C22orf31 chromosome 22 open reading frame 31

Information
Symbol
C22orf31
Type
protein-coding
Description
chromosome 22 open reading frame 31
Entrez Gene ID
25770
Genome
hg19
Position
chr22:29,454,660-29,457,819
Genome
hg38
Position
chr22:29,058,672-29,061,831
HGNC
HGNC:26931 HGNC
Ensembl
ENSG00000100249 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
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
[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 HS747E2A
SYNONYM bK747E2.1
HGNC HGNC:26931 HGNC
Ensembl ENSG00000100249 Ensembl
AllianceGenome HGNC:26931
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000216071.5 hg38 chr22 29,058,672 29,061,831 3,160
ENST00000216071.5 hg19 chr22 29,454,660 29,457,819 3,160
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