RPS17 ribosomal protein S17

Information
Symbol
RPS17
Type
protein-coding
Description
ribosomal protein S17
Entrez Gene ID
6218
Genome
hg19
Position
chr15:83,205,501-83,209,208
Genome
hg38
Position
chr15:82,536,750-82,540,457
MIM
180472 OMIM
HGNC
HGNC:10397 HGNC
Ensembl
ENSG00000182774 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 4
Likely pathogenic 0 1
Benign 0 2
Likely benign 0 6
Conflicting classifications of pathogenicity 0 1
Uncertain significance 0 2
Ranking
ClinVar
0
0
2
12
1
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 DBA4
SYNONYM RPS17L
SYNONYM RPS17L1
SYNONYM RPS17L2
SYNONYM S17
SYNONYM eS17
MIM 180472 OMIM
HGNC HGNC:10397 HGNC
Ensembl ENSG00000182774 Ensembl
AllianceGenome HGNC:10397
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000647841.1 hg38 chr15 82,536,750 82,540,457 3,708
ENST00000561157.5 hg38 chr15 82,536,755 82,540,459 3,705
ENST00000647841.1 hg19 chr15 83,205,501 83,209,208 3,708
ENST00000561157.5 hg19 chr15 83,205,506 83,209,210 3,705
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