URGCP-MRPS24 URGCP-MRPS24 readthrough

Information
Symbol
URGCP-MRPS24
Type
protein-coding
Description
URGCP-MRPS24 readthrough
Entrez Gene ID
100534592
Genome
hg19
Position
chr7:43,906,157-43,946,188
Genome
hg38
Position
chr7:43,866,558-43,906,589
HGNC
HGNC:49188 HGNC
Ensembl
ENSG00000270617 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 16
Likely benign 0 6
Uncertain significance 0 78
Ranking
ClinVar
0
0
0
100
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:49188 HGNC
Ensembl ENSG00000270617 Ensembl
AllianceGenome HGNC:49188
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000603700.1 hg38 chr7 43,866,558 43,906,589 40,032
ENST00000603700.1 hg19 chr7 43,906,157 43,946,188 40,032
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