CNFN cornifelin

Information
Symbol
CNFN
Type
protein-coding
Description
cornifelin
Entrez Gene ID
84518
Genome
hg19
Position
chr19:42,891,171-42,894,449
Genome
hg38
Position
chr19:42,387,019-42,390,297
MIM
611764 OMIM
HGNC
HGNC:30183 HGNC
Ensembl
ENSG00000105427 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 1 0
Uncertain significance 0 8
Ranking
ClinVar
0
0
0
8
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
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
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 PLAC8L2
MIM 611764 OMIM
HGNC HGNC:30183 HGNC
Ensembl ENSG00000105427 Ensembl
AllianceGenome HGNC:30183
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000222032.10 hg38 chr19 42,387,019 42,390,297 3,279
ENST00000597255.1 hg38 chr19 42,387,101 42,390,268 3,168
ENST00000222032.10 hg19 chr19 42,891,171 42,894,449 3,279
ENST00000597255.1 hg19 chr19 42,891,253 42,894,420 3,168
Genome browser