P62270 · RS18_MOUSE
- ProteinSmall ribosomal subunit protein uS13
- GeneRps18
- StatusUniProtKB reviewed (Swiss-Prot)
- Organism
- Amino acids152 (go to sequence)
- Protein existenceEvidence at protein level
- Annotation score5/5
Variants
Variant ID(s) | Position(s) | Change | Description | Clinical significance | Provenance | ||
---|---|---|---|---|---|---|---|
rs3389447841 | 15 | V>I | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated - low confidence (0.13) Somatic: No Accession: NC_000083.7:g.34174111C>T Codon: GTA/ATA Consequence type: missense Cytogenetic band: 17q Genomic location: NC_000083.7:g.34174111C>T Locations: - p.Val15Ile (Ensembl:ENSMUST00000008812) - c.43G>A (Ensembl:ENSMUST00000008812) Source type: large scale study Cross-references: | |||||||
rs3389449236 | 59 | L>F | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious - low confidence (0.01) Somatic: No Accession: NC_000083.7:g.34171493G>A Codon: CTC/TTC Consequence type: missense Cytogenetic band: 17q Genomic location: NC_000083.7:g.34171493G>A Locations: - p.Leu59Phe (Ensembl:ENSMUST00000008812) - c.175C>T (Ensembl:ENSMUST00000008812) Source type: large scale study Cross-references: | |||||||
rs3389449217 | 77 | Y>N | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious - low confidence (0) Somatic: No Accession: NC_000083.7:g.34171439A>T Codon: TAC/AAC Consequence type: missense Cytogenetic band: 17q Genomic location: NC_000083.7:g.34171439A>T Locations: - p.Tyr77Asn (Ensembl:ENSMUST00000008812) - c.229T>A (Ensembl:ENSMUST00000008812) Source type: large scale study Cross-references: | |||||||
rs3389444972 | 89 | D>N | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious - low confidence (0.01) Somatic: No Accession: NC_000083.7:g.34171403C>T Codon: GAT/AAT Consequence type: missense Cytogenetic band: 17q Genomic location: NC_000083.7:g.34171403C>T Locations: - p.Asp89Asn (Ensembl:ENSMUST00000008812) - c.265G>A (Ensembl:ENSMUST00000008812) Source type: large scale study Cross-references: | |||||||
rs3389432549 | 97 | Q>H | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious - low confidence (0.04) Somatic: No Accession: NC_000083.7:g.34171377C>A Codon: CAG/CAT Consequence type: missense Cytogenetic band: 17q Genomic location: NC_000083.7:g.34171377C>A Locations: - p.Gln97His (Ensembl:ENSMUST00000008812) - c.291G>T (Ensembl:ENSMUST00000008812) Source type: large scale study Cross-references: |