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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot P02766: Variant p.Tyr136Ser

Transthyretin
Gene: TTR
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Variant information Variant position: help 136 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 Tyrosine (Y) to Serine (S) at position 136 (Y136S, p.Tyr136Ser). 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 aromatic (Y) to small size and polar (S) 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 AMYL-TTR; amyloid polyneuropathy. Any additional useful information about the variant.
Other resources: help Links to websites of interest for the variant.


Sequence information Variant position: help 136 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 147 The length of the canonical sequence.
Location on the sequence: help TANDSGPRRYTIAALLSPYS Y STTAVVTNPKE 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                         TANDSGPRRYTIAALLSPYSYSTTAVVTNPKE---

Chimpanzee                    TANDSGPRRYTIAALLSPYSYSTTAVVTIPKE

Mouse                         TANDSGHRHYTIAALLSPYSYSTTAVVSNPQN

Rat                           TANDSGHRHYTIAALLSPYSYSTTAVVSNPQN

Pig                           TANDSGRRHYTIAALLSPYSYSTTALVSSPKE

Bovine                        TANDSGPRHYTIAALLSPYSYSTTALVSSPKA

Rabbit                        TANDSGHRSYTIAALLSPFSYSTTAVVSNPQE

Sheep                         TANDSGLRHYTIAALLSPYSYSTTALVSSPKE

Chicken                       TANDSGHRHYTIAALLSPFSYSTTAVVSDPQE

Xenopus laevis                TANDAGHRHYTIAVLLTPYSFSSTAIVSEPHD

Xenopus tropicalis            SANDAGHRHYTIAVLLTPYSISSTAVVSEPHD

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 21 – 147 Transthyretin
Binding site 137 – 137
Glycosylation 118 – 118 N-linked (GlcNAc...) asparagine
Mutagenesis 130 – 130 L -> M. Loss of tetramerization; when associated with M-107.
Beta strand 135 – 143



Literature citations
New transthyretin variants Ser 91 and Ser 116 associated with familial amyloidotic polyneuropathy.
Misrahi A.M.; Plante V.; Lalu T.; Serre I.; Adams D.; Lacroix D.C.; Said G.;
Hum. Mutat. 12:71-71(1998)
Cited for: VARIANTS AMYL-TTR SER-111 AND SER-136;
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.