Details for CHD7:c.2750C>T, p.Thr917Met

CHROMOSOME 8
GENOMIC COORDINATES
hg19hg38
6173440160821842
VARIANT EFFECT None
ANNOTATION FLAG None
GENE CHD7
REFERENCE ALLELE C
ALTERNATE ALLELE T
TRANSCRIPT N.A.
CDNA CHANGE c.2750C>T
PROTEIN CHANGE p.Thr917Met
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
0.00.00.00.00.00.00.00.00.0

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
DeleteriousDamaging4.096635Disease causing
DBSNP ID NA
1 combination linked to CHD7:c.2750C>T, p.Thr917Met OLI1652
1 disease linked to CHD7:c.2750C>T, p.Thr917Met Kallmann syndrome

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