Variant position: 1768 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 1980 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 SYIIISFLIVVNMYIAIILE NFSVATEESADPLSEDDFETF
Mouse SYIIISFLIVVNMYIAIILE NFSVATEESADPLSEDDFETF
Rat SYIIISFLIVVNMYIAIILE NFSVATEESADPLSEDDFETF
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.
de novo pathogenic SCN8A mutation identified by whole-genome sequencing of a family quartet affected by infantile epileptic encephalopathy and SUDEP.
Veeramah K.R.; O'Brien J.E.; Meisler M.H.; Cheng X.; Dib-Hajj S.D.; Waxman S.G.; Talwar D.; Girirajan S.; Eichler E.E.; Restifo L.L.; Erickson R.P.; Hammer M.F.;
Am. J. Hum. Genet. 90:502-510(2012)
Cited for: VARIANT DEE13 ASP-1768; CHARACTERIZATION OF VARIANT DEE13 ASP-1768;
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