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Gene TP53
Variant N210Kfs*37
Impact List frameshift
Protein Effect loss of function
Gene Variant Descriptions TP53 N210Kfs*37 indicates a shift in the reading frame starting at amino acid 210 and terminating 37 residues downstream causing a premature truncation of the 393 amino acid Tp53 protein (UniProt.org). N210Kfs*37 is associated with loss of Tp53 expression and increased proliferation in cultured patient-derived cells, and with tumor formation in mouse models (PMID: 32784519), and due to the loss of the oligomerization domain (UniProt.org), is predicted to lead to a loss of Tp53 protein function.
Associated Drug Resistance
Category Variants Paths

TP53 mutant TP53 exon6 TP53 N210Kfs*37

TP53 mutant TP53 inact mut TP53 N210Kfs*37

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Transcript NM_000546.6
gDNA chr17:g.7674901delG
cDNA c.630delC
Protein p.N210Kfs*37
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_001126114.2 chr17:g.7674901delG c.630delC p.N210Kfs*37 RefSeq GRCh38/hg38
NM_001407266.1 chr17:g.7674901delG c.630delC p.N210Kfs*37 RefSeq GRCh38/hg38
NM_001126113.3 chr17:g.7674901delG c.630delC p.N210Kfs*37 RefSeq GRCh38/hg38
NM_001126114.3 chr17:g.7674901delG c.630delC p.N210Kfs*37 RefSeq GRCh38/hg38
NM_001407270.1 chr17:g.7674901delG c.630delC p.N210Kfs*37 RefSeq GRCh38/hg38
NM_001407264.1 chr17:g.7674901delG c.630delC p.N210Kfs*37 RefSeq GRCh38/hg38
NM_001407268.1 chr17:g.7674901delG c.630delC p.N210Kfs*37 RefSeq GRCh38/hg38
NM_000546.5 chr17:g.7674901delG c.630delC p.N210Kfs*37 RefSeq GRCh38/hg38
NM_001126112.2 chr17:g.7674901delG c.630delC p.N210Kfs*37 RefSeq GRCh38/hg38
NM_000546.6 chr17:g.7674901delG c.630delC p.N210Kfs*37 RefSeq GRCh38/hg38
NM_001126113.2 chr17:g.7674901delG c.630delC p.N210Kfs*37 RefSeq GRCh38/hg38
NM_001126112.3 chr17:g.7674901delG c.630delC p.N210Kfs*37 RefSeq GRCh38/hg38
NM_001407262.1 chr17:g.7674901delG c.630delC p.N210Kfs*37 RefSeq GRCh38/hg38

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Sorting

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Clinical Trial Phase Therapies Title Recruitment Status Covered Countries Other Countries