WormBase Tree Display for Variation: WBVar02004947

WBVar02004947 Name: Public_name: WBVar02004947
    Other_name (16)
    HGVSg: CHROMOSOME_V:g.4503213_4503214insTTGAG
  Sequence_details: SMap: S_parent: Sequence: T28F12
    Flanking_sequences: CTAATTCGGCAAACTCTTATATTTCAAAAT ACACCACCAGCAAACTGAACGTCAAATTTC
    Mapping_target: T28F12
    Source_location: 225 CHROMOSOME_V 4503199 4503200 From_analysis: Million_mutation_project_reanalysis
    Type_of_mutation: Insertion: TTGAG
    SeqStatus: Sequenced
  Variation_type: Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00006637 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023072 From_analysis: Million_mutation_project_reanalysis
    Laboratory: VC
    Analysis: Million_mutation_project_reanalysis
    Status: Live
  Affects: Gene: WBGene00006796
    Transcript: T28F12.2h.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T28F12.2h.1:c.600+373_600+374insTTGAG
        Intron_number: 4/8
      T28F12.2e.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T28F12.2e.1:c.711+373_711+374insTTGAG
        Intron_number: 5/9
      T28F12.2d.4 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T28F12.2d.4:c.-526+373_-526+374insTTGAG
        Intron_number: 5/11
      T28F12.2d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T28F12.2d.1:c.-526+373_-526+374insTTGAG
        Intron_number: 5/11
      T28F12.2d.7 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T28F12.2d.7:c.-526+373_-526+374insTTGAG
        Intron_number: 1/7
      T28F12.2a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T28F12.2a.1:c.822+373_822+374insTTGAG
        Intron_number: 6/11
      T28F12.2b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T28F12.2b.1:c.711+373_711+374insTTGAG
        Intron_number: 6/11
      T28F12.2d.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T28F12.2d.2:c.-544+373_-544+374insTTGAG
        Intron_number: 5/11
      T28F12.2d.5 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T28F12.2d.5:c.-538+373_-538+374insTTGAG
        Intron_number: 4/10
      T28F12.2c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T28F12.2c.1:c.-1108+373_-1108+374insTTGAG
        Intron_number: 5/10
      T28F12.2d.3 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T28F12.2d.3:c.-544+373_-544+374insTTGAG
        Intron_number: 5/11
      T28F12.2d.6 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T28F12.2d.6:c.-538+373_-538+374insTTGAG
        Intron_number: 2/8
      T28F12.2g.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T28F12.2g.1:c.600+373_600+374insTTGAG
        Intron_number: 4/8
      T28F12.2c.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T28F12.2c.2:c.-724+373_-724+374insTTGAG
        Intron_number: 5/10
      T28F12.2f.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T28F12.2f.1:c.822+373_822+374insTTGAG
        Intron_number: 6/10
  Method: WGS_Flibotte