CYP4F8 cytochrome P450 family 4 subfamily F member 8

Information
Symbol
CYP4F8
Type
protein-coding
Description
cytochrome P450 family 4 subfamily F member 8
Entrez Gene ID
11283
Genome
hg19
Position
chr19:15,726,029-15,741,449
Genome
hg38
Position
chr19:15,615,218-15,630,639
MIM
611545 OMIM
HGNC
HGNC:2648 HGNC
Ensembl
ENSG00000186526 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 6
Uncertain significance 0 36
Ranking
ClinVar
0
0
0
42
0
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
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Variant name Gene AA change CDS Japanese
frequency		 TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence		 Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
SYNONYM CPF8
SYNONYM CYPIVF8
MIM 611545 OMIM
HGNC HGNC:2648 HGNC
Ensembl ENSG00000186526 Ensembl
AllianceGenome HGNC:2648
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000612078.5 hg38 chr19 15,615,218 15,630,639 15,422
ENST00000612078.5 hg19 chr19 15,726,029 15,741,449 15,421
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