BRAF (p.G466R)

Variant Data

Location

  • HGVS: ENST00000288602:c.1396G>A
  • Reference Version: GRCh37
  • Chromosome: 7
  • Start: 140481412
  • Stop: 140481412
  • Strand: -1
  • Transcript: ENST00000288602 (ensembl - 74_37)
  • Gene: BRAF ( View drug interactions on DGIdb )

Information

  • Reference: C
  • Variant: T
  • Amino Acid: p.G466R
  • Mutation Type: missense
  • Variant Type: SNV (SO:0001483)
  • cDNA Change: c.1396
  • Tags: likely pathogenic

Disease Data

Disease Source Batch Tags External Links
ovarian cancer MacConaill et al., 2014, J Mol Diagn Oncomap Variants (View variants) likely pathogenic