Details for TRIM42:p.Gly456Ser

CHROMOSOME 3
GENOMIC COORDINATES
hg19hg38
140406890140688048
VARIANT EFFECT None
ANNOTATION FLAG None
GENE TRIM42
REFERENCE ALLELE G
ALTERNATE ALLELE A
TRANSCRIPT N.A.
CDNA CHANGE None
PROTEIN CHANGE p.Gly456Ser
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
0.00640.01740.01010.00.0020.0

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
0.0036110.010160.0059580.010455.44e-054.621e-050.0024540.0084940.003201

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
ToleratedPossibly Damaging2.311415Polymorphism
DBSNP ID NA
1 combination linked to TRIM42:p.Gly456Ser OLI1306
1 disease linked to TRIM42:p.Gly456Ser Juvenile amyotrophic lateral sclerosis
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