RPS5 ribosomal protein S5

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Information
Clinical Significance
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Frequency
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Information

Symbol: RPS5
Type: protein-coding
Description: ribosomal protein S5
Entrez Gene ID: 6193
Genome: hg19
Position: chr19:58,898,656-58,906,173
Genome: hg38
Position: chr19:58,387,289-58,394,806
MIM: 603630 OMIM
HGNC: HGNC:10426 HGNC
Ensembl: ENSG00000083845 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Uncertain significance	0	10

Ranking

	ClinVar
	0
	0
	0
	10
	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

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Target data	:	MGeND data only
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Variant name	Gene	AA change	CDS	Japanese frequency	TogoVar	MGeND				Genome	ClinVar			CIViC evidence	DisGeNET entry	COSMIC occurrence	Prediction
Variant name	Gene	AA change	CDS	Japanese frequency	TogoVar	Entry	Origin	Type	Annotation	Genome	Entry	Origin	Annotation	CIViC evidence	DisGeNET entry	COSMIC occurrence	Prediction

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Target data	:	MGeND data only
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Name	MGeND				Type	Genome	Size	Chromosome	Start	Stop	Ref	Alt	ClinVar	Origin	Entry	CIViC evidence	DisGeNET entry
Name	Entry	Origin	Type	Annotation	Type	Genome	Size	Chromosome	Start	Stop	Ref	Alt	ClinVar	Origin	Entry	CIViC evidence	DisGeNET entry

Search Word

Target data	:	MGeND data only
Category	:
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Filtering	:

Name	MGeND				Type	Genome	Gene symbol	Chromosome	Genomic start	Genomic stop	Strand	Ref	Alt	ClinVar	Origin	Entry	CIViC evidence	DisGeNET entry
Name	Entry	Origin	Type	Annotation	Type	Genome	Gene symbol	Chromosome	Genomic start	Genomic stop	Strand	Ref	Alt	ClinVar	Origin	Entry	CIViC evidence	DisGeNET entry

Type	ID
SYNONYM	S5
SYNONYM	uS7
MIM	603630 OMIM
HGNC	HGNC:10426 HGNC
Ensembl	ENSG00000083845 Ensembl
AllianceGenome	HGNC:10426

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000598495.5	hg38	chr19	58,387,269	58,394,800	7,532
ENST00000598098.5	hg38	chr19	58,387,264	58,394,804	7,541
ENST00000596046.1	hg38	chr19	58,387,289	58,394,806	7,518
ENST00000196551.8	hg38	chr19	58,387,269	58,394,804	7,536
ENST00000601521.5	hg38	chr19	58,386,400	58,394,806	8,407
ENST00000601521.5	hg19	chr19	58,897,767	58,906,173	8,407
ENST00000598098.5	hg19	chr19	58,898,631	58,906,171	7,541
ENST00000598495.5	hg19	chr19	58,898,636	58,906,167	7,532
ENST00000196551.8	hg19	chr19	58,898,636	58,906,171	7,536
ENST00000596046.1	hg19	chr19	58,898,656	58,906,173	7,518

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