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Gene TP53
Variant H178Tfs*69
Impact List frameshift
Protein Effect loss of function - predicted
Gene Variant Descriptions TP53 H178Tfs*69 indicates a shift in the reading frame starting at amino acid 178 and terminating 69 residues downstream causing a premature truncation of the 393 amino acid Tp53 protein (UniProt.org). H178Tfs*69 has not been biochemically characterized however, due to the effects of truncation mutations downstream of H178 (PMID: 31081129, PMID: 34045312), is predicted to lead to a loss of Tp53 protein function.
Associated Drug Resistance
Category Variants Paths

TP53 mutant TP53 exon5 TP53 H178Tfs*69

TP53 mutant TP53 inact mut TP53 H178Tfs*69

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Transcript NM_000546.6
gDNA chr17:g.7675084delG
cDNA c.532delC
Protein p.H178Tfs*69
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_001126112.2 chr17:g.7675084delG c.532delC p.H178Tfs*69 RefSeq GRCh38/hg38
NM_001407270.1 chr17:g.7675084delG c.532delC p.H178Tfs*69 RefSeq GRCh38/hg38
NM_000546.6 chr17:g.7675084delG c.532delC p.H178Tfs*69 RefSeq GRCh38/hg38
NM_001126113.2 chr17:g.7675084delG c.532delC p.H178Tfs*69 RefSeq GRCh38/hg38
NM_001126114.2 chr17:g.7675084delG c.532delC p.H178Tfs*69 RefSeq GRCh38/hg38
NM_001126112.3 chr17:g.7675084delG c.532delC p.H178Tfs*69 RefSeq GRCh38/hg38
NM_001407262.1 chr17:g.7675084delG c.532delC p.H178Tfs*69 RefSeq GRCh38/hg38
NM_001407268.1 chr17:g.7675084delG c.532delC p.H178Tfs*69 RefSeq GRCh38/hg38
NM_001407264.1 chr17:g.7675084delG c.532delC p.H178Tfs*69 RefSeq GRCh38/hg38
NM_000546.5 chr17:g.7675084delG c.532delC p.H178Tfs*69 RefSeq GRCh38/hg38
NM_001126114.3 chr17:g.7675084delG c.532delC p.H178Tfs*69 RefSeq GRCh38/hg38
NM_001126113.3 chr17:g.7675084delG c.532delC p.H178Tfs*69 RefSeq GRCh38/hg38
NM_001407266.1 chr17:g.7675084delG c.532delC p.H178Tfs*69 RefSeq GRCh38/hg38

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Molecular Profile Indication/Tumor Type Response Type Therapy Name Approval Status Evidence Type Efficacy Evidence References