Gene Variant Detail

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Gene TP53
Variant T118fs
Impact List frameshift
Protein Effect loss of function - predicted
Gene Variant Descriptions TP53 T118fs results in a change in the amino acid sequence of the Tp53 protein beginning at aa 118 of 393, likely resulting in premature truncation of the functional protein (UniProt.org). T118fs has not been biochemically characterized however, due to the effects of truncation mutations downstream of T118 (PMID: 31081129, PMID: 34045312), is predicted to lead to a loss of Tp53 protein function.
Associated Drug Resistance
Category Variants Paths

TP53 mutant TP53 exon4 TP53 T118fs

TP53 mutant TP53 inact mut TP53 T118fs

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Transcript NM_000546.6
gDNA chr17:g.(7676017_7676018)
cDNA c.(352_351)
Protein p.T118fs
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_001407266.1 chr17:g.(7676017_7676018) c.(352_351) p.T118fs RefSeq GRCh38/hg38
NM_001126112.2 chr17:g.(7676017_7676018) c.(352_351) p.T118fs RefSeq GRCh38/hg38
NM_001126112 chr17:g.(7676017_7676018) c.(352_351) p.T118fs RefSeq GRCh38/hg38
NM_001126114.3 chr17:g.(7676017_7676018) c.(352_351) p.T118fs RefSeq GRCh38/hg38
NM_001126114 chr17:g.(7676017_7676018) c.(352_351) p.T118fs RefSeq GRCh38/hg38
NM_000546.5 chr17:g.(7676017_7676018) c.(352_351) p.T118fs RefSeq GRCh38/hg38
NM_001126113 chr17:g.(7676017_7676018) c.(352_351) p.T118fs RefSeq GRCh38/hg38
NM_001126113.3 chr17:g.(7676017_7676018) c.(352_351) p.T118fs RefSeq GRCh38/hg38
NM_000546.6 chr17:g.(7676017_7676018) c.(352_351) p.T118fs RefSeq GRCh38/hg38
NM_001126114.2 chr17:g.(7676017_7676018) c.(352_351) p.T118fs RefSeq GRCh38/hg38
NM_001407270.1 chr17:g.(7676017_7676018) c.(352_351) p.T118fs RefSeq GRCh38/hg38
NM_001407268.1 chr17:g.(7676017_7676018) c.(352_351) p.T118fs RefSeq GRCh38/hg38
NM_001126112.3 chr17:g.(7676017_7676018) c.(352_351) p.T118fs RefSeq GRCh38/hg38
NM_001407262.1 chr17:g.(7676017_7676018) c.(352_351) p.T118fs RefSeq GRCh38/hg38
NM_000546 chr17:g.(7676017_7676018) c.(352_351) p.T118fs RefSeq GRCh38/hg38
NM_001126113.2 chr17:g.(7676017_7676018) c.(352_351) p.T118fs RefSeq GRCh38/hg38
NM_001407264.1 chr17:g.(7676017_7676018) c.(352_351) p.T118fs RefSeq GRCh38/hg38

Filtering

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  • Separate multiple filter terms with a space. Any order may be used (i. e. a b c and c b a are equivalent )
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  • Use quotes to match on a longer phrase with spaces (i.e. "mtor c1483f")

Sorting

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  • Click on any column header arrows to sort by that column
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Clinical Trial Phase Therapies Title Recruitment Status Covered Countries Other Countries