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 | S65P |
Impact List | missense |
Protein Effect | loss of function |
Gene Variant Descriptions | VHL S65P does not lie within any known functional domains of the Vhl protein (UniProt.org). S65P results in reduced Vhl protein stability and impaired binding to Hif2a, leading to increased Hif2a stability, upregulation of EMT markers, and increased migration and invasion in cell culture (PMID: 35505422). |
Associated Drug Resistance | |
Category Variants Paths |
VHL mutant VHL inact mut VHL S65P |
Transcript | NM_000551.4 |
gDNA | chr3:g.10142040T>C |
cDNA | c.193T>C |
Protein | p.S65P |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_001354723.2 | chr3:g.10142040T>C | c.193T>C | p.S65P | RefSeq | GRCh38/hg38 |
NM_000551.3 | chr3:g.10142040T>C | c.193T>C | p.S65P | RefSeq | GRCh38/hg38 |
NM_198156.3 | chr3:g.10142040T>C | c.193T>C | p.S65P | RefSeq | GRCh38/hg38 |
NM_198156.2 | chr3:g.10142040T>C | c.193T>C | p.S65P | RefSeq | GRCh38/hg38 |
NM_001354723.1 | chr3:g.10142040T>C | c.193T>C | p.S65P | RefSeq | GRCh38/hg38 |
NM_000551.4 | chr3:g.10142040T>C | c.193T>C | p.S65P | RefSeq | GRCh38/hg38 |
Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
---|