WormBase Tree Display for Variation: WBVar01408481

WBVar01408481 Evidence: Paper_evidence: WBPaper00037807
  Name: Public_name: WBVar01408481
    Other_name: T08A11.1g.1:c.175-260_175-259insCT
      T08A11.1e.1:c.175-260_175-259insCT
      T08A11.1a.1:c.175-260_175-259insCT
      T08A11.1c.1:c.175-260_175-259insCT
      T08A11.1d.1:c.175-260_175-259insCT
      T08A11.1f.1:c.175-260_175-259insCT
      T08A11.1h.1:c.175-260_175-259insCT
      T08A11.1b.1:c.175-260_175-259insCT
    HGVSg: CHROMOSOME_III:g.4262274_4262275insAG
  Sequence_details: SMap: S_parent: Sequence: T08A11
    Flanking_sequences: AAAAACTAAAATAAAATAAATCAAAATTACAAAAAGACTGAATTTCAAAA TGAAGCATCATAAAAATGCCTAAAAATGAAAAAAGAATGCTAAAGGGAGG
    Mapping_target: T08A11
    Type_of_mutation: Insertion: AG Paper_evidence: WBPaper00037807
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00006642 From_analysis: WGS_De_Bono
    Laboratory: AX
    Analysis: WGS_De_Bono
    DB_info: Database: dbSNP_ss ss 539122953
    Status: Live
  Affects: Gene: WBGene00011604
    Transcript: T08A11.1e.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T08A11.1e.1:c.175-260_175-259insCT
        Intron_number: 1/17
      T08A11.1g.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T08A11.1g.1:c.175-260_175-259insCT
        Intron_number: 2/18
      T08A11.1h.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T08A11.1h.1:c.175-260_175-259insCT
        Intron_number: 2/18
      T08A11.1d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T08A11.1d.1:c.175-260_175-259insCT
        Intron_number: 2/18
      T08A11.1f.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T08A11.1f.1:c.175-260_175-259insCT
        Intron_number: 1/17
      T08A11.1c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T08A11.1c.1:c.175-260_175-259insCT
        Intron_number: 1/17
      T08A11.1b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T08A11.1b.1:c.175-260_175-259insCT
        Intron_number: 2/18
      T08A11.1a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T08A11.1a.1:c.175-260_175-259insCT
        Intron_number: 2/18
  Reference: WBPaper00037807
  Method: WGS_De_Bono