Expasy logo

UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot P20908: Variant p.Ala114Asp

Collagen alpha-1(V) chain
Gene: COL5A1
Feedback?
Variant information Variant position: help 114 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Type of variant: help LB/B 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 Alanine (A) to Aspartate (D) at position 114 (A114D, p.Ala114Asp). 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 small size and hydrophobic (A) to medium size and acidic (D) 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

Other resources: help Links to websites of interest for the variant.


Sequence information Variant position: help 114 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 1838 The length of the canonical sequence.
Location on the sequence: help SAFPEDFSILTTVKAKKGSQ A FLVSIYNEQGIQQIGLELGR 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                         SAFPEDFSILTTVKAKKGSQAFLVSIYNEQGIQQIGLELGR

Mouse                         SGFPEDFSILTTVKAKKGSQAFLVSIYNEQGIQQLGLELGR

Rat                           SDFPEDFSILTTVKAKKGSQAFLVSVYNEQGIQQLGLELGR

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 38 – 1605 Collagen alpha-1(V) chain
Domain 72 – 244 Laminin G-like



Literature citations
The molecular basis of classic Ehlers-Danlos syndrome: a comprehensive study of biochemical and molecular findings in 48 unrelated patients.
Malfait F.; Coucke P.; Symoens S.; Loeys B.; Nuytinck L.; De Paepe A.;
Hum. Mutat. 25:28-37(2005)
Cited for: VARIANTS EDSCL1 SER-530 AND CYS-1486; VARIANTS ASP-114; ASN-192 AND SER-951; A novel recurrent COL5A1 genetic variant is associated with a dysplasia-associated arterial disease exhibiting dissections and fibromuscular dysplasia.
Richer J.; Hill H.L.; Wang Y.; Yang M.L.; Hunker K.L.; Lane J.; Blackburn S.; Coleman D.M.; Eliason J.; Sillon G.; D'Agostino M.D.; Jetty P.; Mongeon F.P.; Laberge A.M.; Ryan S.E.; Fendrikova-Mahlay N.; Coutinho T.; Mathis M.R.; Zawistowski M.; Hazen S.L.; Katz A.E.; Gornik H.L.; Brummett C.M.; Abecasis G.; Bergin I.L.; Stanley J.C.; Li J.Z.; Ganesh S.K.;
Arterioscler. Thromb. Vasc. Biol. 40:2686-2699(2020)
Cited for: VARIANT ASP-114; VARIANTS FMDMF GLU-123; SER-514; TRP-611; LEU-1164 AND SER-1400; INVOLVEMENT IN FMDMF;
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.