VHL R161P
Gene Variant Detail

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Gene VHL
Variant R161P
Impact List missense
Protein Effect loss of function
Gene Variant Descriptions VHL R161P lies within the Elongin BC complex interaction region of the Vhl protein (UniProt.org). R161P confers a loss of function to the Vhl protein as indicated by loss of binding to the elongin BC complex and destabilization of microtubule in culture (PMID: 10587522, PMID: 20855504).
Associated Drug Resistance
Category Variants Paths

VHL mutant VHL inact mut VHL R161P

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Transcript NM_000551.4
gDNA chr3:g.10149805G>C
cDNA c.482G>C
Protein p.R161P
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_000551.3 chr3:g.10149805G>C c.482G>C p.R161P RefSeq GRCh38/hg38
NM_000551.4 chr3:g.10149805G>C c.482G>C p.R161P RefSeq GRCh38/hg38
NM_000551 chr3:g.10149805G>C c.482G>C p.R161P 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 )
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  • 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