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KRAS (p.Q22K)

Variant Data

Location

  • HGVS: ENST00000256078:c.64C>A
  • Reference Version: GRCh37
  • Chromosome: 12
  • Start: 25398255
  • Stop: 25398255
  • Strand: -1
  • Transcript: ENST00000256078 (ensembl - 74_37)
  • Gene: KRAS ( View drug interactions on DGIdb )

Information

  • Reference: G
  • Variant: T
  • Amino Acid: p.Q22K
  • Mutation Type: missense
  • Variant Type: SNV (SO:0001483)
  • cDNA Change: c.64
  • Tags: likely pathogenic

Disease Data

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