RPL26 ribosomal protein L26

Information
Symbol
RPL26
Type
protein-coding
Description
ribosomal protein L26
Entrez Gene ID
6154
Genome
hg19
Position
chr17:8,280,839-8,286,482
Genome
hg38
Position
chr17:8,377,521-8,383,164
MIM
603704 OMIM
HGNC
HGNC:10327 HGNC
Ensembl
ENSG00000161970 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 4
Likely pathogenic 0 4
Benign 0 24
Likely benign 0 76
not provided 0 2
Uncertain significance 0 58
Ranking
ClinVar
0
0
22
136
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
SYNONYM DBA11
SYNONYM L26
SYNONYM uL24
MIM 603704 OMIM
HGNC HGNC:10327 HGNC
Ensembl ENSG00000161970 Ensembl
AllianceGenome HGNC:10327
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000584164.6 hg38 chr17 8,377,521 8,383,164 5,644
ENST00000648839.1 hg38 chr17 8,377,516 8,383,193 5,678
ENST00000578812.5 hg38 chr17 8,379,145 8,383,193 4,049
ENST00000583011.6 hg38 chr17 8,377,523 8,383,213 5,691
ENST00000582556.5 hg38 chr17 8,377,549 8,383,166 5,618
ENST00000648839.1 hg19 chr17 8,280,834 8,286,511 5,678
ENST00000584164.6 hg19 chr17 8,280,839 8,286,482 5,644
ENST00000583011.6 hg19 chr17 8,280,841 8,286,531 5,691
ENST00000582556.5 hg19 chr17 8,280,867 8,286,484 5,618
ENST00000578812.5 hg19 chr17 8,282,463 8,286,511 4,049
Genome browser