Details for FGF10:c.-33G>A,

CHROMOSOME 5
GENOMIC COORDINATES
hg19hg38
4438881744388715
VARIANT EFFECT unknown
ANNOTATION FLAG manually_attributed
GENE FGF10
REFERENCE ALLELE C
ALTERNATE ALLELE T
TRANSCRIPT NM_004465.2
CDNA CHANGE c.-33G>A
PROTEIN CHANGE None
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
0.01820.06810.00140.00.00.0

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
0.0036390.051860.0019760.00030160.00.00.0001010.0024843.288e-05

ESP
AAEA
0.043150.0001168
PREDICTORS
siftpp2 hvarcaddmutationtaster
NoneNone1.841402Polymorphism
DBSNP ID rs17233910
1 combination linked to FGF10:c.-33G>A, OLI601
1 disease linked to FGF10:c.-33G>A, Disorder of sex development
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