WormBase Tree Display for Variation: WBVar01328456

WBVar01328456 Evidence: Paper_evidence: WBPaper00037807
  Name: Public_name: WBVar01328456
    Other_name: cewivar00378406
      H19M22.2b.1:c.11692+614A>C
      H19M22.2a.1:c.11693-550A>C
    HGVSg: CHROMOSOME_III:g.2675997A>C
  Sequence_details: SMap: S_parent: Sequence: Y71H2AL
    Flanking_sequences: TGCAAGCCTAGGCTTATTGGACCCTGAAAACAAGTTTTCTCTAAGGTTCT GAAAACTAATCCTTTAAGGACCTCTTCCGGAAGAAACAGGTGGCCCTGTA
    Mapping_target: Y71H2AL
    Type_of_mutation: Substitution: a C Paper_evidence: WBPaper00037807
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00006640 From_analysis: Million_mutation_project_reanalysis
      WBStrain00008273 From_analysis: Million_mutation_project_reanalysis
      WBStrain00022850 From_analysis: Million_mutation_project_reanalysis
          WGS_De_Bono
      WBStrain00022886 From_analysis: Million_mutation_project_reanalysis
      WBStrain00022930 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023138 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023191 From_analysis: Million_mutation_project_reanalysis
    Laboratory: AX
    Analysis: WGS_De_Bono
      Million_mutation_project_reanalysis
    DB_info: Database: dbSNP_ss ss 539183891
    Status: Live
  Affects: Gene: WBGene00002915
    Transcript: H19M22.2a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: H19M22.2a.1:c.11693-550A>C
        Intron_number: 19/26
      H19M22.2b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: H19M22.2b.1:c.11692+614A>C
        Intron_number: 19/28
  Reference: WBPaper00037807
  Method: WGS_De_Bono