CWC25 CWC25 spliceosome associated protein homolog

Information
Symbol
CWC25
Type
protein-coding
Description
CWC25 spliceosome associated protein homolog
Entrez Gene ID
54883
Genome
hg19
Position
chr17:36,956,694-36,981,574
Genome
hg38
Position
chr17:38,800,441-38,825,321
HGNC
HGNC:25989 HGNC
Ensembl
ENSG00000273559 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 4
Uncertain significance 0 52
Ranking
ClinVar
0
0
0
56
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 CCDC49
HGNC HGNC:25989 HGNC
Ensembl ENSG00000273559 Ensembl
AllianceGenome HGNC:25989
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000614790.5 hg38 chr17 38,800,441 38,825,321 24,881
ENST00000614790.5 hg19 chr17 36,956,694 36,981,574 24,881
Genome browser