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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot P12883: Variant p.Thr124Ile

Myosin-7
Gene: MYH7
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Variant information Variant position: help 124 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 Threonine (T) to Isoleucine (I) at position 124 (T124I, p.Thr124Ile). 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 (T) to medium size and hydrophobic (I) 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 CMH1. Any additional useful information about the variant.
Other resources: help Links to websites of interest for the variant.


Sequence information Variant position: help 124 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 1935 The length of the canonical sequence.
Location on the sequence: help NLKDRYGSWMIYTYSGLFCV T VNPYKWLPVYTPEVVAAYRG 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                         NLKDRYGSWMIYTYSGLFCVTVNPYKWLPVYTPEVVAAYRG

                              NLKERYASWMIYTYSGLFCVTVNPYKWLPVYNAEVVAAYRG

Mouse                         NLKERYASWMIYTYSGLFCVTVNPYKWLPVYNAEVVAAYRG

Rat                           NLKERYASWMIYTYSGLFCVTVNPYKWLPVYNAQVVAAYRG

Pig                           NLKERYASWMIYTYSGLFCVTINPYKWLPVYNAEVVAAYRG

Bovine                        NLKERYASWMIYTYSGLFCVTINPYKWLPVYNAEVVAAYRG

Horse                         NLKDRYAAWMIYTYSGLFCVTINPYKWLPVYTAEVVAAYRG
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 – 1935 Myosin-7
Domain 85 – 778 Myosin motor
Modified residue 129 – 129 N6,N6,N6-trimethyllysine
Beta strand 121 – 125



Literature citations
Structural interpretation of the mutations in the beta-cardiac myosin that have been implicated in familial hypertrophic cardiomyopathy.
Rayment I.; Holden H.M.; Sellers J.R.; Fananapazir L.; Epstein N.D.;
Proc. Natl. Acad. Sci. U.S.A. 92:3864-3868(1995)
Cited for: VARIANTS CMH1 ILE-124; CYS-162; LYS-187; LYS-222; LEU-244; HIS-663; ASN-782 AND HIS-870;
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.