WormBase Tree Display for Variation: WBVar01387893

WBVar01387893 Evidence: Paper_evidence: WBPaper00037807
  Name: Public_name: WBVar01387893
    Other_name: cewivar00191041
      C29F9.6.3:c.135+199G>T
      C29F9.6.1:c.135+199G>T
      C29F9.6.2:c.135+199G>T
    HGVSg: CHROMOSOME_III:g.115586G>T
  Sequence_details: SMap: S_parent: Sequence: C29F9
    Flanking_sequences: AGTGCAACTTGCTTAAGGAGTTCTAGAGCGTGTGCGGGGGCCGAGATGGA GCTTTAGCGTCCCAGTTGTGATCTTGACTCCCTATAGAGCGCCTTGGGCT
    Mapping_target: C29F9
    Type_of_mutation: Substitution: g T Paper_evidence: WBPaper00037807
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00004602 From_analysis: Million_mutation_project_reanalysis
          WGS_De_Bono
      WBStrain00023191 From_analysis: Million_mutation_project_reanalysis
      WBStrain00027647 From_analysis: Million_mutation_project_reanalysis
    Laboratory: AX
    Analysis: WGS_De_Bono
      Million_mutation_project_reanalysis
    DB_info: Database: dbSNP_ss ss 539063344
    Status: Live
  Affects: Gene: WBGene00016221
    Transcript: C29F9.6.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C29F9.6.1:c.135+199G>T
        Intron_number: 5/8
      C29F9.6.3 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C29F9.6.3:c.135+199G>T
        Intron_number: 4/7
      C29F9.6.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C29F9.6.2:c.135+199G>T
        Intron_number: 3/6
  Reference: WBPaper00037807
  Method: WGS_De_Bono