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Gene | TP53 |
Variant | P191fs |
Impact List | frameshift |
Protein Effect | loss of function - predicted |
Gene Variant Descriptions | TP53 P191fs results in a change in the amino acid sequence of the Tp53 protein beginning at aa 191 of 393, likely resulting in premature truncation of the functional protein (UniProt.org). P191fs has not been biochemically characterized however, due to the effects of truncation mutations downstream of P191 (PMID: 31081129, PMID: 34045312), is predicted to lead to a loss of Tp53 protein function. |
Associated Drug Resistance | |
Category Variants Paths |
TP53 mutant TP53 exon6 TP53 P191fs TP53 mutant TP53 inact mut TP53 P191fs |
Transcript | NM_000546.6 |
gDNA | chr17:g.(7674960_7674961) |
cDNA | c.(571_570) |
Protein | p.P191fs |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_000546.6 | chr17:g.(7674960_7674961) | c.(571_570) | p.P191fs | RefSeq | GRCh38/hg38 |
NM_001407264.1 | chr17:g.(7674960_7674961) | c.(571_570) | p.P191fs | RefSeq | GRCh38/hg38 |
NM_001126113.2 | chr17:g.(7674960_7674961) | c.(571_570) | p.P191fs | RefSeq | GRCh38/hg38 |
NM_001407270.1 | chr17:g.(7674960_7674961) | c.(571_570) | p.P191fs | RefSeq | GRCh38/hg38 |
NM_001126113.3 | chr17:g.(7674960_7674961) | c.(571_570) | p.P191fs | RefSeq | GRCh38/hg38 |
NM_001126112.3 | chr17:g.(7674960_7674961) | c.(571_570) | p.P191fs | RefSeq | GRCh38/hg38 |
NM_001407262.1 | chr17:g.(7674960_7674961) | c.(571_570) | p.P191fs | RefSeq | GRCh38/hg38 |
NM_001126112 | chr17:g.(7674960_7674961) | c.(571_570) | p.P191fs | RefSeq | GRCh38/hg38 |
NM_001126114.2 | chr17:g.(7674960_7674961) | c.(571_570) | p.P191fs | RefSeq | GRCh38/hg38 |
NM_001126114.3 | chr17:g.(7674960_7674961) | c.(571_570) | p.P191fs | RefSeq | GRCh38/hg38 |
NM_001126112.2 | chr17:g.(7674960_7674961) | c.(571_570) | p.P191fs | RefSeq | GRCh38/hg38 |
NM_001126113 | chr17:g.(7674960_7674961) | c.(571_570) | p.P191fs | RefSeq | GRCh38/hg38 |
NM_000546.5 | chr17:g.(7674960_7674961) | c.(571_570) | p.P191fs | RefSeq | GRCh38/hg38 |
NM_001407266.1 | chr17:g.(7674960_7674961) | c.(571_570) | p.P191fs | RefSeq | GRCh38/hg38 |
NM_001126114 | chr17:g.(7674960_7674961) | c.(571_570) | p.P191fs | RefSeq | GRCh38/hg38 |
NM_001407268.1 | chr17:g.(7674960_7674961) | c.(571_570) | p.P191fs | RefSeq | GRCh38/hg38 |
NM_000546 | chr17:g.(7674960_7674961) | c.(571_570) | p.P191fs | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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