Sequence information
Variant position: 1173 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 1390 The length of the canonical sequence.
Location on the sequence:
PLVVLPYMKHGDLRNFIRNE
T HNPTVKDLIGFGLQVAKGMK
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 PLVVLPYMKHGDLRNFIRNET HNPTVKDLIGFGLQVAKGMK
Gorilla PLVVLPYMKHGDLRNFIRNET HNPTVKDLIGFGLQVAKGMK
Chimpanzee PLVVLPYMKHGDLRNFIRNET HNPTVKDLIGFGLQVAKGMK
Mouse PLVVLPYMKHGDLRNFIRNET HNPTVKDLIGFGLQVAKGMK
Rat PLVVLPYMKHGDLRNFIRNET HNPTVKDLIGFGLQVAKGMK
Pig PLVVLPYMKHGDLRNFIRNET HNPTVKDLIGFGLQVAKGMK
Bovine PLVVLPYMKHGDLRNFIRNET HNPTVKDLIGFGLQVAKGME
Rabbit PLVVLPYMKHGDLRNFIRNET HNPTVKDLIGFGLQVAKGMK
Sheep PLVVLPYMKHGDLRNFIRNET HNPTVKDLIGFGLQVAKGME
Cat PLVVLPYMKHGDLRNFIRNET HNPTVKDLIGFGLQVAKGMK
Horse PLVVLPYMKHGDLRNFIRNET HNPTVKDLIGFGLQVAKGMK
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.
Literature citations
Somatic mutations in the kinase domain of the Met/hepatocyte growth factor receptor gene in childhood hepatocellular carcinomas.
Park W.S.; Dong S.M.; Kim S.Y.; Na E.Y.; Shin M.S.; Pi J.H.; Kim B.J.; Bae J.H.; Hong Y.K.; Lee K.S.; Lee S.H.; Yoo N.J.; Jang J.J.; Pack S.; Zhuang Z.; Schmidt L.; Zbar B.; Lee J.Y.;
Cancer Res. 59:307-310(1999)
Cited for: VARIANTS HCC ILE-1173; ARG-1244 AND ILE-1250;
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.