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Gene | VHL |
Variant | W117C |
Impact List | missense |
Protein Effect | loss of function |
Gene Variant Descriptions | VHL W117C lies within the CCT complex-binding region of the Vhl protein (UniProt.org). W117C confers a loss of function to the Vhl protein as demonstrated by weak binding with CCT resulting in improper folding of the VHL-elongin BC complex (PMID: 14636579). |
Associated Drug Resistance | |
Category Variants Paths |
VHL mutant VHL inact mut VHL W117C |
Transcript | NM_000551.4 |
gDNA | chr3:g.10146524G>T |
cDNA | c.351G>T |
Protein | p.W117C |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_000551.3 | chr3:g.10146524G>T | c.351G>T | p.W117C | RefSeq | GRCh38/hg38 |
NM_000551.4 | chr3:g.10146524G>T | c.351G>T | p.W117C | RefSeq | GRCh38/hg38 |
NM_000551 | chr3:g.10146524G>T | c.351G>T | p.W117C | RefSeq | GRCh38/hg38 |
Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
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