WormBase Tree Display for Variation: WBVar01443182

WBVar01443182 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01443182
    Other_name: cewivar00618985
      C09F5.1b.1:c.685-6T>C
      C09F5.1a.1:c.1264-6T>C
    HGVSg: CHROMOSOME_III:g.661750T>C
  Sequence_details: SMap: S_parent: Sequence: C09F5
    Flanking_sequences: TCTAAGAAAAAAATCTCCTAACCTGCATTT AACAGATCCAATCTACTTTCGGCTGGCAAG
    Mapping_target: C09F5
    Type_of_mutation: Substitution: t c
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00005303 From_analysis: WGS_Andersen
      WBStrain00005312 From_analysis: WGS_Andersen
      WBStrain00027647 From_analysis: Million_mutation_project_reanalysis
          WGS_Andersen
      WBStrain00031279 From_analysis: WGS_Andersen
      WBStrain00031284 From_analysis: WGS_Andersen
    Laboratory: QX
    Person: WBPerson1730
    Analysis: Million_mutation_project_reanalysis
      WGS_Andersen
    DB_info: Database: dbSNP_rs rs 193330343
        dbSNP_ss ss 295506262
    Status: Live
  Affects: Gene: WBGene00015647
    Transcript: C09F5.1a.1 VEP_consequence: splice_region_variant,intron_variant
        VEP_impact: LOW
        HGVSc: C09F5.1a.1:c.1264-6T>C
        Intron_number: 7/10
      C09F5.1b.1 VEP_consequence: splice_region_variant,intron_variant
        VEP_impact: LOW
        HGVSc: C09F5.1b.1:c.685-6T>C
        Intron_number: 5/8
  Reference: WBPaper00040707
  Method: WGS_Andersen