WormBase Tree Display for Variation: WBVar01266477

WBVar01266477 Evidence: Paper_evidence: WBPaper00037807
  Name: Public_name: WBVar01266477
    Other_name: cewivar00388034
      B0523.5.1:c.2028+107T>G
    HGVSg: CHROMOSOME_III:g.8678795A>C
  Sequence_details: SMap: S_parent: Sequence: B0523
    Flanking_sequences: TAAAATTTTTTATCTCATGTTCTGAAACGATTTTGCAATACTACATATTC ATGAGATGAAAAGTCAAACTACAGTACCCCTCCATAAATAAGATAATGGG
    Mapping_target: B0523
    Type_of_mutation: Substitution: a C Paper_evidence: WBPaper00037807
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00006642 From_analysis: WGS_De_Bono
      WBStrain00006643 From_analysis: Million_mutation_project_reanalysis
      WBStrain00006645 From_analysis: Million_mutation_project_reanalysis
    Laboratory: AX
    Analysis: WGS_De_Bono
      Million_mutation_project_reanalysis
    DB_info: Database: dbSNP_ss ss 539101772
    Status: Live
  Affects: Gene: WBGene00001443
    Transcript: B0523.5.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: B0523.5.1:c.2028+107T>G
        Intron_number: 9/14
  Reference: WBPaper00037807
  Method: WGS_De_Bono