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Gene | TP53 |
Variant | Y236F |
Impact List | missense |
Protein Effect | unknown |
Gene Variant Descriptions | TP53 Y236F lies within the DNA-binding domain of the Tp53 protein (PMID: 21760703). Y236F results in reduced DNA-binding affinity compared to wild-type Tp53 when combined with M133L, V203A, and N268D in an in vitro assay (PMID: 25584637), but has not been individually characterized and therefore, its effect on Tp53 protein function is unknown. |
Associated Drug Resistance | |
Category Variants Paths |
TP53 mutant TP53 exon7 TP53 Y236F |
Transcript | NM_000546.6 |
gDNA | chr17:g.7674256T>A |
cDNA | c.707A>T |
Protein | p.Y236F |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_000546.6 | chr17:g.7674256T>A | c.707A>T | p.Y236F | RefSeq | GRCh38/hg38 |
NM_001126113.2 | chr17:g.7674256T>A | c.707A>T | p.Y236F | RefSeq | GRCh38/hg38 |
NM_001126113.3 | chr17:g.7674256T>A | c.707A>T | p.Y236F | RefSeq | GRCh38/hg38 |
NM_001407266.1 | chr17:g.7674256T>A | c.707A>T | p.Y236F | RefSeq | GRCh38/hg38 |
NM_000546.5 | chr17:g.7674256T>A | c.707A>T | p.Y236F | RefSeq | GRCh38/hg38 |
NM_001407268.1 | chr17:g.7674256T>A | c.707A>T | p.Y236F | RefSeq | GRCh38/hg38 |
NM_001407262.1 | chr17:g.7674256T>A | c.707A>T | p.Y236F | RefSeq | GRCh38/hg38 |
NM_001126112 | chr17:g.7674256T>A | c.707A>T | p.Y236F | RefSeq | GRCh38/hg38 |
NM_001126112.3 | chr17:g.7674256T>A | c.707A>T | p.Y236F | RefSeq | GRCh38/hg38 |
NM_001126113 | chr17:g.7674256T>A | c.707A>T | p.Y236F | RefSeq | GRCh38/hg38 |
NM_001126114 | chr17:g.7674256T>A | c.707A>T | p.Y236F | RefSeq | GRCh38/hg38 |
NM_001407270.1 | chr17:g.7674256T>A | c.707A>T | p.Y236F | RefSeq | GRCh38/hg38 |
NM_001407264.1 | chr17:g.7674256T>A | c.707A>T | p.Y236F | RefSeq | GRCh38/hg38 |
NM_001126114.2 | chr17:g.7674256T>A | c.707A>T | p.Y236F | RefSeq | GRCh38/hg38 |
NM_001126114.3 | chr17:g.7674256T>A | c.707A>T | p.Y236F | RefSeq | GRCh38/hg38 |
NM_000546 | chr17:g.7674256T>A | c.707A>T | p.Y236F | RefSeq | GRCh38/hg38 |
NM_001126112.2 | chr17:g.7674256T>A | c.707A>T | p.Y236F | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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