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Gene | VHL |
Variant | Y98N |
Impact List | missense |
Protein Effect | loss of function |
Gene Variant Descriptions | VHL Y98N does not lie within any known functional domains of the Vhl protein (UniProt.org). Y98N confers a loss of function to the Vhl protein as demonstrated by failure to completely suppress Glut1 and defects in Hif1-alpha ubiquitination (PMID: 10823831). |
Associated Drug Resistance | |
Category Variants Paths |
VHL mutant VHL inact mut VHL Y98N |
Transcript | NM_000551.4 |
gDNA | chr3:g.10142139T>A |
cDNA | c.292T>A |
Protein | p.Y98N |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_001354723.2 | chr3:g.10142139T>A | c.292T>A | p.Y98N | RefSeq | GRCh38/hg38 |
NM_198156 | chr3:g.10142139T>A | c.292T>A | p.Y98N | RefSeq | GRCh38/hg38 |
NM_001354723.1 | chr3:g.10142139T>A | c.292T>A | p.Y98N | RefSeq | GRCh38/hg38 |
NM_198156.3 | chr3:g.10142139T>A | c.292T>A | p.Y98N | RefSeq | GRCh38/hg38 |
NM_198156.2 | chr3:g.10142139T>A | c.292T>A | p.Y98N | RefSeq | GRCh38/hg38 |
NM_000551.4 | chr3:g.10142139T>A | c.292T>A | p.Y98N | RefSeq | GRCh38/hg38 |
NM_000551.3 | chr3:g.10142139T>A | c.292T>A | p.Y98N | RefSeq | GRCh38/hg38 |
NM_000551 | chr3:g.10142139T>A | c.292T>A | p.Y98N | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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