C22orf15 chromosome 22 open reading frame 15

Information
Symbol
C22orf15
Type
protein-coding
Description
chromosome 22 open reading frame 15
Entrez Gene ID
150248
Genome
hg19
Position
chr22:24,105,394-24,108,048
Genome
hg38
Position
chr22:23,763,207-23,765,861
HGNC
HGNC:15558 HGNC
Ensembl
ENSG00000169314 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 4
not provided 5 0
Uncertain significance 0 8
Ranking
ClinVar
0
0
0
12
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
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 N27C7-3
HGNC HGNC:15558 HGNC
Ensembl ENSG00000169314 Ensembl
AllianceGenome HGNC:15558
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000382821.3 hg38 chr22 23,763,223 23,765,861 2,639
ENST00000305199.9 hg38 chr22 23,763,207 23,765,861 2,655
ENST00000402217.8 hg38 chr22 23,762,990 23,765,863 2,874
ENST00000402217.8 hg19 chr22 24,105,177 24,108,050 2,874
ENST00000305199.9 hg19 chr22 24,105,394 24,108,048 2,655
ENST00000382821.3 hg19 chr22 24,105,410 24,108,048 2,639
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