UniProtKB/SwissProt variant VAR

Variant information

Variant position:

197

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 Lysine (K) to Glutamate (E) at position 197 (K197E, p.Lys197Glu).

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 (K) to medium size and acidic (E)

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 FA7D.

Any additional useful information about the variant.

Other resources:

Links to websites of interest for the variant.

Variant rs1250204261 [ dbSNP | Ensembl ]

Sequence information

Variant position:

197

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

Protein sequence length:

466

The length of the canonical sequence.

Location on the sequence:

GYSLLADGVSCTPTVEYPCG K IPILEKRNASKPQGRIVGGK

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                         GYSLLADGVSCTPTVEYPCGKIPILEKRNASKPQGRIVGGK

Chimpanzee                    GYSLLADGVSCTPTVEYPCGKIPILEKRNASKPQGRIVGGK

Mouse                         DYTLQPDEVSCKPKVEYPCGRIPVVEKRNSSSRQGRIVGGN

Rat                           DYVLQPDEVSCKPKVEYPCGRIPVVEKRNFSRPQGRIVGGY

Bovine                        GYALQADGVSCAPTVEYPCGKIPVLEKRNGSKPQGRIVGGH

Rabbit                        GYTLLPNGVSCTPTVDYPCGKVPALEKRGASNPQGRIVGGK

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	61 – 212	Factor VII light chain
Glycosylation	205 – 205	N-linked (GlcNAc...) asparagine
Disulfide bond	195 – 322

Literature citations

Detection of missense mutations by single-strand conformational polymorphism (SSCP) analysis in five dysfunctional variants of coagulation factor VII.
Takamiya O.; Kemball-Cook G.; Martin D.M.A.; Cooper D.N.; von Felten A.; Meili E.; Hahn I.; Prangnell D.R.; Lumley H.; Tuddenham E.G.D.; McVey J.H.;
Hum. Mol. Genet. 2:1355-1359(1993)
Cited for: VARIANTS FA7D GLN-139; TRP-139; ARG-160; GLU-197 AND GLN-364;

UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot P08709: Variant p.Lys197Glu