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| Gene | VHL |
| Variant | F91L |
| Impact List | missense |
| Protein Effect | loss of function - predicted |
| Gene Variant Descriptions | VHL F91L does not lie within any known functional domains of the Vhl protein (UniProt.org). F91L results in impaired binding to Hif1a and Hif2a in an in vitro assay (PMID: 31337753), 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 F91L |
| Transcript | NM_000551.4 |
| gDNA | chr3:g.10142118T>C |
| cDNA | c.271T>C |
| Protein | p.F91L |
| Source Database | RefSeq |
| Genome Build | GRCh38/hg38 |
| Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
|---|---|---|---|---|---|
| NM_198156.3 | chr3:g.10142118T>C | c.271T>C | p.F91L | RefSeq | GRCh38/hg38 |
| NM_001354723.2 | chr3:g.10142118T>C | c.271T>C | p.F91L | RefSeq | GRCh38/hg38 |
| NM_001354723.1 | chr3:g.10142118T>C | c.271T>C | p.F91L | RefSeq | GRCh38/hg38 |
| NM_198156.2 | chr3:g.10142118T>C | c.271T>C | p.F91L | RefSeq | GRCh38/hg38 |
| NM_000551 | chr3:g.10142118T>C | c.271T>C | p.F91L | RefSeq | GRCh38/hg38 |
| NM_198156 | chr3:g.10142118T>C | c.271T>C | p.F91L | RefSeq | GRCh38/hg38 |
| NM_000551.4 | chr3:g.10142118T>C | c.271T>C | p.F91L | RefSeq | GRCh38/hg38 |
| NM_000551.3 | chr3:g.10142118T>C | c.271T>C | p.F91L | RefSeq | GRCh38/hg38 |
| Molecular Profile | Protein Effect | Treatment Approaches |
|---|---|---|
| VHL F91L | loss of function - predicted |