WormBase Tree Display for Variation: WBVar01639608

WBVar01639608 Name: Public_name: WBVar01639608
    Other_name: cewivar00321595
      M02A10.2e.1:c.1284+40T>C
      M02A10.2f.1:c.1275+49T>C
      M02A10.2b.1:c.1176+49T>C
      M02A10.2a.1:c.1185+40T>C
      M02A10.2c.1:c.1185+40T>C
      M02A10.2a.2:c.1185+40T>C
      M02A10.2d.1:c.1176+49T>C
    HGVSg: CHROMOSOME_X:g.704276A>G
  Sequence_details: SMap: S_parent: Sequence: M02A10
    Flanking_sequences: AGTCTTCAACTCTGGTTCTATAATATCTGG CGGCTCATTGCAAGCATTTCTCCATCAGCT
    Mapping_target: M02A10
    Source_location: 225 CHROMOSOME_X 704275 704275 From_analysis: Million_mutation_project_reanalysis
    Type_of_mutation: Substitution: A G
    SeqStatus: Sequenced
  Variation_type: Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00006625 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023139 From_analysis: Million_mutation_project_reanalysis
      WBStrain00027648 From_analysis: Million_mutation_project_reanalysis
      WBStrain00027660 From_analysis: Million_mutation_project_reanalysis
      WBStrain00027662 From_analysis: Million_mutation_project_reanalysis
    Laboratory: VC
    Analysis: Million_mutation_project_reanalysis
    Status: Live
  Affects: Gene: WBGene00002150
    Transcript: M02A10.2e.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: M02A10.2e.1:c.1284+40T>C
        Intron_number: 13/15
      M02A10.2d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: M02A10.2d.1:c.1176+49T>C
        Intron_number: 13/15
      M02A10.2f.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: M02A10.2f.1:c.1275+49T>C
        Intron_number: 13/15
      M02A10.2b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: M02A10.2b.1:c.1176+49T>C
        Intron_number: 12/15
      M02A10.2c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: M02A10.2c.1:c.1185+40T>C
        Intron_number: 14/17
      M02A10.2a.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: M02A10.2a.2:c.1185+40T>C
        Intron_number: 14/16
      M02A10.2a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: M02A10.2a.1:c.1185+40T>C
        Intron_number: 13/15
  Method: WGS_Flibotte