WormBase Tree Display for Variation: WBVar01430330

WBVar01430330 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01430330
    Other_name: Y71G12B.11b.1:c.*287-288T>C
      Y71G12B.11a.1:c.2982-288T>C
      Y71G12B.11c.1:c.993-288T>C
      Y71G12B.11e.1:c.1887-288T>C
      Y71G12B.11d.1:c.-145-288T>C
    HGVSg: CHROMOSOME_I:g.1734159T>C
  Sequence_details: SMap: S_parent: Sequence: Y71G12B
    Flanking_sequences: GCGCTTCAGCTGTAGAATTCCCTTTAAATC CACTTTTCATAACAACCACAGGGCTCATTT
    Mapping_target: Y71G12B
    Type_of_mutation: Substitution: t c
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023224 From_analysis: WGS_Andersen
      WBStrain00023234 From_analysis: WGS_Andersen
      WBStrain00023280 From_analysis: WGS_Andersen
      WBStrain00023281 From_analysis: WGS_Andersen
    Laboratory: QX
    Person: WBPerson1730
    Analysis: WGS_Andersen
    DB_info: Database: dbSNP_rs rs 193318393
        dbSNP_ss ss 295494310
    Status: Live
  Affects: Gene: WBGene00006771
    Transcript: Y71G12B.11c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y71G12B.11c.1:c.993-288T>C
        Intron_number: 4/6
      Y71G12B.11e.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y71G12B.11e.1:c.1887-288T>C
        Intron_number: 4/6
      Y71G12B.11a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y71G12B.11a.1:c.2982-288T>C
        Intron_number: 8/11
      Y71G12B.11d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y71G12B.11d.1:c.-145-288T>C
        Intron_number: 1/5
      Y71G12B.11b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y71G12B.11b.1:c.*287-288T>C
        Intron_number: 10/12
  Reference: WBPaper00040707
  Method: WGS_Andersen