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Gene TP53
Variant R282W
Impact List missense
Protein Effect loss of function
Gene Variant Descriptions TP53 R282W is a hotspot mutation that lies within the DNA binding domain of the Tp53 protein (PMID: 22713868). R282W results in increased proliferation, migration, invasion, and protein stability and altered subcellular localization in culture (PMID: 37030635), decreased activation of Tp53 target genes, leads to resistance to apoptosis and failure of G1arrest in culture (PMID: 31395785), and additionally acquires neomorphic DNA binding sites (PMID: 31395785), inhibits Ampk signaling, leading to invasive growth and altered cell metabolism in culture and promotes tumor development in mouse models (PMID: 24857548).
Associated Drug Resistance
Category Variants Paths

TP53 mutant TP53 exon8 TP53 R282W

TP53 mutant TP53 inact mut TP53 R282W

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Transcript NM_000546.6
gDNA chr17:g.7673776G>A
cDNA c.844C>T
Protein p.R282W
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_001407266.1 chr17:g.7673776G>A c.844C>T p.R282W RefSeq GRCh38/hg38
NM_001126113.3 chr17:g.7673776G>A c.844C>T p.R282W RefSeq GRCh38/hg38
NM_000546.6 chr17:g.7673776G>A c.844C>T p.R282W RefSeq GRCh38/hg38
NM_000546 chr17:g.7673776G>A c.844C>T p.R282W RefSeq GRCh38/hg38
NM_001126113 chr17:g.7673776G>A c.844C>T p.R282W RefSeq GRCh38/hg38
NM_001126112.3 chr17:g.7673776G>A c.844C>T p.R282W RefSeq GRCh38/hg38
NM_001126113.2 chr17:g.7673776G>A c.844C>T p.R282W RefSeq GRCh38/hg38
NM_001126112 chr17:g.7673776G>A c.844C>T p.R282W RefSeq GRCh38/hg38
NM_001407268.1 chr17:g.7673776G>A c.844C>T p.R282W RefSeq GRCh38/hg38
NM_001126114 chr17:g.7673776G>A c.844C>T p.R282W RefSeq GRCh38/hg38
NM_001407264.1 chr17:g.7673776G>A c.844C>T p.R282W RefSeq GRCh38/hg38
NM_001126114.3 chr17:g.7673776G>A c.844C>T p.R282W RefSeq GRCh38/hg38
NM_000546.5 chr17:g.7673776G>A c.844C>T p.R282W RefSeq GRCh38/hg38
NM_001407262.1 chr17:g.7673776G>A c.844C>T p.R282W RefSeq GRCh38/hg38
NM_001407270.1 chr17:g.7673776G>A c.844C>T p.R282W RefSeq GRCh38/hg38
NM_001126112.2 chr17:g.7673776G>A c.844C>T p.R282W RefSeq GRCh38/hg38
NM_001126114.2 chr17:g.7673776G>A c.844C>T p.R282W RefSeq GRCh38/hg38

Filtering

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  • Separate multiple filter terms with a space. Any order may be used (i. e. a b c and c b a are equivalent )
  • Filtering will only apply to rows that are already loaded on the page. Filtering has no impact on query parameters.
  • Use quotes to match on a longer phrase with spaces (i.e. "mtor c1483f")

Sorting

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  • Click on any column header arrows to sort by that column
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Molecular Profile Indication/Tumor Type Response Type Therapy Name Approval Status Evidence Type Efficacy Evidence References