P82926 · RT33_BOVIN
- ProteinSmall ribosomal subunit protein mS33
- GeneMRPS33
- StatusUniProtKB reviewed (Swiss-Prot)
- Organism
- Amino acids106 (go to sequence)
- Protein existenceEvidence at protein level
- Annotation score3/5
Variants
Variant ID(s) | Position(s) | Change | Description | Clinical significance | Provenance | ||
---|---|---|---|---|---|---|---|
rs450082866 | 17 | R>W | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.04) Somatic: No Accession: NC_037331.1:g.104268999G>A Codon: CGG/TGG Consequence type: missense Cytogenetic band: Genomic location: NC_037331.1:g.104268999G>A Locations: - p.Arg17Trp (Ensembl:ENSBTAT00000006954) - c.49C>T (Ensembl:ENSBTAT00000006954) Source type: large scale study Cross-references: | |||||||
rs1115256398 | 20 | S>N | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.02) Somatic: No Accession: NC_037331.1:g.104268989C>T Codon: AGT/AAT Consequence type: missense Cytogenetic band: Genomic location: NC_037331.1:g.104268989C>T Locations: - p.Ser20Asn (Ensembl:ENSBTAT00000006954) - c.59G>A (Ensembl:ENSBTAT00000006954) Source type: large scale study Cross-references: | |||||||
rs445090230 | 62 | M>I | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.05) Somatic: No Accession: NC_037331.1:g.104268862C>G Codon: ATG/ATC Consequence type: missense Cytogenetic band: Genomic location: NC_037331.1:g.104268862C>G Locations: - p.Met62Ile (Ensembl:ENSBTAT00000006954) - c.186G>C (Ensembl:ENSBTAT00000006954) Source type: large scale study Cross-references: | |||||||
rs459389396 | 64 | I>R | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.38) Somatic: No Accession: NC_037331.1:g.104268857A>C Codon: ATA/AGA Consequence type: missense Cytogenetic band: Genomic location: NC_037331.1:g.104268857A>C Locations: - p.Ile64Arg (Ensembl:ENSBTAT00000006954) - c.191T>G (Ensembl:ENSBTAT00000006954) Source type: large scale study Cross-references: | |||||||
rs439730713 | 78 | F>V | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.04) Somatic: No Accession: NC_037331.1:g.104265086A>C Codon: TTC/GTC Consequence type: missense Cytogenetic band: Genomic location: NC_037331.1:g.104265086A>C Locations: - p.Phe78Val (Ensembl:ENSBTAT00000006954) - c.232T>G (Ensembl:ENSBTAT00000006954) Source type: large scale study Cross-references: | |||||||
rs470944828 | 87 | K>E | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.42) Somatic: No Accession: NC_037331.1:g.104265059T>C Codon: AAG/GAG Consequence type: missense Cytogenetic band: Genomic location: NC_037331.1:g.104265059T>C Locations: - p.Lys87Glu (Ensembl:ENSBTAT00000006954) - c.259A>G (Ensembl:ENSBTAT00000006954) Source type: large scale study Cross-references: |