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Gene VHL
Variant R167Q
Impact List missense
Protein Effect loss of function
Gene Variant Descriptions VHL R167Q does not lie within any known functional domains of the Vhl protein (UniProt.org). R167Q leads to a loss of Vhl function as indicated by impaired Elongin C binding and inhibition of Hif2a expression in cell culture (PMID: 15574766).
Associated Drug Resistance
Category Variants Paths

VHL mutant VHL inact mut VHL R167Q

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Transcript NM_000551.4
gDNA chr3:g.10149823G>A
cDNA c.500G>A
Protein p.R167Q
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_000551 chr3:g.10149823G>A c.500G>A p.R167Q RefSeq GRCh38/hg38
NM_000551.3 chr3:g.10149823G>A c.500G>A p.R167Q RefSeq GRCh38/hg38
NM_000551.4 chr3:g.10149823G>A c.500G>A p.R167Q RefSeq 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
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Molecular Profile Indication/Tumor Type Response Type Therapy Name Approval Status Evidence Type Efficacy Evidence References