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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot Q8WYA6: Variant p.Met466Val

Beta-catenin-like protein 1
Gene: CTNNBL1
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Variant information Variant position: help 466 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 Methionine (M) to Valine (V) at position 466 (M466V, p.Met466Val). 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 Similar physico-chemical property. Both residues are medium size and hydrophobic. The physico-chemical property of the reference and variant residues and the change implicated.
BLOSUM score: help 1 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 IMD99; when expressed in a B lymphocyte cell line, leads to decreased frequencies of somatic hypermutations, a process involved in the production of isotype-switched high-affinity antibodies, the defect that can be rescued by the wild-type protein; decrease interaction with AICDA, hence impairs AICDA nuclear localization; may decrease protein stability; no effect on interaction with CDC5L. Any additional useful information about the variant.
Other resources: help Links to websites of interest for the variant.


Sequence information Variant position: help 466 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 563 The length of the canonical sequence.
Location on the sequence: help FKYLGAMQVADKKIEGEKHD M VRRGEIIDNDTEEEFYLRRL 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                         FKYLGAMQVADKKIEGEKH-DMVRRGEIIDNDTEEEFYLRRL

Mouse                         FKYLSAMQVADKKIEGEKH-DIVRRGEIIDNDMEDEFYLRR

Rat                           FKYLGAMQVADKKIEGEKH-DIVRRGEIIDNDMEDEFYLRR

Bovine                        FKYLDAVQVADKKIEGEKH-DMVRRGEIIDNDIEDEFYLRR

Fission yeast                 FKIYDRLRIQLKGIDQSRKLDFSPDSE----EKSTKWFLQQ
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 1 – 563 Beta-catenin-like protein 1
Helix 432 – 469



Literature citations
Disease-associated CTNNBL1 mutation impairs somatic hypermutation by decreasing nuclear AID.
Kuhny M.; Forbes L.R.; Cakan E.; Vega-Loza A.; Kostiuk V.; Dinesh R.K.; Glauzy S.; Stray-Pedersen A.; Pezzi A.E.; Hanson I.C.; Vargas-Hernandez A.; Xu M.L.; Coban-Akdemir Z.H.; Jhangiani S.N.; Muzny D.M.; Gibbs R.A.; Lupski J.R.; Chinn I.K.; Schatz D.G.; Orange J.S.; Meffre E.;
J. Clin. Invest. 130:4411-4422(2020)
Cited for: INVOLVEMENT IN IMD9; VARIANT IMD99 VAL-466; FUNCTION; INTERACTION WITH AICDA AND CDC5L; CHARACTERIZATION OF VARIANT IMD99 VAL-466;
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.