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Gene | TP53 |
Variant | R158H |
Impact List | missense |
Protein Effect | loss of function |
Gene Variant Descriptions | TP53 R158H lies within the DNA binding domain of the Tp53 protein (UniProt.org). R158H results in decreased Tp53 transactivation activity and reduced ability to suppress colony formation in cell culture (PMID: 25584008). |
Associated Drug Resistance | |
Category Variants Paths |
TP53 mutant TP53 exon5 TP53 R158H TP53 mutant TP53 inact mut TP53 R158H |
Transcript | NM_000546.6 |
gDNA | chr17:g.7675139C>T |
cDNA | c.473G>A |
Protein | p.R158H |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_001407268.1 | chr17:g.7675139C>T | c.473G>A | p.R158H | RefSeq | GRCh38/hg38 |
NM_001126116.1 | chr17:g.7673751C>T | c.473G>A | p.R158H | RefSeq | GRCh38/hg38 |
NM_001126117.2 | chr17:g.7673751C>T | c.473G>A | p.R158H | RefSeq | GRCh38/hg38 |
NM_000546 | chr17:g.7675139C>T | c.473G>A | p.R158H | RefSeq | GRCh38/hg38 |
NM_001126112.2 | chr17:g.7675139C>T | c.473G>A | p.R158H | RefSeq | GRCh38/hg38 |
NM_001126116 | chr17:g.7673751C>T | c.473G>A | p.R158H | RefSeq | GRCh38/hg38 |
NM_001126116.2 | chr17:g.7673751C>T | c.473G>A | p.R158H | RefSeq | GRCh38/hg38 |
NM_001126114.3 | chr17:g.7675139C>T | c.473G>A | p.R158H | RefSeq | GRCh38/hg38 |
NM_001126112 | chr17:g.7675139C>T | c.473G>A | p.R158H | RefSeq | GRCh38/hg38 |
NM_001126115 | chr17:g.7673751C>T | c.473G>A | p.R158H | RefSeq | GRCh38/hg38 |
NM_001126114 | chr17:g.7675139C>T | c.473G>A | p.R158H | RefSeq | GRCh38/hg38 |
NM_001126113 | chr17:g.7675139C>T | c.473G>A | p.R158H | RefSeq | GRCh38/hg38 |
NM_000546.5 | chr17:g.7675139C>T | c.473G>A | p.R158H | RefSeq | GRCh38/hg38 |
NM_001126115.2 | chr17:g.7673751C>T | c.473G>A | p.R158H | RefSeq | GRCh38/hg38 |
NM_001126115.1 | chr17:g.7673751C>T | c.473G>A | p.R158H | RefSeq | GRCh38/hg38 |
NM_001126113.2 | chr17:g.7675139C>T | c.473G>A | p.R158H | RefSeq | GRCh38/hg38 |
NM_001126117.1 | chr17:g.7673751C>T | c.473G>A | p.R158H | RefSeq | GRCh38/hg38 |
NM_001126112.3 | chr17:g.7675139C>T | c.473G>A | p.R158H | RefSeq | GRCh38/hg38 |
NM_001126113.3 | chr17:g.7675139C>T | c.473G>A | p.R158H | RefSeq | GRCh38/hg38 |
NM_001407270.1 | chr17:g.7675139C>T | c.473G>A | p.R158H | RefSeq | GRCh38/hg38 |
NM_001126117 | chr17:g.7673751C>T | c.473G>A | p.R158H | RefSeq | GRCh38/hg38 |
NM_000546.6 | chr17:g.7675139C>T | c.473G>A | p.R158H | RefSeq | GRCh38/hg38 |
NM_001407264.1 | chr17:g.7675139C>T | c.473G>A | p.R158H | RefSeq | GRCh38/hg38 |
NM_001126114.2 | chr17:g.7675139C>T | c.473G>A | p.R158H | RefSeq | GRCh38/hg38 |
NM_001407262.1 | chr17:g.7675139C>T | c.473G>A | p.R158H | RefSeq | GRCh38/hg38 |
NM_001407266.1 | chr17:g.7675139C>T | c.473G>A | p.R158H | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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