C2orf81 chromosome 2 open reading frame 81

Information
Symbol
C2orf81
Type
protein-coding
Description
chromosome 2 open reading frame 81
Entrez Gene ID
388963
Genome
hg19
Position
chr2:74,641,304-74,648,746
Genome
hg38
Position
chr2:74,414,177-74,421,619
HGNC
HGNC:34350 HGNC
Ensembl
ENSG00000284308 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
SYNONYM hCG40743
HGNC HGNC:34350 HGNC
Ensembl ENSG00000284308 Ensembl
AllianceGenome HGNC:34350
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000612891.4 hg38 chr2 74,414,176 74,421,560 7,385
ENST00000290390.9 hg38 chr2 74,414,178 74,417,717 3,540
ENST00000640868.1 hg38 chr2 74,414,177 74,416,583 2,407
ENST00000684111.1 hg38 chr2 74,414,177 74,421,619 7,443
ENST00000612891.4 hg19 chr2 74,641,303 74,648,687 7,385
ENST00000640868.1 hg19 chr2 74,641,304 74,643,710 2,407
ENST00000684111.1 hg19 chr2 74,641,304 74,648,746 7,443
ENST00000290390.9 hg19 chr2 74,641,305 74,644,844 3,540
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