Variant position: 190 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 ENQSILITGESGAGKTVNTK RVIQYFAVIAAIGDRSKKDQS
Mouse ENQSILITGESGAGKTVNTK RVIQYFAVIAAIGDRSKKDQT
Rat ENQSILITGESGAGKTVNTK RVIQYFAVIAAIGDRSKKDQT
Pig ENQSILITGESGAGKTVNTK RVIQYFAVIAAIGDRSKKEQT
Bovine ENQSILITGESGAGKTVNTK RVIQYFAVIAAIGDRSKKEQA
Horse ENQSILITGESGAGKTVNTK RVIQYFAVIAAIGDRSKKDQT
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.
Familial hypertrophic cardiomyopathy associated with a novel missense mutation affecting the ATP-binding region of the cardiac beta-myosin heavy chain.
Bundgaard H.; Havndrup O.; Andersen P.S.; Larsen L.A.; Brandt N.J.; Vuust J.; Kjeldsen K.; Christiansen M.;
J. Mol. Cell. Cardiol. 31:745-750(1999)
Cited for: VARIANT CMH1 THR-190;
Outcome of clinical versus genetic family screening in hypertrophic cardiomyopathy with focus on cardiac beta-myosin gene mutations.
Havndrup O.; Bundgaard H.; Andersen P.S.; Larsen L.A.; Vuust J.; Kjeldsen K.; Christiansen M.;
Cardiovasc. Res. 57:347-357(2003)
Cited for: VARIANTS CMH1 THR-190; MET-320; VAL-390; VAL-601; MET-606; CYS-694; GLU-778 AND GLN-846;
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.