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Gene TP53
Variant V157fs
Impact List frameshift
Protein Effect loss of function - predicted
Gene Variant Descriptions TP53 V157fs results in a change in the amino acid sequence of the Tp53 protein beginning at aa 157 of 393, likely resulting in premature truncation of the functional protein (UniProt.org). V157fs results in loss of Tp53 protein expression, and increased proliferation, migration, and invasion in cultured cells (PMID: 33987408), and therefore, is predicted to lead to a loss of Tp53 protein function.
Associated Drug Resistance
Category Variants Paths

TP53 mutant TP53 exon5 TP53 V157fs

TP53 mutant TP53 inact mut TP53 V157fs

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Transcript NM_000546.6
gDNA chr17:g.(7675143_7675144)
cDNA c.(469_468)
Protein p.V157fs
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_001126113.3 chr17:g.(7675143_7675144) c.(469_468) p.V157fs RefSeq GRCh38/hg38
NM_000546.5 chr17:g.(7675143_7675144) c.(469_468) p.V157fs RefSeq GRCh38/hg38
NM_000546.6 chr17:g.(7675143_7675144) c.(469_468) p.V157fs RefSeq GRCh38/hg38
NM_001407268.1 chr17:g.(7675143_7675144) c.(469_468) p.V157fs RefSeq GRCh38/hg38
NM_001407262.1 chr17:g.(7675143_7675144) c.(469_468) p.V157fs RefSeq GRCh38/hg38
NM_001126112.2 chr17:g.(7675143_7675144) c.(469_468) p.V157fs RefSeq GRCh38/hg38
NM_001126113 chr17:g.(7675143_7675144) c.(469_468) p.V157fs RefSeq GRCh38/hg38
NM_001126113.2 chr17:g.(7675143_7675144) c.(469_468) p.V157fs RefSeq GRCh38/hg38
NM_001126114.3 chr17:g.(7675143_7675144) c.(469_468) p.V157fs RefSeq GRCh38/hg38
NM_000546 chr17:g.(7675143_7675144) c.(469_468) p.V157fs RefSeq GRCh38/hg38
NM_001126114.2 chr17:g.(7675143_7675144) c.(469_468) p.V157fs RefSeq GRCh38/hg38
NM_001126114 chr17:g.(7675143_7675144) c.(469_468) p.V157fs RefSeq GRCh38/hg38
NM_001407270.1 chr17:g.(7675143_7675144) c.(469_468) p.V157fs RefSeq GRCh38/hg38
NM_001126112.3 chr17:g.(7675143_7675144) c.(469_468) p.V157fs RefSeq GRCh38/hg38
NM_001407266.1 chr17:g.(7675143_7675144) c.(469_468) p.V157fs RefSeq GRCh38/hg38
NM_001126112 chr17:g.(7675143_7675144) c.(469_468) p.V157fs RefSeq GRCh38/hg38
NM_001407264.1 chr17:g.(7675143_7675144) c.(469_468) p.V157fs 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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Molecular Profile Indication/Tumor Type Response Type Therapy Name Approval Status Evidence Type Efficacy Evidence References