WormBase Tree Display for Variation: WBVar01889165

WBVar01889165 Name: Public_name: WBVar01889165
    Other_name (13)
    HGVSg: CHROMOSOME_X:g.10800939G>A
  Sequence_details: SMap: S_parent: Sequence: F31B12
    Flanking_sequences: TAGTTTTGTTTTTTTTTTCAAACCAAAAGG GAGAAAGATCTTGTTTCTAGAAAAATTAGG
    Mapping_target: F31B12
    Source_location: 225 CHROMOSOME_X 10800874 10800874 From_analysis: Million_mutation_project_reanalysis
    Type_of_mutation: Substitution: G A
    SeqStatus: Sequenced
  Variation_type: Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023072 From_analysis: Million_mutation_project_reanalysis
    Laboratory: VC
    Analysis: Million_mutation_project_reanalysis
    Status: Live
  Affects: Gene: WBGene00004036
    Transcript: F31B12.1j.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F31B12.1j.1:c.8148-99C>T
        Intron_number: 52/63
      F31B12.1f.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F31B12.1f.1:c.3345-99C>T
        Intron_number: 20/31
      F31B12.1h.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F31B12.1h.1:c.8199-99C>T
        Intron_number: 52/63
      F31B12.1c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F31B12.1c.1:c.3291-99C>T
        Intron_number: 19/32
      F31B12.1d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F31B12.1d.1:c.8340-99C>T
        Intron_number: 53/64
      F31B12.1g.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F31B12.1g.1:c.8169-99C>T
        Intron_number: 52/63
      F31B12.1b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F31B12.1b.1:c.3291-99C>T
        Intron_number: 19/31
      F31B12.1a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F31B12.1a.1:c.3291-99C>T
        Intron_number: 20/33
      F31B12.1e.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F31B12.1e.1:c.3321-99C>T
        Intron_number: 19/30
      F31B12.1l.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F31B12.1l.1:c.8178-99C>T
        Intron_number: 52/63
      F31B12.1i.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F31B12.1i.1:c.8319-99C>T
        Intron_number: 53/64
      F31B12.1k.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F31B12.1k.1:c.8349-99C>T
        Intron_number: 53/64
  Method: WGS_Flibotte