C2orf49 chromosome 2 open reading frame 49

Information
Symbol
C2orf49
Type
protein-coding
Description
chromosome 2 open reading frame 49
Entrez Gene ID
79074
Genome
hg19
Position
chr2:105,953,997-105,965,668
Genome
hg38
Position
chr2:105,337,540-105,349,211
HGNC
HGNC:28772 HGNC
Ensembl
ENSG00000135974 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely 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
SYNONYM asw
HGNC HGNC:28772 HGNC
Ensembl ENSG00000135974 Ensembl
AllianceGenome HGNC:28772
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000410049.1 hg38 chr2 105,337,532 105,345,596 8,065
ENST00000258457.7 hg38 chr2 105,337,540 105,349,211 11,672
ENST00000410049.1 hg19 chr2 105,953,989 105,962,053 8,065
ENST00000258457.7 hg19 chr2 105,953,997 105,965,668 11,672
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