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 | HRAS |
Variant | K117N |
Impact List | missense |
Protein Effect | loss of function |
Gene Variant Descriptions | HRAS K117N lies within the GTP binding domain of the Hras protein (UniProt.org). K117N results in decreased nucleotide binding affinity and activation of Hras in culture (PMID: 24247240). |
Associated Drug Resistance | |
Category Variants Paths |
HRAS mutant HRAS act mut HRAS K117N |
Transcript | NM_005343.4 |
gDNA | chr11:g.533552C>G |
cDNA | c.351G>C |
Protein | p.K117N |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_001130442.2 | chr11:g.533552C>G | c.351G>C | p.K117N | RefSeq | GRCh38/hg38 |
NM_176795.4 | chr11:g.533552C>G | c.351G>C | p.K117N | RefSeq | GRCh38/hg38 |
NM_005343.4 | chr11:g.533552C>G | c.351G>C | p.K117N | RefSeq | GRCh38/hg38 |
NM_005343 | chr11:g.533552C>G | c.351G>C | p.K117N | RefSeq | GRCh38/hg38 |
NM_176795 | chr11:g.533552C>G | c.351G>C | p.K117N | RefSeq | GRCh38/hg38 |
NM_001130442 | chr11:g.533552C>G | c.351G>C | p.K117N | RefSeq | GRCh38/hg38 |
NM_176795.5 | chr11:g.533552C>G | c.351G>C | p.K117N | RefSeq | GRCh38/hg38 |
NM_005343.3 | chr11:g.533552C>G | c.351G>C | p.K117N | RefSeq | GRCh38/hg38 |
NM_001130442.3 | chr11:g.533552C>G | c.351G>C | p.K117N | RefSeq | GRCh38/hg38 |
Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
---|