Expasy logo

UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot P16473: Variant p.Arg109Gln

Thyrotropin receptor
Gene: TSHR
Feedback?
Variant information Variant position: help 109 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 Arginine (R) to Glutamine (Q) at position 109 (R109Q, p.Arg109Gln). 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 (Q) 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 CHNG1. Any additional useful information about the variant.


Sequence information Variant position: help 109 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 764 The length of the canonical sequence.
Location on the sequence: help LQQLESHSFYNLSKVTHIEI R NTRNLTYIDPDALKELPLLK 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                         LQQLESHSFYNLSKVTHIEIRNTRNLTYIDPDALKELPLLK

                              LQRLESHSFYNLSKMTHIEIRNTRSLTSIDPDALKELPLLK

Mouse                         LQRLEPHSFYNLSKMTHIEIRNTRSLTYIDPDALTELPLLK

Rat                           LQRLEPHSFYNLSKMTHIEIRNTRSLTYIDPDALTELPLLK

Pig                           LQQLESQSFYNLSKMTHIEIRNTRSLTYINPGALKDLPLLK

Bovine                        LQQLESHSFYNLSKVTHIEIRNTRSLTYIDSGALKELPLLK

Sheep                         LQQLESHSFYNLSKVTHIEIRNTRSLTYIDSGALKELPLLK

Cat                           LQRLESHSFYNLSKMTHIEIRNTRSLTYIDPGALKELPLLK
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 – 764 Thyrotropin receptor
Topological domain 21 – 413 Extracellular
Repeat 100 – 124 LRR 1
Glycosylation 99 – 99 N-linked (GlcNAc...) asparagine
Glycosylation 113 – 113 N-linked (GlcNAc...) asparagine
Beta strand 105 – 111



Literature citations
Two novel mutations in the thyrotropin (TSH) receptor gene in a child with resistance to TSH.
Clifton-Bligh R.J.; Gregory J.W.; Ludgate M.; John R.; Persani L.; Asteria C.; Beck-Peccoz P.; Chatterjee V.K.K.;
J. Clin. Endocrinol. Metab. 82:1094-1100(1997)
Cited for: VARIANT CHNG1 GLN-109;
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.