RNA5SP498 RNA, 5S ribosomal pseudogene 498

Information
Symbol
RNA5SP498
Type
pseudo
Description
RNA, 5S ribosomal pseudogene 498
Entrez Gene ID
106480770
Genome
hg19
Position
chrX:1,419,149-1,419,268
Genome
hg19
Position
chrY:1,369,149-1,369,268
Genome
hg19
Position
chrY:1,369,149-1,369,268
Genome
hg38
Position
chrX:1,300,256-1,300,375
Genome
hg38
Position
chrY:1,300,256-1,300,375
HGNC
HGNC:43398 HGNC
Ensembl
ENSG00000223274 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 7 0
Ranking
ClinVar
0
0
0
0
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 RN5S498
HGNC HGNC:43398 HGNC
Ensembl ENSG00000223274 Ensembl
Ensembl ENSG00000292356 Ensembl
AllianceGenome HGNC:43398
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000411342.6 hg38 chrX 1,300,256 1,300,375 120
ENST00000711139.1 hg38 chrY 1,300,256 1,300,375 120
ENST00000411342.6 hg19 chrX 1,419,149 1,419,268 120
ENST00000411342.1 hg19 chrY 1,369,149 1,369,268 120
ENST00000711139.1 hg19 chrY 1,369,149 1,369,268 120
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