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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot P02461: Variant p.Gly297Arg

Collagen alpha-1(III) chain
Gene: COL3A1
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Variant information Variant position: help 297 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 Arginine (R) at position 297 (G297R, p.Gly297Arg). 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 large size and basic (R) The physico-chemical property of the reference and variant residues and the change implicated.
BLOSUM score: help -2 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.
Other resources: help Links to websites of interest for the variant.


Sequence information Variant position: help 297 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 ETGAPGLKGENGLPGENGAP G PMGPRGAPGERGRPGLPGAA 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                         ETGAPGLKGENGLPGENGAPGPMGPRGAPGERGRPGLPGAA

Mouse                         ETGAPGLKGENGLPGDNGAPGPMGPRGAPGERGRPGLPGAA

Rat                           ETGAPGLKGENGLPGDNGAPGPMGPRGAPGERGRPGLPGAA

Bovine                        EPGAPGLKGENGVPGEDGAPGPMGPRGAPGERGRPGLPGAA
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 281 – 281 4-hydroxyproline
Modified residue 284 – 284 5-hydroxylysine
Modified residue 290 – 290 4-hydroxyproline
Modified residue 296 – 296 4-hydroxyproline
Modified residue 305 – 305 4-hydroxyproline
Modified residue 311 – 311 4-hydroxyproline
Modified residue 314 – 314 4-hydroxyproline



Literature citations
Ehlers-Danlos syndrome type IV: unusual congenital anomalies in a mother and son with a COL3A1 mutation and a normal collagen III protein profile.
Kroes H.Y.; Pals G.; van Essen A.J.;
Clin. Genet. 63:224-227(2003)
Cited for: VARIANT EDSVASC ARG-297;
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.