Variant position: 723 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 1935 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 RICRKGFPNRILYGDFRQRY RILNPAAIPEGQFIDSRKGAE
Mouse RICRKGFPNRILYGDFRQRY RILNPAAIPEGQFIDSRKGAE
Rat RICRKGFPNRILYGDFRQRY RILNPAAIPEGQFIDSRKGAE
Pig RICRKGFPNRILYGDFRQRY RILNPAAIPEGQFIDSRKGAE
Bovine RICRKGFPNRILYGDFRQRY RILNPAAIPEGQFIDSRKGAE
Horse RICRKGFPNRILYGDFRQRY RILNPAAIPEGQFIDSRKGAE
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.
Malignant hypertrophic cardiomyopathy caused by the Arg723Gly mutation in beta-myosin heavy chain gene.
Enjuto M.; Francino A.; Navarro-Lopez F.; Viles D.; Pare J.-C.; Ballesta A.M.;
J. Mol. Cell. Cardiol. 32:2307-2313(2000)
Cited for: VARIANT CMH1 GLY-723;
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