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MAP2K1 (p.P264S)

Variant Data

Location

  • HGVS: ENST00000307102:c.790C>T
  • Reference Version: GRCh37
  • Chromosome: 15
  • Start: 66777424
  • Stop: 66777424
  • Strand: 1
  • Transcript: ENST00000307102 (ensembl - 74_37)
  • Gene: MAP2K1 ( View drug interactions on DGIdb )

Information

  • Reference: C
  • Variant: T
  • Amino Acid: p.P264S
  • Mutation Type: missense
  • Variant Type: SNV (SO:0001483)
  • cDNA Change: c.790
  • Tags: pathogenic

Disease Data

Disease Source Batch Tags External Links
melanoma Nikolaev et al., 2012, Nat. Genet. My Cancer Genome (View variants) pathogenic My Cancer Genome
melanoma Berger et al., 2012, Nature My Cancer Genome (View variants) pathogenic My Cancer Genome
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