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CTNNB1 (p.D32A)

Variant Data

Location

  • HGVS: ENST00000349496:c.95A>C
  • Reference Version: GRCh37
  • Chromosome: 3
  • Start: 41266098
  • Stop: 41266098
  • Strand: 1
  • Transcript: ENST00000349496 (ensembl - 74_37)
  • Gene: CTNNB1 ( View drug interactions on DGIdb )

Information

  • Reference: A
  • Variant: C
  • Amino Acid: p.D32A
  • Mutation Type: missense
  • Variant Type: SNV (SO:0001483)
  • cDNA Change: c.95
  • Tags: likely pathogenic

Disease Data

Disease Source Batch Tags External Links
melanoma MacConaill et al., 2014, J Mol Diagn Oncomap Variants (View variants) likely pathogenic
hepatocellular carcinoma Chang et al., 2016, Nat. Biotechnol. Pan-cancer recurrent hotspots (View variants) likely pathogenic
uterine corpus endometrial carcinoma Chang et al., 2016, Nat. Biotechnol. Pan-cancer recurrent hotspots (View variants) likely pathogenic
medulloblastoma 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
skin melanoma Chang et al., 2016, Nat. Biotechnol. Pan-cancer recurrent hotspots (View variants) likely pathogenic
cervix carcinoma 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
urinary bladder urothelial carcinoma Chang et al., 2016, Nat. Biotechnol. Pan-cancer recurrent hotspots (View variants) likely pathogenic
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