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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot P05362: Variant p.Arg397Gln

Intercellular adhesion molecule 1
Gene: ICAM1
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Variant information Variant position: help 397 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Type of variant: help LB/B 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 Arginine (R) to Glutamine (Q) at position 397 (R397Q, p.Arg397Gln). 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 basic (R) to medium size and polar (Q) 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

Polymorphism: help Variant p.Lys56Met, known as ICAM1-Kilifi, may influence susceptibility to cerebral malaria [MIM:611162]. Additional information on the polymorphism described.
Other resources: help Links to websites of interest for the variant.


Sequence information Variant position: help 397 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 532 The length of the canonical sequence.
Location on the sequence: help VAGQLIHKNQTRELRVLYGP R LDERDCPGNWTWPENSQQTP 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                         VAGQLIHKNQTRELRVLYGPRLDERDCPGNWTWPENSQQTP

Gorilla                       VAGQLIHKNQTRELRVLYGPRLDERDCPGNWTWPENSQQTP

Rhesus macaque                VAGQLVHKNQTRELRVLYGPRLDEKDCPGNWTWPENSQQTP

Chimpanzee                    VAGQLIHKNQTRELRVLYGPRLDERDCPGNWTWPENSQQTP

Mouse                         VAGKFLFKNQTLELHVLYGPRLDETDCLGNWTWQEGSQQTL

Rat                           VDGKSLFKNQTLELHVLYGPHLDKKDCLGNWTWQEGSQQTL

Bovine                        IAGQVVHKHQTLELHVLYGPRLDQRDCPGNWTWQEGSEQTL

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 28 – 532 Intercellular adhesion molecule 1
Topological domain 28 – 480 Extracellular
Glycosylation 385 – 385 N-linked (GlcNAc...) asparagine
Glycosylation 406 – 406 N-linked (GlcNAc...) asparagine
Beta strand 378 – 397



Literature citations
Submission
SeattleSNPs variation discovery resource;
Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA]; VARIANT MET-56; VARIANTS ARG-241; LEU-352; GLN-397 AND TRP-478;
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.