FOXL2 NM_023067.4:c.402C G

Preferred Label : FOXL2 NM_023067.4:c.402C G;

NCIt synonyms : FOXL2 c.402C G; PINTO c.402C G; PFRK c.402C G; NM_023067.4:c.402C G; POF3 c.402C G; Forkhead Box L2 c.402C G;

NCIt definition : A nucleotide substitution at position 402 of the coding sequence of the FOXL2 gene where cytosine has been mutated to guanine.;

NCI Metathesaurus CUI : CL1794143;

SNP ID : rs1057519865;

Details

Origin ID

C189295;

UMLS CUI

C5708350;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
is_molecular_abnormality_of_disease
- FOXL2 c.402C>G (p.Cys134Trp)-Mutant Ovarian Sertoli-Leydig Cell Tumor [NCIt concept]
molecular_abnormality_involves_gene
- FOXL2 Gene [NCIt concept]

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