WormBase Tree Display for Variation: WBVar01418446

WBVar01418446 Evidence: Paper_evidence: WBPaper00037807
  Name: Public_name: WBVar01418446
    Other_name: cewivar00384014
      Y71G12B.11d.1:c.4320+160C>T
      Y71G12B.11b.1:c.*4751+160C>T
      Y71G12B.11e.1:c.6351+160C>T
      Y71G12B.11a.1:c.7446+160C>T
      Y71G12B.11c.1:c.5457+160C>T
    HGVSg: CHROMOSOME_I:g.1739370C>T
  Sequence_details: SMap: S_parent: Sequence: Y71G12B
    Flanking_sequences: TGAACACAGAGACTCCTGGCTTCCCTCATAAATTGAGATGGAAGAGTTTT GCCGAACTAGGCCATTTTGGCTTGGCCATATGTCGCGTCGCGGCTCGAAT
    Mapping_target: Y71G12B
    Type_of_mutation: Substitution: c T Paper_evidence: WBPaper00037807
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain (13)
    Laboratory: AX
    Analysis: WGS_De_Bono
      Million_mutation_project_reanalysis
    DB_info: Database: dbSNP_ss ss 539126053
    Status: Live
  Affects: Gene: WBGene00006771
    Transcript: Y71G12B.11c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y71G12B.11c.1:c.5457+160C>T
        Intron_number: 6/6
      Y71G12B.11e.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y71G12B.11e.1:c.6351+160C>T
        Intron_number: 6/6
      Y71G12B.11a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y71G12B.11a.1:c.7446+160C>T
        Intron_number: 10/11
      Y71G12B.11d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y71G12B.11d.1:c.4320+160C>T
        Intron_number: 4/5
      Y71G12B.11b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y71G12B.11b.1:c.*4751+160C>T
        Intron_number: 12/12
  Reference: WBPaper00037807
  Method: WGS_De_Bono