WormBase Tree Display for Variation: WBVar01311926

WBVar01311926 Evidence: Paper_evidence: WBPaper00037807
  Name: Public_name: WBVar01311926
    Other_name: cewivar00509744
      C05D12.3c.2:c.*1093A>C
      C05D12.3c.1:c.*66-222A>C
      C05D12.3c.3:c.*66-222A>C
    HGVSg: CHROMOSOME_II:g.11431646A>C
  Sequence_details: SMap: S_parent: Sequence: C05D12
    Flanking_sequences: AAGTTGGAACATATAGGTATATATATATAGATGTTACAAGTTCACGACGC GCGGTGATATATCCCGCCTATTTACAGCCACCAGGAGAGACTATAAATAC
    Mapping_target: C05D12
    Type_of_mutation: Substitution: a C Paper_evidence: WBPaper00037807
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00022850 From_analysis: Million_mutation_project_reanalysis
          WGS_De_Bono
    Laboratory: AX
    Analysis: WGS_De_Bono
      Million_mutation_project_reanalysis
    DB_info: Database: dbSNP_ss ss 539169013
    Status: Live
  Affects: Gene: WBGene00014666
    Transcript: C05D12.3c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C05D12.3c.1:c.*66-222A>C
        Intron_number: 17/17
      C05D12.3c.3 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C05D12.3c.3:c.*66-222A>C
        Intron_number: 16/17
      C05D12.3c.2 VEP_consequence: 3_prime_UTR_variant
        VEP_impact: MODIFIER
        HGVSc: C05D12.3c.2:c.*1093A>C
        cDNA_position: 4113
        Exon_number: 17/17
  Reference: WBPaper00037807
  Method: WGS_De_Bono