RPS15A ribosomal protein S15a

Information
Symbol
RPS15A
Type
protein-coding
Description
ribosomal protein S15a
Entrez Gene ID
6210
Genome
hg19
Position
chr16:18,792,617-18,801,656
Genome
hg38
Position
chr16:18,781,295-18,790,334
MIM
603674 OMIM
HGNC
HGNC:10389 HGNC
Ensembl
ENSG00000134419 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 2 2
Benign 0 4
Likely benign 0 22
Uncertain significance 0 4
Ranking
ClinVar
0
0
2
28
2
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 DBA20
SYNONYM S15a
SYNONYM uS8
MIM 603674 OMIM
HGNC HGNC:10389 HGNC
Ensembl ENSG00000134419 Ensembl
AllianceGenome HGNC:10389
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000563390.5 hg38 chr16 18,782,956 18,790,383 7,428
ENST00000322989.8 hg38 chr16 18,781,295 18,790,334 9,040
ENST00000576436.5 hg38 chr16 18,782,968 18,789,137 6,170
ENST00000565420.5 hg38 chr16 18,782,969 18,790,260 7,292
ENST00000569083.1 hg38 chr16 18,784,021 18,789,119 5,099
ENST00000322989.8 hg19 chr16 18,792,617 18,801,656 9,040
ENST00000563390.5 hg19 chr16 18,794,278 18,801,705 7,428
ENST00000576436.5 hg19 chr16 18,794,290 18,800,459 6,170
ENST00000565420.5 hg19 chr16 18,794,291 18,801,582 7,292
ENST00000569083.1 hg19 chr16 18,795,343 18,800,441 5,099
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