UniProtKB/SwissProt variant VAR

Variant information

Variant position:

153

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 Aspartate (D) to Asparagine (N) at position 153 (D153N, p.Asp153Asn).

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 acidic (D) to medium size and polar (N)

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

Variant description:

In ATFB13; the mutant results in reduced sodium currents when coexpressed with SCN5A in a heterologous expression system.

Any additional useful information about the variant.

Other resources:

Links to websites of interest for the variant.

Variant rs72550247 [ dbSNP | Ensembl ]

Sequence information

Variant position:

153

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

Protein sequence length:

218

The length of the canonical sequence.

Location on the sequence:

EHNTSVVKKIHIEVVDKANR D MASIVSEIMMYVLIVVLTIW

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                         EHNTSVVKKIHIEVVDKANRDMASIVSEIMMYVLIVVLTIW

                              EHNTSVVKKIHIEVVDKANRDMASIVSEIMMYVLIVVLTIW

Chimpanzee                    EHNTSVVKKIHIEVVDKANRDMASIVSEIMMYVLIVVLTIW

Mouse                         EHNTSVVKKIHLEVVDKANRDMASIVSEIMMYVLIVVLTIW

Rat                           EHNTSVVKKIHLEVVDKANRDMASIVSEIMMYVLIVVLTIW

Bovine                        EHNTSVVKKIHLEVVDKANRDMASIVSEIMMYVLIVVLTIW

Rabbit                        EHNTSVVKKIHLEVVDKANRDMASIVSEIMMYVLIVVLTIW

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	19 – 218	Sodium channel subunit beta-1
Topological domain	19 – 160	Extracellular
Glycosylation	135 – 135	N-linked (GlcNAc...) asparagine
Alternative sequence	150 – 218	ANRDMASIVSEIMMYVLIVVLTIWLVAEMIYCYKKIAAATETAAQENASEYLAITSESKENCTGVQVAE -> GESGAACPFTVTHRRARWRDRWQAVDRTGWLCAWPANRPQQRAEGEGSSPSCPLQLWPLFLSSPRRGQSMPVPHRRSGYRTQLCHLCCMTSGRCLLSLSQRVVLGLPGIIIRCVSRGVV. In isoform 2.

Literature citations

Mutations in sodium channel beta1- and beta2-subunits associated with atrial fibrillation.
Watanabe H.; Darbar D.; Kaiser D.W.; Jiramongkolchai K.; Chopra S.; Donahue B.S.; Kannankeril P.J.; Roden D.M.;
Circ. Arrhythm. Electrophysiol. 2:268-275(2009)
Cited for: VARIANTS ATFB13 HIS-85 AND ASN-153; CHARACTERIZATION OF VARIANTS ATFB13 HIS-85 AND ASN-153;

UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot Q07699: Variant p.Asp153Asn