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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot P40225: Variant p.Arg99Trp

Thrombopoietin
Gene: THPO
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Variant information Variant position: help 99 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 Tryptophan (W) at position 99 (R99W, p.Arg99Trp). 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 large size and aromatic (W) 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 THC9 and CAMT2; likely pathogenic; results in reduced protein secretion. Any additional useful information about the variant.
Other resources: help Links to websites of interest for the variant.


Sequence information Variant position: help 99 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 353 The length of the canonical sequence.
Location on the sequence: help TKAQDILGAVTLLLEGVMAA R GQLGPTCLSSLLGQLSGQVR 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                         TKAQDILGAVTLLLEGVMAARGQLGPTCLSSLLGQLSGQVR

                              TKAQDVWGAVALLLDGVLAARGQLGPSCLSSLLGQLSGQVR

Mouse                         SKAQDILGAVSLLLEGVMAARGQLEPSCLSSLLGQLSGQVR

Rat                           SKAQDILGAVSLLLEGVMAARGQLEPSCLSSLLGQLSGQVR
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 22 – 353 Thrombopoietin
Disulfide bond 28 – 172
Disulfide bond 50 – 106
Turn 99 – 101



Literature citations
Bone marrow failure unresponsive to bone marrow transplant is caused by mutations in thrombopoietin.
Seo A.; Ben-Harosh M.; Sirin M.; Stein J.; Dgany O.; Kaplelushnik J.; Hoenig M.; Pannicke U.; Lorenz M.; Schwarz K.; Stockklausner C.; Walsh T.; Gulsuner S.; Lee M.K.; Sendamarai A.; Sanchez-Bonilla M.; King M.C.; Cario H.; Kulozik A.E.; Debatin K.M.; Schulz A.; Tamary H.; Shimamura A.;
Blood 130:875-880(2017)
Cited for: VARIANTS CAMT2 TRP-99 AND 157-ARG--GLY-353 DEL; Monoallelic loss-of-function THPO variants cause heritable thrombocytopenia.
Cornish N.; Aungraheeta M.R.; FitzGibbon L.; Burley K.; Alibhai D.; Collins J.; Greene D.; Downes K.; Westbury S.K.; Turro E.; Mumford A.D.;
Blood Adv. 4:920-924(2020)
Cited for: VARIANT THC9 TRP-99; CHARACTERIZATION OF VARIANT THC9 TRP-99; SUBCELLULAR LOCATION;
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.