Gene Variant Detail

Contact

Missing content? – Request curation!

Request curation for specific Genes, Variants, or PubMed publications.

Have questions, comments, or suggestions? - Let us know!

Email us at : ckbsupport@genomenon.com

Gene TP53
Variant R267W
Impact List missense
Protein Effect loss of function
Gene Variant Descriptions TP53 R267W lies within the DNA-binding domain of the Tp53 protein (PMID: 15510160). R267W results in decreased Tp53 transcription activity in a reporter assay, reduced DNA binding, and attenuated ability to induce apoptosis in cell culture (PMID: 24076587).
Associated Drug Resistance
Category Variants Paths

TP53 mutant TP53 exon8 TP53 R267W

TP53 mutant TP53 inact mut TP53 R267W

Filtering

  • Case insensitive filtering will display rows if any text in any cell matches the filter term
  • Use simple literal full or partial string matches
  • 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

  • Generally, the default sort order for tables is set to be first column ascending; however, specific tables may set a different default sort order.
  • Click on any column header arrows to sort by that column
  • Hold down the Shift key and click multiple columns to sort by more than one column. Be sure to set ascending or descending order for a given column before moving on to the next column.

Transcript NM_000546.6
gDNA chr17:g.7673821G>A
cDNA c.799C>T
Protein p.R267W
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_001276696.3 chr17:g.7673702_7673704delCGAinsTGG c.799_801delCGAinsTGG p.R267W RefSeq GRCh38/hg38
NM_001126113.2 chr17:g.7673821G>A c.799C>T p.R267W RefSeq GRCh38/hg38
NM_001126114.2 chr17:g.7673821G>A c.799C>T p.R267W RefSeq GRCh38/hg38
NM_001407263.1 chr17:g.7673702_7673704delCGAinsTGG c.799_801delCGAinsTGG p.R267W RefSeq GRCh38/hg38
NM_001126112 chr17:g.7673821G>A c.799C>T p.R267W RefSeq GRCh38/hg38
NM_001126113 chr17:g.7673821G>A c.799C>T p.R267W RefSeq GRCh38/hg38
NM_001407270.1 chr17:g.7673821G>A c.799C>T p.R267W RefSeq GRCh38/hg38
NM_001276695 chr17:g.7673702_7673704delTCGinsCCA c.799_801delCGAinsTGG p.R267W RefSeq GRCh38/hg38
NM_001126118.1 chr17:g.7673702_7673704delCGAinsTGG c.799_801delCGAinsTGG p.R267W RefSeq GRCh38/hg38
NM_001407266.1 chr17:g.7673821G>A c.799C>T p.R267W RefSeq GRCh38/hg38
NM_001276696.1 chr17:g.7673702_7673704delCGAinsTGG c.799_801delCGAinsTGG p.R267W RefSeq GRCh38/hg38
NM_001276695.3 chr17:g.7673702_7673704delCGAinsTGG c.799_801delCGAinsTGG p.R267W RefSeq GRCh38/hg38
NM_001407265.1 chr17:g.7673702_7673704delCGAinsTGG c.799_801delCGAinsTGG p.R267W RefSeq GRCh38/hg38
NM_001276761 chr17:g.7673702_7673704delTCGinsCCA c.799_801delCGAinsTGG p.R267W RefSeq GRCh38/hg38
NM_001276695.1 chr17:g.7673702_7673704delCGAinsTGG c.799_801delCGAinsTGG p.R267W RefSeq GRCh38/hg38
NM_001276761.3 chr17:g.7673702_7673704delCGAinsTGG c.799_801delCGAinsTGG p.R267W RefSeq GRCh38/hg38
NM_001126112.3 chr17:g.7673821G>A c.799C>T p.R267W RefSeq GRCh38/hg38
NM_001126113.3 chr17:g.7673821G>A c.799C>T p.R267W RefSeq GRCh38/hg38
NM_000546.5 chr17:g.7673821G>A c.799C>T p.R267W RefSeq GRCh38/hg38
NM_001407267.1 chr17:g.7673702_7673704delCGAinsTGG c.799_801delCGAinsTGG p.R267W RefSeq GRCh38/hg38
NM_001276760.1 chr17:g.7673702_7673704delCGAinsTGG c.799_801delCGAinsTGG p.R267W RefSeq GRCh38/hg38
NM_001126118.2 chr17:g.7673702_7673704delCGAinsTGG c.799_801delCGAinsTGG p.R267W RefSeq GRCh38/hg38
NM_001407271.1 chr17:g.7673702_7673704delCGAinsTGG c.799_801delCGAinsTGG p.R267W RefSeq GRCh38/hg38
NM_001276760 chr17:g.7673702_7673704delTCGinsCCA c.799_801delCGAinsTGG p.R267W RefSeq GRCh38/hg38
NM_001276696 chr17:g.7673702_7673704delTCGinsCCA c.799_801delCGAinsTGG p.R267W RefSeq GRCh38/hg38
NM_001126118 chr17:g.7673702_7673704delTCGinsCCA c.799_801delCGAinsTGG p.R267W RefSeq GRCh38/hg38
NM_001407262.1 chr17:g.7673821G>A c.799C>T p.R267W RefSeq GRCh38/hg38
NM_001407269.1 chr17:g.7673702_7673704delCGAinsTGG c.799_801delCGAinsTGG p.R267W RefSeq GRCh38/hg38
NM_001276760.3 chr17:g.7673702_7673704delCGAinsTGG c.799_801delCGAinsTGG p.R267W RefSeq GRCh38/hg38
NM_000546 chr17:g.7673821G>A c.799C>T p.R267W RefSeq GRCh38/hg38
NM_001126114 chr17:g.7673821G>A c.799C>T p.R267W RefSeq GRCh38/hg38
NM_000546.6 chr17:g.7673821G>A c.799C>T p.R267W RefSeq GRCh38/hg38
NM_001126114.3 chr17:g.7673821G>A c.799C>T p.R267W RefSeq GRCh38/hg38
NM_001276761.1 chr17:g.7673702_7673704delCGAinsTGG c.799_801delCGAinsTGG p.R267W RefSeq GRCh38/hg38
NM_001407268.1 chr17:g.7673821G>A c.799C>T p.R267W RefSeq GRCh38/hg38
NM_001407264.1 chr17:g.7673821G>A c.799C>T p.R267W RefSeq GRCh38/hg38
NM_001126112.2 chr17:g.7673821G>A c.799C>T p.R267W RefSeq GRCh38/hg38

Filtering

  • Case insensitive filtering will display rows if any text in any cell matches the filter term
  • Use simple literal full or partial string matches
  • 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

  • Generally, the default sort order for tables is set to be first column ascending; however, specific tables may set a different default sort order.
  • Click on any column header arrows to sort by that column
  • Hold down the Shift key and click multiple columns to sort by more than one column. Be sure to set ascending or descending order for a given column before moving on to the next column.

Clinical Trial Phase Therapies Title Recruitment Status Covered Countries Other Countries