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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot P00492: Variant p.Phe199Val

Hypoxanthine-guanine phosphoribosyltransferase
Gene: HPRT1
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Variant information Variant position: help 199 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 Phenylalanine (F) to Valine (V) at position 199 (F199V, p.Phe199Val). 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 large size and aromatic (F) to medium size and hydrophobic (V) The physico-chemical property of the reference and variant residues and the change implicated.
BLOSUM score: help -1 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 LNS; New Briton/RJK 950. Any additional useful information about the variant.
Other resources: help Links to websites of interest for the variant.


Sequence information Variant position: help 199 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 218 The length of the canonical sequence.
Location on the sequence: help VGFEIPDKFVVGYALDYNEY F RDLNHVCVISETGKAKYKA 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                         VGFEIPDKFVVGYALDYNEYFRDLNHVCVISET---GKAKYKA

                              VGFEIPDKFVVGYALDYNEYFRDLNHVCVISET---GKAK

Chimpanzee                    VGFEIPDKFVVGYALDYNEYFRDLNHVCVISET---GKAK

Mouse                         VGFEIPDKFVVGYALDYNEYFRDLNHVCVISET---GKAK

Rat                           VGFEIPDKFVVGYALDYNEHFRDLNHVCVISES---GKAK

Pig                           VGFEIPDKFVVGYALDYNEYFRDLNHVCVISET---GKAK

Bovine                        VGFEIPDKFVVGYALDYNEYFRDLNHVCVISET---GKAK

Chicken                       VGFEVPDKFVVGYALDYNEYFRDLNHICVISET---GKQK

Slime mold                    MGFDIPMVFIIGYGLDFAENYRELPY---LGEL---KEEC

Baker's yeast                 AAKTVPDKWYA-YPWESTDIVFHTRMAIEQGNDIFIPEQE

Fission yeast                 TGCNTPDCWIM-YPWEAQDIEEHDSHVAKMGDL-------
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 – 218 Hypoxanthine-guanine phosphoribosyltransferase
Binding site 194 – 194
Binding site 194 – 194
Beta strand 198 – 201



Literature citations
Multiplex DNA deletion detection and exon sequencing of the hypoxanthine phosphoribosyltransferase gene in Lesch-Nyhan families.
Gibbs R.A.; Nguyen P.N.; Edwards A.; Civitello A.B.; Caskey C.T.;
Genomics 7:235-244(1990)
Cited for: VARIANTS LNS RJK LYS-45; LEU-74; ASP-130; SER-131; LYS-143; SER-161; TYR-177; ASN-194; VAL-199; ASP-204 AND TYR-206;
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.