UniProtKB/SwissProt variant VAR

Variant information

Variant position:

2110

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

Type of variant:

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:

From Arginine (R) to Tryptophan (W) at position 2110 (R2110W, p.Arg2110Trp).

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 large size and basic (R) to large size and aromatic (W)

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

BLOSUM score:

-3

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:

In EBS5A.

Any additional useful information about the variant.

Other resources:

Links to websites of interest for the variant.

Variant rs80338756 [ dbSNP | Ensembl ]

Sequence information

Variant position:

2110

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

Protein sequence length:

4684

The length of the canonical sequence.

Location on the sequence:

SNAEDTLRSKEQAELEAARQ R QLAAEEERRRREAEERVQKS

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                         SNAEDTLRSKEQAELEAARQRQLAAEEERRRREAEERVQKS

Mouse                         SNAEDTMRSKEQAELEAARQRQLAAEEEQRRREAEERVQRS

Rat                           SNAEDTMRSKELAEQEAARQRQLAAEEEQRRREAEERVQRS

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 – 4684	Plectin
Region	1471 – 2755	Central fibrous rod domain
Region	2105 – 2139	Disordered
Coiled coil	1469 – 2756

Literature citations

A site-specific plectin mutation causes dominant epidermolysis bullosa simplex Ogna: two identical de novo mutations.
Koss-Harnes D.; Hoeyheim B.; Anton-Lamprecht I.; Gjesti A.; Joergensen R.S.; Jahnsen F.L.; Olaisen B.; Wiche G.; Gedde-Dahl T. Jr.;
J. Invest. Dermatol. 118:87-93(2002)
Cited for: VARIANT EBS5A TRP-2110;

UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot Q15149: Variant p.Arg2110Trp