WormBase Tree Display for Variation: WBVar01747189

WBVar01747189 Name: Public_name: WBVar01747189
    Other_name: cewivar00446577
      F26D2.2.1:c.-938T>A
      F13A7.14.1:c.586-7T>A
      F13A7.14.2:c.586-7T>A
    HGVSg: CHROMOSOME_V:g.16404825T>A
  Sequence_details: SMap: S_parent: Sequence: F26D2
    Flanking_sequences: AAAATTTCACGTCTCGGAAATAAATAAAAA TTTCAGCCATTCAACAGCAATTTCTACTTT
    Mapping_target: F26D2
    Source_location: 225 CHROMOSOME_V 16404805 16404805 From_analysis: Million_mutation_project_reanalysis
    Type_of_mutation: Substitution: T A
    SeqStatus: Sequenced
  Variation_type: Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023139 From_analysis: Million_mutation_project_reanalysis
      WBStrain00027648 From_analysis: Million_mutation_project_reanalysis
      WBStrain00027660 From_analysis: Million_mutation_project_reanalysis
      WBStrain00027662 From_analysis: Million_mutation_project_reanalysis
    Laboratory: VC
    Analysis: Million_mutation_project_reanalysis
    Status: Live
  Affects: Gene: WBGene00045357
      WBGene00006375
    Transcript: F26D2.2.1 VEP_consequence: 5_prime_UTR_variant
        VEP_impact: MODIFIER
        HGVSc: F26D2.2.1:c.-938T>A
        cDNA_position: 552
        Exon_number: 1/8
      F13A7.14.1 VEP_consequence: splice_region_variant,intron_variant
        VEP_impact: LOW
        HGVSc: F13A7.14.1:c.586-7T>A
        Intron_number: 4/5
      F13A7.14.2 VEP_consequence: splice_region_variant,intron_variant
        VEP_impact: LOW
        HGVSc: F13A7.14.2:c.586-7T>A
        Intron_number: 3/4
  Method: WGS_Flibotte