UniProtKB/Swiss-Prot P10635 : Variant p.Arg365His
Cytochrome P450 2D6
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Variant information
Variant position:
365
The position of the amino-acid change on the UniProtKB canonical protein sequence.
Type of variant:
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:
365 (R365H, p.Arg365His).
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:
The physico-chemical property of the reference and variant residues and the change implicated.
BLOSUM score:
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).following page
Polymorphism:
608902 ]. The CYP2D6 gene is highly polymorphic. CYP2D6 activity ranges widely within a population comprising ultrarapid (UM), extensive (EM), intermediate (IM) and poor (PM) metabolizer phenotypes. UM and PM are those most at risk for treatment failure or dose-dependent drug toxicity, respectively. Of the Caucasian populations of Europe and North America, 5%-10% are of the PM phenotype and are unable to metabolize the antihypersensitive drug debrisoquine and numerous other drugs. Different alleles are known, including CYP2D6*1 (PubMed:15768052 ), CYP2D6*2 (PubMed:25469868 ), CYP2D6*6B/6C (PubMed:7868129 ), CYP2D6*7 also known CYP2D6E (PubMed:7845481 ), CYP2D6*9 also known CYP2D6C (PubMed:1844820 ), CYP2D6*10 also known CYP2D6J (PubMed:8287064 , PubMed:25469868 ), CYP2D6*12 (PubMed:8655150 ), CYP2D6*14 (PubMed:10064570 ), CYP2D6*17 also known CYP2D6Z (PubMed:8971426 ), CYP2D6*41B (PubMed:15768052 ), CYP2D6*45A (PubMed:15768052 ), CYP2D6*45B (PubMed:15768052 ), CYP2D6*46 (PubMed:15768052 ), CYP2D6*87 (PubMed:25469868 ), CYP2D6*88 (PubMed:25469868 ), CYP2D6*89 (PubMed:25469868 ), CYP2D6*90 (PubMed:25469868 ), CYP2D6*91 (PubMed:25469868 ), CYP2D6*93 (PubMed:25469868 ), C CYP2D6*94 (PubMed:25469868 ), CYP2D6*97 (PubMed:25469868 ) and CYP2D6*98 (PubMed:25469868 ). Isozymes CYP2D6.45 (Lys-155, Cys-296 and Thr-486) and CYP2D6.46 (His-26, Lys-155, Cys-296 and Thr-486) are functional (PubMed:15768052 ). The sequence shown is that of isozyme CYP2D6.1 corresponding to allele CYP2D6*1.
Additional information on the polymorphism described.
Other resources:
Links to websites of interest for the variant.
Sequence information
Variant position:
365
The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length:
497
The length of the canonical sequence.
Location on the sequence:
R FGDIVPLGVTHMTSRDIEVQ
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:
The multiple alignment of the region surrounding the variant against various orthologous sequences.
Human PEMGDQAHMPYTTAVIHEVQR FGDIVPLGVTHMTSRDIEVQ
Chimpanzee PEMGDQARMPYTTAVIHEVQR FGDIVPLGVTHMTSRDIEVQ
Sequence annotation in neighborhood:
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.
Literature citations
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.
