WormBase Tree Display for Variation: WBVar01134598

WBVar01134598 Name: Public_name: gk459608
    Other_name: F56B6.2i.1:c.1702+813A>T
      F56B6.2c.1:c.511+813A>T
      F56B6.2b.1:c.1585+813A>T
      F56B6.2j.1:c.1705+813A>T
      F56B6.2a.1:c.1696+813A>T
      F56B6.2h.1:c.1711+813A>T
      F56B6.2e.1:c.211+813A>T
    HGVSg: CHROMOSOME_X:g.3551084A>T
  Sequence_details: SMap: S_parent: Sequence: F56B6
    Flanking_sequences: TCCTTTCGATTATCGCAACGTGTCTACCGAGTTGTCTACGTCGGCAAAGT TGTTAAAATGGCTCTCCAAAATCACTGTTTGTCATGTGTTCATAGTGTAC
    Mapping_target: F56B6
    Type_of_mutation: Substitution: A T
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00039080
    Laboratory: VC
    Analysis: Million_Mutation_Project
    Status: Live
  Affects: Gene: WBGene00004350
    Transcript: F56B6.2j.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F56B6.2j.1:c.1705+813A>T
        Intron_number: 9/14
      F56B6.2e.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F56B6.2e.1:c.211+813A>T
        Intron_number: 1/7
      F56B6.2i.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F56B6.2i.1:c.1702+813A>T
        Intron_number: 10/16
      F56B6.2b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F56B6.2b.1:c.1585+813A>T
        Intron_number: 9/15
      F56B6.2a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F56B6.2a.1:c.1696+813A>T
        Intron_number: 10/16
      F56B6.2h.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F56B6.2h.1:c.1711+813A>T
        Intron_number: 10/16
      F56B6.2c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F56B6.2c.1:c.511+813A>T
        Intron_number: 4/9
  Reference: WBPaper00042537
  Method: Million_mutation