FGFR2 NP_000132.3:p.V679F

Preferred Label : FGFR2 NP_000132.3:p.V679F;

NCIt synonyms : FGFR2 V564F; Fibroblast Growth Factor Receptor 2 V679F; FGFR2 p.V564F; Keratinocyte Growth Factor Receptor V679F; KGFR Val679Phe; NP_000132.3:p.Val679Phe; FGFR-2 Val679Phe; KGFR V679F; NP_000132.3:p.V679F; CD332 Antigen Val679Phe; FGFR-2 V679F; NP_001138388.1:p.Val564Phe; FGFR2 Val679Phe; FGFR2 p.Val679Phe; FGFR2 Val564Phe; Fibroblast Growth Factor Receptor 2 Val679Phe; FGFR2 p.Val564Phe; NP_001138385.1:p.V564F; CD332 Antigen V679F; Keratinocyte Growth Factor Receptor Val679Phe; FGFR2 NP_000132.3:p.Val679Phe; FGFR2 V679F; FGFR2 p.V679F;

NCIt definition : A change in the amino acid residue at position 679 in the fibroblast growth factor receptor 2 protein where valine has been replaced by phenylalanine.;

NCI Metathesaurus CUI : CL522034;

Details

Origin ID

C134314;

UMLS CUI

C4525146;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
gene_product_sequence_variation_encoded_by_gene_mutant
- FGFR2 Gene Mutation [NCIt concept]
gene_product_variant_of_gene_product
- Fibroblast Growth Factor Receptor 2 [NCIt concept]
molecular_abnormality_involves_gene
- FGFR2 Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

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