WormBase Tree Display for Variation: WBVar01316228

WBVar01316228 Evidence: Paper_evidence: WBPaper00037807
  Name: Public_name: WBVar01316228
    Other_name: cewivar00162141
      Y71G12B.11f.1:c.1813-79G>T
      Y71G12B.11b.1:c.2908-79G>T
      Y71G12B.11a.1:c.2908-584G>T
      Y71G12B.11c.1:c.919-584G>T
      Y71G12B.11e.1:c.1813-584G>T
    HGVSg: CHROMOSOME_I:g.1732713G>T
  Sequence_details: SMap: S_parent: Sequence: Y71G12B
    Flanking_sequences: ATTGAGCGCGGGGCCCTCAATATTTGTTCAAGGTCTGCTCAAGGCTTAAT GTATGAGAGACTCTTGGTTGGTGTTGAGAAGGACCACAGAAGACAGGGTG
    Mapping_target: Y71G12B
    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
    Laboratory: AX
    Analysis: WGS_De_Bono
      Million_mutation_project_reanalysis
    DB_info: Database: dbSNP_ss ss 539013321
    Status: Live
  Affects: Gene: WBGene00006771
    Transcript: Y71G12B.11f.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y71G12B.11f.1:c.1813-79G>T
        Intron_number: 3/3
      Y71G12B.11c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y71G12B.11c.1:c.919-584G>T
        Intron_number: 3/6
      Y71G12B.11e.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y71G12B.11e.1:c.1813-584G>T
        Intron_number: 3/6
      Y71G12B.11a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y71G12B.11a.1:c.2908-584G>T
        Intron_number: 7/11
      Y71G12B.11b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y71G12B.11b.1:c.2908-79G>T
        Intron_number: 7/12
  Reference: WBPaper00037807
  Method: WGS_De_Bono