WormBase Tree Display for Variation: WBVar01461027

WBVar01461027 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01461027
    Other_name: K06C4.6c.1:c.196-471G>T
      K06C4.6b.1:c.196-471G>T
      K06C4.6a.1:c.196-471G>T
    HGVSg: CHROMOSOME_V:g.8913208C>A
  Sequence_details: SMap: S_parent: Sequence: K06C4
    Flanking_sequences: AAGATTGATGGCTTTTGACCCATCTCTTCA TCCCACAACTCCCAATCCAATAATTTTTCA
    Mapping_target: K06C4
    Type_of_mutation: Substitution: c a
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00005299 From_analysis: WGS_Andersen
      WBStrain00005300 From_analysis: WGS_Andersen
      WBStrain00005307 From_analysis: WGS_Andersen
      WBStrain00005310 From_analysis: WGS_Andersen
      WBStrain00030851 From_analysis: WGS_Andersen
    Laboratory: QX
    Person: WBPerson1730
    Analysis: WGS_Andersen
    DB_info: Database: dbSNP_rs rs 193346683
        dbSNP_ss ss 295522602
    Status: Live
  Affects: Gene: WBGene00003386
    Transcript: K06C4.6b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: K06C4.6b.1:c.196-471G>T
        Intron_number: 3/11
      K06C4.6c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: K06C4.6c.1:c.196-471G>T
        Intron_number: 2/8
      K06C4.6a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: K06C4.6a.1:c.196-471G>T
        Intron_number: 3/12
  Reference: WBPaper00040707
  Method: WGS_Andersen