EGFR (p.A289I)

Variant Data

Location

  • HGVS: ENST00000342916:c.865GC>AT
  • Reference Version: GRCh37
  • Chromosome: 7
  • Start: 55221821
  • Stop: 55221822
  • Strand: 1
  • Transcript: ENST00000342916 (ensembl - 74_37)
  • Gene: EGFR ( View drug interactions on DGIdb )

Information

  • Reference: GC
  • Variant: AT
  • Amino Acid: p.A289I
  • Mutation Type: missense
  • Variant Type: DNV (SO:0002007)
  • cDNA Change: c.865
  • Tags: likely pathogenic