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| Gene | TP53 |
| Variant | H214Qfs*7 |
| Impact List | frameshift |
| Protein Effect | loss of function - predicted |
| Gene Variant Descriptions | TP53 H214Qfs*7 indicates a shift in the reading frame starting at amino acid 214 and terminating 7 residues downstream causing a premature truncation of the 393 amino acid Tp53 protein (UniProt.org). H214Qfs*7 has not been biochemically characterized however, due to the effects of other truncation mutations downstream of H214 (PMID: 31081129, PMID: 34045312), is predicted to lead to a loss of Tp53 protein function. |
| Associated Drug Resistance | |
| Category Variants Paths |
TP53 mutant TP53 exon6 TP53 H214Qfs*7 TP53 mutant TP53 inact mut TP53 H214Qfs*7 |
| Transcript | NM_000546.6 |
| gDNA | chr17:g.7674889_7674890delAT |
| cDNA | c.642_643delTA |
| Protein | p.H214Qfs*7 |
| Source Database | RefSeq |
| Genome Build | GRCh38/hg38 |
| Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
|---|---|---|---|---|---|
| NM_000546.6 | chr17:g.7674889_7674890delAT | c.642_643delTA | p.H214Qfs*7 | RefSeq | GRCh38/hg38 |
| NM_001126114.2 | chr17:g.7674889_7674890delAT | c.642_643delTA | p.H214Qfs*7 | RefSeq | GRCh38/hg38 |
| NM_001407268.1 | chr17:g.7674889_7674890delAT | c.642_643delTA | p.H214Qfs*7 | RefSeq | GRCh38/hg38 |
| NM_000546.5 | chr17:g.7674889_7674890delAT | c.642_643delTA | p.H214Qfs*7 | RefSeq | GRCh38/hg38 |
| NM_001407270.1 | chr17:g.7674889_7674890delAT | c.642_643delTA | p.H214Qfs*7 | RefSeq | GRCh38/hg38 |
| NM_001407266.1 | chr17:g.7674889_7674890delAT | c.642_643delTA | p.H214Qfs*7 | RefSeq | GRCh38/hg38 |
| NM_001126113.2 | chr17:g.7674889_7674890delAT | c.642_643delTA | p.H214Qfs*7 | RefSeq | GRCh38/hg38 |
| NM_001126112.3 | chr17:g.7674889_7674890delAT | c.642_643delTA | p.H214Qfs*7 | RefSeq | GRCh38/hg38 |
| NM_001126112.2 | chr17:g.7674889_7674890delAT | c.642_643delTA | p.H214Qfs*7 | RefSeq | GRCh38/hg38 |
| NM_001126113.3 | chr17:g.7674889_7674890delAT | c.642_643delTA | p.H214Qfs*7 | RefSeq | GRCh38/hg38 |
| NM_001126114.3 | chr17:g.7674889_7674890delAT | c.642_643delTA | p.H214Qfs*7 | RefSeq | GRCh38/hg38 |
| NM_001407262.1 | chr17:g.7674889_7674890delAT | c.642_643delTA | p.H214Qfs*7 | RefSeq | GRCh38/hg38 |
| NM_001407264.1 | chr17:g.7674889_7674890delAT | c.642_643delTA | p.H214Qfs*7 | RefSeq | GRCh38/hg38 |
| Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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