RPS11 ribosomal protein S11

Information
Symbol
RPS11
Type
protein-coding
Description
ribosomal protein S11
Entrez Gene ID
6205
Genome
hg19
Position
chr19:49,999,691-50,002,965
Genome
hg38
Position
chr19:49,496,434-49,499,708
MIM
180471 OMIM
HGNC
HGNC:10384 HGNC
Ensembl
ENSG00000142534 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 8
Uncertain significance 0 6
Ranking
ClinVar
0
0
0
14
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 S11
SYNONYM uS17
MIM 180471 OMIM
HGNC HGNC:10384 HGNC
Ensembl ENSG00000142534 Ensembl
AllianceGenome HGNC:10384
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000594493.1 hg38 chr19 49,496,434 49,499,689 3,256
ENST00000270625.7 hg38 chr19 49,496,434 49,499,708 3,275
ENST00000599561.1 hg38 chr19 49,496,454 49,499,689 3,236
ENST00000596873.1 hg38 chr19 49,496,432 49,498,251 1,820
ENST00000596873.1 hg19 chr19 49,999,689 50,001,508 1,820
ENST00000594493.1 hg19 chr19 49,999,691 50,002,946 3,256
ENST00000270625.7 hg19 chr19 49,999,691 50,002,965 3,275
ENST00000599561.1 hg19 chr19 49,999,711 50,002,946 3,236
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