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 | S111R |
Impact List | missense |
Protein Effect | loss of function |
Gene Variant Descriptions | VHL S111R lies within the CCT complex-binding region of the Vhl protein (UniProt.org). S111R leads to a loss of Vhl function as indicated by impaired binding to Hif1a, p300 and Tip60, and failure to transactivate p53 on DNA damage in cell culture (PMID: 22071692). |
Associated Drug Resistance | |
Category Variants Paths |
VHL mutant VHL inact mut VHL S111R |
Transcript | NM_000551.4 |
gDNA | chr3:g.10142180C>G |
cDNA | c.333C>G |
Protein | p.S111R |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_198156 | chr3:g.10142180C>G | c.333C>G | p.S111R | RefSeq | GRCh38/hg38 |
NM_000551 | chr3:g.10142180C>G | c.333C>G | p.S111R | RefSeq | GRCh38/hg38 |
NM_001354723.1 | chr3:g.10142180C>G | c.333C>G | p.S111R | RefSeq | GRCh38/hg38 |
NM_198156.2 | chr3:g.10142180C>G | c.333C>G | p.S111R | RefSeq | GRCh38/hg38 |
NM_001354723.2 | chr3:g.10142180C>G | c.333C>G | p.S111R | RefSeq | GRCh38/hg38 |
NM_000551.3 | chr3:g.10142180C>G | c.333C>G | p.S111R | RefSeq | GRCh38/hg38 |
NM_198156.3 | chr3:g.10142180C>G | c.333C>G | p.S111R | RefSeq | GRCh38/hg38 |
NM_000551.4 | chr3:g.10142180C>G | c.333C>G | p.S111R | RefSeq | GRCh38/hg38 |
Molecular Profile | Protein Effect | Treatment Approaches |
---|---|---|
VHL S111R | loss of function | mTORC1 Inhibitor VEGFR Inhibitor (Pan) VEGFR2 Inhibitor |