C14orf178 chromosome 14 open reading frame 178

Information
Symbol
C14orf178
Type
ncRNA
Description
chromosome 14 open reading frame 178
Entrez Gene ID
283579
Genome
hg19
Position
chr14:78,227,177-78,236,085
Genome
hg38
Position
chr14:77,760,834-77,769,742
HGNC
HGNC:26385 HGNC
Ensembl
ENSG00000197734 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Ranking
ClinVar
0
0
0
0
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
HGNC HGNC:26385 HGNC
Ensembl ENSG00000197734 Ensembl
AllianceGenome HGNC:26385
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000650032.1 hg38 chr14 77,760,834 77,769,742 8,909
ENST00000650032.1 hg19 chr14 78,227,177 78,236,085 8,909
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