PTEN NM_000314.7:c.389G T

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

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

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

NCI Metathesaurus CUI : CL978841;

SNP ID : rs121909229;

Details

Origin ID

C165572;

UMLS CUI

C5237279;

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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