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MAP2K1 (p.K57T)

Variant Data

Location

  • HGVS: ENST00000307102:c.170A>C
  • Reference Version: GRCh37
  • Chromosome: 15
  • Start: 66727454
  • Stop: 66727454
  • Strand: 1
  • Transcript: ENST00000307102 (ensembl - 74_37)
  • Gene: MAP2K1 ( View drug interactions on DGIdb )

Information

  • Reference: A
  • Variant: C
  • Amino Acid: p.K57T
  • Mutation Type: missense
  • Variant Type: SNV (SO:0001483)
  • cDNA Change: c.170
  • Tags: likely pathogenic

Disease Data

Disease Source Batch Tags External Links
lung adenocarcinoma Chang et al., 2016, Nat. Biotechnol. Pan-cancer recurrent hotspots (View variants) likely pathogenic
skin melanoma Chang et al., 2016, Nat. Biotechnol. Pan-cancer recurrent hotspots (View variants) likely pathogenic
gastric adenocarcinoma Chang et al., 2016, Nat. Biotechnol. Pan-cancer recurrent hotspots (View variants) likely pathogenic
prostate adenocarcinoma Chang et al., 2016, Nat. Biotechnol. Pan-cancer recurrent hotspots (View variants) likely pathogenic
head and neck squamous cell carcinoma Chang et al., 2016, Nat. Biotechnol. Pan-cancer recurrent hotspots (View variants) likely pathogenic
non-Hodgkin lymphoma Chang et al., 2016, Nat. Biotechnol. Pan-cancer recurrent hotspots (View variants) likely pathogenic
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