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| Gene | VHL |
| Variant | W88L |
| Impact List | missense |
| Protein Effect | loss of function - predicted |
| Gene Variant Descriptions | VHL W88L does not lie within any known functional domains of the Vhl protein (UniProt.org). W88L results in a HIF-dependent growth defect similar to VHL loss in a high-throughput cell culture assay (PMID: 38969834), and therefore, is predicted to lead to a loss of Vhl protein function. |
| Associated Drug Resistance | |
| Category Variants Paths |
VHL mutant VHL inact mut VHL W88L |
| Transcript | NM_000551.4 |
| gDNA | chr3:g.10142110G>T |
| cDNA | c.263G>T |
| Protein | p.W88L |
| Source Database | RefSeq |
| Genome Build | GRCh38/hg38 |
| Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
|---|---|---|---|---|---|
| NM_000551.3 | chr3:g.10142110G>T | c.263G>T | p.W88L | RefSeq | GRCh38/hg38 |
| NM_001354723.1 | chr3:g.10142110G>T | c.263G>T | p.W88L | RefSeq | GRCh38/hg38 |
| NM_198156.3 | chr3:g.10142110G>T | c.263G>T | p.W88L | RefSeq | GRCh38/hg38 |
| NM_001354723.2 | chr3:g.10142110G>T | c.263G>T | p.W88L | RefSeq | GRCh38/hg38 |
| NM_000551.4 | chr3:g.10142110G>T | c.263G>T | p.W88L | RefSeq | GRCh38/hg38 |
| NM_198156 | chr3:g.10142110G>T | c.263G>T | p.W88L | RefSeq | GRCh38/hg38 |
| NM_000551 | chr3:g.10142110G>T | c.263G>T | p.W88L | RefSeq | GRCh38/hg38 |
| NM_198156.2 | chr3:g.10142110G>T | c.263G>T | p.W88L | RefSeq | GRCh38/hg38 |
| Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
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