105C>G, p.Pro369Ala OLI1593
1 disease linked to CHD7:c.1105C>G, p.Pro369Ala Kallmann syndrome

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