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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot P23945: Variant p.Ser128Tyr

Follicle-stimulating hormone receptor
Gene: FSHR
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Variant information Variant position: help 128 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 Serine (S) to Tyrosine (Y) at position 128 (S128Y, p.Ser128Tyr). 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 small size and polar (S) 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 OHSS; displays increase in affinity and sensitivity toward hCG and does not show any constitutive activity nor promiscuous activation by TSH. Any additional useful information about the variant.
Other resources: help Links to websites of interest for the variant.


Sequence information Variant position: help 128 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 695 The length of the canonical sequence.
Location on the sequence: help LLYINPEAFQNLPNLQYLLI S NTGIKHLPDVHKIHSLQKVL 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                         LLYINPEAFQNLPNLQYLLISNTGIKHLPDVHKIHSLQKVL

Mouse                         LLYINPEAFQNLPSLRYLLISNTGIKHLPAFHKIQSLQKVL

Rat                           LLYINPEAFQNLPSLRYLLISNTGIKHLPAVHKIQSLQKVL

Pig                           LLYIDPDAFQNLPNLRYLLISNTGVKHLPAVHKIQSLQKVL

Bovine                        LLYIDPDAFQNLPNLRYLLISNTGIKHLPAVHKIQSLQKVL

Sheep                         LLYIDPDAFQNLPNLRYLLISNTGIKHLPAVHKIQSLQKVL

Cat                           LLYIDTDAFQNLPNLRYLLISNTGIKHFPAVHKIQSLQKVL

Horse                         LLYIDHDAFQNLPNLQYLLISNTGIKHLPAVHKIQSLQKVL

Chicken                       LMKIDQDAFQHLPSLRYLLISNTGLSFLPVVHKVHSFQKVL

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 18 – 695 Follicle-stimulating hormone receptor
Topological domain 18 – 366 Extracellular
Repeat 119 – 143 LRR 4
Beta strand 124 – 130



Literature citations
Identification of the first germline mutation in the extracellular domain of the follitropin receptor responsible for spontaneous ovarian hyperstimulation syndrome.
De Leener A.; Caltabiano G.; Erkan S.; Idil M.; Vassart G.; Pardo L.; Costagliola S.;
Hum. Mutat. 29:91-98(2008)
Cited for: VARIANT OHSS TYR-128; CHARACTERIZATION OF VARIANT OHSS TYR-128;
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.