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HRAS (p.Q61R)

Variant Data

Location

  • HGVS: ENST00000311189:c.182AG>GA
  • Reference Version: GRCh37
  • Chromosome: 11
  • Start: 533873
  • Stop: 533874
  • Strand: -1
  • Transcript: ENST00000311189 (ensembl - 74_37)
  • Gene: HRAS ( View drug interactions on DGIdb )

Information

  • Reference: CT
  • Variant: TC
  • Amino Acid: p.Q61R
  • Mutation Type: missense
  • Variant Type: DNV (SO:0002007)
  • cDNA Change: c.182
  • Tags: likely pathogenic

Disease Data

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