WormBase Tree Display for Variation: WBVar01309157

WBVar01309157 Evidence: Paper_evidence: WBPaper00037807
  Name: Public_name: WBVar01309157
    Other_name: cewivar00508470
      T24H10.7a.1:c.826-103C>A
      T24H10.7i.1:c.517-103C>A
      T24H10.7g.1:c.394-103C>A
      T24H10.7e.1:c.361-103C>A
      T24H10.7d.1:c.334-103C>A
      T24H10.7h.1:c.628-103C>A
      T24H10.7f.1:c.670-103C>A
      T24H10.7b.1:c.766-103C>A
      T24H10.7c.1:c.172-103C>A
    HGVSg: CHROMOSOME_II:g.9131628C>A
  Sequence_details: SMap: S_parent: Sequence: T24H10
    Flanking_sequences: GTATTAAAAATCTTCTCGTCTATTTTCTACCTGTTAGATTTCCCGCTAGA AGCTAAATGTGCAAAACTAATTAAGTTTAACGAAAAAGTATGTAAAAGTG
    Mapping_target: T24H10
    Type_of_mutation: Substitution: c A Paper_evidence: WBPaper00037807
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00022850 From_analysis: Million_mutation_project_reanalysis
          WGS_De_Bono
    Laboratory: AX
    Analysis: WGS_De_Bono
      Million_mutation_project_reanalysis
    DB_info: Database: dbSNP_ss ss 539166522
    Status: Live
  Affects: Gene: WBGene00012005
    Transcript: T24H10.7g.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T24H10.7g.1:c.394-103C>A
        Intron_number: 3/3
      T24H10.7e.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T24H10.7e.1:c.361-103C>A
        Intron_number: 3/4
      T24H10.7c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T24H10.7c.1:c.172-103C>A
        Intron_number: 3/4
      T24H10.7h.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T24H10.7h.1:c.628-103C>A
        Intron_number: 5/5
      T24H10.7d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T24H10.7d.1:c.334-103C>A
        Intron_number: 3/4
      T24H10.7f.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T24H10.7f.1:c.670-103C>A
        Intron_number: 7/8
      T24H10.7i.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T24H10.7i.1:c.517-103C>A
        Intron_number: 4/4
      T24H10.7a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T24H10.7a.1:c.826-103C>A
        Intron_number: 8/9
      T24H10.7b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T24H10.7b.1:c.766-103C>A
        Intron_number: 8/9
  Reference: WBPaper00037807
  Method: WGS_De_Bono