Details for F5:c.1601A>T, p.Gln534Leu

CHROMOSOME 1
GENOMIC COORDINATES
hg19hg38
169519049169549811
VARIANT EFFECT missense
ANNOTATION FLAG manually_corrected
GENE F5
REFERENCE ALLELE T
ALTERNATE ALLELE A
TRANSCRIPT NM_000130.5
CDNA CHANGE c.1601A>T
PROTEIN CHANGE p.Gln534Leu
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
DeleteriousBenign3.318813Polymorphism
DBSNP ID rs6025
1 combination linked to F5:c.1601A>T, p.Gln534Leu OLI455
1 disease linked to F5:c.1601A>T, p.Gln534Leu Familial exudative vitreoretinopathy

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