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VHL W117C - Gene Variant Detail

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Gene VHL
Variant W117C
Impact List missense
Protein Effect loss of function
Gene Variant Descriptions VHL W117C lies within the CCT complex-binding region of the Vhl protein (UniProt.org). W117C confers a loss of function to the Vhl protein as demonstrated by weak binding with CCT resulting in improper folding of the VHL-elongin BC complex (PMID: 14636579).
Associated Drug Resistance
Category Variants Paths

VHL mutant VHL inact mut VHL W117C

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Transcript NM_000551.4
gDNA chr3:g.10146524G>T
cDNA c.351G>T
Protein p.W117C
Source Database RefSeq
Genome Build GRCh38/hg38

Filtering

  • Case insensitive filtering will display rows if any text in any cell matches the filter term
  • Use simple literal full or partial string matches
  • Separate multiple filter terms with a space. Any order may be used (i. e. a b c and c b a are equivalent )
  • Filtering will only apply to rows that are already loaded on the page. Filtering has no impact on query parameters.
  • Use quotes to match on a longer phrase with spaces (i.e. "mtor c1483f")

Sorting

  • Generally, the default sort order for tables is set to be first column ascending; however, specific tables may set a different default sort order.
  • Click on any column header arrows to sort by that column
  • Hold down the Shift key and click multiple columns to sort by more than one column. Be sure to set ascending or descending order for a given column before moving on to the next column.