PTEN NM_000314.7:c.389G C

Preferred Label : PTEN NM_000314.7:c.389G C;

NCIt synonyms : NM_000314.7:c.389G C; Phosphatase and Tensin Homolog c.389G C; TEP1 c.389G C; MMAC1 c.389G C; PTEN c.389G C; PTEN1 c.389G C; Mutated in Multiple Advanced Cancers 1 c.389G C;

NCIt definition : A nucleotide substitution at position 389 of the coding sequence of the PTEN gene where guanine has been mutated to cytosine.;

NCI Metathesaurus CUI : CL978843;

SNP ID : rs121909229;

Details

Origin ID

C165574;

UMLS CUI

C5237281;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
molecular_abnormality_involves_gene
- PTEN Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

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