C1orf167 chromosome 1 open reading frame 167

Information
Symbol
C1orf167
Type
protein-coding
Description
chromosome 1 open reading frame 167
Entrez Gene ID
284498
Genome
hg19
Position
chr1:11,822,250-11,849,642
Genome
hg38
Position
chr1:11,762,193-11,789,585
HGNC
HGNC:25262 HGNC
Ensembl
ENSG00000215910 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 2
Conflicting classifications of pathogenicity 0 2
Uncertain significance 0 14
Ranking
ClinVar
0
0
0
18
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:25262 HGNC
Ensembl ENSG00000215910 Ensembl
AllianceGenome HGNC:25262
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000433342.6 hg38 chr1 11,761,787 11,789,584 27,798
ENST00000688073.1 hg38 chr1 11,762,193 11,789,585 27,393
ENST00000433342.6 hg19 chr1 11,821,844 11,849,641 27,798
ENST00000688073.1 hg19 chr1 11,822,250 11,849,642 27,393
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