Variant position: 113 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 559 The length of the canonical sequence.
Location on the sequence:
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: The multiple alignment of the region surrounding the variant against various orthologous sequences.
Human PEFVDNTQVPSYCLNARGEG AVRKILLCLANQFPDISFCPA
Mouse PEFVDNTQVPTYCLNTRGEG AVRKILLCIANQFPDISFCPA
Bovine PEFVDNTQVPSYCLNSKGEG AVRKILLCISNQFPDVSFCPA
Xenopus laevis PEFVDDRQIPSYSLNSEGTG AVRKIISCISNQFPDISFCPA
Xenopus tropicalis PEFVDDRQIPSYCLNSEGIG AVRKIITCISNQFPDISFCPA
Sequence annotation in neighborhood: 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.
Type Positions Description
1 – 559 TBC1 domain family member 24
47 – 262 Rab-GAP TBC
Clinical intrafamilial variability in lethal familial neonatal seizure disorder caused by TBC1D24 mutations.
Lozano R.; Herman K.; Rothfuss M.; Rieger H.; Bayrak-Toydemir P.; Aprile D.; Fruscione F.; Zara F.; Fassio A.;
Am. J. Med. Genet. A 170:3207-3214(2016)
Cited for: VARIANTS DEE16 ASP-113 AND PRO-159;
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.