CTNNB1 (p.G34E)

Variant Data

Location

  • HGVS: ENST00000349496:c.101G>A
  • Reference Version: GRCh37
  • Chromosome: 3
  • Start: 41266104
  • Stop: 41266104
  • Strand: 1
  • Transcript: ENST00000349496 (ensembl - 74_37)
  • Gene: CTNNB1 ( View drug interactions on DGIdb )

Information

  • Reference: G
  • Variant: A
  • Amino Acid: p.G34E
  • Mutation Type: missense
  • Variant Type: SNV (SO:0001483)
  • cDNA Change: c.101
  • Tags: likely pathogenic