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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot P62273: Variant p.Ile31Phe

Small ribosomal subunit protein uS14
Gene: RPS29
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Variant information Variant position: help 31 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Type of variant: help LP/P [Disclaimer] The variants are classified into three categories: LP/P, LB/B and US.
  • LP/P: likely pathogenic or pathogenic.
  • LB/B: likely benign or benign.
  • US: uncertain significance
Residue change: help From Isoleucine (I) to Phenylalanine (F) at position 31 (I31F, p.Ile31Phe). Indicates the amino acid change of the variant. The one-letter and three-letter codes for amino acids used in UniProtKB/Swiss-Prot are those adopted by the commission on Biochemical Nomenclature of the IUPAC-IUB.
Physico-chemical properties: help Change from medium size and hydrophobic (I) to large size and aromatic (F) The physico-chemical property of the reference and variant residues and the change implicated.
BLOSUM score: help 0 The score within a Blosum matrix for the corresponding wild-type to variant amino acid change. The log-odds score measures the logarithm for the ratio of the likelihood of two amino acids appearing by chance. The Blosum62 substitution matrix is used. This substitution matrix contains scores for all possible exchanges of one amino acid with another:
  • Lowest score: -4 (low probability of substitution).
  • Highest score: 11 (high probability of substitution).
More information can be found on the following page
Variant description: help In DBA13; results in reduced protein expression; results in pre-rRNA processing defect. Any additional useful information about the variant.
Other resources: help Links to websites of interest for the variant.


Sequence information Variant position: help 31 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 56 The length of the canonical sequence.
Location on the sequence: help PRKFGQGSRSCRVCSNRHGL I RKYGLNMCRQCFRQYAKDIG The residue change on the sequence. Unless the variant is located at the beginning or at the end of the protein sequence, both residues upstream (20) and downstream (20) of the variant will be shown.
Residue conservation: help The multiple alignment of the region surrounding the variant against various orthologous sequences. 
Human                         PRKFGQGSRSCRVCSNRHGLIRKYGLNMCRQCFRQYAKDIG

Mouse                         PRKFGQGSRSCRVCSNRHGLIRKYGLNMCRQCFRQYAKDIG

Rat                           PRKFGQGSRSCRVCSNRHGLIRKYGLNMCRQCFRQYAKDIG

Pig                           PRKFGQGSRSCRVCSNRHGLIRKYGLNMCRQCFRQYAKDIG

Bovine                        PRKFGQGSRSCRVCSNRHGLIRKYGLNMCRQCFRQYAKDIG

Rabbit                        PRKFGQGSRSCRVCSNRHGLIRKYGLNMCRQCFRQYAKDIG

Drosophila                    PRKYGQGSRCCRACSNRHGLIRKYGLNICRQCFREYANDIG

Slime mold                    PRNFGPGSRTCRKCGNHHGIIRKYDLNMCRRCFRTDAEAIG

Fission yeast                 PRKYGKGSRQCAHTGRRLGLIRKYGLNISRQSFREYANDIG
Sequence annotation in neighborhood: help The regions or sites of interest surrounding the variant. In general the features listed are posttranslational modifications, binding sites, enzyme active sites, local secondary structure or other characteristics reported in the cited references. The "Sequence annotation in neighborhood" lines have a fixed format:
  • Type: the type of sequence feature.
  • Positions: endpoints of the sequence feature.
  • Description: contains additional information about the feature.
TypePositionsDescription
Chain 2 – 56 Small ribosomal subunit protein uS14
Binding site 21 – 21
Binding site 24 – 24
Binding site 39 – 39
Binding site 42 – 42
Modified residue 12 – 12 Omega-N-methylarginine
Modified residue 48 – 48 N6-acetyllysine
Beta strand 28 – 31



Literature citations
Whole-exome sequencing and functional studies identify RPS29 as a novel gene mutated in multicase Diamond-Blackfan anemia families.
Mirabello L.; Macari E.R.; Jessop L.; Ellis S.R.; Myers T.; Giri N.; Taylor A.M.; McGrath K.E.; Humphries J.M.; Ballew B.J.; Yeager M.; Boland J.F.; He J.; Hicks B.D.; Burdett L.; Alter B.P.; Zon L.; Savage S.A.;
Blood 124:24-32(2014)
Cited for: INVOLVEMENT IN DBA13; VARIANTS DBA13 PHE-31 AND THR-50; CHARACTERIZATION OF VARIANTS DBA13 PHE-31 AND THR-50;
Disclaimer: Any medical or genetic information present in this entry is provided for research, educational and informational purposes only. They are not in any way intended to be used as a substitute for professional medical advice, diagnostic, treatment or care.