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Gene | HRAS |
Variant | R149Gfs*23 |
Impact List | frameshift |
Protein Effect | loss of function - predicted |
Gene Variant Descriptions | HRAS R149Gfs*23 indicates a shift in the reading frame starting at amino acid 149 and terminating 23 residues downstream causing a premature truncation of the 189 amino acid Hras protein (UniProt.org). R149Gfs*23 has not been biochemically characterized however, due to the loss of the CAXX motif (PMID: 6087162, PMID: 21924373), is predicted to lead to a loss of Hras protein function resulting in inactivation of downstream signaling. |
Associated Drug Resistance | |
Category Variants Paths |
HRAS mutant HRAS inact mut HRAS R149Gfs*23 |
Transcript | NM_005343.4 |
gDNA | chr11:g.533460delG |
cDNA | c.445delC |
Protein | p.R149Gfs*23 |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_001130442.3 | chr11:g.533460delG | c.445delC | p.R149Gfs*23 | RefSeq | GRCh38/hg38 |
NM_005343.3 | chr11:g.533460delG | c.445delC | p.R149Gfs*23 | RefSeq | GRCh38/hg38 |
NM_001130442 | chr11:g.533460delG | c.445delC | p.R149Gfs*23 | RefSeq | GRCh38/hg38 |
NM_176795 | chr11:g.(533458_534325) | c.(445_516) | p.R149Gfs*23 | RefSeq | GRCh38/hg38 |
NM_176795.4 | chr11:g.(533458_534325) | c.(445_516) | p.R149Gfs*23 | RefSeq | GRCh38/hg38 |
NM_005343 | chr11:g.533460delG | c.445delC | p.R149Gfs*23 | RefSeq | GRCh38/hg38 |
NM_005343.4 | chr11:g.533460delG | c.445delC | p.R149Gfs*23 | RefSeq | GRCh38/hg38 |
NM_001130442.2 | chr11:g.533460delG | c.445delC | p.R149Gfs*23 | RefSeq | GRCh38/hg38 |
NM_176795.5 | chr11:g.(533458_534325) | c.(445_516) | p.R149Gfs*23 | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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