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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot Q8WVM0: Variant p.Ala120Pro

Dimethyladenosine transferase 1, mitochondrial
Gene: TFB1M
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Variant information Variant position: help 120 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Type of variant: help LB/B 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 Alanine (A) to Proline (P) at position 120 (A120P, p.Ala120Pro). 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 hydrophobic (A) to medium size and hydrophobic (P) 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

Other resources: help Links to websites of interest for the variant.


Sequence information Variant position: help 120 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 346 The length of the canonical sequence.
Location on the sequence: help AAPGKLRIVHGDVLTFKVEK A FSESLKRPWEDDPPNVHIIG 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                         AAPG---KLRIVHGDVLTFKVEKAFSESLKRP----WED-DPPNVHIIG

Mouse                         AAPG---KLRIVHGDVLTYKIEKAFPGNIRRQ----WED-D

Rat                           AAPG---KLRIVHGDVLTYKIEKAFPDNIRRQ----WED-D

Bovine                        AAPG---KLRIVHGDVLTFKIERAFPESLKRQ----WED-D

Xenopus laevis                ASGG---KVRTVHGDILTYRMDRAFPKHLIKS----WDD-E

Xenopus tropicalis            ASSG---KVQIVHGDILTYRMDRAFPKHLKKP----WDD-D

Caenorhabditis elegans        AADS---RMFIHHQDALRTEIGDIWKNETARPESVDWHDSN

Drosophila                    CASPLNIQFDIHYDDILRFNIEQHIPDTSQR----------

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 28 – 346 Dimethyladenosine transferase 1, mitochondrial
Binding site 111 – 111



Literature citations
Mitochondrial transcription factors TFA, TFB1 and TFB2: a search for DNA variants/haplotypes and the risk of cardiac hypertrophy.
Alonso-Montes C.; Castro M.G.; Reguero J.R.; Perrot A.; Ozcelik C.; Geier C.; Posch M.G.; Moris C.; Alvarez V.; Ruiz-Ortega M.; Coto E.;
Dis. Markers 25:131-139(2008)
Cited for: VARIANTS PRO-120; ALA-211 AND GLN-256;
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.