Gene Variant Detail

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Gene TP53
Variant R158fs
Impact List frameshift
Protein Effect loss of function - predicted
Gene Variant Descriptions TP53 R158fs results in a change in the amino acid sequence of the Tp53 protein beginning at 158 of 393, likely resulting in premature truncation of the functional protein (UniProt.org). R158fs has not been biochemically characterized however, due to the effects of truncation mutations downstream of R158 (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 R158fs

TP53 mutant TP53 inact mut TP53 R158fs

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Transcript NM_000546.6
gDNA chr17:g.(7675140_7675141)
cDNA c.(472_471)
Protein p.R158fs
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_001407270.1 chr17:g.(7675140_7675141) c.(472_471) p.R158fs RefSeq GRCh38/hg38
NM_001126116.2 chr17:g.(7673752_7673753) c.(472_471) p.R158fs RefSeq GRCh38/hg38
NM_001126112.2 chr17:g.(7675140_7675141) c.(472_471) p.R158fs RefSeq GRCh38/hg38
NM_001126114 chr17:g.7675137_7675140delCGCG c.473_476delGCGC p.R158fs*11 RefSeq GRCh38/hg38
NM_000546.5 chr17:g.(7675140_7675141) c.(472_471) p.R158fs RefSeq GRCh38/hg38
NM_001126115.2 chr17:g.(7673752_7673753) c.(472_471) p.R158fs RefSeq GRCh38/hg38
NM_001126112 chr17:g.7675137_7675140delCGCG c.473_476delGCGC p.R158fs*11 RefSeq GRCh38/hg38
NM_001126113 chr17:g.7675137_7675140delCGCG c.473_476delGCGC p.R158fs*11 RefSeq GRCh38/hg38
NM_001126116 chr17:g.7673751_7673752insTACGGGGGGGGGGGGGGGGGGGGGGGGGGGA c.472_473insTCCCCCCCCCCCCCCCCCCCCCCCCCCCGTA p.R158fs*11 RefSeq GRCh38/hg38
NM_001407266.1 chr17:g.(7675140_7675141) c.(472_471) p.R158fs RefSeq GRCh38/hg38
NM_001407268.1 chr17:g.(7675140_7675141) c.(472_471) p.R158fs RefSeq GRCh38/hg38
NM_001126113.3 chr17:g.(7675140_7675141) c.(472_471) p.R158fs RefSeq GRCh38/hg38
NM_001126117.1 chr17:g.(7673752_7673753) c.(472_471) p.R158fs RefSeq GRCh38/hg38
NM_000546.6 chr17:g.(7675140_7675141) c.(472_471) p.R158fs RefSeq GRCh38/hg38
NM_001126115.1 chr17:g.(7673752_7673753) c.(472_471) p.R158fs RefSeq GRCh38/hg38
NM_001407264.1 chr17:g.(7675140_7675141) c.(472_471) p.R158fs RefSeq GRCh38/hg38
NM_001126114.2 chr17:g.(7675140_7675141) c.(472_471) p.R158fs RefSeq GRCh38/hg38
NM_001126112.3 chr17:g.(7675140_7675141) c.(472_471) p.R158fs RefSeq GRCh38/hg38
NM_001126114.3 chr17:g.(7675140_7675141) c.(472_471) p.R158fs RefSeq GRCh38/hg38
NM_001126115 chr17:g.7673751_7673752insTACGGGGGGGGGGGGGGGGGGGGGGGGGGGA c.472_473insTCCCCCCCCCCCCCCCCCCCCCCCCCCCGTA p.R158fs*11 RefSeq GRCh38/hg38
NM_001407262.1 chr17:g.(7675140_7675141) c.(472_471) p.R158fs RefSeq GRCh38/hg38
NM_000546 chr17:g.7675137_7675140delCGCG c.473_476delGCGC p.R158fs*11 RefSeq GRCh38/hg38
NM_001126117 chr17:g.7673751_7673752insTACGGGGGGGGGGGGGGGGGGGGGGGGGGGA c.472_473insTCCCCCCCCCCCCCCCCCCCCCCCCCCCGTA p.R158fs*11 RefSeq GRCh38/hg38
NM_001126117.2 chr17:g.(7673752_7673753) c.(472_471) p.R158fs RefSeq GRCh38/hg38
NM_001126116.1 chr17:g.(7673752_7673753) c.(472_471) p.R158fs RefSeq GRCh38/hg38
NM_001126113.2 chr17:g.(7675140_7675141) c.(472_471) p.R158fs RefSeq GRCh38/hg38

Filtering

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  • Use simple literal full or partial string matches
  • Separate multiple filter terms with a space. Any order may be used (i. e. a b c and c b a are equivalent )
  • Filtering will only apply to rows that are already loaded on the page. Filtering has no impact on query parameters.
  • Use quotes to match on a longer phrase with spaces (i.e. "mtor c1483f")

Sorting

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