Gene Variant Detail

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Gene TP53
Variant F212fs
Impact List frameshift
Protein Effect loss of function - predicted
Gene Variant Descriptions TP53 F212fs results in a change in the amino acid sequence of the Tp53 protein beginning at 212 of 393, likely resulting in premature truncation of the functional protein (UniProt.org). F212fs has not been biochemically characterized however, due to the effects of truncation mutations downstream of F212 (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 F212fs

TP53 mutant TP53 inact mut TP53 F212fs

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Transcript NM_000546.6
gDNA chr17:g.(7674897_7674898)
cDNA c.(634_633)
Protein p.F212fs
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_000546 chr17:g.7674894_7674895delGA c.636_637delTC p.F212fs*3 RefSeq GRCh38/hg38
NM_000546.5 chr17:g.(7674897_7674898) c.(634_633) p.F212fs RefSeq GRCh38/hg38
NM_001126112.3 chr17:g.(7674897_7674898) c.(634_633) p.F212fs RefSeq GRCh38/hg38
NM_001126114.2 chr17:g.(7674897_7674898) c.(634_633) p.F212fs RefSeq GRCh38/hg38
NM_001407264.1 chr17:g.(7674897_7674898) c.(634_633) p.F212fs RefSeq GRCh38/hg38
NM_001126113.2 chr17:g.(7674897_7674898) c.(634_633) p.F212fs RefSeq GRCh38/hg38
NM_001126113 chr17:g.7674894_7674895delGA c.636_637delTC p.F212fs*3 RefSeq GRCh38/hg38
NM_001407262.1 chr17:g.(7674897_7674898) c.(634_633) p.F212fs RefSeq GRCh38/hg38
NM_001126113.3 chr17:g.(7674897_7674898) c.(634_633) p.F212fs RefSeq GRCh38/hg38
NM_001407266.1 chr17:g.(7674897_7674898) c.(634_633) p.F212fs RefSeq GRCh38/hg38
NM_001126112 chr17:g.7674894_7674895delGA c.636_637delTC p.F212fs*3 RefSeq GRCh38/hg38
NM_001126112.2 chr17:g.(7674897_7674898) c.(634_633) p.F212fs RefSeq GRCh38/hg38
NM_001407268.1 chr17:g.(7674897_7674898) c.(634_633) p.F212fs RefSeq GRCh38/hg38
NM_001126114 chr17:g.7674894_7674895delGA c.636_637delTC p.F212fs*3 RefSeq GRCh38/hg38
NM_001126114.3 chr17:g.(7674897_7674898) c.(634_633) p.F212fs RefSeq GRCh38/hg38
NM_001407270.1 chr17:g.(7674897_7674898) c.(634_633) p.F212fs RefSeq GRCh38/hg38
NM_000546.6 chr17:g.(7674897_7674898) c.(634_633) p.F212fs RefSeq GRCh38/hg38

Filtering

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  • Use quotes to match on a longer phrase with spaces (i.e. "mtor c1483f")

Sorting

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Clinical Trial Phase Therapies Title Recruitment Status Covered Countries Other Countries