Details for CCNF:c.591C>G, p.Phe197Leu

CHROMOSOME 16
GENOMIC COORDINATES
hg19hg38
24881212438120
VARIANT EFFECT None
ANNOTATION FLAG None
GENE CCNF
REFERENCE ALLELE C
ALTERNATE ALLELE G
TRANSCRIPT N.A.
CDNA CHANGE c.591C>G
PROTEIN CHANGE p.Phe197Leu
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
ToleratedBenign0.890732Polymorphism
DBSNP ID NA
1 combination linked to CCNF:c.591C>G, p.Phe197Leu OLI1010
1 disease linked to CCNF:c.591C>G, p.Phe197Leu Amyotrophic lateral sclerosis

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