WormBase Tree Display for Variation: WBVar01386807

WBVar01386807 Evidence: Paper_evidence: WBPaper00037807
  Name: Public_name: WBVar01386807
    Other_name: cewivar00189776
      H10E21.3a.1:c.1249-20C>A
      H10E21.3b.1:c.1303-20C>A
    HGVSg: CHROMOSOME_III:g.12421G>T
  Sequence_details: SMap: S_parent: Sequence: H10E21
    Flanking_sequences: TGTGATTTTGCACAAAATCATTGCCGGCAGTCTGGAAAAATTCGATTTTC AGGTGATTTGGGTTTTGGTAAAATTTTGAAAATAAAAATTTCAAAAAAAC
    Mapping_target: H10E21
    Type_of_mutation: Substitution: g T Paper_evidence: WBPaper00037807
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00004602 From_analysis: Million_mutation_project_reanalysis
          WGS_De_Bono
      WBStrain00027647 From_analysis: Million_mutation_project_reanalysis
    Laboratory: AX
    Analysis: WGS_De_Bono
      Million_mutation_project_reanalysis
    DB_info: Database: dbSNP_ss ss 539062258
    Status: Live
  Affects: Gene: WBGene00003670
    Transcript: H10E21.3b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: H10E21.3b.1:c.1303-20C>A
        Intron_number: 5/6
      H10E21.3a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: H10E21.3a.1:c.1249-20C>A
        Intron_number: 7/8
  Reference: WBPaper00037807
  Method: WGS_De_Bono