RPS10 ribosomal protein S10

Information
Symbol
RPS10
Type
protein-coding
Description
ribosomal protein S10
Entrez Gene ID
6204
Genome
hg19
Position
chr6:34,385,231-34,393,803
Genome
hg38
Position
chr6:34,417,454-34,426,026
MIM
603632 OMIM
HGNC
HGNC:10383 HGNC
Ensembl
ENSG00000124614 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 12
Likely pathogenic 0 6
Benign 2 48
Likely benign 0 138
Conflicting classifications of pathogenicity 0 4
Uncertain significance 0 98
Ranking
ClinVar
0
0
50
234
4
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 DBA9
SYNONYM S10
SYNONYM eS10
MIM 603632 OMIM
HGNC HGNC:10383 HGNC
Ensembl ENSG00000124614 Ensembl
AllianceGenome HGNC:10383
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000467531.5 hg38 chr6 34,417,454 34,425,784 8,331
ENST00000648437.1 hg38 chr6 34,417,454 34,426,069 8,616
ENST00000621356.3 hg38 chr6 34,417,454 34,426,026 8,573
ENST00000644393.1 hg38 chr6 34,417,467 34,426,069 8,603
ENST00000344700.8 hg38 chr6 34,417,454 34,426,052 8,599
ENST00000464218.5 hg38 chr6 34,417,454 34,425,580 8,127
ENST00000464218.5 hg19 chr6 34,385,231 34,393,357 8,127
ENST00000467531.5 hg19 chr6 34,385,231 34,393,561 8,331
ENST00000621356.3 hg19 chr6 34,385,231 34,393,803 8,573
ENST00000344700.8 hg19 chr6 34,385,231 34,393,829 8,599
ENST00000648437.1 hg19 chr6 34,385,231 34,393,846 8,616
ENST00000644393.1 hg19 chr6 34,385,244 34,393,846 8,603
Genome browser