Expasy logo

UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot P45379: Variant p.Arg215Leu

Troponin T, cardiac muscle
Gene: TNNT2
Feedback?
Variant information Variant position: help 215 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 Leucine (L) at position 215 (R215L, p.Arg215Leu). 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 hydrophobic (L) 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 CMD1D. Any additional useful information about the variant.
Other resources: help Links to websites of interest for the variant.


Sequence information Variant position: help 215 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 298 The length of the canonical sequence.
Location on the sequence: help GGYIQKQAQTERKSGKRQTE R EKKKKILAERRKVLAIDHLN 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                         GGYIQKQAQTERKSGKRQTEREKKKKILAERRKVLAIDHLN

Mouse                         GGYIQKQAQTERKSGKRQTEREKKKKILAERRKALAIDHLN

Rat                           GGYIQK-AQTERKSGKRQTEREKKKKILAERRKVLAIDHLN

Bovine                        GGYIQK-AQTERKSGKRQTEREKKKKILAERRKVLAIDHLN

Rabbit                        GGYIQKQAQTERKSGKRQTEREKKKKILAERRKVLAIDHLN

Sheep                         GGYIQK-AQAERKSGKRQTEREKKKKILAERRKVLAIDHLN

Chicken                       GGYMQK---SEKKGGKKQTEREKKKKILSERRKPLNIDHLS
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 2 – 298 Troponin T, cardiac muscle
Region 120 – 219 Disordered
Compositional bias 204 – 219 Basic and acidic residues
Modified residue 204 – 204 Phosphothreonine; by PKC/PRKCA
Modified residue 208 – 208 Phosphoserine; by PKC/PRKCA
Modified residue 213 – 213 Phosphothreonine; by PKC/PRKCA and RAF1
Alternative sequence 201 – 201 Missing. In isoform 5.
Helix 210 – 225



Literature citations
Severe disease expression of cardiac troponin C and T mutations in patients with idiopathic dilated cardiomyopathy.
Mogensen J.; Murphy R.T.; Shaw T.; Bahl A.; Redwood C.; Watkins H.; Burke M.; Elliott P.M.; McKenna W.J.;
J. Am. Coll. Cardiol. 44:2033-2040(2004)
Cited for: VARIANTS CMD1D TRP-141; LEU-215 AND LYS-220 DEL;
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.