WormBase Tree Display for Variation: WBVar00272041

WBVar00272041 Name: Public_name: WBVar00272041
    Other_name: uCE5-1378
      haw166333
      cewivar00234018
      C14C11.8a.1:c.171+22A>G
      C14C11.8b.1:c.171+22A>G
    HGVSg: CHROMOSOME_V:g.5675890T>C
  Sequence_details: SMap: S_parent: Sequence: C14C11
    Flanking_sequences: CCGAGCACTGGTTTTTGAAAAAGGAGAGAACACAAAAACCAAGTGCAAACAGACACGCGATGTTTTGTTTTTTGGTTTCTTTTTTTTTCGTGATTTTTTT ACTCAAAGCAAAGCAACATACCTCTTCTTTAACTGTTTCCTTGATTGCCGAAGCAGTCGTCGTCTTCGTGGATTCTGTCGTGGATTCGGAAGTGGCTACC
    Mapping_target: C14C11
    Type_of_mutation: Substitution: T C
    SeqStatus: Sequenced
  Variation_type: SNP
    Predicted_SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00004602 From_analysis: SNP_Swan
          WGS_Yanai
          Million_mutation_project_reanalysis
      WBStrain00006629 From_analysis: Million_mutation_project_reanalysis
      WBStrain00022850 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023139 From_analysis: Million_mutation_project_reanalysis
      WBStrain00027648 From_analysis: Million_mutation_project_reanalysis
      WBStrain00027660 From_analysis: Million_mutation_project_reanalysis
      WBStrain00027662 From_analysis: Million_mutation_project_reanalysis
    Person: WBPerson4037
    Analysis: SNP_Swan
      WGS_Yanai
      Million_mutation_project_reanalysis
    History: Acquires_merge: WBVar00586198
    Status: Live
  Affects: Gene: WBGene00004104
    Transcript: C14C11.8b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C14C11.8b.1:c.171+22A>G
        Intron_number: 2/12
      C14C11.8a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C14C11.8a.1:c.171+22A>G
        Intron_number: 2/11
  Reference: WBPaper00038208
    WBPaper00005369
  Method: SNP_Swan