UniProtKB/SwissProt variant VAR

Variant information

Variant position:

119

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 Cysteine (C) to Glycine (G) at position 119 (C119G, p.Cys119Gly).

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 polar (C) to glycine (G)

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 C9D.

Any additional useful information about the variant.

Other resources:

Links to websites of interest for the variant.

Variant rs121909593 [ dbSNP | Ensembl ]

Sequence information

Variant position:

119

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

Protein sequence length:

559

The length of the canonical sequence.

Location on the sequence:

DDCGNDFQCSTGRCIKMRLR C NGDNDCGDFSDEDDCESEPR

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                         DDCGND-FQCSTGRCIKMRLRCNGDNDCGDFSDEDDCESEPR

Mouse                         ENCGND-FQCETGRCIKRRLLCNGDNDCGDYSDENDCDDDP

Rat                           ENCGND-FQCETGRCIKRKLLCNGDNDCGDFSDESDCESDP

Bovine                        EGCGND-FQCGTGRCIKNRLLCNEDNDCGDYSDEDNCEQDP

Rabbit                        EDCEKDEFHCGTGRCIKRRLLCNGDNDCGDFSDEDDCETEP

Horse                         DDCGND-FQCGTGRCIKKRLLCNGDNDCGDFSDEDDCENDP

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	22 – 559	Complement component C9
Chain	22 – 265	Complement component C9a
Domain	99 – 136	LDL-receptor class A
Disulfide bond	107 – 125
Disulfide bond	119 – 134

Literature citations

Heterogeneity in the genetic basis of human complement C9 deficiency.
Witzel-Schloemp K.; Hobart M.J.; Fernie B.A.; Orren A.; Wuerzner R.; Rittner C.; Kaufmann T.; Schneider P.M.;
Immunogenetics 48:144-147(1998)
Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA] OF 27-559; VARIANT C9D GLY-119; FUNCTION; SUBCELLULAR LOCATION; TISSUE SPECIFICITY;

UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot P02748: Variant p.Cys119Gly