WormBase Tree Display for Variation: WBVar01281334

WBVar01281334 Evidence: Paper_evidence: WBPaper00037807
  Name: Public_name: WBVar01281334
    Other_name: cewivar00505218
      F55C7.7b.1:c.21+314T>A
      F55C7.7a.1:c.21+314T>A
      F55C7.7i.1:c.21+314T>A
      F55C7.7i.2:c.21+314T>A
    HGVSg: CHROMOSOME_I:g.4031293A>T
  Sequence_details: SMap: S_parent: Sequence: C09D1
    Flanking_sequences: CACATAAATTTAAACAAATATAGAGAAAAAAATCAATAATCAACTAAACT CAGTAATCTTTAAAGGCTCATCAAAAATTTGTAGTATCGAGACCGAATAC
    Mapping_target: C09D1
    Type_of_mutation: Substitution: a T 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
    Laboratory: AX
    Analysis: WGS_De_Bono
      Million_mutation_project_reanalysis
    DB_info: Database: dbSNP_ss ss 539141481
    Status: Live
  Affects: Gene: WBGene00006805
    Transcript: F55C7.7i.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F55C7.7i.1:c.21+314T>A
        Intron_number: 1/25
      F55C7.7b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F55C7.7b.1:c.21+314T>A
        Intron_number: 1/20
      F55C7.7a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F55C7.7a.1:c.21+314T>A
        Intron_number: 2/33
      F55C7.7i.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F55C7.7i.2:c.21+314T>A
        Intron_number: 1/24
  Reference: WBPaper00037807
  Method: WGS_De_Bono