EGFR (p.R108G)

Variant Data

Location

  • HGVS: ENST00000275493:c.322A>G
  • Reference Version: GRCh37
  • Chromosome: 7
  • Start: 55211079
  • Stop: 55211079
  • Strand: 1
  • Transcript: ENST00000275493 (ensembl - 74_37)
  • Gene: EGFR ( View drug interactions on DGIdb )

Information

  • Reference: A
  • Variant: G
  • Amino Acid: p.R108G
  • Mutation Type: missense
  • Variant Type: SNV (SO:0001483)
  • cDNA Change: c.322
  • Tags: likely pathogenic