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Gene | TP53 |
Variant | C277F |
Impact List | missense |
Protein Effect | loss of function |
Gene Variant Descriptions | TP53 C277F lies within the DNA-binding domain of the Tp53 protein (UniProt.org). C277F results in decreased DNA binding, reduced activation of Tp53 target genes, and reduced growth suppression activity in cultured cells (PMID: 12034820, PMID: 19850740, PMID: 18524770). |
Associated Drug Resistance | |
Category Variants Paths |
TP53 mutant TP53 exon8 TP53 C277F TP53 mutant TP53 inact mut TP53 C277F |
Transcript | NM_000546.6 |
gDNA | chr17:g.7673790C>A |
cDNA | c.830G>T |
Protein | p.C277F |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_001126113 | chr17:g.7673790C>A | c.830G>T | p.C277F | RefSeq | GRCh38/hg38 |
NM_001407264.1 | chr17:g.7673790C>A | c.830G>T | p.C277F | RefSeq | GRCh38/hg38 |
NM_001407266.1 | chr17:g.7673790C>A | c.830G>T | p.C277F | RefSeq | GRCh38/hg38 |
NM_001126114.2 | chr17:g.7673790C>A | c.830G>T | p.C277F | RefSeq | GRCh38/hg38 |
NM_001126113.2 | chr17:g.7673790C>A | c.830G>T | p.C277F | RefSeq | GRCh38/hg38 |
NM_001126112 | chr17:g.7673790C>A | c.830G>T | p.C277F | RefSeq | GRCh38/hg38 |
NM_000546 | chr17:g.7673790C>A | c.830G>T | p.C277F | RefSeq | GRCh38/hg38 |
NM_001407262.1 | chr17:g.7673790C>A | c.830G>T | p.C277F | RefSeq | GRCh38/hg38 |
NM_000546.6 | chr17:g.7673790C>A | c.830G>T | p.C277F | RefSeq | GRCh38/hg38 |
NM_001126114 | chr17:g.7673790C>A | c.830G>T | p.C277F | RefSeq | GRCh38/hg38 |
NM_001126114.3 | chr17:g.7673790C>A | c.830G>T | p.C277F | RefSeq | GRCh38/hg38 |
NM_001126112.2 | chr17:g.7673790C>A | c.830G>T | p.C277F | RefSeq | GRCh38/hg38 |
NM_001407270.1 | chr17:g.7673790C>A | c.830G>T | p.C277F | RefSeq | GRCh38/hg38 |
NM_001126112.3 | chr17:g.7673790C>A | c.830G>T | p.C277F | RefSeq | GRCh38/hg38 |
NM_000546.5 | chr17:g.7673790C>A | c.830G>T | p.C277F | RefSeq | GRCh38/hg38 |
NM_001407268.1 | chr17:g.7673790C>A | c.830G>T | p.C277F | RefSeq | GRCh38/hg38 |
NM_001126113.3 | chr17:g.7673790C>A | c.830G>T | p.C277F | RefSeq | GRCh38/hg38 |
Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
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