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ERBB2 (p.G776CX)

Variant Data

Location

  • HGVS: ENST00000269571:c.2326insTGT
  • Reference Version: GRCh37
  • Chromosome: 17
  • Start: 37880997
  • Stop: 37880998
  • Strand: 1
  • Transcript: ENST00000269571 (ensembl - 74_37)
  • Gene: ERBB2 ( View drug interactions on DGIdb )

Information

  • Reference: -
  • Variant: TGT
  • Amino Acid: p.G776CX
  • Mutation Type: frameshift
  • Variant Type: INS (SO:0000667)
  • cDNA Change: c.2326
  • Tags: likely pathogenic

Disease Data

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