Details for SETX:c.8C>T, p.Thr3Ile

CHROMOSOME 9
GENOMIC COORDINATES
hg19hg38
135224808132349421
VARIANT EFFECT None
ANNOTATION FLAG None
GENE SETX
REFERENCE ALLELE G
ALTERNATE ALLELE A
TRANSCRIPT NM_015046.7
CDNA CHANGE c.8C>T
PROTEIN CHANGE p.Thr3Ile
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
DeleteriousDamaging3.657804Disease causing
DBSNP ID NA
1 combination linked to SETX:c.8C>T, p.Thr3Ile OLI1633
1 disease linked to SETX:c.8C>T, p.Thr3Ile Amyotrophic lateral sclerosis

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