Details for NDUFS8:c.484G>T, p.Val162Leu

CHROMOSOME 11
GENOMIC COORDINATES
hg19hg38
6780383168036364
VARIANT EFFECT None
ANNOTATION FLAG None
GENE NDUFS8
REFERENCE ALLELE G
ALTERNATE ALLELE T
TRANSCRIPT N.A.
CDNA CHANGE c.484G>T
PROTEIN CHANGE p.Val162Leu
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
DeleteriousDamaging2.981681Polymorphism
DBSNP ID NA
1 combination linked to NDUFS8:c.484G>T, p.Val162Leu OLI1589
1 disease linked to NDUFS8:c.484G>T, p.Val162Leu Leigh syndrome

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