WormBase Tree Display for Variation: WBVar01316262

WBVar01316262 Evidence: Paper_evidence: WBPaper00037807
  Name: Public_name: WBVar01316262
    Other_name: cewivar00162144
      Y71G12B.11b.1:c.*286+258C>T
      Y71G12B.11d.1:c.-146+258C>T
      Y71G12B.11c.1:c.992+258C>T
      Y71G12B.11e.1:c.1886+258C>T
      Y71G12B.11a.1:c.2981+258C>T
    HGVSg: CHROMOSOME_I:g.1733628C>T
  Sequence_details: SMap: S_parent: Sequence: Y71G12B
    Flanking_sequences: CGAAACAAAAAGTTTGGGCCAAAGTTTGGCAAGAGTTGGGTGAAACTTGG TTAAACTTTGATTTCACCCGAATCCAAGTTTTGCCAAAGTCTTGCCCAAC
    Mapping_target: Y71G12B
    Type_of_mutation: Substitution: c 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 539013325
    Status: Live
  Affects: Gene: WBGene00006771
    Transcript: Y71G12B.11c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y71G12B.11c.1:c.992+258C>T
        Intron_number: 4/6
      Y71G12B.11e.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y71G12B.11e.1:c.1886+258C>T
        Intron_number: 4/6
      Y71G12B.11a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y71G12B.11a.1:c.2981+258C>T
        Intron_number: 8/11
      Y71G12B.11d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y71G12B.11d.1:c.-146+258C>T
        Intron_number: 1/5
      Y71G12B.11b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y71G12B.11b.1:c.*286+258C>T
        Intron_number: 10/12
  Reference: WBPaper00037807
  Method: WGS_De_Bono