WormBase Tree Display for Variation: WBVar01468665

WBVar01468665 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01468665
    Other_name: cewivar00341920
      F43C9.4b.1:c.799+50G>A
      F43C9.4a.2:c.817+50G>A
      F43C9.4a.1:c.817+50G>A
    HGVSg: CHROMOSOME_X:g.4797681C>T
  Sequence_details: SMap: S_parent: Sequence: F43C9
    Flanking_sequences: TGAAATTGAGGCCCATTGGGGCATTATGTG TTATTGCGAATTAACTGTGTATGCGTTCTT
    Mapping_target: F43C9
    Type_of_mutation: Substitution: c t
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00006629 From_analysis: Million_mutation_project_reanalysis
          WGS_Andersen
    Laboratory: QX
    Person: WBPerson1730
    Analysis: WGS_Andersen
      Million_mutation_project_reanalysis
    DB_info: Database: dbSNP_rs rs 193353967
        dbSNP_ss ss 295529886
    Status: Live
  Affects: Gene: WBGene00003245
    Transcript: F43C9.4b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F43C9.4b.1:c.799+50G>A
        Intron_number: 5/6
      F43C9.4a.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F43C9.4a.2:c.817+50G>A
        Intron_number: 8/10
      F43C9.4a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F43C9.4a.1:c.817+50G>A
        Intron_number: 7/9
  Reference: WBPaper00040707
  Method: WGS_Andersen