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FOXL2 (p.C134W)

Variant Data

Location

  • HGVS: ENST00000330315:c.402C>G
  • Reference Version: GRCh37
  • Chromosome: 3
  • Start: 138665163
  • Stop: 138665163
  • Strand: -1
  • Transcript: ENST00000330315 (ensembl - 74_37)
  • Gene: FOXL2 ( View drug interactions on DGIdb )

Information

  • Reference: G
  • Variant: C (Civic logo View in CIViC)
  • Amino Acid: p.C134W
  • Mutation Type: missense
  • Variant Type: SNV (SO:0001483)
  • cDNA Change: c.402
  • Tags:

Disease Data

Disease Source Batch Tags External Links
granulosa cell tumor Jamieson et al., 2010, Mod. Pathol. CIViC Knowledgebase (View variants) Civic logo CIViC
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