TP53 NM_000546.5:c.659A G

Preferred Label : TP53 NM_000546.5:c.659A G;

NCIt synonyms : P53 c.659A G; Li-Fraumeni Syndrome c.659A G; Tumor Protein p53 c.659A G; TP53 c.659A G; LFS1 c.659A G; NM_000546.5:c.659A G;

NCIt definition : A nucleotide substitution at position 659 of the coding sequence of the TP53 gene where adenine has been mutated to guanine.;

NCI Metathesaurus CUI : CL544916;

SNP ID : rs121912666;

Details

Origin ID

C146889;

UMLS CUI

C4687542;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
concept_is_in_subset
- CTRP Biomarker Terminology [NCIt concept]
- CTRP Molecular Genetic Biomarker Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
gene_mutant_encodes_gene_product_sequence_variation
- TP53 NP_000537.3:p.Y220C [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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