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 | TP53 |
| Variant | G279Pfs*69 |
| Impact List | frameshift |
| Protein Effect | loss of function - predicted |
| Gene Variant Descriptions | TP53 G279Pfs*69 indicates a shift in the reading frame starting at amino acid 279 and terminating 69 residues downstream causing a premature truncation of the 393 amino acid Tp53 protein (UniProt.org). G279Pfs*69 has not been biochemically characterized however, due to the effects of other truncation mutations downstream of G279 (PMID: 31081129, PMID: 34045312), is predicted to lead to a loss of Tp53 protein function. |
| Associated Drug Resistance | |
| Category Variants Paths |
TP53 mutant TP53 exon8 TP53 G279fs TP53 G279Pfs*69 TP53 mutant TP53 inact mut TP53 G279fs TP53 G279Pfs*69 |
| Transcript | NM_000546.6 |
| gDNA | chr17:g.7673785_7673786insTTTGGGGG |
| cDNA | c.834_835insCCCCCAAA |
| Protein | p.G279Pfs*69 |
| Source Database | RefSeq |
| Genome Build | GRCh38/hg38 |
| Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
|---|---|---|---|---|---|
| NM_000546.5 | chr17:g.7673785_7673786insTTTGGGGG | c.834_835insCCCCCAAA | p.G279Pfs*69 | RefSeq | GRCh38/hg38 |
| NM_001407268.1 | chr17:g.7673785_7673786insTGGGGGGGGGGGGGG | c.834_835insCCCCCCCCCCCCCCA | p.G279Pfs*69 | RefSeq | GRCh38/hg38 |
| NM_001126114.3 | chr17:g.7673785_7673786insTGGGGGGGGGGGGGG | c.834_835insCCCCCCCCCCCCCCA | p.G279Pfs*69 | RefSeq | GRCh38/hg38 |
| NM_001126112.2 | chr17:g.7673785_7673786insTTTGGGGG | c.834_835insCCCCCAAA | p.G279Pfs*69 | RefSeq | GRCh38/hg38 |
| NM_001126114.2 | chr17:g.7673785_7673786insTGGGGGGGGGGGGGG | c.834_835insCCCCCCCCCCCCCCA | p.G279Pfs*69 | RefSeq | GRCh38/hg38 |
| NM_001407262.1 | chr17:g.7673785_7673786insTTTGGGGG | c.834_835insCCCCCAAA | p.G279Pfs*69 | RefSeq | GRCh38/hg38 |
| NM_001126113.3 | chr17:g.7673785_7673786insTTTGGGGGGGGGGG | c.834_835insCCCCCCCCCCCAAA | p.G279Pfs*69 | RefSeq | GRCh38/hg38 |
| NM_001407264.1 | chr17:g.7673785_7673786insTTTGGGGG | c.834_835insCCCCCAAA | p.G279Pfs*69 | RefSeq | GRCh38/hg38 |
| NM_001407270.1 | chr17:g.7673785_7673786insTGGGGGGGGGGGGGG | c.834_835insCCCCCCCCCCCCCCA | p.G279Pfs*69 | RefSeq | GRCh38/hg38 |
| NM_000546.6 | chr17:g.7673785_7673786insTTTGGGGG | c.834_835insCCCCCAAA | p.G279Pfs*69 | RefSeq | GRCh38/hg38 |
| NM_001126113.2 | chr17:g.7673785_7673786insTTTGGGGGGGGGGG | c.834_835insCCCCCCCCCCCAAA | p.G279Pfs*69 | RefSeq | GRCh38/hg38 |
| NM_001407266.1 | chr17:g.7673785_7673786insTTTGGGGG | c.834_835insCCCCCAAA | p.G279Pfs*69 | RefSeq | GRCh38/hg38 |
| NM_001126112.3 | chr17:g.7673785_7673786insTTTGGGGG | c.834_835insCCCCCAAA | p.G279Pfs*69 | RefSeq | GRCh38/hg38 |
| Molecular Profile | Protein Effect | Treatment Approaches |
|---|---|---|
| TP53 G279Pfs*69 | loss of function - predicted |