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Gene TP53
Variant R333Vfs*12
Impact List frameshift
Protein Effect loss of function - predicted
Gene Variant Descriptions TP53 R333Vfs*12 indicates a shift in the reading frame starting at amino acid 333 and terminating 12 residues downstream causing a premature truncation of the 393 amino acid Tp53 protein (UniProt.org). R333Vfs*12 has not been biochemically characterized however, due to the effects of truncation mutations downstream of R333 (PMID: 31081129, PMID: 34045312), is predicted to lead to a loss of Tp53 protein function.
Associated Drug Resistance
Category Variants Paths

TP53 mutant TP53 exon10 TP53 R333fs TP53 R333Vfs*12

TP53 mutant TP53 inact mut TP53 R333fs TP53 R333Vfs*12

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Transcript NM_000546.6
gDNA chr17:g.7670713delG
cDNA c.997delC
Protein p.R333Vfs*12
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_001126112 chr17:g.7670713delG c.997delC p.R333Vfs*12 RefSeq GRCh38/hg38
NM_001407264.1 chr17:g.7670713delG c.997delC p.R333Vfs*12 RefSeq GRCh38/hg38
NM_001126112.3 chr17:g.7670713delG c.997delC p.R333Vfs*12 RefSeq GRCh38/hg38
NM_001407266.1 chr17:g.7670713delG c.997delC p.R333Vfs*12 RefSeq GRCh38/hg38
NM_001407262.1 chr17:g.7670713delG c.997delC p.R333Vfs*12 RefSeq GRCh38/hg38
NM_000546.6 chr17:g.7670713delG c.997delC p.R333Vfs*12 RefSeq GRCh38/hg38
NM_000546.5 chr17:g.7670713delG c.997delC p.R333Vfs*12 RefSeq GRCh38/hg38
NM_000546 chr17:g.7670713delG c.997delC p.R333Vfs*12 RefSeq GRCh38/hg38
NM_001126112.2 chr17:g.7670713delG c.997delC p.R333Vfs*12 RefSeq GRCh38/hg38

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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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Clinical Trial Phase Therapies Title Recruitment Status Covered Countries Other Countries