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NRAS NM_002524.4:c.35G>T

MedGen UID:: 1646191
•Concept ID:: C4682811
•: Cell or Molecular Dysfunction

Synonyms:

N-ras c.35G>T; Neuroblastoma RAS Viral (v-ras) Oncogene Homolog c.35G>T; NM_002524.4:c.35G>T; NRAS c.35G>T; NRAS1 c.35G>T

Definition

A nucleotide substitution at position 35 of the coding sequence of the NRAS gene where guanine has been mutated to thymine. [from NCI]

Term Hierarchy

GTR
MeSH

CClinical test, RResearch test, OOMIM, GGeneReviews, VClinVar

CROGVNRAS NM_002524.4:c.35G>T

Molecular Sequence Variation
- Molecular Genetic Variation
  - Gene Abnormality
    - RAS Family Gene Mutation
      - NRAS Gene Mutation
        NRAS Exon 2 Mutation
        NRAS NM_002524.4:c.35G>T

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