TP53 NM_000546.5:c.843_844delinsTT

Preferred Label : TP53 NM_000546.5:c.843_844delinsTT;

NCIt synonyms : Li-Fraumeni Syndrome c.843_844delCCinsTT; P53 c.843_844delCCinsTT; Tumor Protein p53 c.843_844CC TT; NM_000546.5:c.843_844delCCinsTT; TP53 c.843_844CC TT; LFS1 c.843_844delCCinsTT; LFS1 c.843_844CC TT; TP53 c.843_844delCCinsTT; NM_000546.5:c.843_844CC TT; Tumor Protein p53 c.843_844delCCinsTT; P53 c.843_844CC TT; Li-Fraumeni Syndrome c.843_844CC TT; TP53 NM_000546.5:c.843_844CC TT; NM_000546.5:c.843_844delinsTT; TP53 NM_000546.5:c.843_844delCCinsTT;

NCIt definition : A complex substitution where the nucleotide sequence at positions 843 and 844 of the coding sequence of the TP53 gene has changed from cytosine-cytosine to thymine-thymine.;

NCI Metathesaurus CUI : CL544886;

Details

Origin ID

C146922;

UMLS CUI

C4687571;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
gene_mutant_encodes_gene_product_sequence_variation
- TP53 NP_000537.3:p.R282W [NCIt concept]
- TP53 Protein Variant [NCIt concept]
molecular_abnormality_involves_gene
- TP53 Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

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