WormBase Tree Display for Variation: WBVar01438345

WBVar01438345 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01438345
    Other_name: cewivar00418319
      C52E12.2a.1:c.2346-737G>T
      C52E12.2b.1:c.2346-243G>T
      C52E12.2a.2:c.2346-737G>T
    HGVSg: CHROMOSOME_II:g.7005733G>T
  Sequence_details: SMap: S_parent: Sequence: C52E12
    Flanking_sequences: AATAAATAATAACCGGAGAGTAATTGGTGC AGGGAATAAAGGAATTTAAAATATAAACTA
    Mapping_target: C52E12
    Type_of_mutation: Substitution: g t
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00005834 From_analysis: WGS_Andersen
      WBStrain00023139 From_analysis: Million_mutation_project_reanalysis
          WGS_Andersen
      WBStrain00027648 From_analysis: Million_mutation_project_reanalysis
          WGS_Andersen
      WBStrain00027660 From_analysis: Million_mutation_project_reanalysis
          WGS_Andersen
      WBStrain00027661 From_analysis: WGS_Andersen
      WBStrain00027662 From_analysis: Million_mutation_project_reanalysis
          WGS_Andersen
      WBStrain00027669 From_analysis: WGS_Andersen
    Laboratory: QX
    Person: WBPerson1730
    Analysis: Million_mutation_project_reanalysis
      WGS_Andersen
    DB_info: Database: dbSNP_rs rs 193326406
        dbSNP_ss ss 295502325
    Status: Live
  Affects: Gene: WBGene00006831
    Transcript: C52E12.2a.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C52E12.2a.2:c.2346-737G>T
        Intron_number: 13/23
      C52E12.2b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C52E12.2b.1:c.2346-243G>T
        Intron_number: 13/24
      C52E12.2a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C52E12.2a.1:c.2346-737G>T
        Intron_number: 13/23
  Reference: WBPaper00040707
  Method: WGS_Andersen