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Gene | TP53 |
Variant | F212fs |
Impact List | frameshift |
Protein Effect | loss of function - predicted |
Gene Variant Descriptions | TP53 F212fs results in a change in the amino acid sequence of the Tp53 protein beginning at 212 of 393, likely resulting in premature truncation of the functional protein (UniProt.org). F212fs has not been biochemically characterized however, due to the effects of truncation mutations downstream of F212 (PMID: 31081129, PMID: 34045312), is predicted to lead to a loss of Tp53 protein function. |
Associated Drug Resistance | |
Category Variants Paths |
TP53 mutant TP53 exon6 TP53 F212fs TP53 mutant TP53 inact mut TP53 F212fs |
Transcript | NM_000546.6 |
gDNA | chr17:g.(7674897_7674898) |
cDNA | c.(634_633) |
Protein | p.F212fs |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_001126112 | chr17:g.7674894_7674895delGA | c.636_637delTC | p.F212fs*3 | RefSeq | GRCh38/hg38 |
NM_001126113 | chr17:g.7674894_7674895delGA | c.636_637delTC | p.F212fs*3 | RefSeq | GRCh38/hg38 |
NM_000546.6 | chr17:g.(7674897_7674898) | c.(634_633) | p.F212fs | RefSeq | GRCh38/hg38 |
NM_000546 | chr17:g.7674894_7674895delGA | c.636_637delTC | p.F212fs*3 | RefSeq | GRCh38/hg38 |
NM_001126114 | chr17:g.7674894_7674895delGA | c.636_637delTC | p.F212fs*3 | RefSeq | GRCh38/hg38 |
NM_001407270.1 | chr17:g.(7674897_7674898) | c.(634_633) | p.F212fs | RefSeq | GRCh38/hg38 |
NM_001407266.1 | chr17:g.(7674897_7674898) | c.(634_633) | p.F212fs | RefSeq | GRCh38/hg38 |
NM_000546.5 | chr17:g.(7674897_7674898) | c.(634_633) | p.F212fs | RefSeq | GRCh38/hg38 |
NM_001126112.2 | chr17:g.(7674897_7674898) | c.(634_633) | p.F212fs | RefSeq | GRCh38/hg38 |
NM_001126112.3 | chr17:g.(7674897_7674898) | c.(634_633) | p.F212fs | RefSeq | GRCh38/hg38 |
NM_001407264.1 | chr17:g.(7674897_7674898) | c.(634_633) | p.F212fs | RefSeq | GRCh38/hg38 |
NM_001126114.2 | chr17:g.(7674897_7674898) | c.(634_633) | p.F212fs | RefSeq | GRCh38/hg38 |
NM_001126114.3 | chr17:g.(7674897_7674898) | c.(634_633) | p.F212fs | RefSeq | GRCh38/hg38 |
NM_001126113.2 | chr17:g.(7674897_7674898) | c.(634_633) | p.F212fs | RefSeq | GRCh38/hg38 |
NM_001126113.3 | chr17:g.(7674897_7674898) | c.(634_633) | p.F212fs | RefSeq | GRCh38/hg38 |
NM_001407262.1 | chr17:g.(7674897_7674898) | c.(634_633) | p.F212fs | RefSeq | GRCh38/hg38 |
NM_001407268.1 | chr17:g.(7674897_7674898) | c.(634_633) | p.F212fs | RefSeq | GRCh38/hg38 |
Molecular Profile | Protein Effect | Treatment Approaches |
---|---|---|
TP53 F212fs | loss of function - predicted | p53 Gene Therapy |