RNASEL ribonuclease L

Information
Symbol
RNASEL
Type
protein-coding
Description
ribonuclease L
Entrez Gene ID
6041
Genome
hg19
Position
chr1:182,542,769-182,558,391
Genome
hg38
Position
chr1:182,573,634-182,589,256
MIM
180435 OMIM
HGNC
HGNC:10050 HGNC
Ensembl
ENSG00000135828 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 2
Likely pathogenic 0 4
Benign 18 20
Likely benign 0 18
Conflicting classifications of pathogenicity 0 2
Uncertain significance 0 192
Ranking
ClinVar
0
0
4
94
138
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 PRCA1
SYNONYM RNS4
MIM 180435 OMIM
HGNC HGNC:10050 HGNC
Ensembl ENSG00000135828 Ensembl
AllianceGenome HGNC:10050
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000539397.1 hg38 chr1 182,578,121 182,589,256 11,136
ENST00000367559.7 hg38 chr1 182,573,634 182,589,256 15,623
ENST00000367559.7 hg19 chr1 182,542,769 182,558,391 15,623
ENST00000539397.1 hg19 chr1 182,547,256 182,558,391 11,136
Genome browser