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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 |
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_001407266.1 | 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 | 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 |
NM_001126112.3 | 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_001407262.1 | 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_001126112 | chr17:g.7670713delG | c.997delC | p.R333Vfs*12 | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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