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Gene TP53
Variant E339*
Impact List nonsense
Protein Effect loss of function - predicted
Gene Variant Descriptions TP53 E339* results in a premature truncation of the Tp53 protein at amino acid 339 of 393 (UniProt.org). E339* has not been biochemically characterized however, due to the effects of truncation mutations downstream of E339 (PMID: 31081129, PMID: 34045312), is predicted to lead to a loss of Tp53 protein function.
Associated Drug Resistance
Category Variants Paths

TP53 mutant TP53 exon10 TP53 E339*

TP53 mutant TP53 inact mut TP53 E339*

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Transcript NM_000546.6
gDNA chr17:g.7670694C>A
cDNA c.1015G>T
Protein p.E339*
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_000546 chr17:g.7670694C>A c.1015G>T p.E339* RefSeq GRCh38/hg38
NM_001126112.2 chr17:g.7670694C>A c.1015G>T p.E339* RefSeq GRCh38/hg38
NM_001407268.1 chr17:g.7673318C>A c.1015G>T p.E339* RefSeq GRCh38/hg38
NM_000546.6 chr17:g.7670694C>A c.1015G>T p.E339* RefSeq GRCh38/hg38
NM_001126112.3 chr17:g.7670694C>A c.1015G>T p.E339* RefSeq GRCh38/hg38
NM_001407270.1 chr17:g.7673318C>A c.1015G>T p.E339* RefSeq GRCh38/hg38
NM_001407262.1 chr17:g.7670694C>A c.1015G>T p.E339* RefSeq GRCh38/hg38
NM_001407266.1 chr17:g.7670694C>A c.1015G>T p.E339* RefSeq GRCh38/hg38
NM_001126112 chr17:g.7670694C>A c.1015G>T p.E339* RefSeq GRCh38/hg38
NM_001126114.2 chr17:g.7673318C>A c.1015G>T p.E339* RefSeq GRCh38/hg38
NM_001126114 chr17:g.7673318C>A c.1015G>T p.E339* RefSeq GRCh38/hg38
NM_001126114.3 chr17:g.7673318C>A c.1015G>T p.E339* RefSeq GRCh38/hg38
NM_000546.5 chr17:g.7670694C>A c.1015G>T p.E339* RefSeq GRCh38/hg38
NM_001407264.1 chr17:g.7670694C>A c.1015G>T p.E339* RefSeq GRCh38/hg38

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