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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot Q04671: Variant p.Trp679Cys

P protein
Gene: OCA2
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Variant information Variant position: help 679 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 Tryptophan (W) to Cysteine (C) at position 679 (W679C, p.Trp679Cys). 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 (W) to medium size and polar (C) The physico-chemical property of the reference and variant residues and the change implicated.
BLOSUM score: help -2 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 OCA2. Any additional useful information about the variant.
Other resources: help Links to websites of interest for the variant.


Sequence information Variant position: help 679 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 838 The length of the canonical sequence.
Location on the sequence: help IWLLILADIHDFEIILHRVE W ATLLFFAALFVLMEALAHLH 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                         IWLLILADIHDFEIILHRVEWATLLFFAALFVLMEALAHLH

Mouse                         IWLLILADIHDFEIILHRVEWATLLFFAALFVLMEALTHLH

Pig                           IWLLILADIHDFEIILHRVEWATLLFFAALFILMEALAHLH
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 1 – 838 P protein
Topological domain 665 – 679 Cytoplasmic
Alternative sequence 669 – 838 Missing. In isoform 3.



Literature citations
Novel and recurrent mutations in the tyrosinase gene and the P gene in the German albino population.
Passmore L.A.; Kaesmann-Kellner B.; Weber B.H.F.;
Hum. Genet. 105:200-210(1999)
Cited for: VARIANTS OCA2 GLY-290; ILE-443; GLU-614; LEU-617; CYS-679; CYS-720; ARG-795 AND VAL-833 DEL; VARIANTS TRP-305 AND GLN-419; MC1R mutations modify the classic phenotype of oculocutaneous albinism type 2 (OCA2).
King R.A.; Willaert R.K.; Schmidt R.M.; Pietsch J.; Savage S.; Brott M.J.; Fryer J.P.; Summers C.G.; Oetting W.S.;
Am. J. Hum. Genet. 73:638-645(2003)
Cited for: VARIANTS OCA2 GLY-290; ILE-443; ASP-489; CYS-679 AND LEU-743; DNA variations in oculocutaneous albinism: an updated mutation list and current outstanding issues in molecular diagnostics.
Simeonov D.R.; Wang X.; Wang C.; Sergeev Y.; Dolinska M.; Bower M.; Fischer R.; Winer D.; Dubrovsky G.; Balog J.Z.; Huizing M.; Hart R.; Zein W.M.; Gahl W.A.; Brooks B.P.; Adams D.R.;
Hum. Mutat. 34:827-835(2013)
Cited for: VARIANTS OCA2 MET-404; TRP-419; ILE-633; CYS-679 AND CYS-684;
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.