WormBase Tree Display for Variation: WBVar01451441

WBVar01451441 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01451441
    Other_name: cewivar00154320
      Y54G2A.11a.1:c.505+386G>A
      Y54G2A.11b.2:c.-720+386G>A
      Y54G2A.11b.1:c.-2360+386G>A
    HGVSg: CHROMOSOME_IV:g.2770283C>T
  Sequence_details: SMap: S_parent: Sequence: Y54G2A
    Flanking_sequences: CTCGAAGCGAAAATCTGAAAATTCGAGACC AAAATCTATCAAAACTTCGATTTTTGCATT
    Mapping_target: Y54G2A
    Type_of_mutation: Substitution: c t
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00004600 From_analysis: Million_mutation_project_reanalysis
          WGS_Andersen
      WBStrain00005832 From_analysis: WGS_Andersen
      WBStrain00023018 From_analysis: Million_mutation_project_reanalysis
          WGS_Andersen
      WBStrain00023191 From_analysis: Million_mutation_project_reanalysis
          WGS_Andersen
    Laboratory: QX
    Person: WBPerson1730
    Analysis: Million_mutation_project_reanalysis
      WGS_Andersen
    DB_info: Database: dbSNP_rs rs 193337098
        dbSNP_ss ss 295513017
    Status: Live
  Affects: Gene: WBGene00021876
    Transcript: Y54G2A.11b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y54G2A.11b.1:c.-2360+386G>A
        Intron_number: 2/6
      Y54G2A.11a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y54G2A.11a.1:c.505+386G>A
        Intron_number: 3/7
      Y54G2A.11b.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y54G2A.11b.2:c.-720+386G>A
        Intron_number: 1/6
  Reference: WBPaper00040707
  Method: WGS_Andersen