C2orf15 chromosome 2 open reading frame 15

Information
Symbol
C2orf15
Type
protein-coding
Description
chromosome 2 open reading frame 15
Entrez Gene ID
150590
Genome
hg19
Position
chr2:99,758,170-99,768,132
Genome
hg38
Position
chr2:99,141,707-99,151,669
HGNC
HGNC:28436 HGNC
Ensembl
ENSG00000273045 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Uncertain significance 0 4
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:28436 HGNC
Ensembl ENSG00000273045 Ensembl
AllianceGenome HGNC:28436
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000409684.2 hg38 chr2 99,141,750 99,151,047 9,298
ENST00000650052.2 hg38 chr2 99,141,707 99,151,669 9,963
ENST00000650052.2 hg19 chr2 99,758,170 99,768,132 9,963
ENST00000409684.2 hg19 chr2 99,758,213 99,767,510 9,298
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