EGFR (p.P733L)

Variant Data

Location

  • HGVS: ENST00000275493:c.2198C>T
  • Reference Version: GRCh37
  • Chromosome: 7
  • Start: 55242428
  • Stop: 55242428
  • Strand: 1
  • Transcript: ENST00000275493 (ensembl - 74_37)
  • Gene: EGFR ( View drug interactions on DGIdb )

Information

  • Reference: C
  • Variant: T
  • Amino Acid: p.P733L
  • Mutation Type: missense
  • Variant Type: SNV (SO:0001483)
  • cDNA Change: c.2198
  • Tags: likely pathogenic

Disease Data