Details for SETX:c.*849G>T,

CHROMOSOME 9
GENOMIC COORDINATES
hg19hg38
135138777132263390
VARIANT EFFECT None
ANNOTATION FLAG None
GENE SETX
REFERENCE ALLELE C
ALTERNATE ALLELE A
TRANSCRIPT N.A.
CDNA CHANGE c.*849G>T
PROTEIN CHANGE None
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
0.00860.00080.02450.0010.02090.0031

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
NoneNone0.058168Polymorphism
DBSNP ID NA
1 combination linked to SETX:c.*849G>T, OLI970
1 disease linked to SETX:c.*849G>T, Amyotrophic lateral sclerosis

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