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Gene | TP53 |
Variant | S227Lfs*20 |
Impact List | frameshift |
Protein Effect | loss of function |
Gene Variant Descriptions | TP53 S227Lfs*20 indicates a shift in the reading frame starting at amino acid 227 and terminating 20 residues downstream causing a premature truncation of the 393 amino acid Tp53 protein (UniProt.org). S227Lfs*20 results in caspase-3 induction similar to wild-type Tp53, but confers a loss of function to Tp53 as indicated by failure to induce apoptosis in cultured cells, minimal transactivation activity in a reporter assay, and altered subcellular localization and decreased Puma and Bax expression in cultured cells (PMID: 31081129). |
Associated Drug Resistance | |
Category Variants Paths |
TP53 mutant TP53 exon7 TP53 S227fs TP53 S227Lfs*20 TP53 mutant TP53 inact mut TP53 S227fs TP53 S227Lfs*20 |
Transcript | NM_000546.6 |
gDNA | chr17:g.7674283delG |
cDNA | c.680delC |
Protein | p.S227Lfs*20 |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_001126112.3 | chr17:g.7674283delG | c.680delC | p.S227Lfs*20 | RefSeq | GRCh38/hg38 |
NM_001126112.2 | chr17:g.7674283delG | c.680delC | p.S227Lfs*20 | RefSeq | GRCh38/hg38 |
NM_001126113.3 | chr17:g.7674283delG | c.680delC | p.S227Lfs*20 | RefSeq | GRCh38/hg38 |
NM_000546.5 | chr17:g.7674283delG | c.680delC | p.S227Lfs*20 | RefSeq | GRCh38/hg38 |
NM_001407262.1 | chr17:g.7674283delG | c.680delC | p.S227Lfs*20 | RefSeq | GRCh38/hg38 |
NM_001126114.3 | chr17:g.7674283delG | c.680delC | p.S227Lfs*20 | RefSeq | GRCh38/hg38 |
NM_001407264.1 | chr17:g.7674283delG | c.680delC | p.S227Lfs*20 | RefSeq | GRCh38/hg38 |
NM_001126114.2 | chr17:g.7674283delG | c.680delC | p.S227Lfs*20 | RefSeq | GRCh38/hg38 |
NM_001407266.1 | chr17:g.7674283delG | c.680delC | p.S227Lfs*20 | RefSeq | GRCh38/hg38 |
NM_001126113.2 | chr17:g.7674283delG | c.680delC | p.S227Lfs*20 | RefSeq | GRCh38/hg38 |
NM_000546.6 | chr17:g.7674283delG | c.680delC | p.S227Lfs*20 | RefSeq | GRCh38/hg38 |
NM_001407268.1 | chr17:g.7674283delG | c.680delC | p.S227Lfs*20 | RefSeq | GRCh38/hg38 |
NM_001407270.1 | chr17:g.7674283delG | c.680delC | p.S227Lfs*20 | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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