Header logo

HRAS (p.G12C)

Variant Data

Location

  • HGVS: ENST00000311189:c.34G>T
  • Reference Version: GRCh37
  • Chromosome: 11
  • Start: 534289
  • Stop: 534289
  • Strand: -1
  • Transcript: ENST00000311189 (ensembl - 74_37)
  • Gene: HRAS ( View drug interactions on DGIdb )

Information

  • Reference: C
  • Variant: A
  • Amino Acid: p.G12C
  • Mutation Type: missense
  • Variant Type: SNV (SO:0001483)
  • cDNA Change: c.34
  • Tags: likely pathogenic

Disease Data

Disease Source Batch Tags External Links
bladder carcinoma MacConaill et al., 2014, J Mol Diagn Oncomap Variants (View variants) likely pathogenic
Produced by The McDonnell Genome Institute at the Washington University School of Medicine

DoCM by The McDonnell Genome Institute at Washington University School of Medicine is licensed under a Creative Commons Attribution 4.0 International License. Questions? Comments? Concerns? You can contact us here.