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Gene | TP53 |
Variant | R282G |
Impact List | missense |
Protein Effect | loss of function |
Gene Variant Descriptions | TP53 R282G is a hotspot mutation that lies within the DNA-binding domain of the Tp53 protein (PMID: 22713868). R282G results in subcellular localization similar to wild-type in Tp53-null cells, but leads to increased cellular growth rate, decreased transactivation of Tp53 target genes (PMID: 23246812), increased Nek2 expression in cell culture (PMID: 35088582), and reduced apoptotic function in cell culture (PMID: 23246812). |
Associated Drug Resistance | |
Category Variants Paths |
TP53 mutant TP53 exon8 TP53 R282G TP53 mutant TP53 inact mut TP53 R282G |
Transcript | NM_000546.6 |
gDNA | chr17:g.7673776G>C |
cDNA | c.844C>G |
Protein | p.R282G |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_001126112 | chr17:g.7673776G>C | c.844C>G | p.R282G | RefSeq | GRCh38/hg38 |
NM_001126112.3 | chr17:g.7673776G>C | c.844C>G | p.R282G | RefSeq | GRCh38/hg38 |
NM_000546 | chr17:g.7673776G>C | c.844C>G | p.R282G | RefSeq | GRCh38/hg38 |
NM_001126113 | chr17:g.7673776G>C | c.844C>G | p.R282G | RefSeq | GRCh38/hg38 |
NM_001126113.3 | chr17:g.7673776G>C | c.844C>G | p.R282G | RefSeq | GRCh38/hg38 |
NM_001126114.3 | chr17:g.7673776G>C | c.844C>G | p.R282G | RefSeq | GRCh38/hg38 |
NM_001126112.2 | chr17:g.7673776G>C | c.844C>G | p.R282G | RefSeq | GRCh38/hg38 |
NM_001407264.1 | chr17:g.7673776G>C | c.844C>G | p.R282G | RefSeq | GRCh38/hg38 |
NM_001126114.2 | chr17:g.7673776G>C | c.844C>G | p.R282G | RefSeq | GRCh38/hg38 |
NM_001407262.1 | chr17:g.7673776G>C | c.844C>G | p.R282G | RefSeq | GRCh38/hg38 |
NM_001126113.2 | chr17:g.7673776G>C | c.844C>G | p.R282G | RefSeq | GRCh38/hg38 |
NM_001407270.1 | chr17:g.7673776G>C | c.844C>G | p.R282G | RefSeq | GRCh38/hg38 |
NM_000546.6 | chr17:g.7673776G>C | c.844C>G | p.R282G | RefSeq | GRCh38/hg38 |
NM_001407266.1 | chr17:g.7673776G>C | c.844C>G | p.R282G | RefSeq | GRCh38/hg38 |
NM_001407268.1 | chr17:g.7673776G>C | c.844C>G | p.R282G | RefSeq | GRCh38/hg38 |
NM_000546.5 | chr17:g.7673776G>C | c.844C>G | p.R282G | RefSeq | GRCh38/hg38 |
NM_001126114 | chr17:g.7673776G>C | c.844C>G | p.R282G | RefSeq | GRCh38/hg38 |
Molecular Profile | Protein Effect | Treatment Approaches |
---|---|---|
TP53 R282G | loss of function |