CEP295NL CEP295 N-terminal like

Information
Symbol
CEP295NL
Type
protein-coding
Description
CEP295 N-terminal like
Entrez Gene ID
100653515
Genome
hg19
Position
chr17:76,886,661-76,899,283
Genome
hg38
Position
chr17:78,890,579-78,903,201
HGNC
HGNC:44659 HGNC
Ensembl
ENSG00000178404 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Ranking
ClinVar
0
0
0
2
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 :
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 DDC8
SYNONYM KIAA1731NL
HGNC HGNC:44659 HGNC
Ensembl ENSG00000178404 Ensembl
AllianceGenome HGNC:44659
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000322630.3 hg38 chr17 78,890,579 78,903,201 12,623
ENST00000322630.3 hg19 chr17 76,886,661 76,899,283 12,623
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