WormBase Tree Display for Variation: WBVar01328444

WBVar01328444 Evidence: Paper_evidence: WBPaper00037807
  Name: Public_name: WBVar01328444
    Other_name: cewivar00378403
      H19M22.2a.1:c.3005-135A>G
      H19M22.2b.1:c.3005-135A>G
    HGVSg: CHROMOSOME_III:g.2666194A>G
  Sequence_details: SMap: S_parent: Sequence: H19M22
    Flanking_sequences: AAATTTGAGTAATACTAGGCAACGCCCCGAAAATGGGCGTGGTTTTTCAC GCTCGAATGTCCAAAAATATTACAATTTTAAGAGAGAAACAATTTTTTTG
    Mapping_target: H19M22
    Type_of_mutation: Substitution: a G 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 539183880
    Status: Live
  Affects: Gene: WBGene00002915
    Transcript: H19M22.2a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: H19M22.2a.1:c.3005-135A>G
        Intron_number: 15/26
      H19M22.2b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: H19M22.2b.1:c.3005-135A>G
        Intron_number: 15/28
  Reference: WBPaper00037807
  Method: WGS_De_Bono