WormBase Tree Display for Variation: WBVar01681596

WBVar01681596 Name: Public_name: WBVar01681596
    Other_name: cewivar00372139
      Y43H11AL.1a.3:c.1083+1505G>A
      Y43H11AL.1b.1:c.1244+183G>A
      Y43H11AL.1a.1:c.1083+1505G>A
      Y43H11AL.1a.4:c.1083+1505G>A
      Y43H11AL.1c.1:c.1202+183G>A
      Y43H11AL.1d.1:c.269+183G>A
      Y43H11AL.1a.2:c.1083+1505G>A
    HGVSg: CHROMOSOME_II:g.226431C>T
  Sequence_details: SMap: S_parent: Sequence: Y43H11AL
    Flanking_sequences: AAAATTTTGTGACTATTGTCAAATGAAAGA CATGGTTGATAACCTAAATTCCCACAGTTT
    Mapping_target: Y43H11AL
    Source_location: 225 CHROMOSOME_II 226431 226431 From_analysis: Million_mutation_project_reanalysis
    Type_of_mutation: Substitution: C T
    SeqStatus: Sequenced
  Variation_type: Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00006640 From_analysis: Million_mutation_project_reanalysis
      WBStrain00022850 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023018 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023138 From_analysis: Million_mutation_project_reanalysis
    Laboratory: VC
    Analysis: Million_mutation_project_reanalysis
    Status: Live
  Affects: Gene: WBGene00021545
    Transcript: Y43H11AL.1a.3 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y43H11AL.1a.3:c.1083+1505G>A
        Intron_number: 7/10
      Y43H11AL.1c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y43H11AL.1c.1:c.1202+183G>A
        Intron_number: 6/8
      Y43H11AL.1d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y43H11AL.1d.1:c.269+183G>A
        Intron_number: 2/4
      Y43H11AL.1b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y43H11AL.1b.1:c.1244+183G>A
        Intron_number: 8/11
      Y43H11AL.1a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y43H11AL.1a.1:c.1083+1505G>A
        Intron_number: 7/10
      Y43H11AL.1a.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y43H11AL.1a.2:c.1083+1505G>A
        Intron_number: 7/8
      Y43H11AL.1a.4 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y43H11AL.1a.4:c.1083+1505G>A
        Intron_number: 7/9
  Method: WGS_Flibotte