WormBase Tree Display for Variation: WBVar01307300

WBVar01307300 Evidence: Paper_evidence: WBPaper00037807
  Name: Public_name: WBVar01307300
    Other_name: cewivar00355783
      F22D3.2d.1:c.1102-257C>G
      F22D3.2e.1:c.1093-257C>G
      F22D3.2g.1:c.1102-257C>G
      F22D3.2j.1:c.1093-257C>G
    HGVSg: CHROMOSOME_II:g.6942455C>G
  Sequence_details: SMap: S_parent: Sequence: F22D3
    Flanking_sequences: CGAATATATTATGTGGAAAAAACGCGCTTCGCGGACATTTTAAAAGGCTC GCCTCCTACAGTTGGGTCTCGTTAGGTGTTTGATGGCAACGCTGTAAAAT
    Mapping_target: F22D3
    Type_of_mutation: Substitution: c G Paper_evidence: WBPaper00037807
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00006637 From_analysis: Million_mutation_project_reanalysis
      WBStrain00022850 From_analysis: Million_mutation_project_reanalysis
          WGS_De_Bono
      WBStrain00023286 From_analysis: Million_mutation_project_reanalysis
    Laboratory: AX
    Analysis: WGS_De_Bono
      Million_mutation_project_reanalysis
    DB_info: Database: dbSNP_ss ss 539164850
    Status: Live
  Affects: Gene: WBGene00017699
    Transcript: F22D3.2g.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F22D3.2g.1:c.1102-257C>G
        Intron_number: 13/18
      F22D3.2e.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F22D3.2e.1:c.1093-257C>G
        Intron_number: 13/18
      F22D3.2d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F22D3.2d.1:c.1102-257C>G
        Intron_number: 13/18
      F22D3.2j.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F22D3.2j.1:c.1093-257C>G
        Intron_number: 13/18
  Reference: WBPaper00037807
  Method: WGS_De_Bono