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| Gene | TP53 |
| Variant | P191del |
| Impact List | deletion |
| Protein Effect | unknown |
| Gene Variant Descriptions | TP53 P191del results in the deletion of an amino acid in the DNA-binding domain of the Tp53 protein at amino acid 191 (UniProt.org). P191del has been identified in the scientific literature (PMID: 12010886, PMID: 39649724), but has not been biochemically characterized and therefore, its effect on Tp53 protein function is unknown (PubMed, Jul 2025). |
| Associated Drug Resistance | |
| Category Variants Paths |
TP53 mutant TP53 exon6 TP53 P191del |
| Transcript | NM_000546.6 |
| gDNA | chr17:g.7674961_7674963delAGG |
| cDNA | c.572_574delCTC |
| Protein | p.P191del |
| Source Database | RefSeq |
| Genome Build | GRCh38/hg38 |
| Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
|---|---|---|---|---|---|
| NM_001407264.1 | chr17:g.7674961_7674963delAGG | c.572_574delCTC | p.P191del | RefSeq | GRCh38/hg38 |
| NM_001407268.1 | chr17:g.7674961_7674963delAGG | c.572_574delCTC | p.P191del | RefSeq | GRCh38/hg38 |
| NM_001126112.3 | chr17:g.7674961_7674963delAGG | c.572_574delCTC | p.P191del | RefSeq | GRCh38/hg38 |
| NM_001126113.3 | chr17:g.7674961_7674963delAGG | c.572_574delCTC | p.P191del | RefSeq | GRCh38/hg38 |
| NM_001407270.1 | chr17:g.7674961_7674963delAGG | c.572_574delCTC | p.P191del | RefSeq | GRCh38/hg38 |
| NM_001407266.1 | chr17:g.7674961_7674963delAGG | c.572_574delCTC | p.P191del | RefSeq | GRCh38/hg38 |
| NM_001407262.1 | chr17:g.7674961_7674963delAGG | c.572_574delCTC | p.P191del | RefSeq | GRCh38/hg38 |
| NM_001126114.3 | chr17:g.7674961_7674963delAGG | c.572_574delCTC | p.P191del | RefSeq | GRCh38/hg38 |
| NM_000546.6 | chr17:g.7674961_7674963delAGG | c.572_574delCTC | p.P191del | RefSeq | GRCh38/hg38 |
| Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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