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MTHFR (p.A222V)

Variant Data

Location

  • HGVS: ENST00000376592:c.665C>T
  • Reference Version: GRCh37
  • Chromosome: 1
  • Start: 11856378
  • Stop: 11856378
  • Strand: -1
  • Transcript: ENST00000376592 (ensembl - 74_37)
  • Gene: MTHFR ( View drug interactions on DGIdb )

Information

  • Reference: G
  • Variant: A (Civic logo View in CIViC)
  • Amino Acid: p.A222V
  • Mutation Type: missense
  • Variant Type: SNV (SO:0001483)
  • cDNA Change: c.665
  • Tags:

Disease Data

Disease Source Batch Tags External Links
stomach cancer Huang et al., 2009, Cancer Chemother. Pharmacol. CIViC Knowledgebase (View variants) Civic logo CIViC
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