C2orf73 chromosome 2 open reading frame 73

Information
Symbol
C2orf73
Type
protein-coding
Description
chromosome 2 open reading frame 73
Entrez Gene ID
129852
Genome
hg19
Position
chr2:54,558,021-54,588,718
Genome
hg38
Position
chr2:54,330,884-54,361,581
HGNC
HGNC:26861 HGNC
Ensembl
ENSG00000177994 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 6
Ranking
ClinVar
0
0
0
6
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:26861 HGNC
Ensembl ENSG00000177994 Ensembl
AllianceGenome HGNC:26861
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000398634.7 hg38 chr2 54,330,884 54,361,581 30,698
ENST00000615983.1 hg38 chr2 54,330,965 54,361,387 30,423
ENST00000405749.5 hg38 chr2 54,330,902 54,383,194 52,293
ENST00000398634.7 hg19 chr2 54,558,021 54,588,718 30,698
ENST00000405749.5 hg19 chr2 54,558,039 54,610,331 52,293
ENST00000615983.1 hg19 chr2 54,558,102 54,588,524 30,423
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