Missing content? – Request curation!
Request curation for specific Genes, Variants, or PubMed publications.
Have questions, comments, or suggestions? - Let us know!
Email us at : ckbsupport@genomenon.com
Gene | VHL |
Variant | G93V |
Impact List | missense |
Protein Effect | unknown |
Gene Variant Descriptions | VHL G93V does not lie within any known functional domains of the Vhl protein (UniProt.org). G93V has been identified in the scientific literature (PMID: 24969085, Journal of Clinical Oncology 28, no. 15_suppl e15024), but has not been biochemically characterized and therefore, its effect on Vhl protein function is unknown (PubMed, Apr 2024). |
Associated Drug Resistance | |
Category Variants Paths |
VHL mutant VHL G93V |
Transcript | NM_000551.4 |
gDNA | chr3:g.10142125G>T |
cDNA | c.278G>T |
Protein | p.G93V |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_000551 | chr3:g.10142125G>T | c.278G>T | p.G93V | RefSeq | GRCh38/hg38 |
NM_198156.3 | chr3:g.10142125G>T | c.278G>T | p.G93V | RefSeq | GRCh38/hg38 |
NM_198156.2 | chr3:g.10142125G>T | c.278G>T | p.G93V | RefSeq | GRCh38/hg38 |
NM_198156 | chr3:g.10142125G>T | c.278G>T | p.G93V | RefSeq | GRCh38/hg38 |
NM_001354723.1 | chr3:g.10142125G>T | c.278G>T | p.G93V | RefSeq | GRCh38/hg38 |
NM_000551.3 | chr3:g.10142125G>T | c.278G>T | p.G93V | RefSeq | GRCh38/hg38 |
NM_001354723.2 | chr3:g.10142125G>T | c.278G>T | p.G93V | RefSeq | GRCh38/hg38 |
NM_000551.4 | chr3:g.10142125G>T | c.278G>T | p.G93V | RefSeq | GRCh38/hg38 |
Molecular Profile | Protein Effect | Treatment Approaches |
---|---|---|
VHL G93V | unknown |