RPS26 ribosomal protein S26

Information
Symbol
RPS26
Type
protein-coding
Description
ribosomal protein S26
Entrez Gene ID
6231
Genome
hg19
Position
chr12:56,435,135-56,438,460
Genome
hg38
Position
chr12:56,041,351-56,044,676
MIM
603701 OMIM
HGNC
HGNC:10414 HGNC
Ensembl
ENSG00000197728 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 4 38
Likely pathogenic 0 20
Benign 2 28
Likely benign 0 116
Conflicting classifications of pathogenicity 0 8
Uncertain significance 0 72
Ranking
ClinVar
0
0
60
194
12
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 DBA10
SYNONYM S26
SYNONYM eS26
MIM 603701 OMIM
HGNC HGNC:10414 HGNC
Ensembl ENSG00000197728 Ensembl
AllianceGenome HGNC:10414
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000356464.10 hg38 chr12 56,041,351 56,044,676 3,326
ENST00000552361.1 hg38 chr12 56,041,893 56,044,223 2,331
ENST00000646449.2 hg38 chr12 56,041,918 56,044,697 2,780
ENST00000356464.10 hg19 chr12 56,435,135 56,438,460 3,326
ENST00000552361.1 hg19 chr12 56,435,677 56,438,007 2,331
ENST00000646449.2 hg19 chr12 56,435,702 56,438,481 2,780
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