WormBase Tree Display for Variation: WBVar01291307

WBVar01291307 Evidence: Paper_evidence: WBPaper00037807
  Name: Public_name: WBVar01291307
    Other_name: cewivar00506381
      K01A2.4a.1:c.642-33T>C
      K01A2.4b.1:c.267-33T>C
      K01A2.4a.2:c.642-33T>C
    HGVSg: CHROMOSOME_II:g.309167T>C
  Sequence_details: SMap: S_parent: Sequence: K01A2
    Flanking_sequences: GCGTAAGCCTAGGCCTGAACCTAAACCAGAGAAAAAGCTTACGGCTAAAA CAATCTCAATCAAGCTTTAAAGGTATTTTCAGACTCCCCCTGTTCAACAT
    Mapping_target: K01A2
    Type_of_mutation: Substitution: t 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
      WBStrain00023018 From_analysis: Million_mutation_project_reanalysis
    Laboratory: AX
    Analysis: WGS_De_Bono
      Million_mutation_project_reanalysis
    DB_info: Database: dbSNP_ss ss 539150456
    Status: Live
  Affects: Gene: WBGene00019279
    Transcript: K01A2.4a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: K01A2.4a.1:c.642-33T>C
        Intron_number: 9/11
      K01A2.4b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: K01A2.4b.1:c.267-33T>C
        Intron_number: 3/4
      K01A2.4a.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: K01A2.4a.2:c.642-33T>C
        Intron_number: 9/12
  Reference: WBPaper00037807
  Method: WGS_De_Bono