Gene Variant Detail

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Gene TP53
Variant C176F
Impact List missense
Protein Effect loss of function - predicted
Gene Variant Descriptions TP53 C176F lies within the DNA-binding domain of the Tp53 protein (PMID: 22713868). C176F results in similar mitotic rate and apoptotic activity as wild-type Tp53 but decreased tumor initiation and proliferation in a zebrafish model also expressing KRAS G12D (PMID: 37266578), results in the inability to induce CDKN1A (p21) transcription in cell culture (PMID: 22090360), and leads to increased proliferation, migration, invasion, and Tp53 protein stability in culture (PMID: 37030635), and therefore, is predicted to lead to a loss of Tp53 protein function.
Associated Drug Resistance
Category Variants Paths

TP53 mutant TP53 exon5 TP53 C176F

TP53 mutant TP53 inact mut TP53 C176F

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Transcript NM_000546.6
gDNA chr17:g.7675085C>A
cDNA c.527G>T
Protein p.C176F
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_000546.6 chr17:g.7675085C>A c.527G>T p.C176F RefSeq GRCh38/hg38
NM_001407264.1 chr17:g.7675085C>A c.527G>T p.C176F RefSeq GRCh38/hg38
NM_001126113 chr17:g.7675085C>A c.527G>T p.C176F RefSeq GRCh38/hg38
NM_001126114.2 chr17:g.7675085C>A c.527G>T p.C176F RefSeq GRCh38/hg38
NM_000546 chr17:g.7675085C>A c.527G>T p.C176F RefSeq GRCh38/hg38
NM_001126114.3 chr17:g.7675085C>A c.527G>T p.C176F RefSeq GRCh38/hg38
NM_001407266.1 chr17:g.7675085C>A c.527G>T p.C176F RefSeq GRCh38/hg38
NM_001126114 chr17:g.7675085C>A c.527G>T p.C176F RefSeq GRCh38/hg38
NM_001126113.2 chr17:g.7675085C>A c.527G>T p.C176F RefSeq GRCh38/hg38
NM_001126112.2 chr17:g.7675085C>A c.527G>T p.C176F RefSeq GRCh38/hg38
NM_001407270.1 chr17:g.7675085C>A c.527G>T p.C176F RefSeq GRCh38/hg38
NM_001407262.1 chr17:g.7675085C>A c.527G>T p.C176F RefSeq GRCh38/hg38
NM_001407268.1 chr17:g.7675085C>A c.527G>T p.C176F RefSeq GRCh38/hg38
NM_000546.5 chr17:g.7675085C>A c.527G>T p.C176F RefSeq GRCh38/hg38
NM_001126113.3 chr17:g.7675085C>A c.527G>T p.C176F RefSeq GRCh38/hg38
NM_001126112 chr17:g.7675085C>A c.527G>T p.C176F RefSeq GRCh38/hg38
NM_001126112.3 chr17:g.7675085C>A c.527G>T p.C176F RefSeq GRCh38/hg38

Filtering

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  • 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

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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