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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 |
| Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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