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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot P54259: Variant p.His1060Tyr

Atrophin-1
Gene: ATN1
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Variant information Variant position: help 1060 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 Histidine (H) to Tyrosine (Y) at position 1060 (H1060Y, p.His1060Tyr). 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 medium size and polar (H) to large size and aromatic (Y) 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 CHEDDA; the mutation resulted in a perturbation of the structural and functional integrity of the HX repeat; altered zinc-binding properties of the HX repeat. Any additional useful information about the variant.


Sequence information Variant position: help 1060 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 1190 The length of the canonical sequence.
Location on the sequence: help ARLQMLNVTPHHHQHSHIHS H LHLHQQDAIHAASASVHPLI 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.
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 – 1190 Atrophin-1
Region 1049 – 1065 HX repeat



Literature citations
De novo variants disrupting the HX repeat motif of ATN1 cause a recognizable non-progressive neurocognitive syndrome.
Palmer E.E.; Hong S.; Al Zahrani F.; Hashem M.O.; Aleisa F.A.; Ahmed H.M.J.; Kandula T.; Macintosh R.; Minoche A.E.; Puttick C.; Gayevskiy V.; Drew A.P.; Cowley M.J.; Dinger M.; Rosenfeld J.A.; Xiao R.; Cho M.T.; Yakubu S.F.; Henderson L.B.; Guillen Sacoto M.J.; Begtrup A.; Hamad M.; Shinawi M.; Andrews M.V.; Jones M.C.; Lindstrom K.; Bristol R.E.; Kayani S.; Snyder M.; Villanueva M.M.; Schteinschnaider A.; Faivre L.; Thauvin C.; Vitobello A.; Roscioli T.; Kirk E.P.; Bye A.; Merzaban J.; Jaremko L.; Jaremko M.; Sachdev R.K.; Alkuraya F.S.; Arold S.T.;
Am. J. Hum. Genet. 104:542-552(2019)
Cited for: INVOLVEMENT IN CHEDDA; VARIANTS CHEDDA ASN-1054; TYR-1058; 1059-SER-HIS-1060 DELINS ASN-LEU; 1059-SER-HIS-1060 DELINS ASP-LEU; TYR-1060; ARG-1062; ASP-1062 AND ARG-1063; CHARACTERIZATION OF VARIANT CHEDDA TYR-1060; REGION;
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.