UniProtKB/SwissProt variant VAR

Variant information

Variant position:

163

The position of the amino-acid change on the UniProtKB canonical protein sequence.

Type of variant:

Polymorphism

The variants are classified into three categories: Disease, Polymorphism and Unclassified.

Disease: Variants implicated in disease according to literature reports.
Polymorphism: Variants not reported to be implicated in disease.
Unclassified: Variants with uncertain implication in disease according to literature reports. Evidence against or in favor of a pathogenic role is limited and/or conflicting.

Residue change:

From Isoleucine (I) to Threonine (T) at position 163 (I163T, p.Ile163Thr).

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:

Change from medium size and hydrophobic (I) to medium size and polar (T)

The physico-chemical property of the reference and variant residues and the change implicated.

BLOSUM score:

-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

Other resources:

Links to websites of interest for the variant.

Variant rs1965208 [ dbSNP | Ensembl ]

Sequence information

Variant position:

163

The position of the amino-acid change on the UniProtKB canonical protein sequence.

Protein sequence length:

308

The length of the canonical sequence.

Location on the sequence:

QLATGSWTSGILVSVVDTTF I LRLPYRGSNSIAHFFCEAPA

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.

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.

Type	Positions	Description
Chain	1 – 308	Olfactory receptor 2D2
Topological domain	159 – 195	Extracellular

Literature citations

Genomic analysis of orthologous mouse and human olfactory receptor loci.
Lane R.P.; Cutforth T.; Young J.; Athanasiou M.; Friedman C.; Rowen L.; Evans G.; Axel R.; Hood L.; Trask B.J.;
Proc. Natl. Acad. Sci. U.S.A. 98:7390-7395(2001)
Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA]; VARIANTS THR-163 AND THR-202;

Submission
Mural R.J.; Istrail S.; Sutton G.G.; Florea L.; Halpern A.L.; Mobarry C.M.; Lippert R.; Walenz B.; Shatkay H.; Dew I.; Miller J.R.; Flanigan M.J.; Edwards N.J.; Bolanos R.; Fasulo D.; Halldorsson B.V.; Hannenhalli S.; Turner R.; Yooseph S.; Lu F.; Nusskern D.R.; Shue B.C.; Zheng X.H.; Zhong F.; Delcher A.L.; Huson D.H.; Kravitz S.A.; Mouchard L.; Reinert K.; Remington K.A.; Clark A.G.; Waterman M.S.; Eichler E.E.; Adams M.D.; Hunkapiller M.W.; Myers E.W.; Venter J.C.;
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA]; VARIANT THR-163;

The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).
The MGC Project Team;
Genome Res. 14:2121-2127(2004)
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA]; VARIANT THR-163;

Organization and evolution of olfactory receptor genes on human chromosome 11.
Buettner J.A.; Glusman G.; Ben-Arie N.; Ramos P.; Lancet D.; Evans G.A.;
Genomics 53:56-68(1998)
Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA] OF 67-283; VARIANTS THR-163 AND THR-202;

DEFOG: a practical scheme for deciphering families of genes.
Fuchs T.; Malecova B.; Linhart C.; Sharan R.; Khen M.; Herwig R.; Shmulevich D.; Elkon R.; Steinfath M.; O'Brien J.K.; Radelof U.; Lehrach H.; Lancet D.; Shamir R.;
Genomics 80:295-302(2002)
Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA] OF 68-281; VARIANTS THR-163 AND THR-202;

UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot Q9H210: Variant p.Ile163Thr