HRAS NM_005343.3:c.35_36delinsAT

Preferred Label : HRAS NM_005343.3:c.35_36delinsAT;

NCIt synonyms : H-ras c.35_36delGCinsAT; RASH1 c.35_36GC AT; NM_005343.3:c.35_36GC AT; RASH1 c.35_36delGCinsAT; Ha-ras c.35_36delGCinsAT; H-ras c.35_36GC AT; v-Ha-ras Harvey Rat Sarcoma Viral Oncogene Homolog c.35_36GC AT; HRAS c.35_36GC AT; C-H-RAS c.35_36delGCinsAT; HRAS1 c.35_36delGCinsAT; C-HA-RAS1 c.35_36delGCinsAT; Harvey Rat Sarcoma Viral Oncogene Homolog c.35_36delGCinsAT; HRAS c.35_36delGCinsAT; v-Ha-ras Harvey Rat Sarcoma Viral Oncogene Homolog c.35_36delGCinsAT; Ha-ras c.35_36GC AT; HRas Proto-Oncogene, GTPase c.35_36GC AT; NM_005343.3:c.35_36delGCinsAT; HRAS NM_005343.3:c.35_36GC AT; HRas Proto-Oncogene, GTPase c.35_36delGCinsAT; C-HA-RAS1 c.35_36GC AT; Harvey Rat Sarcoma Viral Oncogene Homolog c.35_36GC AT; C-H-RAS c.35_36GC AT; HRAS1 c.35_36GC AT; NM_005343.3:c.35_36delinsAT;

NCIt related terms : HRAS NM_005343.3:c.35_36delGCinsAT;

NCIt definition : A complex substitution where the nucleotide sequence at positions 35 and 36 of the coding sequence of the HRAS gene has changed from guanine-cytosine to adenine-thymine.;

NCI Metathesaurus CUI : CL935996;

SNP ID : rs727503094;

Détails

Origin ID

C156887;

UMLS CUI

C4745147;

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]
molecular_abnormality_involves_gene
- HRAS Gene [NCIt concept]

Position du mot-clé dans l'(les) arborescence(s) :

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