VHL C162R - Gene Variant Detail

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Gene VHL
Variant C162R
Impact List missense
Protein Effect unknown
Gene Variant Descriptions VHL C162R lies within the Elongin BC complex-interacting region of the Vhl protein (UniProt.org). C162R has been identified in the scientific literature (PMID: 27530247, PMID: 27034166, PMID: 38619811), but has not been biochemically characterized and therefore, its effect on Vhl protein function is unknown (PubMed, May 2024).
Associated Drug Resistance
Category Variants Paths

VHL mutant VHL C162R

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Transcript NM_000551.4
gDNA chr3:g.10149807T>C
cDNA c.484T>C
Protein p.C162R
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_000551.4 chr3:g.10149807T>C c.484T>C p.C162R RefSeq GRCh38/hg38
NM_000551 chr3:g.10149807T>C c.484T>C p.C162R RefSeq GRCh38/hg38
NM_000551.3 chr3:g.10149807T>C c.484T>C p.C162R 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

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Molecular Profile Indication/Tumor Type Response Type Therapy Name Approval Status Evidence Type Efficacy Evidence References