Gene Variant Detail

Contact

Missing content? – Request curation!

Request curation for specific Genes, Variants, or PubMed publications.

Have questions, comments, or suggestions? - Let us know!

Email us at : ckbsupport@genomenon.com

Gene VHL
Variant H110L
Impact List missense
Protein Effect unknown
Gene Variant Descriptions VHL H110L lies within the CCT complex-binding region of the Vhl protein (UniProt.org). H110L has been identified in the scientific literature (PMID: 36329119), but has not been biochemically characterized and therefore, its effect on Vhl protein function is unknown (PubMed, Apr 2024).
Associated Drug Resistance
Category Variants Paths

VHL mutant VHL H110L

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.

Transcript NM_000551.4
gDNA chr3:g.10142176A>T
cDNA c.329A>T
Protein p.H110L
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_001354723.2 chr3:g.10142176A>T c.329A>T p.H110L RefSeq GRCh38/hg38
NM_198156.3 chr3:g.10142176A>T c.329A>T p.H110L RefSeq GRCh38/hg38
NM_000551.3 chr3:g.10142176A>T c.329A>T p.H110L RefSeq GRCh38/hg38
NM_000551.4 chr3:g.10142176A>T c.329A>T p.H110L RefSeq GRCh38/hg38
NM_198156.2 chr3:g.10142176A>T c.329A>T p.H110L RefSeq GRCh38/hg38
NM_001354723.1 chr3:g.10142176A>T c.329A>T p.H110L 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
  • 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.

Molecular Profile Indication/Tumor Type Response Type Therapy Name Approval Status Evidence Type Efficacy Evidence References
VHL H110L colon carcinoma sensitive ARV-771 Preclinical - Cell culture Actionable In a preclinical study, ARV-771 inhibited viability in a colon carcinoma cell line expressing VHL H110L in culture (PMID: 36329119). 36329119