WormBase Tree Display for Variation: WBVar01307364

WBVar01307364 Evidence: Paper_evidence: WBPaper00037807
  Name: Public_name: WBVar01307364
    Other_name: cewivar00355790
      C52E12.2b.1:c.4767+124C>T
      C52E12.2a.1:c.4635+124C>T
      C52E12.2a.2:c.4635+124C>T
    HGVSg: CHROMOSOME_II:g.7009900C>T
  Sequence_details: SMap: S_parent: Sequence: C52E12
    Flanking_sequences: TCAATTTTGTATTTCATTAAATTTCTAAATGATTGGTTTTTTGACACAAA TTTTTTTGAAATCAGATTATGTTTGTATTTTTTCTGATTAGATTTACTTA
    Mapping_target: C52E12
    Type_of_mutation: Substitution: c T Paper_evidence: WBPaper00037807
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00006637 From_analysis: Million_mutation_project_reanalysis
      WBStrain00022850 From_analysis: Million_mutation_project_reanalysis
          WGS_De_Bono
      WBStrain00023286 From_analysis: Million_mutation_project_reanalysis
    Laboratory: AX
    Analysis: WGS_De_Bono
      Million_mutation_project_reanalysis
    DB_info: Database: dbSNP_ss ss 539164907
    Status: Live
  Affects: Gene: WBGene00006831
    Transcript: C52E12.2a.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C52E12.2a.2:c.4635+124C>T
        Intron_number: 22/23
      C52E12.2b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C52E12.2b.1:c.4767+124C>T
        Intron_number: 23/24
      C52E12.2a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C52E12.2a.1:c.4635+124C>T
        Intron_number: 22/23
  Reference: WBPaper00037807
  Method: WGS_De_Bono