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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot P02461: Variant p.Gly762Cys

Collagen alpha-1(III) chain
Gene: COL3A1
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Variant information Variant position: help 762 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Type of variant: help 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: help From Glycine (G) to Cysteine (C) at position 762 (G762C, p.Gly762Cys). 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: help Change from glycine (G) to medium size and polar (C) The physico-chemical property of the reference and variant residues and the change implicated.
BLOSUM score: help -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: help In EDSVASC. Any additional useful information about the variant.


Sequence information Variant position: help 762 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 1466 The length of the canonical sequence.
Location on the sequence: help DKGEPGGPGADGVPGKDGPR G PTGPIGPPGPAGQPGDKGEG 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: help The multiple alignment of the region surrounding the variant against various orthologous sequences. 
Human                         DKGEPGGPGADGVPGKDGPRGPTGPIGPPGPAGQPGDKGEG

Mouse                         EKGEPGGAGADGVPGKDGPRGPAGPIGPPGPAGQPGDKGEG

Rat                           EKGEPGGAGADGVPGKDGPRGPAGPIGPPGPAGQPGDKGEG

Bovine                        DKGEPGSSGVDGAPGKDGPRGPTGPIGPPGPAGQPGDKGES
Sequence annotation in neighborhood: help 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.
TypePositionsDescription
Chain 154 – 1221 Collagen alpha-1(III) chain
Region 95 – 1194 Disordered
Region 168 – 1196 Triple-helical region
Modified residue 746 – 746 4-hydroxyproline
Modified residue 749 – 749 4-hydroxyproline
Modified residue 755 – 755 4-hydroxyproline
Modified residue 770 – 770 4-hydroxyproline
Modified residue 776 – 776 4-hydroxyproline



Literature citations
Ehlers-Danlos syndrome type IV caused by Gly400Glu, Gly595Cys and Gly1003Asp substitutions in collagen III: clinical features, biochemical screening, and molecular confirmation.
Mackay K.; Raghunath M.; Superti-Furga A.; Steinmann B.; Dalgleish R.;
Clin. Genet. 49:286-295(1996)
Cited for: VARIANTS EDSVASC GLU-567; CYS-762 AND ASP-1170;
Disclaimer: Any medical or genetic information present in this entry is provided for research, educational and informational purposes only. They are not in any way intended to be used as a substitute for professional medical advice, diagnostic, treatment or care.