Details for CDH23:c.3625A>G, p.Thr1209Ala

CHROMOSOME 10
GENOMIC COORDINATES
hg19hg38
7349027171730514
VARIANT EFFECT missense
ANNOTATION FLAG automatically_attributed
GENE CDH23
REFERENCE ALLELE A
ALTERNATE ALLELE G
TRANSCRIPT NM_001171930.1
CDNA CHANGE c.3625A>G
PROTEIN CHANGE p.Thr1209Ala
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
0.04930.1740.02310.00.0010.0

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
0.010540.1450.0076810.00.00.00051070.00062920.0057879.805e-05

ESP
AAEA
0.14170.0005988
PREDICTORS
siftpp2 hvarcaddmutationtaster
ToleratedBenign1.973061Polymorphism
DBSNP ID rs41281314
1 combination linked to CDH23:c.3625A>G, p.Thr1209Ala OLI267
1 disease linked to CDH23:c.3625A>G, p.Thr1209Ala Usher syndrome type 1

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