WormBase Tree Display for Variation: WBVar01134576

WBVar01134576 Name: Public_name: gk484707
    Other_name: F56B6.2a.1:c.1485+946C>T
      F56B6.2c.1:c.300+946C>T
      F56B6.2b.1:c.1374+946C>T
      F56B6.2j.1:c.1494+946C>T
      F56B6.2i.1:c.1491+946C>T
      F56B6.2h.1:c.1500+946C>T
    HGVSg: CHROMOSOME_X:g.3548865C>T
  Sequence_details: SMap: S_parent: Sequence: F56B6
    Flanking_sequences: AACTTCAGTTGAAACACTAGAGCAATTTCAAATTTCAACTATTCCATTCG TTATCAGTTTCGTTTCATGATAAGTGGTTTGCGACTCCTAAATTCAATTT
    Mapping_target: F56B6
    Type_of_mutation: Substitution: C T
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00039130
    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.1494+946C>T
        Intron_number: 8/14
      F56B6.2i.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F56B6.2i.1:c.1491+946C>T
        Intron_number: 9/16
      F56B6.2b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F56B6.2b.1:c.1374+946C>T
        Intron_number: 8/15
      F56B6.2a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F56B6.2a.1:c.1485+946C>T
        Intron_number: 9/16
      F56B6.2h.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F56B6.2h.1:c.1500+946C>T
        Intron_number: 9/16
      F56B6.2c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F56B6.2c.1:c.300+946C>T
        Intron_number: 3/9
  Reference: WBPaper00042537
  Method: Million_mutation