RN7SL614P RNA, 7SL, cytoplasmic 614, pseudogene

Information
Symbol
RN7SL614P
Type
pseudo
Description
RNA, 7SL, cytoplasmic 614, pseudogene
Entrez Gene ID
106481089
Genome
hg19
Position
chr1:10,676,893-10,677,170
Genome
hg38
Position
chr1:10,616,836-10,617,115
HGNC
HGNC:46630 HGNC
Ensembl
ENSG00000243267 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
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
[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:46630 HGNC
Ensembl ENSG00000243267 Ensembl
AllianceGenome HGNC:46630
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000461850.3 hg38 chr1 10,616,836 10,617,115 280
ENST00000461850.2 hg19 chr1 10,676,893 10,677,170 278
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