MYC (p.N101T)

Variant Data

Location

  • HGVS: ENST00000377970:c.302A>C
  • Reference Version: GRCh37
  • Chromosome: 8
  • Start: 128750765
  • Stop: 128750765
  • Strand: 1
  • Transcript: ENST00000377970 (ensembl - 74_37)
  • Gene: MYC ( View drug interactions on DGIdb )

Information

  • Reference: A
  • Variant: C
  • Amino Acid: p.N101T
  • Mutation Type: missense
  • Variant Type: SNV (SO:0001483)
  • cDNA Change: c.302
  • 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