Variant position: 135 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 213 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 HLWLFRDAGTHDG--LLVNQTE LFVP--------SLNVDGQPIFAN---ITLPV
Mouse HLWLFRDAGTHDG--LLVNQTE LFVP--------SLNVDGQ
Rat HLWLFRDAGTHDG--LLVNQTE LFVP--------SLNVDGQ
Caenorhabditis elegans HPWVARR--SFDGCKVLVNEKE VFWP--------EPAPRMN
Drosophila HSWLFRD--YYTGERMHVRSQR IFQPIRVRVPKSQQSPDQL
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 – 213 von Hippel-Lindau disease tumor suppressor
100 – 155 Involved in binding to CCT complex
114 – 154 Missing. In isoform 2.
Somatic mutations of the von Hippel-Lindau tumor suppressor gene in sporadic central nervous system hemangioblastomas.
Kanno H.; Kondo K.; Ito S.; Yamamoto I.; Fujii S.; Torigoe S.; Sakai N.; Hosaka M.; Shuin T.; Yao M.;
Cancer Res. 54:4845-4847(1994)
Cited for: VARIANT HEMANGIOBLASTOMA PHE-135;
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