RN7SL812P RNA, 7SL, cytoplasmic 812, pseudogene

Information
Symbol
RN7SL812P
Type
pseudo
Description
RNA, 7SL, cytoplasmic 812, pseudogene
Entrez Gene ID
106479518
Genome
hg19
Position
chr22:20,836,224-20,836,497
Genome
hg38
Position
chr22:20,481,935-20,482,213
HGNC
HGNC:46828 HGNC
Ensembl
ENSG00000242876 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 15 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 :
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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:46828 HGNC
Ensembl ENSG00000242876 Ensembl
AllianceGenome HGNC:46828
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000493791.3 hg38 chr22 20,481,935 20,482,213 279
ENST00000493791.2 hg19 chr22 20,836,224 20,836,497 274
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