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BRAF (p.G464R)

Variant Data

Location

  • HGVS: ENST00000288602:c.1390G>A
  • Reference Version: GRCh37
  • Chromosome: 7
  • Start: 140481418
  • Stop: 140481418
  • Strand: -1
  • Transcript: ENST00000288602 (ensembl - 74_37)
  • Gene: BRAF ( View drug interactions on DGIdb )

Information

  • Reference: C
  • Variant: T
  • Amino Acid: p.G464R
  • Mutation Type: missense
  • Variant Type: SNV (SO:0001483)
  • cDNA Change: c.1390
  • Tags: likely pathogenic

Disease Data

Disease Source Batch Tags External Links
melanoma Carlino et al., 2014, Br. J. Cancer Literature (View variants) likely pathogenic
melanoma MacConaill et al., 2014, J Mol Diagn Oncomap Variants (View variants) likely pathogenic
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