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| Gene | TP53 |
| Variant | P151H |
| Impact List | missense |
| Protein Effect | loss of function |
| Gene Variant Descriptions | TP53 P151H lies within the DNA binding domain of the Tp53 protein (PMID: 22713868). P151H confers a loss of function to the Tp53 protein as demonstrated by decreased transactivation of select Tp53 targets and inability to repress autophagy in cell culture (PMID: 22673234, PMID: 18818522, PMID: 27533082). |
| Associated Drug Resistance | |
| Category Variants Paths |
TP53 mutant TP53 exon5 TP53 P151H TP53 mutant TP53 inact mut TP53 P151H |
| Transcript | NM_000546.6 |
| gDNA | chr17:g.7675160G>T |
| cDNA | c.452C>A |
| Protein | p.P151H |
| Source Database | RefSeq |
| Genome Build | GRCh38/hg38 |
| Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
|---|---|---|---|---|---|
| NM_001276761.3 | chr17:g.7674962G>T | c.452C>A | p.P151H | RefSeq | GRCh38/hg38 |
| NM_001126114.3 | chr17:g.7675160G>T | c.452C>A | p.P151H | RefSeq | GRCh38/hg38 |
| NM_001126118.1 | chr17:g.7674962G>T | c.452C>A | p.P151H | RefSeq | GRCh38/hg38 |
| NM_001126112.3 | chr17:g.7675160G>T | c.452C>A | p.P151H | RefSeq | GRCh38/hg38 |
| NM_001126118 | chr17:g.7674962G>T | c.452C>A | p.P151H | RefSeq | GRCh38/hg38 |
| NM_001276761.1 | chr17:g.7674962G>T | c.452C>A | p.P151H | RefSeq | GRCh38/hg38 |
| NM_001126113.2 | chr17:g.7675160G>T | c.452C>A | p.P151H | RefSeq | GRCh38/hg38 |
| NM_001407267.1 | chr17:g.7674962G>T | c.452C>A | p.P151H | RefSeq | GRCh38/hg38 |
| NM_001126114 | chr17:g.7675160G>T | c.452C>A | p.P151H | RefSeq | GRCh38/hg38 |
| NM_001276696.1 | chr17:g.7674962G>T | c.452C>A | p.P151H | RefSeq | GRCh38/hg38 |
| NM_001276696.3 | chr17:g.7674962G>T | c.452C>A | p.P151H | RefSeq | GRCh38/hg38 |
| NM_001407265.1 | chr17:g.7674962G>T | c.452C>A | p.P151H | RefSeq | GRCh38/hg38 |
| NM_000546 | chr17:g.7675160G>T | c.452C>A | p.P151H | RefSeq | GRCh38/hg38 |
| NM_000546.6 | chr17:g.7675160G>T | c.452C>A | p.P151H | RefSeq | GRCh38/hg38 |
| NM_001126113 | chr17:g.7675160G>T | c.452C>A | p.P151H | RefSeq | GRCh38/hg38 |
| NM_001276760.3 | chr17:g.7674962G>T | c.452C>A | p.P151H | RefSeq | GRCh38/hg38 |
| NM_001276695.3 | chr17:g.7674962G>T | c.452C>A | p.P151H | RefSeq | GRCh38/hg38 |
| NM_001276696 | chr17:g.7674962G>T | c.452C>A | p.P151H | RefSeq | GRCh38/hg38 |
| NM_001126118.2 | chr17:g.7674962G>T | c.452C>A | p.P151H | RefSeq | GRCh38/hg38 |
| NM_001407266.1 | chr17:g.7675160G>T | c.452C>A | p.P151H | RefSeq | GRCh38/hg38 |
| NM_001126112.2 | chr17:g.7675160G>T | c.452C>A | p.P151H | RefSeq | GRCh38/hg38 |
| NM_001276695 | chr17:g.7674962G>T | c.452C>A | p.P151H | RefSeq | GRCh38/hg38 |
| NM_001126113.3 | chr17:g.7675160G>T | c.452C>A | p.P151H | RefSeq | GRCh38/hg38 |
| NM_001407268.1 | chr17:g.7675160G>T | c.452C>A | p.P151H | RefSeq | GRCh38/hg38 |
| NM_001407263.1 | chr17:g.7674962G>T | c.452C>A | p.P151H | RefSeq | GRCh38/hg38 |
| NM_001276760 | chr17:g.7674962G>T | c.452C>A | p.P151H | RefSeq | GRCh38/hg38 |
| NM_001126112 | chr17:g.7675160G>T | c.452C>A | p.P151H | RefSeq | GRCh38/hg38 |
| NM_001407271.1 | chr17:g.7674962G>T | c.452C>A | p.P151H | RefSeq | GRCh38/hg38 |
| NM_001407264.1 | chr17:g.7675160G>T | c.452C>A | p.P151H | RefSeq | GRCh38/hg38 |
| NM_001407270.1 | chr17:g.7675160G>T | c.452C>A | p.P151H | RefSeq | GRCh38/hg38 |
| NM_001407269.1 | chr17:g.7674962G>T | c.452C>A | p.P151H | RefSeq | GRCh38/hg38 |
| NM_001126114.2 | chr17:g.7675160G>T | c.452C>A | p.P151H | RefSeq | GRCh38/hg38 |
| NM_001276760.1 | chr17:g.7674962G>T | c.452C>A | p.P151H | RefSeq | GRCh38/hg38 |
| NM_001276695.1 | chr17:g.7674962G>T | c.452C>A | p.P151H | RefSeq | GRCh38/hg38 |
| NM_000546.5 | chr17:g.7675160G>T | c.452C>A | p.P151H | RefSeq | GRCh38/hg38 |
| NM_001407262.1 | chr17:g.7675160G>T | c.452C>A | p.P151H | RefSeq | GRCh38/hg38 |
| NM_001276761 | chr17:g.7674962G>T | c.452C>A | p.P151H | RefSeq | GRCh38/hg38 |
| Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
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