RPS16 ribosomal protein S16

Information
Symbol
RPS16
Type
protein-coding
Description
ribosomal protein S16
Entrez Gene ID
6217
Genome
hg19
Position
chr19:39,923,847-39,926,576
Genome
hg38
Position
chr19:39,433,207-39,435,936
MIM
603675 OMIM
HGNC
HGNC:10396 HGNC
Ensembl
ENSG00000105193 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Uncertain significance 0 10
Ranking
ClinVar
0
0
0
12
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 S16
SYNONYM uS9
MIM 603675 OMIM
HGNC HGNC:10396 HGNC
Ensembl ENSG00000105193 Ensembl
AllianceGenome HGNC:10396
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000599539.5 hg38 chr19 39,433,207 39,435,915 2,709
ENST00000339471.8 hg38 chr19 39,433,207 39,435,936 2,730
ENST00000251453.8 hg38 chr19 39,433,137 39,435,949 2,813
ENST00000601655.5 hg38 chr19 39,433,217 39,435,941 2,725
ENST00000251453.8 hg19 chr19 39,923,777 39,926,589 2,813
ENST00000599539.5 hg19 chr19 39,923,847 39,926,555 2,709
ENST00000339471.8 hg19 chr19 39,923,847 39,926,576 2,730
ENST00000601655.5 hg19 chr19 39,923,857 39,926,581 2,725
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