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STK11 (p.Q37*)

Variant Data

Location

  • HGVS: ENST00000326873:c.109C>T
  • Reference Version: GRCh37
  • Chromosome: 19
  • Start: 1207021
  • Stop: 1207021
  • Strand: 1
  • Transcript: ENST00000326873 (ensembl - 74_37)
  • Gene: STK11 ( View drug interactions on DGIdb )

Information

  • Reference: C
  • Variant: T
  • Amino Acid: p.Q37*
  • Mutation Type: stop_lost
  • Variant Type: SNV (SO:0001483)
  • cDNA Change: c.109
  • 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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