Details for WNT10A:c.637G>A, p.Gly213Ser

CHROMOSOME 2
GENOMIC COORDINATES
hg19hg38
219754966218890244
VARIANT EFFECT None
ANNOTATION FLAG None
GENE WNT10A
REFERENCE ALLELE G
ALTERNATE ALLELE A
TRANSCRIPT NM_025216.3
CDNA CHANGE c.637G>A
PROTEIN CHANGE p.Gly213Ser
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
0.00280.00.00.01390.00.0

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
0.0020796.328e-055.8e-050.00.027540.03.546e-050.00065790.0001308

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
DeleteriousDamaging3.939693Polymorphism
DBSNP ID NA
1 combination linked to WNT10A:c.637G>A, p.Gly213Ser OLI1737
1 disease linked to WNT10A:c.637G>A, p.Gly213Ser Amelogenesis imperfecta
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