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| Gene | TP53 |
| Variant | R196G |
| Impact List | missense |
| Protein Effect | loss of function - predicted |
| Gene Variant Descriptions | TP53 R196G lies within the DNA-binding domain of the Tp53 protein (PMID: 22713868). R196G is predicted to confer a loss of function to the Tp53 protein, as demonstrated by decreased transactivation activity of Tp53 in culture (PMID: 22710932). |
| Associated Drug Resistance | |
| Category Variants Paths |
TP53 mutant TP53 exon6 TP53 R196G TP53 mutant TP53 inact mut TP53 R196G |
| Transcript | NM_000546.6 |
| gDNA | chr17:g.7674945G>C |
| cDNA | c.586C>G |
| Protein | p.R196G |
| Source Database | RefSeq |
| Genome Build | GRCh38/hg38 |
| Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
|---|---|---|---|---|---|
| NM_001126114.3 | chr17:g.7674945G>C | c.586C>G | p.R196G | RefSeq | GRCh38/hg38 |
| NM_001407262.1 | chr17:g.7674945G>C | c.586C>G | p.R196G | RefSeq | GRCh38/hg38 |
| NM_001407270.1 | chr17:g.7674945G>C | c.586C>G | p.R196G | RefSeq | GRCh38/hg38 |
| NM_000546 | chr17:g.7674945G>C | c.586C>G | p.R196G | RefSeq | GRCh38/hg38 |
| NM_001126112.2 | chr17:g.7674945G>C | c.586C>G | p.R196G | RefSeq | GRCh38/hg38 |
| NM_001126113.3 | chr17:g.7674945G>C | c.586C>G | p.R196G | RefSeq | GRCh38/hg38 |
| NM_001407266.1 | chr17:g.7674945G>C | c.586C>G | p.R196G | RefSeq | GRCh38/hg38 |
| NM_001407264.1 | chr17:g.7674945G>C | c.586C>G | p.R196G | RefSeq | GRCh38/hg38 |
| NM_001126112 | chr17:g.7674945G>C | c.586C>G | p.R196G | RefSeq | GRCh38/hg38 |
| NM_000546.6 | chr17:g.7674945G>C | c.586C>G | p.R196G | RefSeq | GRCh38/hg38 |
| NM_000546.5 | chr17:g.7674945G>C | c.586C>G | p.R196G | RefSeq | GRCh38/hg38 |
| NM_001126113 | chr17:g.7674945G>C | c.586C>G | p.R196G | RefSeq | GRCh38/hg38 |
| NM_001126114 | chr17:g.7674945G>C | c.586C>G | p.R196G | RefSeq | GRCh38/hg38 |
| NM_001407268.1 | chr17:g.7674945G>C | c.586C>G | p.R196G | RefSeq | GRCh38/hg38 |
| NM_001126112.3 | chr17:g.7674945G>C | c.586C>G | p.R196G | RefSeq | GRCh38/hg38 |
| NM_001126113.2 | chr17:g.7674945G>C | c.586C>G | p.R196G | RefSeq | GRCh38/hg38 |
| NM_001126114.2 | chr17:g.7674945G>C | c.586C>G | p.R196G | RefSeq | GRCh38/hg38 |
| Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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