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Gene | TP53 |
Variant | R110P |
Impact List | missense |
Protein Effect | loss of function |
Gene Variant Descriptions | TP53 R110P lies within the DNA-binding domain of the Tp53 protein (PMID: 15510160). R110P confers a loss of function on the Tp53 protein as indicated by increased aggregation, including aggregation with Tp63, and Tp73, decreased DNA binding and transactivation of Tp53 targets, and decreased Caspase 3/7 activity in culture (PMID: 21445056, PMID: 24076587). |
Associated Drug Resistance | |
Category Variants Paths |
TP53 mutant TP53 exon4 TP53 R110P TP53 mutant TP53 inact mut TP53 R110P |
Transcript | NM_000546.6 |
gDNA | chr17:g.7676040C>G |
cDNA | c.329G>C |
Protein | p.R110P |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_001126113.3 | chr17:g.7676040C>G | c.329G>C | p.R110P | RefSeq | GRCh38/hg38 |
NM_001126114.3 | chr17:g.7676040C>G | c.329G>C | p.R110P | RefSeq | GRCh38/hg38 |
NM_001407266.1 | chr17:g.7676040C>G | c.329G>C | p.R110P | RefSeq | GRCh38/hg38 |
NM_001407268.1 | chr17:g.7676040C>G | c.329G>C | p.R110P | RefSeq | GRCh38/hg38 |
NM_000546 | chr17:g.7676040C>G | c.329G>C | p.R110P | RefSeq | GRCh38/hg38 |
NM_001126112 | chr17:g.7676040C>G | c.329G>C | p.R110P | RefSeq | GRCh38/hg38 |
NM_001407264.1 | chr17:g.7676040C>G | c.329G>C | p.R110P | RefSeq | GRCh38/hg38 |
NM_001126114 | chr17:g.7676040C>G | c.329G>C | p.R110P | RefSeq | GRCh38/hg38 |
NM_001126112.3 | chr17:g.7676040C>G | c.329G>C | p.R110P | RefSeq | GRCh38/hg38 |
NM_001126113 | chr17:g.7676040C>G | c.329G>C | p.R110P | RefSeq | GRCh38/hg38 |
NM_001126112.2 | chr17:g.7676040C>G | c.329G>C | p.R110P | RefSeq | GRCh38/hg38 |
NM_001407270.1 | chr17:g.7676040C>G | c.329G>C | p.R110P | RefSeq | GRCh38/hg38 |
NM_001126113.2 | chr17:g.7676040C>G | c.329G>C | p.R110P | RefSeq | GRCh38/hg38 |
NM_001126114.2 | chr17:g.7676040C>G | c.329G>C | p.R110P | RefSeq | GRCh38/hg38 |
NM_000546.5 | chr17:g.7676040C>G | c.329G>C | p.R110P | RefSeq | GRCh38/hg38 |
NM_001407262.1 | chr17:g.7676040C>G | c.329G>C | p.R110P | RefSeq | GRCh38/hg38 |
NM_000546.6 | chr17:g.7676040C>G | c.329G>C | p.R110P | RefSeq | GRCh38/hg38 |
Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
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