Details for ARHGEF28:c.1180G>T, p.Glu394Ter

CHROMOSOME 5
GENOMIC COORDINATES
hg19hg38
7313633873840513
VARIANT EFFECT None
ANNOTATION FLAG None
GENE ARHGEF28
REFERENCE ALLELE G
ALTERNATE ALLELE T
TRANSCRIPT NM_001080479.2
CDNA CHANGE c.1180G>T
PROTEIN CHANGE p.Glu394Ter
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
4.026e-060.00.00.00.00.08.894e-060.00.0

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
NoneNone7.557651Disease causing
DBSNP ID NA
1 combination linked to ARHGEF28:c.1180G>T, p.Glu394Ter OLI1634
1 disease linked to ARHGEF28:c.1180G>T, p.Glu394Ter Amyotrophic lateral sclerosis

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