COMMD2 COMM domain containing 2

Information
Symbol
COMMD2
Type
protein-coding
Description
COMM domain containing 2
Entrez Gene ID
51122
Genome
hg19
Position
chr3:149,456,259-149,470,276
Genome
hg38
Position
chr3:149,738,472-149,752,489
MIM
616699 OMIM
HGNC
HGNC:24993 HGNC
Ensembl
ENSG00000114744 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 30
Ranking
ClinVar
0
0
0
32
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 HSPC042
MIM 616699 OMIM
HGNC HGNC:24993 HGNC
Ensembl ENSG00000114744 Ensembl
AllianceGenome HGNC:24993
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000473414.6 hg38 chr3 149,738,472 149,752,489 14,018
ENST00000473414.6 hg19 chr3 149,456,259 149,470,276 14,018
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