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Gene | VHL |
Variant | C77* |
Impact List | nonsense |
Protein Effect | loss of function - predicted |
Gene Variant Descriptions | VHL C77* results in a premature truncation of the Vhl protein at amino acid 77 of 213 (UniProt.org). C77* has not been characterized, however, due to the effects of other truncation mutations downstream of C77 (PMID: 14691445), is predicted to lead to a loss of Vhl protein function. |
Associated Drug Resistance | |
Category Variants Paths |
VHL mutant VHL inact mut VHL C77* |
Transcript | NM_000551.4 |
gDNA | chr3:g.10142078C>A |
cDNA | c.231C>A |
Protein | p.C77* |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_001354723.1 | chr3:g.10142078C>A | c.231C>A | p.C77* | RefSeq | GRCh38/hg38 |
NM_198156 | chr3:g.10142078C>A | c.231C>A | p.C77* | RefSeq | GRCh38/hg38 |
NM_198156.2 | chr3:g.10142078C>A | c.231C>A | p.C77* | RefSeq | GRCh38/hg38 |
NM_000551.3 | chr3:g.10142078C>A | c.231C>A | p.C77* | RefSeq | GRCh38/hg38 |
NM_000551.4 | chr3:g.10142078C>A | c.231C>A | p.C77* | RefSeq | GRCh38/hg38 |
NM_000551 | chr3:g.10142078C>A | c.231C>A | p.C77* | RefSeq | GRCh38/hg38 |
NM_198156.3 | chr3:g.10142078C>A | c.231C>A | p.C77* | RefSeq | GRCh38/hg38 |
NM_001354723.2 | chr3:g.10142078C>A | c.231C>A | p.C77* | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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