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Gene | TP53 |
Variant | N235D |
Impact List | missense |
Protein Effect | loss of function |
Gene Variant Descriptions | TP53 N235D lies within the DNA binding domain and the HIPK1, ZNF385A, FBXO42 and AXIN1 interaction region of the Tp53 protein (UniProt.org). N235D results in decreased Tp53 transactivation activity and fails to suppress colony formation in cell culture (PMID: 25584008). |
Associated Drug Resistance | |
Category Variants Paths |
TP53 mutant TP53 exon7 TP53 N235D TP53 mutant TP53 inact mut TP53 N235D |
Transcript | NM_000546.6 |
gDNA | chr17:g.7674260T>C |
cDNA | c.703A>G |
Protein | p.N235D |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_001407266.1 | chr17:g.7674260T>C | c.703A>G | p.N235D | RefSeq | GRCh38/hg38 |
NM_001126113 | chr17:g.7674260T>C | c.703A>G | p.N235D | RefSeq | GRCh38/hg38 |
NM_000546.5 | chr17:g.7674260T>C | c.703A>G | p.N235D | RefSeq | GRCh38/hg38 |
NM_001126112.2 | chr17:g.7674260T>C | c.703A>G | p.N235D | RefSeq | GRCh38/hg38 |
NM_001126112 | chr17:g.7674260T>C | c.703A>G | p.N235D | RefSeq | GRCh38/hg38 |
NM_001407268.1 | chr17:g.7674260T>C | c.703A>G | p.N235D | RefSeq | GRCh38/hg38 |
NM_001407264.1 | chr17:g.7674260T>C | c.703A>G | p.N235D | RefSeq | GRCh38/hg38 |
NM_001126112.3 | chr17:g.7674260T>C | c.703A>G | p.N235D | RefSeq | GRCh38/hg38 |
NM_001126113.3 | chr17:g.7674260T>C | c.703A>G | p.N235D | RefSeq | GRCh38/hg38 |
NM_001407270.1 | chr17:g.7674260T>C | c.703A>G | p.N235D | RefSeq | GRCh38/hg38 |
NM_000546 | chr17:g.7674260T>C | c.703A>G | p.N235D | RefSeq | GRCh38/hg38 |
NM_001126114.3 | chr17:g.7674260T>C | c.703A>G | p.N235D | RefSeq | GRCh38/hg38 |
NM_001407262.1 | chr17:g.7674260T>C | c.703A>G | p.N235D | RefSeq | GRCh38/hg38 |
NM_001126114 | chr17:g.7674260T>C | c.703A>G | p.N235D | RefSeq | GRCh38/hg38 |
NM_001126114.2 | chr17:g.7674260T>C | c.703A>G | p.N235D | RefSeq | GRCh38/hg38 |
NM_001126113.2 | chr17:g.7674260T>C | c.703A>G | p.N235D | RefSeq | GRCh38/hg38 |
NM_000546.6 | chr17:g.7674260T>C | c.703A>G | p.N235D | RefSeq | GRCh38/hg38 |
Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
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