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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot Q07954: Variant p.Arg3760His

Prolow-density lipoprotein receptor-related protein 1
Gene: LRP1
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Variant information Variant position: help 3760 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Type of variant: help US 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 Arginine (R) to Histidine (H) at position 3760 (R3760H, p.Arg3760His). 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 large size and basic (R) to medium size and polar (H) The physico-chemical property of the reference and variant residues and the change implicated.
BLOSUM score: help 0 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 a colorectal cancer sample; somatic mutation. Any additional useful information about the variant.
Other resources: help Links to websites of interest for the variant.


Sequence information Variant position: help 3760 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 4544 The length of the canonical sequence.
Location on the sequence: help HCKDKKEFLCRNQRCLSSSL R CNMFDDCGDGSDEEDCSIDP 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                         HC-KDKKEFLCRNQRCLSSSLRCNMFDDCGDGSDEEDCSIDP

Mouse                         HC-KDKKEFLCRNQRCLSSSLRCNMFDDCGDGSDEEDCSID

Rat                           HC-KDKKEFLCRNQRCLSSSLRCNMFDDCGDGSDEEDCSID

Chicken                       SCSQDKNEFLCENKKCISANLRCNFFDDCGDGSDEKSCSHE

Baker's yeast                 -----------------------------------------

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 20 – 4544 Prolow-density lipoprotein receptor-related protein 1
Chain 20 – 3943 Low-density lipoprotein receptor-related protein 1 515 kDa subunit
Topological domain 20 – 4419 Extracellular
Domain 3739 – 3778 LDL-receptor class A 31
Disulfide bond 3749 – 3767
Alternative sequence 293 – 4544 Missing. In isoform 2.



Literature citations
The consensus coding sequences of human breast and colorectal cancers.
Sjoeblom T.; Jones S.; Wood L.D.; Parsons D.W.; Lin J.; Barber T.D.; Mandelker D.; Leary R.J.; Ptak J.; Silliman N.; Szabo S.; Buckhaults P.; Farrell C.; Meeh P.; Markowitz S.D.; Willis J.; Dawson D.; Willson J.K.V.; Gazdar A.F.; Hartigan J.; Wu L.; Liu C.; Parmigiani G.; Park B.H.; Bachman K.E.; Papadopoulos N.; Vogelstein B.; Kinzler K.W.; Velculescu V.E.;
Science 314:268-274(2006)
Cited for: VARIANTS [LARGE SCALE ANALYSIS] LYS-869 AND HIS-3760;
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.