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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot Q92823: Variant p.Gly1116Val

Neuronal cell adhesion molecule
Gene: NRCAM
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Variant information Variant position: help 1116 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 Glycine (G) to Valine (V) at position 1116 (G1116V, p.Gly1116Val). 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 hydrophobic (V) 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 a breast cancer sample; somatic mutation. Any additional useful information about the variant.


Sequence information Variant position: help 1116 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 1304 The length of the canonical sequence.
Location on the sequence: help FYVEYGVAGSKEEWRKEIVN G SRSFFGLKGLMPGTAYKVRV 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                         FYVEYGVAGSKEEWRKEIVNGSRSFFGLKGLMPGTAYKVRV

Mouse                         ---------GKEEWRKEIVNGSRSFFGLKGLMPGTAYKVRV

Rat                           -----------------------------------------

Chicken                       FYVEYGVAGSKEDWKKEIVNGSRSFFVLKGLTPGTAYKVRV

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 25 – 1304 Neuronal cell adhesion molecule
Topological domain 25 – 1167 Extracellular
Domain 1064 – 1156 Fibronectin type-III 5
Glycosylation 1115 – 1115 N-linked (GlcNAc...) asparagine
Alternative sequence 1051 – 1155 Missing. In isoform 3 and isoform 4.
Alternative sequence 1063 – 1155 Missing. In isoform 6.



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] PRO-1093 AND VAL-1116;
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.