RPS5 ribosomal protein S5
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 10 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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10 |
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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
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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
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 | |||
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Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
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Category | : |
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Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | S5 |
SYNONYM | uS7 |
MIM | 603630 OMIM |
HGNC | HGNC:10426 HGNC |
Ensembl | ENSG00000083845 Ensembl |
AllianceGenome | HGNC:10426 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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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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