WormBase Tree Display for Variation: WBVar01452491

WBVar01452491 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01452491
    Other_name: B0273.4c.1:c.208-3128C>G
      B0273.4b.1:c.124-3128C>G
      B0273.4a.1:c.124-3128C>G
    HGVSg: CHROMOSOME_IV:g.5512029G>C
  Sequence_details: SMap: S_parent: Sequence: B0273
    Flanking_sequences: ATTTATTTTTCAATAACAGCATTTGCTTAT TGTTCTATCCGACTTATGGTAAAGGTTTGA
    Mapping_target: B0273
    Type_of_mutation: Substitution: g 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 193338148
        dbSNP_ss ss 295514067
    Status: Live
  Affects: Gene: WBGene00006745
    Transcript: B0273.4c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: B0273.4c.1:c.208-3128C>G
        Intron_number: 2/9
      B0273.4a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: B0273.4a.1:c.124-3128C>G
        Intron_number: 2/9
      B0273.4b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: B0273.4b.1:c.124-3128C>G
        Intron_number: 1/5
  Reference: WBPaper00040707
  Method: WGS_Andersen